Adult-onset type 1 diabetes with DIDMOAD syndrome-like manifestations

Archives of Internal Medicine

Volumn 161, Issue 5, 2001, Pages 767-768

  Fukui, M ^a   Kitagawa, Y ^a   Nakamura, N ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; C PEPTIDE; GLUTAMATE DECARBOXYLASE; GLYCOSYLATED HEMOGLOBIN; HLA ANTIGEN; HYPOPHYSIS HORMONE; INSULIN; ORAL ANTIDIABETIC AGENT; VASOPRESSIN;

AGED; ARTICLE; CASE REPORT; DIET THERAPY; FEMALE; HUMAN; MATURITY ONSET DIABETES MELLITUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WOLFRAM SYNDROME;

EID: 0035848344     PISSN: 00039926     EISSN: None     Source Type: Journal    
DOI: 10.1001/archinte.161.5.767-a     Document Type: Article

References (7)

1. Recessive inheritance of diabetes: The syndrome of diabetes insipidus, diabetes mellitus, opuc atrophy and deafness
2. Association of diabetes insipidus, diabetes mellitus, optic atrophy and deafness
3. Morbidity and mortality m the Wolfram syndrome
4. GAD antibodtes in NIDDM
5. - diabetes with residual β-cell function
6. HLA type and islet cell antibody status in family with DIDMOAD syndrome
7. HLA-DRB 1 alleles contribute to determining the prognosis of Japanese diabetes mellitus positive for antibodies to glutamate decarboxylase