M. D. de Vroede

发表

Neonatal cardiac hypertrophy: the role of hyperinsulinism—a review of literature

J. Breur, M. de Vroede, R. Stegeman, 2019, European Journal of Pediatrics.

Fetal Sex Determination From Maternal Plasma in Pregnancies at Risk for Congenital Adrenal Hyperplasia

R. Rijnders, C. E. van der Schoot, G. Christiaens, 2001, Obstetrics and gynecology.

Bone mineral density in children with moderate to severe atopic dermatitis.

M. D. de Bruin‐Weller, M. Knol, S. Pasmans, 2010, Journal of the American Academy of Dermatology.

Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism

P. Macchia, M. Zannini, C. Ris-Stalpers, 2010, Clinical endocrinology.

An amino-terminal DAX1 (NROB1) missense mutation associated with isolated mineralocorticoid deficiency.

R. Sinke, J. Giltay, J. Jameson, 2007, The Journal of clinical endocrinology and metabolism.

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.

L. Notarangelo, V. Lougaris, A. Plebani, 2011, Clinical immunology.

Insulin-like growth factor receptors.

M. Rechler, S. Nissley, M. de Vroede, 1985, Journal of cell science. Supplement.

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

P. Donohoue, M. Fassnacht, L. Dunkel, 2005, The Journal of clinical endocrinology and metabolism.

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.

J. Drouin, C. Deal, A. Pulichino, 2003, Genes & development.

[Discovery of fructose intolerance in a case of acute liver failure in a 16-month-old child].

S. Cadranel, H. Loeb, R. Heimann, 1980, Pediatrie.

A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction.

E. Kalkhoven, R. Berger, N. Verhoeven-Duif, 2012, JIMD reports.

Modulation of insulinlike growth factor I binding to human fibroblast monolayer cultures by insulinlike growth factor carrier proteins released to the incubation media.

M. Rechler, S. Nissley, P. Katsoyannis, 1986, The Journal of clinical investigation.

Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findings.

W. Feremans, P. Fondu, E. Vamos, 2009, Scandinavian journal of haematology.

Cardiovascular and metabolic outcome in 6-8 year old offspring of women with type 1 diabetes with near-optimal glycaemic control during pregnancy.

G. Visser, H. D. de Valk, C. Heijnen, 2011, Early human development.

Hypertrophic cardiomyopathy in Donohue syndrome

J. Breur, M. de Vroede, J. Termote, 2015, Cardiology in the Young.

Interaction of insulin-like growth factors with a nonfusing mouse muscle cell line: binding, action, and receptor down-regulation.

M. Rechler, S. Nissley, M. Standaert, 1984, Endocrinology.

Laparoscopic Diagnosis and Cure of Hyperinsulinism in Two Cases of Focal Adenomatous Hyperplasia in Infancy

F. Groenendaal, K. Brusgaard, M. Dunne, 2004, Pediatrics.

Hybrid molecules containing the B-domain of insulin-like growth factor I are recognized by carrier proteins of the growth factor.

M. Rechler, S. Nissley, P. Katsoyannis, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Insulin-Like Growth Factor Receptors

M. Rechler, S. Nissley, M. de Vroede, 1985, Journal of Cell Science.

Risk Factors for Childhood Overweight in Offspring of Type 1 Diabetic Women With Adequate Glycemic Control During Pregnancy

G. Visser, H. D. de Valk, C. Heijnen, 2009, Diabetes Care.

Hypertrophic cardiomyopathy in Donohue syndrome

J. Breur, J. Termote, M. D. de Vroede, 2015, Cardiology in the Young.