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In antibody-positive first-degree relatives of patients with type 1 diabetes, HLA-A24 and HLA-B18, but not HLA-B39, are predictors of impending diabetes with distinct HLA-DQ interactions

Diabetologia, 2013-09, Vol.56 (9), p.1964-1970

2013

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Male-to-female excess in diabetes diagnosed in early adulthood is not specific for the immune-mediated form nor is it HLA-DQ restricted : possible relation to increased body mass index

Diabetologia, 2001-01, Vol.44 (1), p.40-47

2001

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Non-transmitted maternal HLA DQ2 or DQ8 alleles and risk of Type I diabetes in offspring: the importance of fetal or post partum exposure to diabetogenic molecules

Diabetologia, 2002-09, Vol.45 (9), p.1340-1343

2002

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DQ-LTR13 modifies Type 1 diabetes (IDDM) susceptibility on high risk DQ haplotypes: reply to the comments of Pascual et al

Diabetologia, 2003-06, Vol.46 (6), p.870-871

2003

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Proinsulin and its conversion intermediates in human pancreas and isolated islet tissue: kinetics and steady-state analysis

Pancreas, 1997-08, Vol.15 (2), p.113-121

1997

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CTLA-4 gene polymorphism confers susceptibility to insulin-dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers

Clinical and experimental immunology, 1997-10, Vol.110 (1), p.98-103

1997

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IFIH1 gene polymorphisms in type 1 diabetes: Genetic association analysis and genotype–phenotype correlation in the Belgian population

Human immunology, 2009-09, Vol.70 (9), p.706-710

2009

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CTLA‐4 gene polymorphism confers susceptibility to insulin‐dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers

Clinical and experimental immunology, 2003-10, Vol.110 (1), p.98-103

2003

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5' insulin gene polymorphism confers risk to IDDM independently of HLA class II susceptibility

Diabetes (New York, N.Y.), 1993-06, Vol.42 (6), p.851-854

1993

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Monozygotic twins discordant for spondylocostal dysostosis

American journal of medical genetics, 1994-10, Vol.52 (4), p.483-486

1994

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5' insulin gene polymorphism confers risk to IDDM independently of HLA class II susceptibility

Diabetes (New York, N.Y.), 1993-06, Vol.42 (6), p.851-854

1993

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The rare HLA-DQA103-DQB102 haplotype confers susceptibility to type 1 diabetes in whites and is preferentially associated with early clinical disease onset in male subjects

Human immunology, 2004-07, Vol.65 (7), p.729-736

2004

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Relative and absolute HLA-DQA1-DQB1 linked risk for developing type I diabetes before 40 years of age in the Belgian population: implications for future prevention studies

Human immunology, 2002-01, Vol.63 (1), p.40-50

2002

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Authors' reply

Diabetologia, 2003-04, Vol.46 (4), p.592-593

2003

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Authors' reply

Diabetologia, 2003-04, Vol.46 (4), p.592

2003

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Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family

Archives of neurology (Chicago), 1990-06, Vol.47 (6), p.665-669

1990

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BclI RFLP in fucosidase pseudogene (FUCA1P)

Nucleic acids research, 1990-09, Vol.18 (18), p.5583-5583

1990

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Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients

Clinical genetics, 1991-02, Vol.39 (2), p.89-92

1991

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Distribution of HERV-LTR elements in HLA-DQB1 alleles: comments on the article by Bieda et al

Diabetologia, 2003-06, Vol.46 (6), p.869-870

2003

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to: Pani MA, Van Autreve J, Van Der Auwera BJ, Gorus FK, Badenhoop K (2002) Non-transmitted maternal HLA DQ2 or DQ8 alleles and risk of Type I diabetes in offspring: the importance of foetal or post partum exposure to diabetogenic molecules. Diabetologia 45:1340-1343

Diabetologia, 2003-04, Vol.46 (4), p.588-589

2003

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Two brothers with mental retardation discordant for the Fragile-X syndrome

American journal of medical genetics, 1990-05, Vol.36 (1), p.122-125

1990

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Assignment of X-linked hydrocephalus to Xq28 by linkage analysis

Genomics (San Diego, Calif.), 1990-10, Vol.8 (2), p.367-370

1990

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CTLA-4 gene polymorphism confers susceptibility to insulin-dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers. The Belgian Diabetes Registry

Clinical and experimental immunology, 1997-10, Vol.110 (1), p.98-103

1997

Volltextzugriff (PDF)

Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22

Genomics (San Diego, Calif.), 1991-04, Vol.9 (4), p.565-569

1991

Volltextzugriff (PDF)

BcII RFLP in fucosidase pseudogene (FUCA1P)

Nucleic acids research, 1990-09, Vol.18 (18), p.5583-5583

1990

Volltextzugriff (PDF)

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In antibody-positive first-degree relatives of patients with type 1 diabetes, HLA-A24 and HLA-B18, but not HLA-B39, are predictors of impending diabetes with distinct HLA-DQ interactions

Male-to-female excess in diabetes diagnosed in early adulthood is not specific for the immune-mediated form nor is it HLA-DQ restricted : possible relation to increased body mass index

Non-transmitted maternal HLA DQ2 or DQ8 alleles and risk of Type I diabetes in offspring: the importance of fetal or post partum exposure to diabetogenic molecules

DQ-LTR13 modifies Type 1 diabetes (IDDM) susceptibility on high risk DQ haplotypes: reply to the comments of Pascual et al

Proinsulin and its conversion intermediates in human pancreas and isolated islet tissue: kinetics and steady-state analysis

CTLA-4 gene polymorphism confers susceptibility to insulin-dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers

IFIH1 gene polymorphisms in type 1 diabetes: Genetic association analysis and genotype–phenotype correlation in the Belgian population

CTLA‐4 gene polymorphism confers susceptibility to insulin‐dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers

5' insulin gene polymorphism confers risk to IDDM independently of HLA class II susceptibility

Monozygotic twins discordant for spondylocostal dysostosis

5' insulin gene polymorphism confers risk to IDDM independently of HLA class II susceptibility

The rare HLA-DQA103-DQB102 haplotype confers susceptibility to type 1 diabetes in whites and is preferentially associated with early clinical disease onset in male subjects

Relative and absolute HLA-DQA1-DQB1 linked risk for developing type I diabetes before 40 years of age in the Belgian population: implications for future prevention studies

Authors' reply

Authors' reply

Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family

BclI RFLP in fucosidase pseudogene (FUCA1P)

Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients

Distribution of HERV-LTR elements in HLA-DQB1 alleles: comments on the article by Bieda et al

to: Pani MA, Van Autreve J, Van Der Auwera BJ, Gorus FK, Badenhoop K (2002) Non-transmitted maternal HLA DQ2 or DQ8 alleles and risk of Type I diabetes in offspring: the importance of foetal or post partum exposure to diabetogenic molecules. Diabetologia 45:1340-1343

Two brothers with mental retardation discordant for the Fragile-X syndrome

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis

CTLA-4 gene polymorphism confers susceptibility to insulin-dependent diabetes mellitus (IDDM) independently from age and from other genetic or immune disease markers. The Belgian Diabetes Registry

Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22

BcII RFLP in fucosidase pseudogene (FUCA1P)

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