Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Monique A. M. J. de Vroede"'
Autor:
Johannes M.P.J. Breur, Nina D. Paauw, Matthias W. Freund, Jacqueline U.M. Termote, Monique A. M. J. de Vroede, Raymond Stegeman
Publikováno v:
European Journal of Pediatrics
European Journal of Pediatrics, 179(1), 39. Springer Verlag
European Journal of Pediatrics, 179(1), 39. Springer Verlag
Hypertrophic cardiomyopathy (HCM) in neonates is a rare and heterogeneous disorder which is characterized by hypertrophy of heart with histological and functional disruption of the myocardial structure/composition. The prognosis of HCM depends on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb67cf9d8b5ff62b630aeefa27179905
https://doi.org/10.1007/s00431-019-03521-6
https://doi.org/10.1007/s00431-019-03521-6
Publikováno v:
Cardiology in the Young. 26:815-818
We report the case of a patient with Donohue syndrome who died of heart failure due to obstructive hypertrophic cardiomyopathy. A literature survey revealed that hypertrophic cardiomyopathy was present in 30% of these patients and was often fatal. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7dc5709969ee08db5e88e58e5937741
https://doi.org/10.1017/s1047951115002437
https://doi.org/10.1017/s1047951115002437
Autor:
Paolo Emidio Macchia, Carrie Ris-Stalpers, Mariastella Zannini, Maria Grazia Filippone, Monique A. M. J. de Vroede, Tina Di Palma, Emilia Zampella
Publikováno v:
Clinical Endocrinology. 73:808-814
Summary Background Congenital hypothyroidism (CH) is a common endocrine disease that occurs in about 1:3000 newborns. In 80–85% of the cases, CH is presumably secondary to thyroid dysgenesis (TD), a defect in the organogenesis of the gland leading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86afb20c6556c9613edda2f990e8936d
https://doi.org/10.1111/j.1365-2265.2010.03851.x
https://doi.org/10.1111/j.1365-2265.2010.03851.x
Autor:
Monique A. M. J. de Vroede, Cobi Jacoba Johanna Heijnen, Inge M. Evers, Maarten Rijpert, Gerard H. A. Visser, Harold W. de Valk
Publikováno v:
Diabetes Care
OBJECTIVE Pregnancy in type 1 diabetic women remains a high-risk situation for both mother and child. In this study, we investigated long-term effects on body composition, prevalence of overweight, and insulin resistance in children of type 1 diabeti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacc574c1c44a66fef9ef9294b86698f
https://doi.org/10.2337/dc09-0652
https://doi.org/10.2337/dc09-0652
Autor:
Klara Flipsen-ten Berg, P F Ron Hochstenbach, Martin Poot, Marc J. Eleveld, Frits A. Beemer, Peter M. van Hasselt, Suzanne E van der Wijst, Monique A. M. J. de Vroede, Frans A. Hol
Publikováno v:
European Journal of Human Genetics, 15, 11, pp. 1132-8
European Journal of Human Genetics, 15, 1132-8
European Journal of Human Genetics, 15, 1132-8
Contains fulltext : 36655.pdf (Publisher’s version ) (Closed access) The Wolf-Hirschhorn syndrome (WHS (MIM 194190)), which is characterized by growth delay, mental retardation, epilepsy, facial dysmorphisms, and midline fusion defects, shows exten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::300afc8fc920bad9ff181a0eb8981020
https://doi.org/10.1038/sj.ejhg.5201899
https://doi.org/10.1038/sj.ejhg.5201899
Publikováno v:
Pediatrics. 114:e520-e522
Persistent hyperinsulinemic hypoglycemia of infancy or congenital hyperinsulinism of the neonate is a rare condition that may cause severe neurologic damage if the disease is unrecognized or inadequately treated. Cur- rent treatment aims to restore n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b6601ae4f8d0cf422aa48cbde61644
https://doi.org/10.1542/peds.2003-1180-l
https://doi.org/10.1542/peds.2003-1180-l
Autor:
Ruud Berger, Monique A. M. J. de Vroede, Johannes M.P.J. Breur, Ellen H. Jeninga, Nanda M. Verhoeven-Duif, Eric Kalkhoven, Nicole Hamers
Publikováno v:
JIMD Reports ISBN: 9783642257513
Congenital generalized lipodystrophy (CGL) results from mutations in AGPAT2, encoding 1-acyl-glycerol-3-phosphate-acyltransferase 2 (CGL1; MIM 608594), BSCL2, encoding seipin (CGL2; MIM 269700), CAV1, encoding caveolin1 (CGL3; MIM 612526) or PTRF, en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::786bb231e913d96e23f29218253b3c61
https://europepmc.org/articles/PMC3509903/
https://europepmc.org/articles/PMC3509903/
Autor:
Inge M. Evers, Monique A. M. J. de Vroede, Marijke Tersteeg-Kamperman, Gerard H. A. Visser, Cobi J. Heijnen, Maarten Rijpert, Harold W. de Valk
Publikováno v:
Early human development. 87(1)
Background High maternal glucose concentrations during diabetic pregnancy may lead to health problems in the offspring later in life. We showed in a previous nationwide study on pregnancy outcome in type 1 diabetic women that prepregnancy care was go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::968efed5db24f9274be1c099d04f542a
https://pubmed.ncbi.nlm.nih.gov/21095079
https://pubmed.ncbi.nlm.nih.gov/21095079
Autor:
Suzanne G.M.A. Pasmans, Marjolein S. de Bruin-Weller, Sara G.A. van Velsen, Tim C. de Wit, Marnix G.E.H. Lam, Monique A. M. J. de Vroede, Carla A.F.M. Bruijnzeel-Koomen, Inge Haeck, Mirjam J. Knol, Rachel L.A. van Eijk
Publikováno v:
Journal of the American Academy of Dermatology, 63(5), 824-831. Mosby Inc.
BACKGROUND: Low bone mineral density (BMD) has been reported in 30.4% of adult patients with atopic dermatitis (AD). OBJECTIVE: The aim of this study was to determine the prevalence of low BMD in children with moderate to severe AD and to investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbce0c2169e3fd8f624b6be0eea8eeb5
https://pubmed.ncbi.nlm.nih.gov/20850893
https://pubmed.ncbi.nlm.nih.gov/20850893