Results 101 to 110 of about 7,382 (203)

Senear-Usher Syndrome—I [PDF]

Proceedings of the Royal Society of Medicine, 1939
openaire   +2 more sources

MCV/Q, Medical College of Virginia Quarterly, Vol. 13 No. 4 [PDF]

, 1977

core   +1 more source

From Usher syndrome to Bardet-Biedl syndrome: Diagnosis after an atypical presentation. [PDF]

Clin Nephrol Case Stud
Milheiro J, Pinto R, Veiga C, Dias A, Pêgo C, Lemos S.   +5 more
europepmc   +1 more source

Application of smooth OWA operators to classification of retinitis pigmentosa. [PDF]

Sci Rep
Rachwał A, Rachwał A, Powroźnik P, Skublewska-Paszkowska M, Nowomiejska K, Rejdak R, Jonak K, Karczmarek P.   +7 more
europepmc   +1 more source

Usher syndrome [PDF]

, 2020
openaire   +3 more sources

From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2A. [PDF]

Otol Neurotol
Wijn DH, Fehrmann MLA, Robijn SMM, Velde HM, Smits JJ, van Wijk E, Beynon AJ, Cals FLJ, Hoyng CB, Yzer S, Lanting CP, Pennings RJE.   +11 more
europepmc   +1 more source

Identification of a variant in the USH1G gene in a family with Usher syndrome [PDF]

Biomedica
Gélvez N, López G, Tamayo ML.
europepmc   +1 more source

Editorial: Pain in the older adult patient. [PDF]

Front Med (Lausanne)
Tagliafico L, Penfold R, Duque S, Cacciatore S.   +3 more
europepmc   +1 more source

Epidemiological and genetic insights of Usher syndrome in Turkish population: A cross-sectional preliminary study from University of Health Sciences, Turkey. [PDF]

J Int Med Res
Alkan AA, Güven D, Kaçar H, Türk B, Arslan GD, Karataş G, Karataş ME, Al Saadoni H, Kutucu OK, Karapapak M, Şendül Y, Düzgün E.   +11 more
europepmc   +1 more source

A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F. [PDF]

Mol Genet Genomic Med
Ma Q, Xu C, Xu X, Xiang Y.
europepmc   +1 more source