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Marielle Alders

Showing results (1-10 of 76) with videos related to

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American Journal of Medical Genetics. Part A|December 15, 2012
Increase in central striatal dopamine transporters in patients with Shwachman-Diamond syndrome: additional evidence of a brain phenotypeJan Booij, Liesbeth Reneman, Marielle Alders, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysisMarielle Alders, Jet Bliek, Karin vd Lip, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 4, 2011
[Premature sudden death--consider serious familial heart rhythm disturbances]Pieter G Postema, Imke Christiaans, Marielle Alders, et al.
Journal of Hepatology|December 15, 2015
A de novo mutation in KCNN3 associated with autosomal dominant idiopathic non-cirrhotic portal hypertensionBart G P Koot, Marielle Alders, Joanne Verheij, et al.
Journal of Cardiovascular Electrophysiology|September 4, 2010
Sodium channelopathies: do we really understand what's going on?Pieter G Postema, Arend Mosterd, Nynke Hofman, et al.
Pediatrics|September 3, 2004
Congenital aplastic anemia caused by mutations in the SBDS gene: a rare presentation of Shwachman-Diamond syndromeTaco W Kuijpers, Eline Nannenberg, Marielle Alders, et al.
Journal of Pediatric Genetics|September 15, 2016
A STAT3 mutation in hyper-immunoglobulin E syndrome: A case reportFilip Haenen, Marielle Alders, Elke Dierckx, et al.
Journal of the American College of Cardiology|June 2, 2010
Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?Nynke Hofman, Hanno L Tan, Marielle Alders, et al.
Clinical Epigenetics|July 7, 2025
ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disordersFrédéric Brioude, Martin A Haagmans, Marcel Mannens, et al.
Cancer Chemotherapy and Pharmacology|February 15, 2008
Topotecan distribution in an anephric infant with therapy-resistant bilateral Wilms tumor with a novel germline WT1 gene mutationRieneke T Lugtenberg, Karlien Cransberg, Walter J Loos, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|December 15, 2012
Increase in central striatal dopamine transporters in patients with Shwachman-Diamond syndrome: additional evidence of a brain phenotypeJan Booij, Liesbeth Reneman, Marielle Alders, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysisMarielle Alders, Jet Bliek, Karin vd Lip, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 4, 2011
[Premature sudden death--consider serious familial heart rhythm disturbances]Pieter G Postema, Imke Christiaans, Marielle Alders, et al.
Journal of Hepatology|December 15, 2015
A de novo mutation in KCNN3 associated with autosomal dominant idiopathic non-cirrhotic portal hypertensionBart G P Koot, Marielle Alders, Joanne Verheij, et al.
Journal of Cardiovascular Electrophysiology|September 4, 2010
Sodium channelopathies: do we really understand what's going on?Pieter G Postema, Arend Mosterd, Nynke Hofman, et al.
Pediatrics|September 3, 2004
Congenital aplastic anemia caused by mutations in the SBDS gene: a rare presentation of Shwachman-Diamond syndromeTaco W Kuijpers, Eline Nannenberg, Marielle Alders, et al.
Journal of Pediatric Genetics|September 15, 2016
A STAT3 mutation in hyper-immunoglobulin E syndrome: A case reportFilip Haenen, Marielle Alders, Elke Dierckx, et al.
Journal of the American College of Cardiology|June 2, 2010
Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?Nynke Hofman, Hanno L Tan, Marielle Alders, et al.
Clinical Epigenetics|July 7, 2025
ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disordersFrédéric Brioude, Martin A Haagmans, Marcel Mannens, et al.
Cancer Chemotherapy and Pharmacology|February 15, 2008
Topotecan distribution in an anephric infant with therapy-resistant bilateral Wilms tumor with a novel germline WT1 gene mutationRieneke T Lugtenberg, Karlien Cransberg, Walter J Loos, et al.
Pageof 8