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472401 to 472500 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Correlating factors and clinical significance of flexible flatfoot in preschool children.
Corrective shoes and inserts as treatment for flexible flatfoot in infants and children.
Consistency of visual assessments of arch height among clinicians.
Rupture of the posterior tibial tendon causing flat foot. Surgical treatment.
Calcaneal lengthening for valgus deformity of the hindfoot. Results in children who had severe, symptomatic flatfoot and skewfoot.
Acquired adult flat foot secondary to posterior tibial-tendon pathology.
The influence of footwear on the prevalence of flat foot. A survey of 2300 children.
THE ROLE OF MUSCLES IN ARCH SUPPORT OF THE FOOT.
Prevalence of flat foot in preschool-aged children.
An extra-articular arthrodesis of the subastragalar joint for correction of paralytic flat feet in children.
The distributed plantar vertical force of neutrally aligned and pes planus feet.
Acquired prion disease: iatrogenic CJD, variant CJD, kuru.
Transmissible and non-transmissible amyloidoses: autocatalytic post-translational conversion of host precursor proteins to beta-pleated sheet configurations.
Experimental subacute spongiform virus encephalopathies in primates and other laboratory animals.
Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue.
Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents.
Infection-specific particle from the unconventional slow virus diseases.
Getting out of shape.
Sonya D Zabludoff
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
Pathology of Kuru.
Typing prion isoforms.
Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population.
Kuru in the 21st century--an acquired human prion disease with very long incubation periods.
Genetic influence on the structural variations of the abnormal prion protein.
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.
Effects of dextromethorphan/quinidine on auditory event-related potentials in multiple sclerosis patients with pseudobulbar affect.
Dextromethorphan/quinidine (Nuedexta) for pseudobulbar affect.
A clinical overview of pseudobulbar affect.
[Atypical CADASIL phenotypes and pathological findings in two new French families].
Recognizing and treating common psychiatric disorders in multiple sclerosis.
Quantitative voice analysis in the assessment of bulbar involvement in amyotrophic lateral sclerosis.
Pseudobulbar syndrome in two patients with human immunodeficiency virus infection.
Adeno-associated virus transfer of a gene encoding SNAP-25 resistant to botulinum toxin A attenuates neuromuscular paralysis associated with botulism.
Pseudobulbar affect: an under-recognized and under-treated neurological disorder.
Measuring pseudobulbar affect in ALS.
Dextromethorphan/quinidine sulfate for pseudobulbar affect.
The differential diagnosis of pseudobulbar affect (PBA). Distinguishing PBA among disorders of mood and affect. Proceedings of a roundtable meeting.
Pseudobulbar crying induced by stimulation in the region of the subthalamic nucleus.
Botulinum neurotoxin A: an unusual systemic effect.
Review of pseudobulbar affect including a novel and potential therapy.
The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings.
SUPRANUCLEAR OPHTHALMOPLEGIA, PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA. A CLINICAL REPORT ON EIGHT CASES OF "HETEROGENOUS SYSTEM DEGENERATION".
Treatment of pseudobulbar affect in ALS with dextromethorphan/quinidine: a randomized trial.
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
Sunlight and the 10-year incidence of age-related maculopathy: the Beaver Dam Eye Study.
Beta-carotene, carotenoids, and disease prevention in humans.
Serological findings in patients with "ANA-negative" systemic lupus erythematosus.
Side effects of long-term amiodarone therapy.
Haematococcus astaxanthin: applications for human health and nutrition.
Past exposure to sun, skin phenotype, and risk of multiple sclerosis: case-control study.
DNA repair. Engagement with transcription.
Azathioprine and UVA light generate mutagenic oxidative DNA damage.
Light-induced cross-linking of DNA in the presence of a furocoumarin (psoralen). Studies with phage lambda, Escherichia coli, and mouse leukemia cells.
Caspase-14 protects against epidermal UVB photodamage and water loss.
Oxidative stress in the pathogenesis of skin disease.
Nucleotide excision repair. II: From yeast to mammals.
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.
Oxidative damage and age-related macular degeneration.
What looks like alopecia areata is not always alopecia areata.
Short anagen syndrome.
Poorly growing hair in a child.
Phenotypic variability associated with the invariant SHOC2 c.4A>G (p.Ser2Gly) missense mutation.
Moyamoya syndrome in a patient with Noonan-like syndrome with loose anagen hair.
Minoxidil 5% solution for topical treatment of loose anagen hair syndrome.
Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type.
Loose anagen hair syndrome in black-haired Indian children.
Hydrops fetalis in a preterm newborn heterozygous for the c.4A>G SHOC2 mutation.
GH Therapy and first final height data in Noonan-like syndrome with loose anagen hair (Mazzanti syndrome).
Coarctation of the aorta in Noonan-like syndrome with loose anagen hair.
A 3-year-old girl with thin hair.
[Loose anagen hair syndrome. Diagnostic use of the trichogram].
Short anagen syndrome in an African American woman.
Otitis Media, Tetanus, tachycardia
Abnormal inner root sheath of the hair follicle in the loose anagen hair syndrome: an ultrastructural study.
Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations.
Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service.
A mouse model for medulloblastoma and basal cell nevus syndrome.
PTCH mutations: distribution and analyses.
Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
Location of gene for Gorlin syndrome.
Mutations of the PATCHED gene in several types of sporadic extracutaneous tumors.
Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9.
Inhibiting the hedgehog pathway in patients with the basal-cell nevus syndrome.
Rhabdomyosarcomas and radiation hypersensitivity in a mouse model of Gorlin syndrome.
Genetic elimination of Suppressor of fused reveals an essential repressor function in the mammalian Hedgehog signaling pathway.
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.
Human homolog of patched, a candidate gene for the basal cell nevus syndrome.
Dependent Rubor post foot surgery
Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine.
Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.
Sox2 and Pou2f1 interact to control lens and olfactory placode development.
Multiple roles of the eyes absent gene in Drosophila.
Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus.
SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.
The phosphatidylserine receptor has essential functions during embryogenesis but not in apoptotic cell removal.