메뉴 건너뛰기




Volumn 41, Issue 10, 1999, Pages 729-731

MRI of Wolfram syndrome (DIDMOAD)

Author keywords

DIDMOAD syndrome; Magnetic resonance imaging; Substantia nigra; Wolfram syndrome

Indexed keywords

ARTICLE; BRAIN ATROPHY; BRAIN CORTEX; BRAIN STEM; CASE REPORT; CEREBELLUM; FEMALE; HUMAN; HYPOTHALAMUS; NEUROHYPOPHYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; SCHOOL CHILD; SUBSTANTIA NIGRA; WOLFRAM SYNDROME;

EID: 0033406686     PISSN: 00283940     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002340050832     Document Type: Article
Times cited : (48)

References (16)
  • 1
    • 0000804149 scopus 로고
    • Diabetes mellitus and simple optic atrophy among siblings: Report of four cases
    • Wolfram DJ, Wagener HP (1938) Diabetes mellitus and simple optic atrophy among siblings: report of four cases. Mayo Clin Proc 9: 715-718
    • (1938) Mayo Clin Proc , vol.9 , pp. 715-718
    • Wolfram, D.J.1    Wagener, H.P.2
  • 3
    • 33646273485 scopus 로고
    • Atrofia ottica, diabete mellito, diabete insipido, sordità neurosensoriale (DIDMOAD syndrome): Considerazioni etiopatogenetiche
    • Bardelli AM, Nuti A, Lasorella G (1979) Atrofia ottica, diabete mellito, diabete insipido, sordità neurosensoriale (DIDMOAD syndrome): considerazioni etiopatogenetiche. Ann Ottal E Clin Ocul 105: 81-88
    • (1979) Ann Ottal E Clin Ocul , vol.105 , pp. 81-88
    • Bardelli, A.M.1    Nuti, A.2    Lasorella, G.3
  • 4
    • 0029151131 scopus 로고
    • Growth hormone deficiency and empty sella in DIDMOAD syndrome: An endocrine study
    • Soliman AT, Bappal B, Darwish A, Raiab A, Asfour M (1995) Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study. Arch Dis Child 73: 251-253
    • (1995) Arch Dis Child , vol.73 , pp. 251-253
    • Soliman, A.T.1    Bappal, B.2    Darwish, A.3    Raiab, A.4    Asfour, M.5
  • 5
    • 0017565453 scopus 로고
    • Juvenile diabetes mellitus and optic atrophy
    • Lessell S, Rosman P (1977) Juvenile diabetes mellitus and optic atrophy. Arch Neurol 34: 759-765
    • (1977) Arch Neurol , vol.34 , pp. 759-765
    • Lessell, S.1    Rosman, P.2
  • 6
    • 0021968147 scopus 로고
    • Association of diabetes insipidus, diabetes mellitus, optic atrophy, and defness. The Wolfram or DIDMOAD syndrome
    • Najjar SS, Saikaly MG, Zaytoun GM, Abdelnoor A (1985) Association of diabetes insipidus, diabetes mellitus, optic atrophy, and defness. The Wolfram or DIDMOAD syndrome. Arch Dis Child 60: 823-828
    • (1985) Arch Dis Child , vol.60 , pp. 823-828
    • Najjar, S.S.1    Saikaly, M.G.2    Zaytoun, G.M.3    Abdelnoor, A.4
  • 7
    • 0028350394 scopus 로고
    • Mitochondrial mutation associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD)
    • Pilz D, Quarrell OWJ, Jones EW (1994) Mitochondrial mutation associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD). J Med Genet 31: 328-330
    • (1994) J Med Genet , vol.31 , pp. 328-330
    • Pilz, D.1    Quarrell, O.W.J.2    Jones, E.W.3
  • 8
    • 0029939777 scopus 로고    scopus 로고
    • Wolfram syndrome: Hereditary diabetes mellitus with brainstem and optic atrophy
    • Scolding NJ, Keller-Wood H, Shaw C, Shneerson J, Antoun N (1996) Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy. Ann Neurol 39: 352-360
    • (1996) Ann Neurol , vol.39 , pp. 352-360
    • Scolding, N.J.1    Keller-Wood, H.2    Shaw, C.3    Shneerson, J.4    Antoun, N.5
  • 9
    • 0026755751 scopus 로고
    • Wolfram syndrome: Evidence of a diffuse neurodegenerative disease by magnetic resonance imaging
    • Rando TA, Horton JC, Layzer RB (1992) Wolfram syndrome: evidence of a diffuse neurodegenerative disease by magnetic resonance imaging. Neurology 42: 1220-1224
    • (1992) Neurology , vol.42 , pp. 1220-1224
    • Rando, T.A.1    Horton, J.C.2    Layzer, R.B.3
  • 10
    • 33646314128 scopus 로고    scopus 로고
    • Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4p 16.1 and evidence for heterogeneity
    • Polymeropoulos M, Swift R, Swift M (1996) Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4p 16.1 and evidence for heterogeneity. Am J Hum Genet 59: 855-863
    • (1996) Am J Hum Genet , vol.59 , pp. 855-863
    • Polymeropoulos, M.1    Swift, R.2    Swift, M.3
  • 11
    • 0027275218 scopus 로고
    • Wolfram syndrome: A mitochondrial-mediated disorder?
    • Bu X, Rotter JI (1993) Wolfram syndrome: a mitochondrial-mediated disorder? Lancet 342: 598-600
    • (1993) Lancet , vol.342 , pp. 598-600
    • Bu, X.1    Rotter, J.I.2
  • 12
    • 0031466720 scopus 로고    scopus 로고
    • Optic atrophy in Wolfram (DIDMOAD) syndrome
    • Barrett TG, Bundey S, Fielder AR, Good PA (1997) Optic atrophy in Wolfram (DIDMOAD) syndrome. Eye 11: 882-888
    • (1997) Eye , vol.11 , pp. 882-888
    • Barrett, T.G.1    Bundey, S.2    Fielder, A.R.3    Good, P.A.4
  • 15
    • 0342703121 scopus 로고
    • Wolfram's syndrome with schizophrenia and central hypoventilation: A neuropathological study
    • Gregorios JB (1989) Wolfram's syndrome with schizophrenia and central hypoventilation: a neuropathological study. J Neuropathol Exp Neurol 48: 308
    • (1989) J Neuropathol Exp Neurol , vol.48 , pp. 308
    • Gregorios, J.B.1
  • 16
    • 0017729442 scopus 로고
    • Simultaneous occurrence of diabetes mellitus, and optic atrophy in a brother and sister
    • Carson MJ, Slager UT, Steinberg RM (1977) Simultaneous occurrence of diabetes mellitus, and optic atrophy in a brother and sister. Am J Dis Child 131: 1382-1385
    • (1977) Am J Dis Child , vol.131 , pp. 1382-1385
    • Carson, M.J.1    Slager, U.T.2    Steinberg, R.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.