S. Tenoutasse

发表

Management of familial hypercholesterolemia in children and young adults: consensus paper developed by a panel of lipidologists, cardiologists, paediatricians, nutritionists, gastroenterologists, general practitioners and a patient organization.

C. de Beaufort, G. De Backer, J. Balligand, 2011, Atherosclerosis.

Genetic variation at ERBB3/IKZF4 and sexual dimorphism in epitope spreading in single autoantibody-positive relatives

C. D. De Block, B. Keymeulen, F. Gorus, 2021, Diabetologia.

Diabetic ketoacidosis in children newly diagnosed with type 1 diabetes mellitus: Role of demographic, clinical, and biochemical features along with genetic and immunological markers as risk factors. A 20‐year experience in a tertiary Belgian center

H. Dorchy, S. Tenoutasse, A. Messaaoui, 2019, Pediatric diabetes.

Screening for insulinoma antigen 2 and zinc transporter 8 autoantibodies: a cost‐effective and age‐independent strategy to identify rapid progressors to clinical onset among relatives of type 1 diabetic patients

D. Pipeleers, J. Wenzlau, J. Hutton, 2013, Clinical and experimental immunology.

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.

IGF-I Transcript Levels in Whole-Liver Tissue, in Freshly Isolated Hepatocytes, and in Cultured Hepatocytes from Lean and Obese Zucker Rats

C. Deal, G. Van Vliet, S. Tenoutasse, 2003, Hormone Research in Paediatrics.

L'acidocétose diabétique: diagnostic, prise en charge, prévention.

H. Dorchy, S. Tenoutasse, T. Mouraux, 2010 .

Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.

M. Polak, A. Grüters, Z. Hochberg, 2011, The Journal of clinical endocrinology and metabolism.

[Diabetic ketoacidosis: diagnosis, management, prevention].

H. Dorchy, S. Tenoutasse, T. Mouraux, 2010, Revue medicale de Bruxelles.

Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager.

W. Lissens, G. Andry, C. Heinrichs, 2009, European journal of endocrinology.

Comparison Between Continuous Versus Flash Glucose Monitoring in Children, Adolescents, and Young Adults with Type 1 Diabetes: An 8-Week Prospective Randomized Trial

S. Tenoutasse, A. Messaaoui, L. Crenier, 2022, Diabetes Therapy.

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

Raoul Rooman, J. De Schepper, V. Beauloye, 2019, Front. Endocrinol..

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.

Children With Sickle Cell Disease: Growth and Gonadal Function After Hematopoietic Stem Cell Transplantation

C. Heinrichs, A. Ferster, C. Devalck, 2007, Journal of pediatric hematology/oncology.

Flash Glucose Monitoring Accepted in Daily Life of Children and Adolescents with Type 1 Diabetes and Reduction of Severe Hypoglycemia in Real-Life Use.

S. Tenoutasse, A. Messaaoui, L. Crenier, 2019, Diabetes technology & therapeutics.

Anti-SARS-CoV-2 antibodies in new-onset type 1 diabetes in children during pandemic in Belgium

S. Tenoutasse, A. Messaaoui, L. Hajselova, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Adult final height after GH therapy for irradiation-induced GH deficiency in childhood survivors of brain tumors: the Belgian experience.

J. Jamart, J. De Schepper, M. Thomas, 2010, European journal of endocrinology.

Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.

B. Velkeniers, C. Christophe, J. Rutishauser, 2011, European journal of endocrinology.

Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

A. Janecke, M. Bros, C. Hübner, 2011, Nature Genetics.

Accelerated Progression to Type 1 Diabetes in the Presence of HLA-A*24 and -B*18 Is Restricted to Multiple Islet Autoantibody–Positive Individuals With Distinct HLA-DQ and Autoantibody Risk Profiles

D. Pipeleers, K. Casteels, B. Keymeulen, 2018, Diabetes Care.

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

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

The Retina in Patients With Triple A Syndrome: A Window Into Neurodegeneration?

I. Balikova, C. Heinrichs, C. Vilain, 2021, Frontiers in Endocrinology.

Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty

C. Libioulle, C. Heinrichs, S. Tenoutasse, 2022, Journal of the Endocrine Society.

Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes

C. Dangoisse, L. Larizza, Y. Sznajer, 2008, European Journal of Pediatrics.

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

Raoul Rooman, S. Verhulst, M. Cools, 2023, Frontiers in Endocrinology.

Inverse Relationship between Glomerular Hyperfiltration and C-Peptide Level in Type 1 Diabetes

Anissa Messaaoui, Sylvie Tenoutasse, Christian Melot, 2014 .

CTLA4, SH2B3, and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of Type 1 diabetes patients

C. D. De Block, B. Keymeulen, F. Gorus, 2023, Clinical and experimental immunology.

Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage

C. Heinrichs, G. Van Vliet, S. Tenoutasse, 2016, Hormone Research in Paediatrics.