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503301 to 503400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Intraepithelial lymphocytes of the small intestine.
Outcomes of patients with differentiated thyroid carcinoma following initial therapy.
Prognostic factors for thyroid carcinoma. A population-based study of 15,698 cases from the Surveillance, Epidemiology and End Results (SEER) program 1973-1991.
Acute Respiratory Failure, Complete Blood Count Abnormal, Cyanosis, Hypoxia, Stridor
Focal adhesion kinase as a marker of invasive potential in differentiated human thyroid cancer.
High prevalence of BRAF gene mutation in papillary thyroid carcinomas and thyroid tumor cell lines.
Long-term outcome of 444 patients with distant metastases from papillary and follicular thyroid carcinoma: benefits and limits of radioiodine therapy.
Overexpression and overactivation of Akt in thyroid carcinoma.
Cytogenetic findings in Roberts-SC phocomelia syndrome(s).
Hindlimb deformities (ectromelia, ectrodactyly) in free-living anurans from agricultural habitats.
A zebrafish model of Roberts syndrome reveals that Esco2 depletion interferes with development by disrupting the cell cycle.
Reorganization of cortical blood flow and transcranial magnetic stimulation maps in human subjects after upper limb amputation.
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.
A role for NKG2D in NK cell-mediated resistance to poxvirus disease.
Dreamlike mentations during sleepwalking and sleep terrors in adults.
Evidence of dissociated arousal states during NREM parasomnia from an intracerebral neurophysiological study.
Dynamics of slow-wave activity during the NREM sleep of sleepwalkers and control subjects.
Hereditary factors in sleepwalking and night terrors.
Sleep problems in healthy preadolescents.
Factors that predispose, prime and precipitate NREM parasomnias in adults: clinical and forensic implications.
Night terrors, sleepwalking, and confusional arousals in the general population: their frequency and relationship to other sleep and mental disorders.
A polysomnographic and clinical report on sleep-related injury in 100 adult patients.
Maintenance of wakefulness test: a polysomnographic technique for evaluation treatment efficacy in patients with excessive somnolence.
Prevalence of sleep disorders in the Los Angeles metropolitan area.
Mutation of B-Raf in human choroidal melanoma cells mediates cell proliferation and transformation through the MEK/ERK pathway.
Development of metastatic disease after enrollment in the COMS trials for treatment of choroidal melanoma: Collaborative Ocular Melanoma Study Group Report No. 26.
Does enucleation of the eye containing a malignant melanoma prevent or accelerate the dissemination of tumour cells.
Pathology of human cystoid macular edema.
The prognostic value of tumor blood vessel morphology in primary uveal melanoma.
FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa.
Prevention of rickets and vitamin D deficiency in infants, children, and adolescents.
Vitamin D: A millenium perspective.
Increased skin pigment reduces the capacity of skin to synthesise vitamin D3.
Genetic influences in the aetiology of femoroacetabular impingement: a sibling study.
Correction of tibia vara with six-axis deformity analysis and the Taylor Spatial Frame.
Femoroacetabular impingement and classification of the cam deformity: the reference interval in normal hips.
Allograft reconstruction after proximal tibial resection for bone tumors. An analysis of function and outcome comparing allograft and prosthetic reconstructions.
Prevalence of associated deformities and hip pain in patients with cam-type femoroacetabular impingement.
Perfect balance in total knee arthroplasty: the elusive compromise.
Bone-marrow transplantation in Hurler's syndrome. Effect on skeletal development.
Joint damage and disability in rheumatoid arthritis: an updated systematic review.
Predictors of progression of osteoarthritis in femoroacetabular impingement: a radiological study with a minimum of ten years follow-up.
Dissociation of intra- and extracellular domains of desmosomal cadherins and E-cadherin in Hailey-Hailey disease and Darier's disease.
Poly-(L-alanine) expansions form core beta-sheets that nucleate amyloid assembly.
The role of apoptosis in neuromuscular diseases and prospects for anti-apoptosis therapy.
Prevention of oculopharyngeal muscular dystrophy by muscular expression of Llama single-chain intrabodies in vivo.
PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions.
Hailey-Hailey disease: the clinical features, response to treatment and prognosis.
Myoblast transfer therapy: is there any light at the end of the tunnel?
Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in normal magnocellular neurosecretory neurons of the hypothalamus.
Human keratinocyte ATP2C1 localizes to the Golgi and controls Golgi Ca2+ stores.
Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear polyA-binding protein with a single-domain intracellular antibody.
Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1.
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump.
Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.
Calcium in the Golgi apparatus.
Doxycycline attenuates and delays toxicity of the oculopharyngeal muscular dystrophy mutation in transgenic mice.
Functional expression in yeast of the human secretory pathway Ca(2+), Mn(2+)-ATPase defective in Hailey-Hailey disease.
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease.
The genetics and pathology of oxidative phosphorylation.
Mitochondrial DNA sequence variation in human evolution and disease.
Cholesterol, lipid rafts, and disease.
Increased mitochondrial mass in mitochondrial myopathy mice.
Cardiac mitochondria in heart failure: decrease in respirasomes and oxidative phosphorylation.
Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.
The most infectious prion protein particles.
Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria.
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.
Eight prion strains have PrP(Sc) molecules with different conformations.
Mitochondria take center stage in aging and neurodegeneration.
A controlled study of sleep related disordered breathing in obese children.
Protection against streptococcal pharyngeal colonization with a vaccinia: M protein recombinant.
The host cytokine responses and protective immunity in oropharyngeal candidiasis.
New model of oropharyngeal candidiasis in mice.
The male predisposition to pharyngeal collapse: importance of airway length.
The diagnosis of strep throat in adults in the emergency room.
Granulomatosis with polyangiitis (Wegener's): an alternative name for Wegener's granulomatosis.
The contrasting epidemiology of granulomatosis with polyangiitis (Wegener's) and microscopic polyangiitis.
New advances in the pathogenesis of ANCA-associated vasculitides.
Revisiting the classification of clinical phenotypes of anti-neutrophil cytoplasmic antibody-associated vasculitis: a cluster analysis.
Nomenclature and classification of vasculitis: lessons learned from granulomatosis with polyangiitis (Wegener's granulomatosis).
Pathophysiology of ANCA-associated small vessel vasculitis.
Rituximab maintenance therapy for granulomatosis with polyangiitis and microscopic polyangiitis.
The Five-Factor Score revisited: assessment of prognoses of systemic necrotizing vasculitides based on the French Vasculitis Study Group (FVSG) cohort.
Lipid Metabolism, Inborn Errors
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.
Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly.
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway.
Age-dependent effect of myostatin blockade on disease severity in a murine model of limb-girdle muscular dystrophy.
Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin.
Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro.
Sustained alpha-sarcoglycan gene expression after gene transfer in limb-girdle muscular dystrophy, type 2D.
X-linked myotubular and centronuclear myopathies.
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.