Detalhe da pesquisa
1.
Expression and localization of COL2A1 mRNA and type II collagen in human fetal cochlea.
Hear Res
; 79(1-2): 59-73, 1994 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-7806485
2.
GNAZ in human fetal cochlea: expression, localization, and potential role in inner ear function.
Hear Res
; 90(1-2): 55-64, 1995 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-8975005
3.
DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear.
Laryngoscope
; 110(8): 1379-84, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10942145
4.
Temporal bone findings in a case of bilateral Menière's disease treated by parenteral streptomycin and endolymphatic shunt.
Laryngoscope
; 100(4): 407-14, 1990 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-2319892
5.
Neurotrophin 3, not brain-derived neurotrophic factor or neurotrophin 4, knockout mice have delay in vestibular compensation after unilateral labyrinthectomy.
Laryngoscope
; 108(5): 671-8, 1998 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9591544
6.
COL1A2 and COL2A1 expression in temporal bone of lethal osteogenesis imperfecta.
Arch Otolaryngol Head Neck Surg
; 119(12): 1305-14, 1993 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17431984
7.
Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds.
Arch Otolaryngol Head Neck Surg
; 117(9): 1032-42, 1991 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1910721
8.
Investigations into the cause of vertigo in sudden sensorineural hearing loss.
Otolaryngol Head Neck Surg
; 105(3): 360-71, 1991 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1945420
9.
Idiopathic sudden sensorineural hearing loss and postnatal viral labyrinthitis: a statistical comparison of temporal bone findings.
Ann Otol Rhinol Laryngol
; 99(12): 969-76, 1990 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-2244729
10.
Inner ridge cells may be the main source of tectorial membrane type II collagen: evidence from quantitative mRNA in situ hybridization.
Acta Otolaryngol
; 118(2): 177-84, 1998 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9583784
11.
In search of pathologic correlates for hearing loss and vertigo in Paget's disease. A clinical and histopathologic study of 26 temporal bones.
Ann Otol Rhinol Laryngol Suppl
; 145: 1-16, 1990 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-2106820
12.
Morphological and neurochemical correlates of vestibular compensation.
Auris Nasus Larynx
; 25(2): 193-201, 1998 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9673734
13.
Autosomal dominant sensorineural hearing loss. Further temporal bone findings.
Arch Otolaryngol Head Neck Surg
; 119(1): 106-8, 1993 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8417734
14.
Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.
Genomics
; 23(1): 42-50, 1994 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-7829101
15.
Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiency.
Hum Mutat
; 9(5): 402-8, 1997.
Artigo
em Inglês
| MEDLINE | ID: mdl-9143918
16.
A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.
Hum Mol Genet
; 5(7): 1047-50, 1996 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-8817345