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M De Vroede

Showing results (11-20 of 18) with videos related to

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Surgical Endoscopy|December 23, 2003
Laparoscopic identification and removal of focal lesions in persistent hyperinsulinemic hypoglycemia of infancyN M A Bax, D C van der Zee, M de Vroede, et al.
Scandinavian Journal of Haematology|May 1, 1982
Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findingsM de Vroede, W Feremans, E de Maertelaere-Laurent, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Children with craniopharyngioma, a 'benign' brain tumor with a high morbidity]M J Taphoorn, C van Es, R H Gooskens, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Cortisol resistance in manM B Lipsett, M Tomita, D D Brandon, et al.
European Journal of Pediatrics|March 30, 2001
Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic studyJ C Giltay, M G Ausems, I van Seumeren, et al.
Tijdschrift Voor Psychiatrie|May 12, 2010
[Antipsychotics and metabolic abnormalities in children and adolescents: a review of the literature and some recommendations]W A Overbeek, M A M de Vroede, B E Lahuis, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndromeKlara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, et al.
Hormone Research in Paediatrics|November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type IIM J E Kempers, S N van der Crabben, M de Vroede, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Surgical Endoscopy|December 23, 2003
Laparoscopic identification and removal of focal lesions in persistent hyperinsulinemic hypoglycemia of infancyN M A Bax, D C van der Zee, M de Vroede, et al.
Scandinavian Journal of Haematology|May 1, 1982
Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findingsM de Vroede, W Feremans, E de Maertelaere-Laurent, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Children with craniopharyngioma, a 'benign' brain tumor with a high morbidity]M J Taphoorn, C van Es, R H Gooskens, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Cortisol resistance in manM B Lipsett, M Tomita, D D Brandon, et al.
European Journal of Pediatrics|March 30, 2001
Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic studyJ C Giltay, M G Ausems, I van Seumeren, et al.
Tijdschrift Voor Psychiatrie|May 12, 2010
[Antipsychotics and metabolic abnormalities in children and adolescents: a review of the literature and some recommendations]W A Overbeek, M A M de Vroede, B E Lahuis, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndromeKlara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, et al.
Hormone Research in Paediatrics|November 28, 2013
Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type IIM J E Kempers, S N van der Crabben, M de Vroede, et al.
Pageof 2