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The Leu544Ile polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency

Clinical endocrinology (Oxford), 2007-08, Vol.67 (2), p.212-217

2007

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Long-term prospective study of body composition and lipid profiles during and after growth hormone (GH) treatment in children with GH deficiency : Gender-specific metabolic effects

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.3890-3896

1998

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Premature mortality and hypopituitarism

The Lancet (British edition), 2001-06, Vol.357 (9272), p.1973-1973

2001

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PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children

Human genetics, 2007-04, Vol.121 (2), p.223-232

2007

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Juvenile idiopathic arthritis associated with autoimmune thyroid disorders and autoimmune cholangitis

British journal of rheumatology, 2001-08, Vol.40 (8), p.942-943

2001

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Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese population

Genes and immunity, 2002-04, Vol.3 (2), p.96-101

2002

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A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl‐phosphate synthetase‐1 activity in liver: A pitfall in enzymatic diagnosis for hyperammonaemia

Journal of inherited metabolic disease, 2005-01, Vol.28 (5), p.681-687

2005

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A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes

Immunogenetics (New York), 2003-06, Vol.55 (3), p.149-156

2003

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Body composition, atherogenic risk factors and apolipoproteins following growth hormone treatment

Acta Paediatrica, 1996-08, Vol.85 (8), p.899-901

1996

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Growth hormone treatment and type 2 diabetes

Growth hormone & IGF research, 2001-06, Vol.11 (3), p.196-197

2001

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The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

Human genetics, 1997-02, Vol.99 (2), p.171-176

1997

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Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (α-glucosidase) inhibitor

Acta pædiatrica (Oslo), 1998-05, Vol.87 (5), p.595-598

1998

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Identification of a novel type 1 diabetes susceptibility gene, T-bet

Human genetics, 2004-08, Vol.115 (3), p.177-184

2004

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An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease

European journal of pediatrics, 1997-09, Vol.156 (9), p.713-715

1997

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Late-onset ornithine transcarbamylase deficiency in male patients: Prognostic factors and characteristics of plasma amino acid profile

Pediatrics international, 2006-04, Vol.48 (2), p.105-111

2006

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Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with type 1 diabetes in the Japanese population

Immunogenetics (New York), 2001-08, Vol.53 (6), p.447-454

2001

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Lipoprotein (a) changes during growth hormone treatment

Clinical endocrinology (Oxford), 1995-11, Vol.43 (5), p.655-655

1995

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The Leu54411e polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency

Clinical endocrinology (Oxford), 2007, Vol.67 (2), p.212-217

2007

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Quantification of circulating varicella zoster virus-DNA for the early diagnosis of visceral varicella

The Journal of infection, 2003-08, Vol.47 (2), p.133-138

2003

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Changes in adiposity and excess body weight correlate with growth responses but not with decreases in low-density lipoprotein cholesterol levels during GH treatment in GH-deficient children

Clinical endocrinology (Oxford), 2002-06, Vol.56 (6), p.799-803

2002

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Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus

Endocrine Journal, 2004, Vol.51(5), pp.493-498

2004

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Association between birthweight and body mass index at 3 years of age

Pediatrics international, 2001-12, Vol.43 (6), p.641-646

2001

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Improved diabetes control by using 'close adjustment algorithms'

Pediatrics international, 2004-12, Vol.46 (6), p.678-684

2004

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Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib

Human genetics, 1998-10, Vol.103 (4), p.493-496

1998

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Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes

Immunogenetics (New York), 2002-07, Vol.54 (4), p.282-285

2002

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The Leu544Ile polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency

Long-term prospective study of body composition and lipid profiles during and after growth hormone (GH) treatment in children with GH deficiency : Gender-specific metabolic effects

Premature mortality and hypopituitarism

PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children

Juvenile idiopathic arthritis associated with autoimmune thyroid disorders and autoimmune cholangitis

Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese population

A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl‐phosphate synthetase‐1 activity in liver: A pitfall in enzymatic diagnosis for hyperammonaemia

A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes

Body composition, atherogenic risk factors and apolipoproteins following growth hormone treatment

Growth hormone treatment and type 2 diabetes

The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (α-glucosidase) inhibitor

Identification of a novel type 1 diabetes susceptibility gene, T-bet

An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency detected by newborn screening for maple syrup urine disease

Late-onset ornithine transcarbamylase deficiency in male patients: Prognostic factors and characteristics of plasma amino acid profile

Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with type 1 diabetes in the Japanese population

Lipoprotein (a) changes during growth hormone treatment

The Leu54411e polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency

Quantification of circulating varicella zoster virus-DNA for the early diagnosis of visceral varicella

Changes in adiposity and excess body weight correlate with growth responses but not with decreases in low-density lipoprotein cholesterol levels during GH treatment in GH-deficient children

Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus

Association between birthweight and body mass index at 3 years of age

Improved diabetes control by using 'close adjustment algorithms'

Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib

Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes

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