SCOPUS 정보 검색 플랫폼

Volumn 22, Issue 8, 1999, Pages 1378-1379

Partial wolfram syndrome (DIDMOAD): Two new patients in a family [7]

(8) Hernandez Mijares, Antonio a Morillas, Carlos b Lluch, Irene b Martinez Triguero, Maria Luisa b Muñoz, Maria Luisa b Gomez, Marcelino b Merino, Miguel Angel b Escudero, Manuel b

a HOSPITAL UNIVERSITARIO DR PESET (Spain)

b NONE

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN;

ADULT; CASE REPORT; DIABETES INSIPIDUS; DIABETES MELLITUS; FEMALE; HEARING IMPAIRMENT; HUMAN; LETTER; OPTIC NERVE ATROPHY; POLYDIPSIA; POLYURIA; WOLFRAM SYNDROME;

ADULT; FEMALE; HAPLOTYPES; HLA ANTIGENS; HUMANS; PREVALENCE; WOLFRAM SYNDROME;

EID: 0032792134 PISSN: 01495992 EISSN: None Source Type: Journal
DOI: 10.2337/diacare.22.8.1378 Document Type: Letter

Times cited : (6)

References (8)

1
- 0000804149
- Diabetes mellitus and simple optic atrophy among sibling: Reports of four cases
- Wolfram DJ: Diabetes mellitus and simple optic atrophy among sibling: reports of four cases. Mayo Clin Proc 9:715-718, 1938
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- Wolfram, D.J.¹

2
- 0017764306
- Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram Syndrome): A review of 88 cases from the literature with personal observations on 3 new patients
- Cremers CW, Wijdeveld PG, Pinckers AJ: Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram Syndrome): a review of 88 cases from the literature with personal observations on 3 new patients. Acta Pacdiatr Scand 264 (Suppl.):1-16, 1977
- (1977) Acta Pacdiatr Scand , vol.264 , Issue.SUPPL. , pp. 1-16
- Cremers, C.W.¹ Wijdeveld, P.G.² Pinckers, A.J.³

3
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- Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram Syndrome (DIDMOAD)
- Pilz D, Quarrell OWJ, Jones EW: Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram Syndrome (DIDMOAD). J Med Genet 31: 328-330, 1994
- (1994) J Med Genet , vol.31 , pp. 328-330
- Pilz, D.¹ Quarrell, O.W.J.² Jones, E.W.³

4
- 13344260008
- A nuclear defect in the 4pl6 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome
- Barrientos A, Volpini V, Casedemont J, Gems D, Manzanares JM, Ferrer Y, Corral J, Cardellach F, Urbano-Marquez A, Estivil X, Nunes V: A nuclear defect in the 4pl6 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. J Clin Invest 97:1570-1576, 1996
- (1996) J Clin Invest , vol.97 , pp. 1570-1576
- Barrientos, A.¹ Volpini, V.² Casedemont, J.³ Gems, D.⁴ Manzanares, J.M.⁵ Ferrer, Y.⁶ Corral, J.⁷ Cardellach, F.⁸ Urbano-Marquez, A.⁹ Estivil, X.¹⁰ Nunes, V.¹¹

5
- 0005760504
- HLA type and islet cell antibody status in family with DIDMOAD syndrome
- Monson JP, Boucher BJ: HLA type and islet cell antibody status in family with DIDMOAD syndrome. Lancet i:1398-1399, 1983
- (1983) Lancet , vol.1 , pp. 1398-1399
- Monson, J.P.¹ Boucher, B.J.²

6
- 0023916334
- Contrasting features of insulin dependent diabetes mellitus associated with neuroectodermal defects and classical insulin dependent diabetes mellitus
- Garcia-Luna PP, Villechenous E, Leal-Cerro A: Contrasting features of insulin dependent diabetes mellitus associated with neuroectodermal defects and classical insulin dependent diabetes mellitus. Acta Paediatr Scand 77:413-418, 1988
- (1988) Acta Paediatr Scand , vol.77 , pp. 413-418
- Garcia-Luna, P.P.¹ Villechenous, E.² Leal-Cerro, A.³

7
- 0029939777
- Wolfram syndrome: Hereditary diabetes mellitus with brainstem and optic atrophy
- Scolding NJ, Kellar-Wood HF, Shaw C, Shneerson JM, Antoun N: Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy. Ann Neurol 39:352-360, 1996
- (1996) Ann Neurol , vol.39 , pp. 352-360
- Scolding, N.J.¹ Kellar-Wood, H.F.² Shaw, C.³ Shneerson, J.M.⁴ Antoun, N.⁵

8
- 0021829539
- Sindrome DIDMOADUA (DIDMOAD): Estudio de 3 familias con 5 nuevos caves: diferencia con la diabetes mellitus insulinode-pendiente clasica
- Garcia-Luna P, Leal A, Villamil F: Sindrome DIDMOADUA (DIDMOAD): estudio de 3 familias con 5 nuevos caves: diferencia con la diabetes mellitus insulinode-pendiente clasica. Med Clin (Barc) 85:486-490, 1985
- (1985) Med Clin (Barc) , vol.85 , pp. 486-490
- Garcia-Luna, P.¹ Leal, A.² Villamil, F.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.