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Volumn 16, Issue 3, 2003, Pages 193-195

The importance of brain magnetic resonance in Boucher-Neuhauser Syndrome diagnosis;A importância da neuroimagem no diagnóstico da Síndrome de Boucher-Neuhauser

Author keywords

Autossomal recessive inheritance; Boucher Neuhauser Syndrome (BNS); Brain magnetic resonance imaging (MRI)

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BOUCHER NEUHAUSER SYNDROME; BRAIN DISEASE; CASE REPORT; CEREBELLAR ATAXIA; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; RETINA DYSTROPHY;

EID: 0038464950     PISSN: None     EISSN: 16460758     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (7)
  • 1
    • 0035866017 scopus 로고    scopus 로고
    • New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness
    • AMOR DJ, DELATYCKY MB, GARDNER RJM, STOREY E: New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness. Am J Med Genet 2001;99: 29-33
    • (2001) Am J Med Genet , vol.99 , pp. 29-33
    • Amor, D.J.1    Delatycky, M.B.2    Gardner, R.J.M.3    Storey, E.4
  • 2
    • 0027480982 scopus 로고
    • Heterogeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes'type ataxia)
    • MICHELE G, FILLA A, STRIANO S, RIMOLDI M, CAMPANELLA G: Heterogeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes'type ataxia). Clin Neurol and Neurosurg 1993;95: 23-28
    • (1993) Clin Neurol and Neurosurg , vol.95 , pp. 23-28
    • Michele, G.1    Filla, A.2    Striano, S.3    Rimoldi, M.4    Campanella, G.5
  • 5
    • 0029149805 scopus 로고
    • Ophthalmologic findings in a patient with cerebellar ataxia, hypogonadotropic hypogonadism and chorioretinal dystrophy
    • SALVADOR F, GARCIA-ARUMI J, CORCÓSTEGUI B, MINOVES T, TARRUS F: Ophthalmologic findings in a patient with cerebellar ataxia, hypogonadotropic hypogonadism and chorioretinal dystrophy. Am J of OphtALMOL 1995;120:241-244
    • (1995) Am J of Ophtalmol , vol.120 , pp. 241-244
    • Salvador, F.1    Garcia-Arumi, J.2    Corcóstegui, B.3    Minoves, T.4    Tarrus, F.5
  • 7
    • 0029118994 scopus 로고
    • A new family of Boucher-Neuhauser syndrome: Coexistence of Holmes type cerebellar atrophy, hypogonadotropic hypogonadism and retinochoroidal degeneration: Case report and review of literature
    • TOJO K, ICHINOSE M, NAKAYAMA M, YAMAMOTO H, HASEGAWA T, KAWAGUCHI Y, SEALFON SC, SAKAI O: A new family of Boucher-Neuhauser syndrome: coexistence of Holmes type cerebellar atrophy, hypogonadotropic hypogonadism and retinochoroidal degeneration: case report and review of literature. Endocr J 1995; 42 (3): 367-76
    • (1995) Endocr J , vol.42 , Issue.3 , pp. 367-376
    • Tojo, K.1    Ichinose, M.2    Nakayama, M.3    Yamamoto, H.4    Hasegawa, T.5    Kawaguchi, Y.6    Sealfon, S.C.7    Sakai, O.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.