SCOPUS 정보 검색 플랫폼

Journal of Laryngology and Otology

Volumn 119, Issue 6, 2005, Pages 470-472

Brown-Vialetto-Van Laere syndrome: A rare syndrome in otology - Case report and literature review

(2) Prabhu, H V a Brown, M J K a

a ROYAL GWENT HOSPITAL (United Kingdom)

Author keywords

Bulbar Palsy; Cranial Nerve Diseases; Hearing Loss

Indexed keywords

ADULT; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; BROWN VIALETTO VAN LAERE SYNDROME; BULBAR PARALYSIS; CASE REPORT; CONGENITAL DEAFNESS; CRANIAL NERVE PARALYSIS; CRANIAL NEUROPATHY; EVIDENCE BASED MEDICINE; FACIAL NERVE; FEMALE; HUMAN; MOTONEURON; MOTOR NERVE; PERCEPTION DEAFNESS; RARE DISEASE; REVIEW; SYMPTOMATOLOGY; VAGUS NERVE; X CHROMOSOMAL INHERITANCE;

ADULT; AUDIOMETRY, PURE-TONE; BULBAR PALSY, PROGRESSIVE; FACIAL PARALYSIS; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; SYNDROME; VOCAL CORD PARALYSIS;

EID: 21244438730 PISSN: 00222151 EISSN: None Source Type: Journal
DOI: 10.1258/0022215054273179 Document Type: Review

Times cited : (7)

References (6)

1
- 0025193469
- Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance
- Hawkins SA, Nevin NC, Harding AE. Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. J Med Genet 1990;27:176-9
- (1990) J Med Genet , vol.27 , pp. 176-179
- Hawkins, S.A.¹ Nevin, N.C.² Harding, A.E.³

2
- 0342314442
- Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?
- Megarbane A, Desguerres I, Rizkallah E, Delague V, Nabbout R, Barois A, et al. Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: confirmation of autosomal recessive inheritance? Am J Med Genet 2000;92:117-21
- (2000) Am J Med Genet , vol.92 , pp. 117-121
- Megarbane, A.¹ Desguerres, I.² Rizkallah, E.³ Delague, V.⁴ Nabbout, R.⁵ Barois, A.⁶

3
- 0034278928
- Brown-Vialetto-Van Laere syndrome: Case report and literature review
- Sathasivam S, O'Sullivan S, Nicolson A, Tilley PJ, Shaw PJ. Brown-Vialetto-Van Laere syndrome: case report and literature review. Amyotroph Lateral Scler Other Motor Neuron Disord 2000;1:277-81
- (2000) Amyotroph Lateral Scler Other Motor Neuron Disord , vol.1 , pp. 277-281
- Sathasivam, S.¹ O'Sullivan, S.² Nicolson, A.³ Tilley, P.J.⁴ Shaw, P.J.⁵

4
- 0023390542
- Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-Van Laere syndrome or Madras type motor neuron disease?
- Summers BA, Swash M, Schwartz MS, Ingram DA. Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-Van Laere syndrome or Madras type motor neuron disease? J Neurol 1987;234:440-2
- (1987) J Neurol , vol.234 , pp. 440-442
- Summers, B.A.¹ Swash, M.² Schwartz, M.S.³ Ingram, D.A.⁴

5
- 0027481872
- Brown-Vialetto-Van Laere syndrome
- Francis DA, Ponsford JR, Wiles CM, Thomas PK, Duchen LW. Brown-Vialetto-Van Laere syndrome. Neuropathol Appl Neurobiol 1993;19:91-4
- (1993) Neuropathol Appl Neurobiol , vol.19 , pp. 91-94
- Francis, D.A.¹ Ponsford, J.R.² Wiles, C.M.³ Thomas, P.K.⁴ Duchen, L.W.⁵

6
- 2542464042
- Vilaetto-Van Laere syndrome in two sisters born to consanguineous parents
- Nair RR, Parameshwaran M, Girija AS. Vilaetto-Van Laere syndrome in two sisters born to consanguineous parents. Pediatr Neurol 2004;30:354-5
- (2004) Pediatr Neurol , vol.30 , pp. 354-355
- Nair, R.R.¹ Parameshwaran, M.² Girija, A.S.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.