Results 101 to 110 of about 163,801 (186)

Multimodal imaging and intravitreal faricimab for polypoidal choroidal vasculopathy associated with a choroidal nevus in genetically confirmed Usher syndrome type 2: a case report. [PDF]

BMC Ophthalmol
Kim J, Choi J, Kim K, Yu SY.
europepmc   +1 more source

Rare Case of Esophageal Squamous Cell Carcinoma in an Adolescent with Multiple Congenital Anomalies and Homozygous USH2A Mutation. [PDF]

J Indian Assoc Pediatr Surg
Krishnamurthy A, Vighneshwar N, Balakrishnan G, Radhakrishnan V.   +3 more
europepmc   +1 more source

Ocular findings in pediatric candidates for cochlear implantation with bilateral sensorineural hearing loss: a brief report from northwestern Iran. [PDF]

BMC Ophthalmol
Sobhi N, Vahedi H, Ashayeri H, Razmjooei F, Jafarizadeh A, Nouri A, Ariafar A, Jabbari Moghaddam Y, Naderpour M.   +8 more
europepmc   +1 more source

Challenging neuropathic pain syndromes : evaluation and evidence-based treatment /

Includes bibliographical references and index.Pathophysiology of pain -- Central sensitization, central sensitization syndromes, and chronic neuropathic pain -- A physiatric approach to the treatment of complex regional pain syndrome -- Complex regional ...
Gehret, Jeffrey A.,author., Freedman, Mitchell K.,author., Young, George W.D.O.,author., Kamen, Leonard B.,author.   +3 more
core  

Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations. [PDF]

Clin Genet
Diogo-Cavassana S, Alencar-Coutinho D, Abreu-Oberhuber R, Paramo-Neto ME, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K.   +7 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

Heimler Syndrome Caused by Novel <i>PEX6</i> Variants: Clinical and Genetic Characterization in a Saudi Cohort. [PDF]

Genes (Basel)
AlMoallem B.
europepmc   +1 more source

Multicenter Natural History Study and Long-Term Cochlear Implant Outcomes in Usher Syndrome Subtypes. [PDF]

Ear Hear
Krumpoeck PE, Gadenstaetter AJ, Uehara N, Fujita T, Giarbini N, Pawloff M, Ritter M, Landegger A, Parzefall T, Riss D, Baumgartner WD, Gstoettner W, Arnoldner C, Landegger LD.   +13 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

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics. [PDF]

Mol Med
Koparir A, Carbajal PB, Zamini M, Naghinejad M, Najarzadeh Torbati P, Hofrichter MAH, Tovornik S, Koparir E, Dragicevic Babic N, Rad A, Owrang D, Kalay I, Chamanrou N, Martínez Völter LN, Christophersen N, Baranzehi T, Rajati M, Loum S, Kunstmann E, Shadab M, Abbasi AA, Doosti M, Alidadiani N, Ghaderi S, Haack TB, Alavi S, Doll J, Kremer H, Kordi-Tamandani DM, Murphy D, Mohammad R, Hebestreit H, Ghayoor Karimiani E, Flandin S, Linares P, Villalobos D, Houlden H, Galehdari H, Shehata-Dieler W, Maroofian R, Haaf T, Vona B.   +41 more
europepmc   +1 more source