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Are family factors universally related to metabolic outcomes in adolescents with Type 1 diabetes?

Diabetic medicine, 2008-04, Vol.25 (4), p.463-468

2008

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Insulin management and metabolic control of Type 1 diabetes mellitus in childhood and adolescence in 18 countries

Diabetic medicine, 1998-09, Vol.15 (9), p.752-759

1998

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Panhypopituitarism: genetic versus acquired etiological factors

Journal of pediatric endocrinology & metabolism : JPEM, 2007-01, Vol.20 (1), p.27

2007

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Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus

Autoimmunity (Chur, Switzerland), 2005-09, Vol.38 (6), p.439-444

2005

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Clinical dilemmas arising from the increased intake of iodine in the Spanish population and the recommendation for systematic prescription of potassium iodide in pregnant and lactating women (Consensus of the TDY Working Group of SEEN)

Journal of endocrinological investigation, 2009-02, Vol.32 (2), p.184-191

2009

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Lessons from the Hvidoere International Study Group on childhood diabetes: be dogmatic about outcome and flexible in approach

Pediatric diabetes, 2013-11, Vol.14 (7), p.473-480

2013

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Good Metabolic Control Is Associated With Better Quality of Life in 2,101 Adolescents With Type 1 Diabetes

Diabetes care, 2001-11, Vol.24 (11), p.1923-1928

2001

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Thyroid hormone resistance from newborns to adults: a Spanish experience

Journal of endocrinological investigation, 2019-08, Vol.42 (8), p.941-949

2019

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No Effect of the Altered Peptide Ligand NBI-6024 on β-Cell Residual Function and Insulin Needs in New-Onset Type 1 Diabetes

Diabetes care, 2009-11, Vol.32 (11), p.2036-2040

2009

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Clinical evaluation and health care in childhood and adolescent obesity

Journal of pediatric endocrinology & metabolism : JPEM, 2005-01, Vol.18 Suppl 1, p.1207

2005

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Associations between physical activity, sedentary behavior, and glycemic control in a large cohort of adolescents with type 1 diabetes: the Hvidoere Study Group on Childhood Diabetes

Pediatric diabetes, 2009-06, Vol.10 (4), p.234-239

2009

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Functional Study of a Novel Single Deletion in the TITF1/NKX2.1 Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress

The journal of clinical endocrinology and metabolism, 2006-05, Vol.91 (5), p.1832-1841

2006

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Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trial

European journal of endocrinology, 2012-10, Vol.167 (4), p.523

2012

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Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

Clinical endocrinology (Oxford), 2007-10, Vol.67 (4), p.538-546

2007

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Childhood-onset congenital adrenal hyperplasia: long-term outcome and optimization of therapy

Journal of pediatric endocrinology & metabolism : JPEM, 2004-03, Vol.17 Suppl 3, p.411

2004

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Effect of Cyclic 3′,5′-Adenosine Monophosphate, Glucocorticoids, and Insulin on Leptin Messenger RNA Levels and Leptin Secretion in Cultured Human Trophoblast1

Biology of reproduction, 2001-09, Vol.65 (3), p.814-819

2001

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Dual growth hormone (GH) response to repeated GH releasing hormone stimulus in children and adults

Journal of pediatric endocrinology & metabolism : JPEM, 2004-05, Vol.17 (5), p.743

2004

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Circulating non-22 kDa growth hormone isoforms after a repeated GHRH stimulus in normal subjects

Growth hormone & IGF research, 2005-04, Vol.15 (2), p.123-129

2005

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Prospective Population Screening for Celiac Disease: High Prevalence in the First 3 Years of Life

Journal of pediatric gastroenterology and nutrition, 2004-07, Vol.39 (1), p.80-84

2004

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Insulin injection regimens and metabolic control in an international survey of adolescents with type 1 diabetes over 3 years: results from the Hvidore study group

European journal of pediatrics, 2003, Vol.162 (1), p.22-29

2003

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Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism Genotype Frequencies in Spanish Short Small-for-Gestational-Age (SGA) Children and Adolescents (n = 247) and in an Adult Control Population (n = 289) Show Increased fl/fl in Short SGA

The journal of clinical endocrinology and metabolism, 2006-12, Vol.91 (12), p.5038-5043

2006

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Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family

Journal of pediatric endocrinology & metabolism : JPEM, 2001-03, Vol.14 (3), p.295

2001

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Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis

Journal of pediatric endocrinology & metabolism : JPEM, 2002-07, Vol.15 (7), p.1047

2002

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Hypogonadotrophic hypogonadism with hyposmia, X-linked ichthyosis, and renal malformation syndrome

Clinical endocrinology (Oxford), 1995-02, Vol.42 (2), p.121-128

1995

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Are family factors universally related to metabolic outcomes in adolescents with Type 1 diabetes?

Insulin management and metabolic control of Type 1 diabetes mellitus in childhood and adolescence in 18 countries

Panhypopituitarism: genetic versus acquired etiological factors

Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus

Clinical dilemmas arising from the increased intake of iodine in the Spanish population and the recommendation for systematic prescription of potassium iodide in pregnant and lactating women (Consensus of the TDY Working Group of SEEN)

Lessons from the Hvidoere International Study Group on childhood diabetes: be dogmatic about outcome and flexible in approach

Good Metabolic Control Is Associated With Better Quality of Life in 2,101 Adolescents With Type 1 Diabetes

Thyroid hormone resistance from newborns to adults: a Spanish experience

Persistent Differences Among Centers Over 3 Years in Glycemic Control and Hypoglycemia in a Study of 3,805 Children and Adolescents With Type 1 Diabetes From the Hvidøre Study Group

No Effect of the Altered Peptide Ligand NBI-6024 on β-Cell Residual Function and Insulin Needs in New-Onset Type 1 Diabetes

Clinical evaluation and health care in childhood and adolescent obesity

Associations between physical activity, sedentary behavior, and glycemic control in a large cohort of adolescents with type 1 diabetes: the Hvidoere Study Group on Childhood Diabetes

Functional Study of a Novel Single Deletion in the TITF1/NKX2.1 Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress

Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trial

Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

Childhood-onset congenital adrenal hyperplasia: long-term outcome and optimization of therapy

Effect of Cyclic 3′,5′-Adenosine Monophosphate, Glucocorticoids, and Insulin on Leptin Messenger RNA Levels and Leptin Secretion in Cultured Human Trophoblast1

Dual growth hormone (GH) response to repeated GH releasing hormone stimulus in children and adults

Circulating non-22 kDa growth hormone isoforms after a repeated GHRH stimulus in normal subjects

Prospective Population Screening for Celiac Disease: High Prevalence in the First 3 Years of Life

Insulin injection regimens and metabolic control in an international survey of adolescents with type 1 diabetes over 3 years: results from the Hvidore study group

Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism Genotype Frequencies in Spanish Short Small-for-Gestational-Age (SGA) Children and Adolescents (n = 247) and in an Adult Control Population (n = 289) Show Increased fl/fl in Short SGA

Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family

Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis

Hypogonadotrophic hypogonadism with hyposmia, X-linked ichthyosis, and renal malformation syndrome

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