Zobrazeno 1 - 10 of 28 pro vyhledávání: '"P Ph Forget"'
1
Energy expenditure in infants with congenital heart disease, including a meta-analysis
Autor: Reinoud J. B. J. Gemke, Marije B. Hoos, M van der Kuip, P Ph Forget, K. de Meer, Klaas R. Westerterp
Publikováno v: Acta Paediatrica. 92:921-927
Energy expenditure in infants with congenital heart disease, including a meta-analysis. van der Kuip M, Hoos MB, Forget PP, Westerterp KR, Gemke RJ, de Meer K. Department of Paediatrics, VU University Medical Centre, Amsterdam, The Netherlands. AIM:
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6241e03e186978110fecc1194f9df7a6
https://doi.org/10.1111/j.1651-2227.2003.tb00625.x
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2
Body composition in children with galactosaemia
Autor: Bianca Panis, P Ph Forget, Fred H. M. Nieman, M. J. P. G. van Kroonenburgh, M. E. Rubio-Gozalbo
Publikováno v: Journal of Inherited Metabolic Disease, 28(6), 931-937. Wiley
Body composition in classical galactosaemia has not been studied. Patients with classical galactosaemia, an inherited disorder of galactose metabolism caused by deficiency of galactose-1-phosphate uridyltransferase (GALT, EC 2.7.7.10), might be at ri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fb41b64f154d229b139f6faf8b9d1cf
https://doi.org/10.1007/s10545-005-0189-4
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3
Bone metabolism in galactosemia
Autor: M. J. P. G. van Kroonenburgh, Bianca Panis, M. E. Rubio-Gozalbo, Fred H. M. Nieman, P Ph Forget, Cees Vermeer, Paul P.C.A. Menheere
Publikováno v: Bone, 35(4), 982-987. Elsevier Science
Bone metabolism in galactosemia.Panis B, Forget PP, van Kroonenburgh MJ, Vermeer C, Menheere PP, Nieman FH, Rubio-Gozalbo ME.Department of Pediatrics, Metabolic Diseases, University Hospital Maastricht, 6202 AZ Maastricht, The Netherlands.Classical g
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ad5ddc95539645626fe2d93542c943
https://doi.org/10.1016/j.bone.2004.06.004
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4
Bone mineral density in patients with classic galactosaemia
Autor: S Hamming, Jaap A. Bakker, M. E. Rubio-Gozalbo, Cees Vermeer, P Ph Forget, M. J. P. G. van Kroonenburgh
Publikováno v: Archives of Disease in Childhood, 87(1), 57-60. BMJ Publishing Group
Bone mineral density in patients with classic galactosaemia.Rubio-Gozalbo ME, Hamming S, van Kroonenburgh MJ, Bakker JA, Vermeer C, Forget PP.Department of Pediatrics, Academic Hospital Maastricht, Netherlands. mrub@skin.azm.nlBACKGROUND: Diminished
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1876900eee672097fa7febd40cdb89fa
https://doi.org/10.1136/adc.87.1.57
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5
Long-term growth of children with congenital heart disease: a retrospective study
Autor: C. F. M. Pulles-Heintzberger, P Ph Forget, F. M. Schuurmans, Arnold D. M. Kester, Willem-Jan M. Gerver
Publikováno v: Acta Paediatrica, 87(12), 1250-1255. Wiley
Department of Pediatrics, University Hospital of Maastricht, Maastricht University, The Netherlands.This retrospective study evaluates long-term growth of children with congenital heart disease (CHD) and looks for possible relationships between posts
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255168c7c8fd88fe23e50ce7df31385a
https://cris.maastrichtuniversity.nl/en/publications/654c375d-c6a2-4c57-a89d-9328a20f36e2
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6
Nitrotyrosine in plasma of celiac disease patients as detected by a new sandwich ELISA
Autor: E. A. Van Straaten, L. Koster-Kamphuis, W. A. Buurman, P. Ph. Forget, J. C. A. Ter Steege
Publikováno v: Free Radical Biology and Medicine, 25(8), 953-963. Elsevier Science
Department of Pediatrics, Academic Hospital Maastricht, The Netherlands. W.Buurman@AH.Unimaas.NLInflammation is characterized by increased nitric oxide production. Nitrotyrosine has recently been suggested to be useful as a marker for NO-mediated tis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b69ef1180392ad6081e655342cc19cae
https://doi.org/10.1016/s0891-5849(98)00184-1
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7
Acid steatocrit: a reliable screening tool for steatorrhea
Autor: P. M. V. M. Theunissen, E. M. Kerkvliet, A.M. van den Neucker, P Ph Forget
Publikováno v: Acta Paediatrica. 90:873-875
Acid steatocrit: a reliable screening tool for steatorrhoea. Van den Neucker AM, Kerkvliet EM, Theunissen PM, Forget PP. Department of Pediatrics, University Hospital Maastricht, The Netherlands. AVN@SKIN.AZM.NL This study compared the acid steatocri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::08b30a044e276087949e5665376dacc9
https://doi.org/10.1111/j.1651-2227.2001.tb02448.x
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8
Carnitine-acylcarnitine translocase deficiency: case report and review of the literature
Autor: P. Vos, P Ph Forget, Ronald J.A. Wanders, Jaap A. Bakker, S. B. van der Meer, M. E. Rubio-Gozalbo, Hans R. Waterham
Publikováno v: Scopus-Elsevier
Acta Paediatrica, 92(4), 501-504. Wiley
Acta paediatrica (Oslo, Norway, 92(4), 501-504. Wiley-Blackwell
Carnitine-acylcarnitine translocase deficiency: case report and review of the literature.Rubio-Gozalbo ME, Vos P, Forget PP, Van Der Meer SB, Wanders RJ, Waterham HR, Bakker JA.Departments of Pediatrics, University Hospital Maastricht, The Netherland
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358bd08b61dcec6e48dcc781de22c6ff
https://pubmed.ncbi.nlm.nih.gov/12801121
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9
Urinary NOx:creatinine ratios during gluten challenge in children with celiac disease
Autor: I. M. Y. Bovee-Oudenhoven, W. A. Kors, E. A. Van Straaten, R. Van Der Meer, Linda Koster-Kamphuis, J. E. A. R. De Schrijver, P Ph Forget
Publikováno v: Journal of Pediatric Gastroenterology and Nutrition, 36(3), 372-375. LIPPINCOTT WILLIAMS & WILKINS
Journal of Pediatric Gastroenterology and Nutrition, 36, 3, pp. 372-5
Journal of Pediatric Gastroenterology and Nutrition, 36, 372-5
Urinary NOx:creatinine ratios during gluten challenge in children with celiac disease.Koster-Kamphuis L, van Straaten EA, Kors WA, De Schrijver JE, Bovee-Oudenhoven IM, vandDer Meer R, Forget PP.Department of Pediatrics, University Hospital, Maastric
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416987279895fb1efecae3fcf501bc16
https://pubmed.ncbi.nlm.nih.gov/12604977
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10
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophy
Autor: L. J. M. Spaapen, P. C. A. J. Vroomen, A. Verrips, D. A. van Waardenburg, P Ph Forget, M. E. Rubio-Gozalbo
Publikováno v: Journal of Inherited Metabolic Disease, 24(5), 605-606. Wiley
Journal of Inherited Metabolic Disease, 24, 5, pp. 605--6
Journal of Inherited Metabolic Disease, 24, 605--6
Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophy.Rubio-Gonzalbo ME, van Waardenburg DA, Forget PP, Spaapen LJ, Verrips A, Vroomen PC.Department of Paediatrics, University Hospital Maastricht, The
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a83da912923413549224b8344bd5106
https://cris.maastrichtuniversity.nl/en/publications/6f1eb8db-9599-40be-9dc7-9a0fd9e106ec
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