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Determinants of Early Atherosclerosis in Obese Children and Adolescents

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.3025-3032

2007

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Criteria for First-Year Growth Response to Growth Hormone Treatment in Prepubertal Children With Growth Hormone Deficiency: Do They Predict Poor Adult Height Outcome?

Frontiers in endocrinology (Lausanne), 2019-11, Vol.10, p.792-792

2019

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Longitudinal Changes in Acylated versus Unacylated Ghrelin Levels May Be Involved in the Underlying Mechanisms of the Switch in Nutritional Phases in Prader-Willi Syndrome

Hormone research in paediatrics, 2024-01, Vol.97 (4), p.343-352

2024

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Correlation Between the Responses to Growth Hormone (GH) Treatment During Childhood and Adulthood in a Monocentric Cohort of GH-Deficient Patients

Hormone and metabolic research, 2018-06, Vol.50 (6), p.462-468

2018

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Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Therapeutic advances in endocrinology and metabolism, 2017-01, Vol.8 (1-2), p.3-13

2017

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Characterization of insulin resistance in young adult survivors of childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma

Clinical endocrinology (Oxford), 2013-05, Vol.78 (5), p.790-798

2013

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Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series

Hormone research in paediatrics, 2018-01, Vol.89 (6), p.423-433

2018

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Characteristics and Determinants of Partial Remission in Children with Type 1 Diabetes Using the Insulin-Dose-Adjusted A1C Definition

Journal of Diabetes Research, 2014-01, Vol.2014 (2014), p.1-7

2014

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Long-Term Effects on Bone Mineral Density of Different Therapeutic Schemes for Acute Lymphoblastic Leukemia or Non-Hodgkin Lymphoma during Childhood

Hormone research in paediatrics, 2010-01, Vol.74 (4), p.241-250

2010

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Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22

American journal of medical genetics. Part A, 2013-12, Vol.161A (12), p.3176-3181

2013

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Evaluation of a 5-year multidisciplinary approach for the treatment of childhood obesity

Public health nutrition, 2012-08, Vol.15 (8A), p.1543-1543

2012

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Efficacy and safety of a 4-year combination therapy of growth hormone and gonadotropin-releasing hormone analogue in pubertal girls with short predicted adult height

Frontiers in endocrinology (Lausanne), 2023, Vol.14, p.1113750-1113750

2023

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Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome

The journal of clinical endocrinology and metabolism, 2013-06, Vol.98 (6), p.E1072-E1087

2013

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Multiple neoplasia in a 15-year-old girl with familial adenomatous polyposis

Journal of pediatric hematology/oncology, 2009-07, Vol.31 (7), p.530-532

2009

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Papillary thyroid carcinoma in a 9-year-old girl with ataxia-telangiectasia

Pediatric blood & cancer, 2008-05, Vol.50 (5), p.1058-1060

2008

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Blood urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Therapeutic advances in endocrinology and metabolism, 2017-01, Vol.8

2017

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Prader‐Willi syndrome: A model for understanding the ghrelin system

Journal of neuroendocrinology, 2019-07, Vol.31 (7), p.e12728-n/a

2019

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Impairment of Liver GH Receptor Signaling by Fasting

Endocrinology (Philadelphia), 2002-03, Vol.143 (3), p.792-800

2002

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GHRH excess and blockade in X-LAG syndrome

Endocrine-related cancer, 2016-03, Vol.23 (3), p.161-170

2016

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Effects of maternal protein malnutrition on fetal growth, plasma insulin-like growth factors, insulin-like growth factor binding proteins, and liver insulin-like growth factor gene expression in the rat

Pediatric research, 1995-03, Vol.37 (3), p.334-342

1995

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High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome

Orphanet journal of rare diseases, 2016-05, Vol.11 (1), p.56-56, Article 56

2016

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A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease

Journal of Pediatric Endocrinology and Metabolism, 2014-09, Vol.27 (9-10), p.1005

2014

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Announcement of an updated Belgian consensus on the assessment and management of obesity

Acta clinica belgica (English ed. Online), 2020-09, Vol.75 (5), p.375-377

2020

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Determinants of Early Atherosclerosis in Obese Children and Adolescents

Criteria for First-Year Growth Response to Growth Hormone Treatment in Prepubertal Children With Growth Hormone Deficiency: Do They Predict Poor Adult Height Outcome?

Longitudinal Changes in Acylated versus Unacylated Ghrelin Levels May Be Involved in the Underlying Mechanisms of the Switch in Nutritional Phases in Prader-Willi Syndrome

Correlation Between the Responses to Growth Hormone (GH) Treatment During Childhood and Adulthood in a Monocentric Cohort of GH-Deficient Patients

Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Characterization of insulin resistance in young adult survivors of childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma

Familial Forms of Cushing Syndrome in Primary Pigmented Nodular Adrenocortical Disease Presenting with Short Stature and Insidious Symptoms: A Clinical Series

Characteristics and Determinants of Partial Remission in Children with Type 1 Diabetes Using the Insulin-Dose-Adjusted A1C Definition

Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

Long-Term Effects on Bone Mineral Density of Different Therapeutic Schemes for Acute Lymphoblastic Leukemia or Non-Hodgkin Lymphoma during Childhood

Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22

Evaluation of a 5-year multidisciplinary approach for the treatment of childhood obesity

Efficacy and safety of a 4-year combination therapy of growth hormone and gonadotropin-releasing hormone analogue in pubertal girls with short predicted adult height

Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome

Multiple neoplasia in a 15-year-old girl with familial adenomatous polyposis

Papillary thyroid carcinoma in a 9-year-old girl with ataxia-telangiectasia

Blood urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study

Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

Prader‐Willi syndrome: A model for understanding the ghrelin system

Impairment of Liver GH Receptor Signaling by Fasting

GHRH excess and blockade in X-LAG syndrome

Effects of maternal protein malnutrition on fetal growth, plasma insulin-like growth factors, insulin-like growth factor binding proteins, and liver insulin-like growth factor gene expression in the rat

High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome

A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease

Announcement of an updated Belgian consensus on the assessment and management of obesity

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