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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 syndrome
P 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 study
W 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 gene
P 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 syndrome
P 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 syndrome
P 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 gene
H 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 treatment
N E Bakker, R J Kuppens, E P C Siemensma, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 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 syndrome
P 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 study
W 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 gene
P 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 syndrome
P 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 syndrome
P 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 gene
H 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 treatment
N E Bakker, R J Kuppens, E P C Siemensma, et al.
Page
of 2