Results 181 to 190 of about 31,332 (279)

Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p

, 1998
Theresa Brennan, Daniel Landau, Hana Shalev, Fred S. Lamb, Brian C. Schutte, Roxanne Y. Walder, Allyn L. Mark, Rivka Carmi, Val C. Sheffield   +8 more
openalex   +1 more source

The epigenetic regulation of sensorineural deafness

IOP Conference Series: Earth and Environmental Science, 2019
Ruirui Song, Zhenyu Yun, Qi Wu, Lin Zhao
openaire   +2 more sources

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.

J Am Soc Nephrol, 2021
Schlingmann KP, Renigunta A, Hoorn EJ, Forst AL, Renigunta V, Atanasov V, Mahendran S, Barakat TS, Gillion V, Godefroid N, Brooks AS, Lugtenberg D, Lake J, Debaix H, Rudin C, Knebelmann B, Tellier S, Rousset-Rouvière C, Viering D, de Baaij JHF, Weber S, Palygin O, Staruschenko A, Kleta R, Houillier P, Bockenhauer D, Devuyst O, Vargas-Poussou R, Warth R, Zdebik AA, Konrad M.   +30 more
europepmc   +1 more source

Mitochondrial cytopathy presenting with focal segmental glomerulosclerosis, hypoparathyroidism, sensorineural deafness, and progressive neurological disease [PDF]

, 2001
R. Hameed, F. Raafat, Pratibha Ramani, G. HARRISON GRAY, Helen P. Roper, D V Milford   +5 more
openalex   +1 more source

Sensorineural deafness.4.Two cases of mumps deafness.

, 1995
Hiromi Orihara
openalex   +2 more sources

[A case report of congenital sensorineural deafness caused by novel mutation in Usher1C and related literature analysis]. [PDF]

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi, 2020
Guo M, Han W, Li S.
europepmc   +1 more source

An electrocochleogram. II. Electrocochleogram findings of the sensorineural deafness with the bass failure.

, 1995
Yoshihiro Ueki
openalex   +2 more sources

Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice [PDF]

, 2002
Kimihiko Oishi
openalex   +1 more source

Sensorineural deafness in a child with Prader-Willi Syndrome-A rare case report. [PDF]

J Family Med Prim Care
Saikrishna P, Tripathy SK, Medhagopal RG, Das S, Bharti B, Malik A.   +5 more
europepmc   +1 more source

Sensorineural deafness.3.Examination of idiopathic bilateral sensorineural deafness.

, 1995
MASATOSHI HIRAYAMA
openalex   +2 more sources