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Helen Stewart

Showing results (21-30 of 93) with videos related to

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Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 24, 2006
Polymorphisms of the Bcl-2 family member bfl-1 in children with atopic dermatitisAndrew Gray, Helen Stewart, Vera Pravica, et al.
Hematological Oncology|October 15, 2013
Molecular detection of BRAF-V600E is superior to flow cytometry for disease evaluation in hairy cell leukaemiaTom Rider, Robert Powell, Rebecca Gover, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndromeZahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2013
CLN6 disease caused by the same mutation originating in Pakistan has varying pathologyRita Guerreiro, Jose T Bras, Mariana Vieira, et al.
Journal of Cardiovascular Pharmacology|March 23, 2013
The safety of preoperative vardenafil in patients undergoing coronary artery bypass graft surgeryAsghar Ali, Andrew Binder, Asad Mohmand, et al.
Annals of the New York Academy of Sciences|November 1, 2017
The "CMT Rat": Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22Stephan Niemann, Michael W Sereda, Moritz Rossner, et al.
The Journal of Clinical Endocrinology and Metabolism|October 23, 2012
De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic casesSerap Turan, Jaakko Ignatius, Jukka S Moilanen, et al.
Frontiers in Genetics|July 28, 2025
Two novel cases with PIGQ-CDG: expansion of the genotype-phenotype spectrum and evaluation of GestaltMatcher as a diagnostic toolKatarína Kušíková, Tzung-Chien Hsieh, Mateja Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
Human Genetics|May 31, 2012
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunctionChristelle Borel, Fanny Cheung, Helen Stewart, et al.
Pageof 10

Showing results (21-30 of 93) with videos related to

Sort By:
Pageof 10
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 24, 2006
Polymorphisms of the Bcl-2 family member bfl-1 in children with atopic dermatitisAndrew Gray, Helen Stewart, Vera Pravica, et al.
Hematological Oncology|October 15, 2013
Molecular detection of BRAF-V600E is superior to flow cytometry for disease evaluation in hairy cell leukaemiaTom Rider, Robert Powell, Rebecca Gover, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndromeZahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 6, 2013
CLN6 disease caused by the same mutation originating in Pakistan has varying pathologyRita Guerreiro, Jose T Bras, Mariana Vieira, et al.
Journal of Cardiovascular Pharmacology|March 23, 2013
The safety of preoperative vardenafil in patients undergoing coronary artery bypass graft surgeryAsghar Ali, Andrew Binder, Asad Mohmand, et al.
Annals of the New York Academy of Sciences|November 1, 2017
The "CMT Rat": Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22Stephan Niemann, Michael W Sereda, Moritz Rossner, et al.
The Journal of Clinical Endocrinology and Metabolism|October 23, 2012
De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic casesSerap Turan, Jaakko Ignatius, Jukka S Moilanen, et al.
Frontiers in Genetics|July 28, 2025
Two novel cases with PIGQ-CDG: expansion of the genotype-phenotype spectrum and evaluation of GestaltMatcher as a diagnostic toolKatarína Kušíková, Tzung-Chien Hsieh, Mateja Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
Human Genetics|May 31, 2012
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunctionChristelle Borel, Fanny Cheung, Helen Stewart, et al.
Pageof 10