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On this website you'll find the work of a six-months project for last-year Bachelor's Degree students. You can browse 10,000 medical abstracts concerning orphan diseases. In blue will appear symptoms. Some were known, some are automatically detected by our processing resources and treatments. By clicking on one of them, you will see all diseases presenting the current symptom. As Natural Language Processing isn't a 100% reliable science and can always be improved, some of our "guessed" symptoms aren't actually symptoms. For these new symptom, as an expert of the medical field, you can either validate or signal a symptom as false. By doing so, you will help specialists diagnose but also help us improve our work in the future!

Choosing a letter here will allow you to access every abstract concerning all diseases which name begins with that particular letter

"Clavicular Duplication Causing Thoracic Outlet Obstruction": Unique Presentation of Unreported Association between Clavicular Duplication and Thoracic Outlet Syndrome.

Unusual Case of an Arterial Thoracic Outlet Syndrome due to Srb Anomaly.

Simultaneous bilateral magnetic resonance angiography to evaluate thoracic outlet syndrome.

Coexistence of Arterial Compression in Patients With Neurogenic Thoracic Outlet Syndrome.

Thoracic Outlet Syndrome Caused by Synostosis of the First and Second Thoracic Ribs: 2 Case Reports and Review of the Literature.

C8 and T1 innervation of forearm muscles.

Upper extremity deep vein thrombosis (Paget-Schroetter syndrome) after surfing: A case report.

A wire transposition technique for recanalization of chronic complex central venous occlusions.

Diagnostic value of magnetic resonance imaging in thoracic outlet syndrome.

Atypical thoracic outlet syndrome and reverse flow thromboembolism.

Understanding thoracic outlet syndrome.

Novel axillary approach for brachial plexus in robotic surgery: a cadaveric experiment.

Bilateral Upper Extremity DVT in a 43-Year-Old Man: Is It Thoracic Outlet Syndrome?!

Computed tomography-guided reoperation for neurogenic thoracic outlet syndrome.

Scapular Winging: A Great Masquerader of Shoulder Disorders: AAOS Exhibit Selection.

Hybrid management of Paget-Schroetter syndrome due to thoracic outlet syndrome.

Outcome of trans-axillary approach for surgical decompression of thoracic outlet: a retrospective study in a tertiary care hospital.

Recurrent peripheral embolism following nonunion of the clavicle.

Late onset venous thoracic outlet syndrome following clavicle non-union fracture: A case report.

A Content Analysis of Cognitive and Affective Uses of Patient Support Groups for Rare and Uncommon Vascular Diseases: Comparisons of May Thurner, Thoracic Outlet, and Superior Mesenteric Artery Syndrome.

Brachial plexus lipomata presenting with neurogenic and venous thoracic outlet syndrome: case reports and review of the literature.

Comparison of blood pool and extracellular gadolinium chelate for functional MR evaluation of vascular thoracic outlet syndrome.

Thoracic outlet syndrome in high-performance athletes.

Therapeutic neuroscience education via e-mail: a case report.

Bilateral first rib resection and scalenectomy is effective for treatment of thoracic outlet syndrome.

Nerve entrapment syndromes in musicians.

Neurologic thoracic outlet syndrome: summarizing a complex history and evolution.

Venous thoracic outlet syndrome: approach to diagnosis and treatment with focus on affected athletes.

Arterial thoracic outlet syndrome.

Ultrasonography of the brachial plexus, normal appearance and practical applications.

Neurogenic thoracic outlet syndrome treatment by the supraclavicular approach.

Ulnar tunnel syndrome.

Functional shoulder radiography with use of a dynamic flat panel detector.

Thoracic outlet syndrome in the pediatric population: case series.

The rare case of cervical rib fusion to the second rib.

Thoracic outlet syndrome caused by schwannoma of brachial plexus.

Regrown first rib in patients with recurrent thoracic outlet syndrome.

Diagnostic accuracy of physician and self-referred patients for thoracic outlet syndrome is excellent.

Remaining or residual first ribs are the cause of recurrent thoracic outlet syndrome.

Internal jugular vein stenosis is common in patients presenting with neurogenic thoracic outlet syndrome.

Thoracic outlet syndrome in a patient with absent scalenus anterior muscle.

Axillary artery thrombosis in a major league baseball pitcher: a case report and rehabilitation guide.

Dynamic neuromusculoskeletal ultrasound documentation of brachial plexus/thoracic outlet compression during elevated arm stress testing.

NTOS symptoms and mobility: a case study on neurogenic thoracic outlet syndrome involving massage therapy.

Transient long thoracic nerve injury during posterior spinal fusion for adolescent idiopathic scoliosis: A report of two cases.

Outcomes of surgical paraclavicular thoracic outlet decompression.

McCleery syndrome: etiology and outcome.

Thromboembolic stroke associated with thoracic outlet syndrome.

Relevance of bone anomalies in patients with thoracic outlet syndrome.

Osteoid osteoma of the rib presenting as thoracic outlet syndrome.

Thoracic outlet syndrome in 3T MR neurography-fibrous bands causing discernible lesions of the lower brachial plexus.

Cognitive and Affective Uses of a Thoracic Outlet Syndrome Facebook Support Group.

Distal subclavian artery occlusion causing multiple cerebral infarcts consequence of retrograde flow of a thrombus?

The subclavius posticus muscle: an unusual cause of thoracic outlet syndrome.

Targeting systemic inflammation in patients with obesity-related pain: Neurogenic thoracic outlet syndrome: an often overlooked but treatable condition.

Neurogenic thoracic outlet syndrome associated with cervical rib.

Early versus Late Surgical Treatment for Neurogenic Thoracic Outlet Syndrome.

Specific scapular kinematic patterns to differentiate two forms of dynamic scapular winging.

Thoracic outlet syndromes in sport: a practical review in the face of limited evidence--unusual pain presentation in an athlete.

Electrodiagnostic features of true neurogenic thoracic outlet syndrome.

Peripheral arterial aneurysms: open or endovascular surgery?

Congenital pseudarthrosis of the clavicle causing thoracic outlet syndrome.

Arterial thoracic outlet syndrome: a 32-year experience.

Postfixed brachial plexus radiculopathy due to thoracic disc herniation in a collegiate wrestler: a case report.

Diagnosis of brachial and lumbosacral plexus lesions.

Deep venous thrombosis of the upper extremity. A review.

Imaging of the non-traumatic brachial plexus.

A hand surgeon's advanced experience with thoracic outlet compression syndrome.

Pictorial essay: Role of magnetic resonance imaging in evaluation of brachial plexus pathologies.

Incidence and distribution of extravascular compression of extracranial venous pathway in patients with chronic cerebrospinal venous insufficiency and multiple sclerosis.

Cervical ribs: identification on MRI and clinical relevance.

Thoracic outlet syndrome: A neurological and vascular disorder.

Brachial plexopathy.

Surgical management of vascular thoracic outlet syndrome: a teaching hospital experience.

Paget-Schroetter syndrome in a lacrosse player.

Scalenus minimus muscle: overestimated or not? An anatomical study.

Dancers' and musicians' injuries.

Contemporary vascular smartphone medical applications.

Vascular thoracic outlet syndrome developed after minimally invasive repair of pectus excavatum.

Neurogenic thoracic outlet and pectoralis minor syndromes in children.

Changing strategies to treat venous thrombotic occlusions of the upper and lower extremities secondary to compressive phenomena.

A low energy paediatric clavicle fracture associated with acute brachial plexus injury and subclavian artery compression.

Pharmacomechanical thrombolysis in the management of paget-schroetter syndrome.

Comprehensive management of subclavian vein effort thrombosis.

The significance of cervical ribs in thoracic outlet syndrome.

Vascular thoracic outlet in a competitive swimmer: a case report.

Case report: Thoracic outlet syndrome in an elite archer in full-draw position.

Pseudo-hypotension in patients with ankylosing spondylitis during posterior osteotomy for correction of kyphosis.

Upper extremity venous aneurysm as a source of pulmonary emboli.

Early effectiveness of isolated pectoralis minor tenotomy in selected patients with neurogenic thoracic outlet syndrome.

[Effort thrombosis of the right subclavian vein].

High-definition video-assisted transaxillary first rib resection for thoracic outlet syndrome.

Bilateral thoracic outlet syndrome: An uncommon presentation of a rare condition in children.

Diagnosis and treatment of a patient with bilateral thoracic outlet syndrome secondary to anterior subluxation of bilateral sternoclavicular joints: a case report.

A case of traumatic thoracic outlet syndrome.

[Thoracic outlet syndrome in a child: a rare pediatric diagnosis].

Clinical presentation of cervical ribs in the pediatric population.

Thoracic outlet syndrome of pectoralis minor etiology mimicking cardiac symptoms on activity: a case report.

Paget Schroetter Syndrome: A case study of the chiropractor's role in recognizing and comanaging an important condition.

A review of thoracic outlet syndrome and the possible role of botulinum toxin in the treatment of this syndrome.

Fasciculations in human hereditary disease.

Oxidative stress and adrenocortical insufficiency.

Neurologic complications of disorders of the adrenal glands.

Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction.

A case of late-onset allgrove syndrome presenting with predominant autonomic dysfunction.

Triple A syndrome in Japan.

Deficiency of ALADIN impairs redox homeostasis in human adrenal cells and inhibits steroidogenesis.

Triple A (Allgrove) syndrome: an unusual association with syringomyelia.

Longitudinal neuropsychological profile in a patient with triple a syndrome.

Clinical and genetic characterization of a Chinese patient with triple A syndrome and novel compound heterozygous mutations in the AAAS gene.

Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress.

Familial achalasia in children.

The genetic basis of triple A (Allgrove) syndrome in a Greek family.

Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.

A 12 year old boy with recurrent episodes of pneumonia: triple A syndrome.

Triple A syndrome in a patient with genetic growth hormone insensitivity: phenotypic effects of two genetic disorders.

Neurologic presentation of triple A syndrome.

X-linked mental retardation with alacrima and achalasia-Triple A syndrome or a new syndrome?

Neurological features in adult Triple-A (Allgrove) syndrome.

New ophthalmic features in a family with triple A syndrome.

Mutation spectra of the AAAS gene in Iranian families with Allgrove Syndrome.

Achalasia familiar: report of a family with an autosomal dominant pattern of inherence.

Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.

Intracellular ROS level is increased in fibroblasts of triple A syndrome patients.

Triple-A syndrome.

Adult or late-onset triple A syndrome: case report and literature review.

Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation.

Triple A syndrome: 32 years experience of a single centre (1977-2008).

Two patients with an identical novel mutation in the AAAS gene and similar phenotype of triple A (Allgrove) syndrome.

Premature Loss of Permanent Teeth in Allgrove (4A) Syndrome in Two Related Families.

Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency.

Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism.

The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope.

The transmembrane nucleoporin NDC1 is required for targeting of ALADIN to nuclear pore complexes.

Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome.

Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene.

Allgrove'S syndrome: case report and literature review.

Triple A syndrome: two novel mutations in the AAAS gene.

The molecular basis of adrenocorticotrophin resistance syndrome.

Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management.

Restoration of nuclear-import failure caused by triple A syndrome and oxidative stress.

Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.

Triple A syndrome mimicking ALS.

Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.

Adrenocorticotropin resistance syndromes.

Heterogeneity in the molecular basis of ACTH resistance syndrome.

Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation.

Genetic disorders involving adrenal development.

An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome.

[Allgrove syndrome in the mainland of China: clinical report and mutation analysis].

Dysphagia due to triple A syndrome: successful treatment of achalasia by balloon dilatation.

Triple A syndrome with ophthalmic manifestations in two siblings.

Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes.

Mechanisms of disease: DNA repair defects and neurological disease.

Unusual presentation of triple A syndrome mimicking Sjögren's syndrome.

The genetics of ACTH resistance syndromes.

Heterogeneity of the triple A syndrome and assessment of a case.

Allgrove syndrome with features of familial dysautonomia: a novel mutation in the AAAS gene.

[Allgrove syndrome. Report on a family].

Triple-A syndrome--the first Chinese patient with novel mutations in the AAAS gene.

Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.

Cellular localization of 17 natural mutant variants of ALADIN protein in triple A syndrome - shedding light on an unexpected splice mutation.

A novel AAAS gene mutation (p.R194X) in a patient with triple A syndrome.

Esophageal achalasia and alacrima in siblings.

A novel DNA sequence variation in the first genetically confirmed allgrove syndrome in iran.

Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome.

ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome.

Triple A syndrome.

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.

Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005.

Molecular cloning and characterization of AAAS-V2, a novel splice variant of human AAAS.

Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locus.

Identification of the sites of expression of triple A syndrome mRNA in the rat using in situ hybridisation.

The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex.

Association of chronic symptomatic neutropenia with the triple A syndrome.

Two cases of Allgrove syndrome with mutations in the AAAS gene.

Phenotypic heterogeneity in AAAS gene mutation.

Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report.

Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation.

The nuclear pore complex: disease associations and functional correlations.

Three children with triple A syndrome due to a mutation (R478X) in the AAAS gene.

Oral manifestations of triple A syndrome.

Triple A syndrome--diagnostic and management issues.

Achalasia--alacrima--ACTH insensitivity syndrome (Triple A syndrome).

Triple A syndrome: genotype-phenotype assessment.

The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome.

Achalasia of the cardia in Allgrove's (triple A) syndrome: histopathologic study of 10 cases.

Chromosomal fragility in patients with triple A syndrome.

New insights into the molecular basis of the triple A syndrome.

Advances in the understanding of the genetic basis of adrenal insufficiency.

[From gene to disease; adrenocortical insufficiency, achalasia and disrupted tear secretion: Allgrove syndrome].

Clinical and genetic characterization of families with triple A (Allgrove) syndrome.

A case of Allgrove (Triple A) syndrome associated with renal ectopia.

Analysis of the AAAS gene in a Japanese patient with triple A syndrome.

Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation.

[Allgrove's syndrome].

Clinical and novel molecular findings in a 6.8-year-old Turkish boy with triple A syndrome.

Recurrent vomiting as first symptom of triple-a syndrome--a case report.

Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin.

Ophthalmic manifestations of Allgrove syndrome: report of a case.

Reconstructive surgery for patellofemoral joint incongruency.

Association between patellar cartilage defects and patellofemoral geometry: a matched-pair MRI comparison of patients with and without isolated patellar cartilage defects.

[Patella instability.]

The tibial-tubercle trochlear groove distance in patients with trochlear dysplasia: the influence of the proximally flat trochlea.

Femoral trochlear groove development after patellar subluxation and early reduction in growing rabbits.

Morphological Traits Around Patellofemoral Joint in Indian Femora and their Implications.

The use of rapid prototyped implants to simulate knee joint abnormalities for in vitro testing: a validation study with replica implants of the native trochlea.

[Patellofemoral arthroplasty: indication, technique and results].

Trochlear boss height measurement: A comparison of radiographs and MRI.

Application of an artificial neural network and morphing techniques in the redesign of dysplastic trochlea.

Patellofemoral arthroplasty: outcomes and factors associated with early progression of tibiofemoral arthritis.

Characteristics of femorotibial joint geometry in the trochlear dysplastic femur.

Analysis of failure and clinical outcome after unsuccessful medial patellofemoral ligament reconstruction in young patients.

Trochlear dysplasia and the role of trochleoplasty.

Patellar instability.

Imaging of the patellofemoral joint.

Landmarks of the normal adult human trochlea based on axial MRI measurements: a cross-sectional study.

Measurement of tibial tuberosity-trochlear groove distance: evaluation of inter- and intraobserver correlation dependent on the severity of trochlear dysplasia.

Medial patellofemoral ligament anatomy: is it a predisposing factor for lateral patellar dislocation?

A validated cadaveric model of trochlear dysplasia.

Reconstruction of the Medial Patellofemoral Ligament: Clinical Outcomes and Return to Sports.

Current concepts on trochleoplasty procedures for the surgical treatment of trochlear dysplasia.

Evidence of trochlear dysplasia in patellofemoral arthroplasty designs.

Internal derangement of the knee in fibular hemimelia: radiographic and MRI findings.

Trochleoplasty versus nontrochleoplasty procedures in treating patellar instability caused by severe trochlear dysplasia.

The association of patellofemoral joint morphology with chondromalacia patella: a quantitative MRI analysis.

Guidelines for medial patellofemoral ligament reconstruction in chronic lateral patellar instability.

The incidence of trochlear dysplasia in anterior cruciate ligament tears.

MRI of anterior knee pain.

Does degree of trochlear dysplasia and position of femoral tunnel influence outcome after medial patellofemoral ligament reconstruction?

Does form follow function in trochlear dysplasia? Case report of patellar instability in a below-knee amputee.

Association and impact of patellofemoral dysplasia on patellofemoral arthropathy and arthroplasty.

Multiple osteochondritis dissecans of knee joint in a patient with Wilson disease, focusing on magnetic resonance findings.

Correlation between trochlear dysplasia and the notch index.

A statistical shape model of trochlear dysplasia of the knee.

Femoral tunnel enlargement after medial patellofemoral ligament reconstruction: prevalence, risk factors, and clinical effect.

Axial MRI index of patellar engagement: a new method to assess patellar instability.

Patellar instability with and without trochlear dysplasia: new arthroscopic medial soft tissue plication with pullout technique.

Correlation between trochlear dysplasia and anterior cruciate ligament injury.

Which patellae are likely to redislocate?

Combined trochleoplasty and MPFL reconstruction for treatment of chronic patellofemoral instability: a prospective minimum 2-year follow-up study.

Posterior shape models.

Arthroscopic evaluation of trochlear dysplasia as an aid in decision making for the treatment of patellofemoral instability.

Femoral trochlear dysplasia after patellar dislocation in rabbits.

Association of trochlear dysplasia with degenerative abnormalities in the knee: data from the Osteoarthritis Initiative.

Semi-automated landmark-based 3D analysis reveals new morphometric characteristics in the trochlear dysplastic femur.

Early revisions of the Femoro-Patella Vialla joint replacement.

Treating patella instability in skeletally immature patients.

Lateral patellar dislocation: mechanism of disease, radiographic presentation, and management.

Long-term outcome after operative treatment of traumatic patellar dislocation in adolescents.

Midterm results of comprehensive surgical reconstruction including sulcus-deepening trochleoplasty in recurrent patellar dislocations with high-grade trochlear dysplasia.

Patellofemoral osteoarthritis after Insall's proximal realignment for recurrent patellar dislocation.

[MRI after patellar dislocation: assessment of risk factors and injury to the joint].

Three-dimensional transfer of the tibial tuberosity for patellar instability with patella alta.

Combined trochleoplasty and medial patellofemoral ligament reconstruction for recurrent patellar dislocations in severe trochlear dysplasia: a minimum 2-year follow-up study.

Combined arthroscopic deepening trochleoplasty and reconstruction of the medial patellofemoral ligament for patients with recurrent patella dislocation and trochlear dysplasia.

Predictors of recurrent instability after acute patellofemoral dislocation in pediatric and adolescent patients.

The Lyon's sulcus-deepening trochleoplasty in previous unsuccessful patellofemoral surgery.

Evidence of trochlear dysplasia in femoral component designs.

Evaluation of trochlear dysplasia using MRI: correlation between the classification system of Dejour and objective parameters of trochlear dysplasia.

Prevalence and patterns of anatomical risk factors in patients after patellar dislocation: a case control study using MRI.

Medial patellofemoral ligament reconstruction for patellar instability in patients with hypermobility: a case control study.

[Imaging of patellofemoral instability].

Anatomic reconstruction of the medial patellofemoral ligament in children and adolescents with open growth plates: surgical technique and clinical outcome.

Influence of tibial slope asymmetry on femoral rotation in patients with lateral patellar instability.

Modern management of patellar instability.

Transient lateral patellar dislocation: review of imaging findings, patellofemoral anatomy, and treatment options.

The basic science of the patella: structure, composition, and function.

Reconstruction of medial patellofemoral ligament for chronic patellar instability.

The role of trochleoplasty in patellofemoral instability.

First-time patellar dislocation: surgery or conservative treatment?

Permanent patellar dislocation after a nonoperative treatment of recurrent dislocation of the patella because of trochlear dysplasia: a case report and review of the literature.

[Chronic patellofemoral instability].

The influence of risk factors on clinical outcomes following anatomical medial patellofemoral ligament (MPFL) reconstruction using the gracilis tendon.

Familial association of femoral trochlear dysplasia with recurrent bilateral patellar dislocation.

Trochleoplasty and medial patellofemoral ligament reconstruction for recurrent patellar dislocation.

[Anatomical double-bundle reconstruction of the medial patellofemoral ligament with a gracilis autograft].

Trochleoplasty in major trochlear dysplasia: current concepts.

Open lateral patellar retinacular lengthening versus open retinacular release in lateral patellar hypercompression syndrome: a prospective double-blinded comparative study on complications and outcome.

Radiographic parameters associated with lateral patella degeneration in young patients.

Observer agreement on the Dejour trochlear dysplasia classification: a comparison of true lateral radiographs and axial magnetic resonance images.

Outcomes after trochleoplasty.

Incidence and radiologic predictor of postoperative patellar instability after Fulkerson procedure of the tibial tuberosity for recurrent patellar dislocation.

Tibial tubercle advancement osteotomy with bone allograft for patellofemoral arthritis: a retrospective cohort study of 50 knees.

Recession wedge trochleoplasty as an additional procedure in the surgical treatment of patellar instability with major trochlear dysplasia: early results.

Knee osteochondral fractures in skeletally immature patients: French multicenter study.

Recurrent dislocation of the patella accompanying hypotrochlea of the femur and malalignment of the patella.

Analysis of failed surgery for patellar instability in children with open growth plates.

Radiological criteria for trochlear dysplasia in children and adolescents.

[The treatment of patellar dislocation: a systematic review].

Clinical outcomes of medial patellofemoral ligament repair in recurrent (chronic) lateral patella dislocations.

Gracilis tendon transfer associated with distal alignment for patella alta with recurrent dislocations: an original surgical technique.

Classification of trochlear dysplasia as predictor of clinical outcome after trochleoplasty.

The role of trochlear dysplasia in patellofemoral instability.

Patellar shape can be a predisposing factor in patellar instability.

The lateral condyle index: a new index for assessing the length of the lateral articular trochlea as predisposing factor for patellar instability.

3D representation of the surface topography of normal and dysplastic trochlea using MRI.

Anatomy of lateral patellar instability: trochlear dysplasia and tibial tubercle-trochlear groove distance is more pronounced in women who dislocate the patella.

Patellar dislocations in children, adolescents and adults: a comparative MRI study of medial patellofemoral ligament injury patterns and trochlear groove anatomy.

MR imaging of patellar instability: injury patterns and assessment of risk factors.

Multi-isotype antibody responses against the multimeric Salmonella Typhi hemolysin (HlyE) antigen.

Cost of illness due to typhoid Fever in pemba, zanzibar, East Africa.

Enteric fever imported to the Czech Republic: epidemiology, clinical characteristics and antimicrobial susceptibility.

Genomic Signature of Multi-Drug Resistant Salmonella Typhi related to a Massive Outbreak in Zambia during 2010 - 2012.

Surface Plasmon Resonance Based Label-Free Detection of Salmonella using DNA Self Assembly.

Review of Climate Change and Water-Related Diseases in Cambodia and Findings From Stakeholder Knowledge Assessments.

Complex adaptive immunity to enteric fevers in humans: lessons learned and the path forward.

Medical causes of death in a teaching hospital in South-Eastern Nigeria: A 16 year review.

Suppression of dendritic cell and T-cell activation by the pRST98 Salmonella plasmid.

Trends (2009-2013) in serotype distribution and antimicrobial susceptibility in Belgian human Salmonella isolates: Mind the uncommon.

[Epidemiological characteristics of typhoid fever and antibiotic susceptibility testing of Salmonella Typhi isolates in Guangxi, 1994-2013].

Typhoid outbreak in songkhla, Thailand 2009-2011: clinical outcomes, susceptibility patterns, and reliability of serology tests.

Host hydrogen rather than that produced by the pathogen is important for Salmonella enterica serovar Typhimurium virulence.

Indian Academy of Pediatrics (IAP) Recommended Immunization Schedule for Children Aged 0 through 18 years - India, 2014 and Updates on Immunization.

Multi-drug resistance and reduced susceptibility to ciprofloxacin among Salmonella enterica serovar Typhi isolates from the Middle East and Central Asia.

Immune Response of Thalassemia Major Patients in Indonesia with and without Splenectomy.

ESBL-Producing Salmonella enterica Serovar Typhi in Traveler Returning from Guatemala to Spain.

Salmonella-host interactions - modulation of the host innate immune system.

A novel tool for capture and detection of typhoid fever using Ag-labeled nanocomposites.

Arthritis and adult respiratory distress syndrome: unusual presentations of typhoid fever.

A bivalent typhoid live vector vaccine expressing both chromosomal and plasmid-encoded Y. pestis antigens fully protects against murine lethal pulmonary plague infection.

Evaluation of the timeliness and completeness of communicable disease reporting: Surveillance in The Cuban Hospital, Qatar.

Acid Exposure Induces Multiplication of Salmonella enterica Serovar Typhi.

Typhoid and dengue coinfection: case reports.

The association between malaria and non-typhoid Salmonella bacteraemia in children in sub-Saharan Africa: a literature review.

Safety and Immunogenicity of Typhoid Fever and Yellow Fever Vaccines When Administered Concomitantly With Quadrivalent Meningococcal ACWY Glycoconjugate Vaccine in Healthy Adults.

An AIL family protein promotes Type Three Secretion System-1 independent invasion and pathogenesis of Salmonella enterica serovar Typhi.

Burden of typhoid fever in low-income and middle-income countries: a systematic, literature-based update with risk-factor adjustment.

Possibility of scrub typhus in fever of unknown origin (FUO) cases: An experience from Rajasthan.

Predictors of mortality in children with typhoid ileal perforation in a Nigerian tertiary hospital.

Antityphoid and radical scavenging properties of the methanol extracts and compounds from the aerial part of Paullinia pinnata.

Typhoid Fever surveillance and vaccine use - South-East Asia and Western Pacific regions, 2009-2013.

Anaemia, iron deficiency and susceptibility to infections.

In vitro modeling of gallbladder-associated Salmonella spp. colonization.

Applications of microscopy in salmonella research.

Detecting non-typhoid Salmonella in humans by enzyme-linked immunosorbent assays (ELISAs): practical and epidemiological aspects.

Determination of antimicrobial resistance in Salmonella spp.

A rare neurological complication of typhoid fever: Guillain-Barre' syndrome.

A case of vasculitis, retinitis and macular neurosensory detachment presenting post typhoid fever.

Typhoid glomerulonephritis and intestinal perforation in a Nigerian child.

Comparative evaluation of safety and efficacy of a live Salmonella gallinarum vaccine candidate secreting an adjuvant protein with SG9R in chickens.

Study of baseline Widal titres in a healthy adult population of Wayanad district, Kerala, India.

A comparative study of Widal test with blood culture in the diagnosis of typhoid fever in febrile patients.

[Exanthems and fever in travellers returning from the tropics].

Endovascular treatment of an iliac artery rupture caused by invasive Salmonella spondylodiscitis.

Salmonella enterica serovar Typhi and the pathogenesis of typhoid fever.

Effective Control of Salmonella Infections by Employing Combinations of Recombinant Antimicrobial Human β-Defensins hBD-1 and hBD-2.

Comparison between azithromycin and cefixime in the treatment of typhoid fever in children.

Temporal dimension in reference standard misclassification - a concept note.

Burden of typhoid fever in Sulaimania, Iraqi Kurdistan.

Preparation and testing of a Vi conjugate vaccine using pneumococcal surface protein A (PspA) from Streptococcus pneumoniae as the carrier protein.

WHO Expert Committee on Biological Standardization.

Non-traumatic ileal perforation: a retrospective study.

Genetic dissection of the ity3 locus identifies a role for ncf2 co-expression modules and suggests selp as a candidate gene underlying the ity3.2 locus.

Preparing children for international travel: need for training and pediatric-focused research.

Identification of Protective Antigens for Vaccination against Systemic Salmonellosis.

Effects of Inflammation on Hippocampus and Substantia Nigra Responses to Novelty in Healthy Human Participants.

Acute tubular necrosis (ATN) presenting with an unusually prolonged period of marked polyuria heralded by an abrupt oliguric phase.

Overexpression, Purification and Validation of Antigenic Salmonella enterica Serovar Typhi Proteins Identified from LC-MS/MS.

Investigation of Class I Integron in Salmonella infantis and Its Association With Drug Resistance.

Review on prescription compatibility of shaoyao gancao decoction and reflection on pharmacokinetic compatibility mechanism of traditional chinese medicine prescription based on in vivo drug interaction of main efficacious components.

Dynamic modularity of host protein interaction networks in Salmonella Typhi infection.

Same species, different diseases: how and why typhoidal and non-typhoidal Salmonella enterica serovars differ.

Determinants of patients' choice of provider in accessing brucellosis care among pastoral communities adjacent to lake Mburo National Park in Kiruhura District, Uganda.

Science and society: vaccines and public health.

Vaccination and malaria prophylaxis among Greek international travelers to Asian destinations.

Interactome analyses of Salmonella pathogenicity islands reveal SicA indispensable for virulence.

A Study of Etiological Pattern in an Epidemic of Acute Febrile Illness during Monsoon in a Tertiary Health Care Institute of Uttarakhand, India.

Pyonephrosis Caused by Salmonella Typhi: A Case Report.

Limited role for ASC and NLRP3 during in vivo Salmonella Typhimurium infection.

Immuno-fluorescence based Vi capsular polysaccharide detection for specific recognition of Salmonella enterica serovar Typhi in clinical samples.

The Vi capsular polysaccharide enables Salmonella enterica serovar typhi to evade microbe-guided neutrophil chemotaxis.

Antimicrobial resistance, virulence profiles and molecular subtypes of Salmonella enterica serovars Typhi and Paratyphi A blood isolates from Kolkata, India during 2009-2013.

Indian tick typhus presenting as Purpura fulminans.

Transient Darwinian selection in Salmonella enterica serovar Paratyphi A during 450 years of global spread of enteric fever.

Periappendicitis: our 13 year experience.

Independent bottlenecks characterize colonization of systemic compartments and gut lymphoid tissue by salmonella.

How multidrug resistance in typhoid fever affects treatment options.

[Health problems of combatants during the First World War].

Typhoid fever in Fiji: a reversible plague?

Salmonella chronic carriage: epidemiology, diagnosis, and gallbladder persistence.

[Evaluation on the effects of prevention and control programs regarding typhoid fever and paratyphoid fever in Guizhou province, from 2007 to 2012].

A case report of typhoidal acute acalculous cholecystitis.

[Sanitary and epidemiological supply for the Russian Army during the First World War (1914-1918)].

Multiple ileal perforations and concomitant cholecystitis with gall bladder gangrene as complication of typhoid fever.

Pattern and presentation of acute abdomen in a Nigerian teaching hospital.

Assembly and stability of Salmonella enterica ser. Typhi TolC protein in POPE and DMPE.

Molecular characterization of the Na+/H+-antiporter NhaA from Salmonella Typhimurium.

[Demarcation of infection with Salmonella typhi and S. paratyphi against Salmonella enteritidis in children].

Perforation peritonitis and the developing world.

False positive malaria rapid diagnostic test in returning traveler with typhoid fever.

Formative investigation of acceptability of typhoid vaccine during a typhoid fever outbreak in Neno District, Malawi.

Vaccine-induced inflammation attenuates the vascular responses to mental stress.

Comparative evaluation of various tests for diagnosis of concurrent malaria and typhoid Fever in a tertiary care hospital of northern India.

Retrospective audit of the widal test for diagnosis of typhoid Fever in pediatric patients in an endemic region.

Salmonella enterica Serovar Typhi conceals the invasion-associated type three secretion system from the innate immune system by gene regulation.

Evaluation of protective efficacy of live attenuated Salmonella enterica serovar Gallinarum vaccine strains against fowl typhoid in chickens.

Resistance Patterns of Typhoid Fever in Children: A Longitudinal Community-Based Study.

Honing in on enteric fever.

Vaccination in elite athletes.