G. Massa

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Trends in age at diagnosis of Turner syndrome

F. de Zegher, M. Craen, C. Heinrichs, 2005, Archives of Disease in Childhood.

Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients

C. de Beaufort, Raoul Rooman, C. Mathieu, 2006, Clinical genetics.

Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity

L. V. Van Gaal, S. Verhulst, K. Desager, 2016, Endocrine.

Aberrant Mechanical Efficiency during Exercise Relates to Metabolic Health and Exercise Intolerance in Adolescents with Obesity

D. Hansen, P. Dendale, K. Verboven, 2021, International journal of environmental research and public health.

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations

T. de Ravel, K. Devriendt, R. Sciot, 2009, Genes, chromosomes & cancer.

Comparison of flash glucose monitoring with real time continuous glucose monitoring in children and adolescents with type 1 diabetes treated with continuous subcutaneous insulin infusion.

G. Massa, R. Zeevaert, Inge Gys, 2019, Diabetes research and clinical practice.

Growth hormone deficiency in a girl with the Cohen syndrome.

G. Massa, M. Vanderschueren‐Lodeweyckx, L. Dooms, 1991, Journal of medical genetics.

The Shape of the Plasma Glucose Curve During an Oral Glucose Tolerance Test as an Indicator of Beta Cell Function and Insulin Sensitivity in End-Pubertal Obese Girls

L. Bervoets, G. Massa, A. Mewis, 2014, Hormone and Metabolic Research.

Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene

W. Wuyts, G. Massa, S. Janssens de Varebeke, 2003, European Journal of Pediatrics.

Health and Psychosocial Status of Patients with Turner Syndrome after Transition to Adulthood: The Belgian Experience

M. Craen, C. Heinrichs, G. Massa, 2004, Hormone Research in Paediatrics.

Identification and functional characterization of a missense mutation in resistin in two patients with severe obesity and insulin resistance.

L. V. Van Gaal, S. Verhulst, K. Desager, 2011, European journal of endocrinology.

Body mass index measurements and prevalence of overweight and obesity in school-children living in the province of Belgian Limburg

G. Massa, 2002, European Journal of Pediatrics.

Exercise tolerance in obese vs. lean adolescents: a systematic review and meta‐analysis

T. Takken, F. Cools, D. Hansen, 2014, Obesity reviews : an official journal of the International Association for the Study of Obesity.

Identification and Functional Characterization of Novel Mutations in the Melanocortin-4 Receptor

L. V. Van Gaal, J. Timmermans, S. Verhulst, 2010, Obesity Facts.

Growth hormone therapy in Turner's syndrome: one versus two daily injections.

M. Craen, C. Heinrichs, G. Massa, 1994, The Journal of clinical endocrinology and metabolism.

Five‐year follow‐up of growth hormone antibodies in growth hormone deficient children treated with recombinant human growth hormone

R. Bouillon, G. Massa, M. Vanderschueren‐Lodeweyckx, 1993, Clinical endocrinology.

Cardiac function in adolescents with obesity: cardiometabolic risk factors and impact on physical fitness

D. Hansen, I. Frederix, P. Dendale, 2018, International Journal of Obesity.

Insulin Sensitivity Modulates the Growth Response during the First Year of High-Dose Growth Hormone Treatment in Short Prepubertal Children Born Small for Gestational Age

C. de Beaufort, Raoul Rooman, G. Massa, 2012, Hormone Research in Paediatrics.

Response to letter from Okutucu and Bursa

D. Hansen, L. Bruckers, W. Franssen, 2019, International Journal of Obesity.

Prevalence of the metabolic syndrome and impaired glucose tolerance in Flemish obese children

L. Bervoets, G. Massa, 2011 .

Identification and functional characterization of a missense mutation in resistin in 2 patients with severe obesity and insulin resistance Running Title: A missense mutation in resistin.

W. Hul, S. Verhulst, K. Desager, 2011 .

Prevalence and demographic features of childhood growth hormone deficiency in Belgium during the period 1986-2001.

F. de Zegher, M. Craen, C. Heinrichs, 2004, European journal of endocrinology.

Prevalence of rare MC3R variants in obese cases and lean controls

L. V. Van Gaal, K. Desager, W. Van Hul, 2013, Endocrine.

Classification and clinical characterization of metabolically “healthy” obese children and adolescents

L. Bervoets, G. Massa, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Increased incidence and prevalence of diabetes mellitus in Down’s syndrome

R. Hirasing, G. Massa, J. C. Van Goor, 1997, Archives of disease in childhood.

Serum levels of growth hormone‐binding protein and insulin‐like growth factor‐I during puberty *

R. Bouillon, G. Massa, M. Vanderschueren‐Lodeweyckx, 1992, Clinical endocrinology.

Treatment of osteogenesis imperfecta with the bisphosphonate olpadronate (dimethylaminohydroxypropylidene bisphosphonate)

G. Massa, S. Papapoulos, P. Maaswinkel-Mooy, 1997, European Journal of Pediatrics.

Effect of oestrogen status on serum levels of growth hormone‐binding protein and insulin‐like growth factor‐I in non‐pregnant and pregnant women

A. Igout, G. Massa, F. Frankenne, 1993, Clinical endocrinology.

Serum levels of growth hormone-binding protein and insulin-like growth factor I in children and adolescents with Type 1 (insulin-dependent) diabetes mellitus

R. Bouillon, G. Massa, M. Vanderschueren‐Lodeweyckx, 1993, Diabetologia.

Growth Hormone-Binding Proteins during Human Pregnancy: Maternal, Fetal and Neonatal Data

G. Massa, G. Massa, 1994, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Serum growth hormone (GH)-binding protein and insulin-like growth factor-I levels in Turner's syndrome before and during treatment with recombinant human GH and ethinyl estradiol.

R. Bouillon, G. Massa, M. Vanderschueren‐Lodeweyckx, 1992, The Journal of clinical endocrinology and metabolism.

The influence of age and gender on sensitization to aero‐allergens

K. Verhamme, G. Massa, F. Baets, 2007, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Adult Height after Growth Hormone Treatment at Pubertal Onset in Short Adolescents Born Small for Gestational Age: Results from a Belgian Registry-Based Study

Raoul Rooman, M. Roelants, G. Massa, 2018, International journal of endocrinology.

Concerns, Expectations and Perception Regarding Stature, Physical Appearance and Psychosocial Functioning before and during High-Dose Growth Hormone Treatment of Short Pre-pubertal Children Born Small for Gestational Age

C. de Beaufort, Raoul Rooman, M. Craen, 2008, Hormone Research in Paediatrics.

Effect of 2 years of high-dose growth hormone therapy on cognitive and psychosocial development in short children born small for gestational age.

C. de Beaufort, Raoul Rooman, M. Craen, 2007, European journal of endocrinology.

Late or delayed induced or spontaneous puberty in girls with Turner syndrome treated with growth hormone does not affect final height.

M. Craen, C. Heinrichs, G. Massa, 2003, The Journal of clinical endocrinology and metabolism.

Plasma Levels of Insulin-Like Growth Factor (IGF)-I, IGF-II and IGF-Binding Protein-3 in the Evaluation of Childhood Growth Hormone Deficiency

J. Wit, J. van den Brande, J. van Doorn, 1998, Hormone Research in Paediatrics.

Growth-promoting effect of growth hormone and low dose ethinyl estradiol in girls with Turner's syndrome.

M. Craen, C. Heinrichs, G. Massa, 1990, The Journal of clinical endocrinology and metabolism.

Serum Growth Hormone-Binding Proteins in the Human Fetus and Infant

G. Massa, F. Zegher, M. Vanderschueren‐Lodeweyckx, 1992, Pediatric Research.

Initial characterization and sexual dimorphism of serum growth hormone-binding protein in adult rats.

J. Ketelslegers, G. Massa, M. Maes, 1990, Endocrinology.

Rare Heterozygous PCSK1 Variants in Human Obesity: The Contribution of the p.Y181H Variant and a Literature Review

S. Verhulst, W. Van Hul, K. Van Hoorenbeeck, 2022, Genes.

Effect of nationwide reimbursement of real-time continuous glucose monitoring on HbA1c, hypoglycemia and quality of life in a pediatric type 1 diabetes population: The RESCUE-pediatrics study

C. D. De Block, K. Casteels, P. Gillard, 2022, Frontiers in Pediatrics.

Effect of growth hormone therapy on thyroid status of girls with Turner's syndrome *

G. Massa, F. Zegher, M. Vanderschueren‐Lodeweyckx, 1991, Clinical endocrinology.

Effects of total-body irradiation on growth, thyroid and pituitary gland in rhesus monkeys.

J. J. Broerse, J. Wit, J. Broerse, 1999, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Care delivery and outcomes among Belgian children and adolescents with type 1 diabetes

Raoul Rooman, K. Casteels, H. Dorchy, 2012, European Journal of Pediatrics.

Identification of Three Novel Genetic Variants in the Melanocortin‐3 Receptor of Obese Children

Raoul Rooman, L. V. Van Gaal, J. Timmermans, 2011, Obesity.

Hypothalamo-pituitary dysfunction in congenital toxoplasmosis

E. Eggermont, M. Craen, G. Massa, 1989, European Journal of Pediatrics.

Needle detachment from the Sure-T® infusion set in two young children with diabetes mellitus (DM) treated with continuous subcutaneous insulin infusion (CSII) and unexplained hyperglycaemia

G. Massa, Inge Gys, Anniek Op’t Eyndt, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Isolated GH deficiency with dominant inheritance: new mutations, new insights.

G. Binder, J. Wit, M. Ranke, 2001, The Journal of clinical endocrinology and metabolism.

Growth Hormone (GH) Secretion in Patients with Childhood-Onset GH Deficiency: Retesting after One Year of Therapy and at Final Height

M. Craen, C. Heinrichs, G. Massa, 2003, Hormone Research in Paediatrics.

Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).

J. Fryns, H. van den Berghe, G. Massa, 1993, Genetic counseling.

Pubertal development and growth after total-body irradiation and bone marrow transplantation for haematological malignancies

J. Wit, G. Massa, J. Vossen, 2000, European Journal of Pediatrics.

Altered gas-exchange at peak exercise in obese adolescents: implications for verification of effort during cardiopulmonary exercise testing.

T. Takken, D. Hansen, L. Bervoets, 2017, The Journal of sports medicine and physical fitness.

Nucleotide variation of sFRP5 gene is not associated with obesity in children and adolescents

L. V. Van Gaal, S. Verhulst, K. Desager, 2016, Molecular Biology Reports.

Gonadal function and bone marrow transplantation.

J. Wit, G. Massa, J. Vossen, 1997, The Journal of pediatrics.

Protein malnutrition due to replacement of milk by rice drink

G. Massa, P. Gillis, P. Alliet, 2001, European Journal of Pediatrics.

Metabolic profiling of type 1 diabetes mellitus in children and adolescents: a case–control study

P. Adriaensens, E. Louis, L. Bervoets, 2017, Diabetology & Metabolic Syndrome.

Deletion of the short arm of the X chromosome: A hereditary form of Turner syndrome

J. Fryns, G. Massa, M. Vanderschueren‐Lodeweyckx, 1992, European Journal of Pediatrics.

Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents

L. V. Van Gaal, S. Verhulst, W. Van Hul, 2018, Annals of Human Genetics.

Genetic and structural variation in the SH2B1 gene in the Belgian population.

Raoul Rooman, L. V. Van Gaal, S. Verhulst, 2015, Molecular genetics and metabolism.

Identification of mutations in the NUCB2/nesfatin gene in children with severe obesity.

Raoul Rooman, L. V. Van Gaal, K. Desager, 2012, Molecular genetics and metabolism.

Final Height in Children with Idiopathic Growth Hormone Deficiency Treated with Recombinant Human Growth Hormone: The Belgian Experience

Raoul Rooman, F. de Zegher, M. Craen, 2001, Hormone Research in Paediatrics.

CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity

L. V. Van Gaal, S. Verhulst, W. Van Hul, 2016, Obesity.

Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.

L. V. Van Gaal, S. Verhulst, W. Van Hul, 2016, Molecular genetics and metabolism.

46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.

H. van den Berghe, G. Massa, J. Fryns, 1992, Annales de genetique.

Steroid 11-Beta-Hydroxylase Deficiency Caused by Compound Heterozygosity for a Novel Mutation, p.G314R, in One CYP11B1 Allele, and a Chimeric CYP11B2/CYP11B1 in the Other Allele

B. Wolffenbuttel, J. Wit, Y. Shizuta, 2005, Hormone Research in Paediatrics.

Screening for genetic variants in BDNF that contribute to childhood obesity

Raoul Rooman, W. Hul, L. V. Van Gaal, 2014, Pediatric obesity.

Copy number variant analysis and expression profiling of the olfactory receptor-rich 11q11 region in obesity predisposition

L. V. Van Gaal, S. Verhulst, W. Van Hul, 2020, Molecular genetics and metabolism reports.

Germline mutation in the STK11 gene in a girl with an ovarian Sertoli cell tumour

J. Gille, M. Renard, G. Massa, 2007, European Journal of Pediatrics.

Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity

Raoul Rooman, W. Hul, S. Verhulst, 2014, International Journal of Obesity.

with the Cohen syndrome . Growth hormone deficiency in a girl

G. Massa, M. Vanderschueren‐Lodeweyckx, L. Dooms, 2022 .

Clinical, hormonal and imaging findings in 27 children with central diabetes insipidus

C. Christophe, C. Heinrichs, G. Massa, 2006, European Journal of Pediatrics.

Serum levels of immunoreactive inhibin, FSH, and LH in human infants at preterm and term birth.

F. de Zegher, G. Massa, F. Zegher, 1992, Biology of the neonate.

Identification of metabolic phenotypes in childhood obesity by 1H NMR metabolomics of blood plasma

P. Adriaensens, G. Reekmans, L. Bervoets, 2018, Future science OA.

Psychosocial Functioning, Self-Perception and Body Image and Their Auxologic Correlates in Growth Hormone and Oestrogen-Treated Young Adult Women with Turner Syndrome

M. Craen, G. Massa, J. De Schepper, 2006, Hormone Research in Paediatrics.

Long‐term results of growth hormone therapy in children with short stature, subnormal growth rate and normal growth hormone response to secretagogues

H. Delemarre-van de Waal, J. Wit, B. Otten, 1995 .

Final height in girls with Turner’s syndrome treated with once or twice daily growth hormone injections

T. Stijnen, A. Hokken-Koelega, S. Drop, 1999, Archives of disease in childhood.

Treatment with two growth hormone regimens in girls with Turner syndrome: final height results. Dutch Growth Hormone Working Group.

H. Delemarre-van de Waal, B. Otten, S. de Muinck Keizer-Schrama, 1995, Hormone research.

Linear growth in patients with Turner syndrome: Influence of spontaneous puberty and parental height

G. Massa, P. Malvaux, M. Vanderschueren‐Lodeweyckx, 2005, European Journal of Pediatrics.

Age and height at diagnosis in Turner syndrome: influence of parental height.

G. Massa, G G Massa, M Vanderschueren-Lodeweyckx, 1991, Pediatrics.

Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: results of a randomized dose-response trial.

T. Stijnen, B. Otten, S. Drop, 1999, The Journal of clinical endocrinology and metabolism.

Aetiology of growth hormone deficiency

E. Eggermont, G. Massa, M. Vanderschueren‐Lodeweyckx, 1988 .

Evaluation of the FreeStyle® Libre Flash Glucose Monitoring System in Children and Adolescents with Type 1 Diabetes

G. Massa, Renate Zeevaert, Guy G. Massa, 2018, Hormone Research in Paediatrics.

CMO I deficiency caused by a point mutation in exon 8 of the human CYP11B2 gene encoding steroid 18-hydroxylase (P450C18).

S. Onishi, H. Imura, J. Fukata, 1997, Biochemical and biophysical research communications.

Quality of life and retrospective perception of the effect of growth hormone treatment in adult patients with childhood growth hormone deficiency.

F. de Zegher, M. Craen, C. Heinrichs, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

A de-novo 15q24.2 deletion involving SIN3A is associated with emotional, behavioural, motor problems and hypersensitivity in a girl with above average intelligence and typical facial features.

H. Peeters, G. Massa, A. Swillen, 2020, Clinical dysmorphology.

Severe weight gain in 2 boys treated with risperidone

L. Bervoets, G. Massa, Sanne Nelissen, 2010 .

Hyperthyroidism accelerates growth in Turner's syndrome

G. Massa, F. Zegher, M. Vanderschueren‐Lodeweyckx, 1992, Acta paediatrica.

Defining morbid obesity in children based on BMI 40 at age 18 using the extended international (IOTF) cut‐offs

L. Bervoets, G. Massa, G Massa, 2014, Pediatric obesity.

Ontogeny and nutritional regulation of the serum growth hormone-binding protein in the rat.

J. Ketelslegers, G. Massa, M. Maes, 1991, Acta endocrinologica.

The Belgian Genotropin Turner Trial: Preliminary Results

G. Massa, M. Maes, M. VANDERSCHUEREN‐LODEWEYCKX, 1989 .

Prognosis in fetal valproate syndrome.

P. Casaer, G. Massa, D. Lecoutere, 1987, The Journal of pediatrics.

[Micropenis in children: etiology, diagnosis and therapy].

J. Wit, G. Massa, W. Oostdijk, 1997, Nederlands tijdschrift voor geneeskunde.

A valuable improvement of adult height prediction methods in short normal children.

J. Bourguignon, G. Massa, J. Bourguignon, 1997, Hormone research.

European Obesity Summit (EOS) – Joint Congress of EASO and IFSO-EC, Gothenburg, Sweden, June 1 – 4, 2016: Abstracts

Parashu Ram Pal, S. A. Todd, Jimmy D Bell, 2016, Obesity Facts.

Final height of short normal children treated with growth hormone

J. Wit, G. Massa, Lyset TM Rakers-Mombarg, 1996, The Lancet.

Chronotropic incompetence is more frequent in obese adolescents and relates to systemic inflammation and exercise intolerance.

D. Hansen, P. Dendale, K. Verboven, 2021, Journal of sport and health science.

Length Velocity Acceleration at 9 Months of Age in a Representative Birth Cohort of Dutch Infants

J. van den Broeck, J. Wit, R. Brand, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Fear of Hypoglycemia, Parenting Stress, and Metabolic Control for Children with Type 1 Diabetes and Their Parents

T. Van Daele, G. Massa, A. Viaene, 2017, Journal of Clinical Psychology in Medical Settings.

Mutation analysis of WNT10B in obese children, adolescents and adults

W. Hul, S. Verhulst, K. Desager, 2013, Endocrine.

C. de Beaufort, Raoul Rooman, M. Craen, 2008, Hormone Research in Paediatrics.

Influence of spontaneous or induced puberty on the growth promoting effect of treatment with growth hormone in girls with Turner's syndrome

M. Craen, C. Heinrichs, G. Massa, 1993, Clinical endocrinology.

Spondyloepiphyseal Dysplasia Tarda in Turner Syndrome

G. Massa, M. Vanderschueren‐Lodeweyckx, 1989, Acta paediatrica Scandinavica.

Screening for genetic variants in BDNF that contribute to childhood obesity

Raoul Rooman, W. Hul, L. Gaal, 2014, Pediatric obesity.

Differentiation of the plasma metabolite profile detected with 1H-NMR spectroscopy of obese and normal-weight children and adolescents

P. Adriaensens, G. Reekmans, L. Bervoets, 2013 .

Maternal determinants of child survival in a rural African community.

J. van den Broeck, G. Massa, G. Massa, 1996, International journal of epidemiology.