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517101 to 517200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Hereditary deaf mutism, with particular reference to Northern Ireland.
Anatomical correlates of early mutism in progressive nonfluent aphasia.
Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections.
The neural basis of language.
Field trial for autistic disorder in DSM-IV.
Incidence and severity of postoperative cerebellar mutism syndrome in children with medulloblastoma: a prospective study by the Children's Oncology Group.
The Vineland Adaptive Behavior Scales: supplementary norms for individuals with autism.
The role of arousal and "gating" systems in the neurology of impaired consciousness.
A note on deaf mutism.
Contributions of intrinsic membrane dynamics to fast network oscillations with irregular neuronal discharges.
Acquisition of imitative speech by schizophrenic children.
The cerebellum contributes to higher functions during development: evidence from a series of children surgically treated for posterior fossa tumours.
Prevalence and risk factors for anal human papillomavirus infection in human immunodeficiency virus (HIV)-positive and high-risk HIV-negative women.
Ocular Bobbing, Trigeminal Neuralgia
Diagnosis of Chlamydia trachomatis endocervical infections by a commercial polymerase chain reaction assay.
The polymerase chain reaction: a new epidemiological tool for investigating cervical human papillomavirus infection.
Cervical intraepithelial neoplasia.
Nogo-A-specific antibody treatment enhances sprouting and functional recovery after cervical lesion in adult primates.
Relationships of vaginal Lactobacillus species, cervical Chlamydia trachomatis, and bacterial vaginosis to preterm birth.
Natural history of genital warts.
Ligase chain reaction to detect Chlamydia trachomatis infection of the cervix.
Design and methods of a population-based natural history study of cervical neoplasia in a rural province of Costa Rica: the Guanacaste Project.
The natural history of type-specific human papillomavirus infections in female university students.
A longitudinal study of genital human papillomavirus infection in a cohort of closely followed adolescent women.
Incidence, duration, and determinants of cervical human papillomavirus infection in a cohort of Colombian women with normal cytological results.
Epidemiology of acquisition and clearance of cervical human papillomavirus infection in women from a high-risk area for cervical cancer.
A general primer GP5+/GP6(+)-mediated PCR-enzyme immunoassay method for rapid detection of 14 high-risk and 6 low-risk human papillomavirus genotypes in cervical scrapings.
Genital human papillomavirus infection in female university students as determined by a PCR-based method.
Comparison of PCR detection methods for B1, P30, and 18S rDNA genes of T. gondii in aqueous humor.
Aqueous humor interleukin-6 levels in uveitis.
Ocular sequelae of congenital toxoplasmosis in Brazil compared with Europe.
Uveitis and systemic disease.
Toxoplasmosis in the non-AIDS immunocompromised host.
Ocular toxoplasmosis; pathogenesis, diagnosis and treatment.
Ocular toxoplasmosis in patients with the acquired immunodeficiency syndrome.
Changing patterns of uveitis.
Foodborne outbreaks of human toxoplasmosis.
Ocular toxoplasmosis: a global reassessment. Part I: epidemiology and course of disease.
Genetic divergence of Toxoplasma gondii strains associated with ocular toxoplasmosis, Brazil.
An unusually high prevalence of ocular toxoplasmosis in southern Brazil.
Toxoplasmosis: A history of clinical observations.
Highly endemic, waterborne toxoplasmosis in north Rio de Janeiro state, Brazil.
Unusual abundance of atypical strains associated with human ocular toxoplasmosis.
Immediate early and early lytic cycle proteins are frequent targets of the Epstein-Barr virus-induced cytotoxic T cell response.
Antibodies to polynucleotides in human sera: antigenic specificity and relation to disease.
Large clonal expansions of CD8+ T cells in acute infectious mononucleosis.
Cytotoxic effector cells specific for B Cell lines transformed by Epstein-Barr virus are present in patients with infectious mononucleosis.
B cells under influence: transformation of B cells by Epstein-Barr virus.
DNA of Epstein-Barr virus VIII: B95-8, the previous prototype, is an unusual deletion derivative.
Tan See Wei
Tay Seok Wei
Differences between laboratory strains of Epstein-Barr virus based on immortalization, abortive infection, and interference.
Epstein-Barr virus replication in oropharyngeal epithelial cells.
Latent murine gamma-herpesvirus infection is established in activated B cells, dendritic cells, and macrophages.
Cellular responses to viral infection in humans: lessons from Epstein-Barr virus.
Direct visualization of antigen-specific CD8+ T cells during the primary immune response to Epstein-Barr virus In vivo.
Progressive loss of CD8+ T cell-mediated control of a gamma-herpesvirus in the absence of CD4+ T cells.
Release of infectious Epstein-Barr virus by transformed marmoset leukocytes.
Imaging of macular diseases with optical coherence tomography.
Toward the generation of rod and cone photoreceptors from mouse, monkey and human embryonic stem cells.
State-of-the-art retinal optical coherence tomography.
Retinal angiogenesis in development and disease.
RPE lipofuscin and its role in retinal pathobiology.
Therapeutic in vivo gene transfer for genetic disease using AAV: progress and challenges.
Delta-like ligand 4 (Dll4) is induced by VEGF as a negative regulator of angiogenic sprouting.
Retinopathy and attenuated circadian entrainment in Crx-deficient mice.
Increased dietary intake of omega-3-polyunsaturated fatty acids reduces pathological retinal angiogenesis.
Dark adaptation and the retinoid cycle of vision.
Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair.
Müller cells in the healthy and diseased retina.
Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms.
IgA antibodies for diagnosis of acute congenital and acquired toxoplasmosis.
The infectious origins of stillbirth.
Toxoplasmosis: the time has come.
Toxoplasma gondii: epidemiology, feline clinical aspects, and prevention.
Toxoplasmosis snapshots: global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis.
Prenatal management of 746 pregnancies at risk for congenital toxoplasmosis.
Neonatal serologic screening and early treatment for congenital Toxoplasma gondii infection. The New England Regional Toxoplasma Working Group.
Mother-to-child transmission of toxoplasmosis: risk estimates for clinical counselling.
Early and longitudinal evaluations of treated infants and children and untreated historical patients with congenital toxoplasmosis: the Chicago Collaborative Treatment Trial.
Development of adverse sequelae in children born with subclinical congenital Toxoplasma infection.
Prenatal diagnosis of congenital toxoplasmosis with a polymerase-chain-reaction test on amniotic fluid.
Management of Toxoplasma gondii infection during pregnancy.
Toxoplasmosis in pregnancy.
Genotype of 86 Toxoplasma gondii isolates associated with human congenital toxoplasmosis, and correlation with clinical findings.
Toxoplasma gondii infection in humans and animals in the United States.
Congenital toxoplasmosis. A prospective study of 378 pregnancies.
Prenatal infection and schizophrenia: a review of epidemiologic and translational studies.
X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele.
Autosomal ichthyosis with hypotrichosis syndrome displays low matriptase proteolytic activity and is phenocopied in ST14 hypomorphic mice.
Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.
Stratum corneum moisturization at the molecular level.
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.
Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.
Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase.
Regional assignment of the steroid sulfatase-X-linked ichthyosis locus: implications for a noninactivated region on the short arm of human X chromosome.
X-linked ichthyosis due to steroid-sulphatase deficiency.
CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.