Usher's syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity.
about
Early diagnosis of Usher syndrome in childrenUSH1A: chronicle of a slow deathUsher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapyUsher syndrome in the city of Birmingham--prevalence and clinical classificationClinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumIdentification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.Molecular genetics of retinitis pigmentosaMouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.Diagnosis and treatment of a severe psychotic illness in a man with dual severe sensory impairments caused by the presence of Usher syndrome.Clinical variability and genetic heterogeneity within the Acadian Usher population.Retinal disease course in Usher syndrome 1B due to MYO7A mutationsEvidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type IRetinitis pigmentosa, pigmentary retinopathies, and neurologic diseases.Pre-mRNA splicing and retinitis pigmentosaThe use of carbonic anhydrase inhibitors in the retreatment of cystic macular lesions in retinitis pigmentosa and X-linked retinoschisis.Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.Usher's syndrome.Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis.Usher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers.[Usher syndrome: about a case].Prevalence of retinitis pigmentosa and allied disorders in Denmark. II. Systemic involvement and age at onset.Prevalence of cystic macular lesions in patients with Usher II syndrome.Evaluation of visual impairment in Usher syndrome 1b and Usher syndrome 2a.Ultra-widefield fundus autofluorescence patterns in retinitis pigmentosa and other retinal dystrophies.Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?Ophthalmologic findings in Usher syndrome type 2A.Ocular abnormalities in deaf children: a discussion of deafness and retinal pigment changes.Vestibular and auditory function in Usher's syndrome.Visual impairment in Finnish Usher syndrome type III.Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in NorwayPostural Control in Blinds and in Usher's Syndrome
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P2860
Usher's syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity.
description
1983 nî lūn-bûn
@nan
1983 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1983 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
name
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@ast
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@en
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@nl
type
label
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@ast
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@en
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@nl
prefLabel
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@ast
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@en
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@nl
P2093
P1433
P1476
Usher's syndrome. Ophthalmic a ...... gesting genetic heterogeneity.
@en
P2093
P304
P356
10.1001/ARCHOPHT.1983.01040020369005
P407
P577
1983-09-01T00:00:00Z