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P E Jira

Showing results (1-10 of 11) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|August 3, 1996
[Theophylline poisoning in children]P E Jira, B A Semmekrot, T B Vree, et al.
Clinical Chemistry|January 1, 1997
Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndromeP E Jira, J G de Jong, F S Janssen-Zijlstra, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 30, 1998
[Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease]M A Willemsen, P E Jira, F J Gabreëls, et al.
Journal of Pediatric Urology|March 13, 2020
SENS-U: continuous home monitoring of natural nocturnal bladder filling in children with nocturnal enuresis - a feasibility studyW M J Kwinten, P G van Leuteren, M van Duren-van Iersel, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 13, 1996
[Smith-Lemli-Opitz syndrome; a special defect in cholesterol metabolism]C M Aalfs, R C Hennekam, R J Wanders, et al.
Annals of Human Genetics|August 14, 2003
Smith-Lemli-Opitz syndrome and the DHCR7 geneP E Jira, H R Waterham, R J A Wanders, et al.
Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
Annals of Human Genetics|June 28, 2001
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndromeP E Jira, R J Wanders, J A Smeitink, et al.
American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.
The Journal of Clinical Endocrinology and Metabolism|February 11, 2015
Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatmentN E Bakker, R J Kuppens, E P C Siemensma, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Nederlands Tijdschrift Voor Geneeskunde|August 3, 1996
[Theophylline poisoning in children]P E Jira, B A Semmekrot, T B Vree, et al.
Clinical Chemistry|January 1, 1997
Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndromeP E Jira, J G de Jong, F S Janssen-Zijlstra, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 30, 1998
[Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease]M A Willemsen, P E Jira, F J Gabreëls, et al.
Journal of Pediatric Urology|March 13, 2020
SENS-U: continuous home monitoring of natural nocturnal bladder filling in children with nocturnal enuresis - a feasibility studyW M J Kwinten, P G van Leuteren, M van Duren-van Iersel, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 13, 1996
[Smith-Lemli-Opitz syndrome; a special defect in cholesterol metabolism]C M Aalfs, R C Hennekam, R J Wanders, et al.
Annals of Human Genetics|August 14, 2003
Smith-Lemli-Opitz syndrome and the DHCR7 geneP E Jira, H R Waterham, R J A Wanders, et al.
Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
Annals of Human Genetics|June 28, 2001
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndromeP E Jira, R J Wanders, J A Smeitink, et al.
American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.
The Journal of Clinical Endocrinology and Metabolism|February 11, 2015
Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatmentN E Bakker, R J Kuppens, E P C Siemensma, et al.
Pageof 2