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Volumn 4, Issue 1, 2003, Pages 52-53

Mental retardation associated with Brown-Vialetto-Van Laere syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; BODY DYSMORPHIC DISORDER; CASE REPORT; CEREBELLUM ATROPHY; DAILY LIFE ACTIVITY; DISEASE ASSOCIATION; DYSPHAGIA; ELECTROMYOGRAPHY; FACIAL NERVE PARALYSIS; HUMAN; HYPERPIGMENTATION; LABORATORY TEST; LETTER; MALE; MENTAL DEFICIENCY; MOTOR NERVE CONDUCTION; MOTOR NEURON DISEASE; MUSCLE ATROPHY; MUSCLE HYPOTONIA; MUSCLE WEAKNESS; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION DEAFNESS; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PROGRESSIVE BULBAR PALSY; RETINA MACULOPATHY; TONGUE DISEASE;

EID: 0037799433     PISSN: 14660822     EISSN: None     Source Type: Journal    
DOI: 10.1080/14660820301170     Document Type: Letter
Times cited : (8)

References (6)
  • 2
    • 0019431614 scopus 로고
    • Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome)
    • Gallai V, Hockaday JM, Hughes JT, et al. Ponto-bulbar palsy with deafness (Brown-Vialetto-Van Laere syndrome). J Neurol Sci 1981; 50: 259-275.
    • (1981) J. Neurol. Sci. , vol.50 , pp. 259-275
    • Gallai, V.1    Hockaday, J.M.2    Hughes, J.T.3
  • 3
    • 0342314442 scopus 로고    scopus 로고
    • Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?
    • Megarbane A, Desguerres I, Rizkallah E, et al. Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?. American Journal of Medical Genetics 2000; 92: 117-121.
    • (2000) American Journal of Medical Genetics , vol.92 , pp. 117-121
    • Megarbane, A.1    Desguerres, I.2    Rizkallah, E.3
  • 4
    • 0025193469 scopus 로고
    • 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: 176-179.
    • (1990) J. Med. Genet. , vol.27 , pp. 176-179
    • Hawkins, S.A.1    Nevin, N.C.2    Harding, A.E.3
  • 5
    • 0026629712 scopus 로고
    • Recovery from respiratory muscle failure in a sporadic case of Brown-Vialetto-Van Laere syndrome with unusually late onset
    • Piccolo G, Marchioni E, Maurelli E, et al. Recovery from respiratory muscle failure in a sporadic case of Brown-Vialetto-Van Laere syndrome with unusually late onset. J Neurol 1992; 239: 355-356.
    • (1992) J. Neurol. , vol.239 , pp. 355-356
    • Piccolo, G.1    Marchioni, E.2    Maurelli, E.3
  • 6
    • 0019510555 scopus 로고
    • Progressive ponto-bulbar palsy with deafness. Clinical and pathological study of two cases
    • Brucher JM, Dom R, Lombaert A, et al. Progressive ponto-bulbar palsy with deafness. Clinical and pathological study of two cases. Arch Neurol 1981; 38: 186-190.
    • (1981) Arch. Neurol. , vol.38 , pp. 186-190
    • Brucher, J.M.1    Dom, R.2    Lombaert, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.