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Brian Fowler

Showing results (71-80 of 138) with videos related to

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Molecular Genetics and Metabolism Reports|March 26, 2016
Successful intrauterine treatment of a patient with cobalamin C defectFriedrich K Trefz, Dagmar Scheible, Georg Frauendienst-Egger, et al.
JIMD Reports|April 13, 2013
Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC TypePaul Hoff Backe, Mari Ytre-Arne, Asmund Kjendseth Røhr, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutationMustafa Kılıç, Rıza Köksal Özgül, Ali Dursun, et al.
Metabolism: Clinical and Experimental|May 28, 2004
Propionic acidemia: unusual course with late onset and fatal outcomeThomas Lücke, Celia Pérez-Cerdá, Matthias Baumgartner, et al.
Plant Physiology|July 19, 2005
TaVRT-2, a member of the StMADS-11 clade of flowering repressors, is regulated by vernalization and photoperiod in wheatNdjido A Kane, Jean Danyluk, Guylaine Tardif, et al.
Pediatric Pulmonology|July 5, 2021
EVALI versus MIS-C, one more overlapping diagnosis to considerDiego A Cruz-Vidal, Eric S Mull, Jeanette Taveras, et al.
The Plant Genome|July 11, 2019
Genome-Wide Identification and Characterization of the Wheat Remorin (<i>Ta</i>REM) Family during Cold AcclimationMohamed A Badawi, Zahra Agharbaoui, Muhammad Zayed, et al.
Orphanet Journal of Rare Diseases|November 16, 2014
Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancyMartina Huemer, Sabine Scholl-Bürgi, Karine Hadaya, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Lack of genetic dispositions to hyperhomocysteinemia in Alzheimer diseaseMichael Linnebank, Anja Linnebank, Monika Jeub, et al.
The New England Journal of Medicine|April 4, 2008
Gene identification for the cblD defect of vitamin B12 metabolismDavid Coelho, Terttu Suormala, Martin Stucki, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
Molecular Genetics and Metabolism Reports|March 26, 2016
Successful intrauterine treatment of a patient with cobalamin C defectFriedrich K Trefz, Dagmar Scheible, Georg Frauendienst-Egger, et al.
JIMD Reports|April 13, 2013
Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC TypePaul Hoff Backe, Mari Ytre-Arne, Asmund Kjendseth Røhr, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Cobalamin C defect: a patient of late-onset type with homozygous p.R132* mutationMustafa Kılıç, Rıza Köksal Özgül, Ali Dursun, et al.
Metabolism: Clinical and Experimental|May 28, 2004
Propionic acidemia: unusual course with late onset and fatal outcomeThomas Lücke, Celia Pérez-Cerdá, Matthias Baumgartner, et al.
Plant Physiology|July 19, 2005
TaVRT-2, a member of the StMADS-11 clade of flowering repressors, is regulated by vernalization and photoperiod in wheatNdjido A Kane, Jean Danyluk, Guylaine Tardif, et al.
Pediatric Pulmonology|July 5, 2021
EVALI versus MIS-C, one more overlapping diagnosis to considerDiego A Cruz-Vidal, Eric S Mull, Jeanette Taveras, et al.
The Plant Genome|July 11, 2019
Genome-Wide Identification and Characterization of the Wheat Remorin (<i>Ta</i>REM) Family during Cold AcclimationMohamed A Badawi, Zahra Agharbaoui, Muhammad Zayed, et al.
Orphanet Journal of Rare Diseases|November 16, 2014
Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancyMartina Huemer, Sabine Scholl-Bürgi, Karine Hadaya, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Lack of genetic dispositions to hyperhomocysteinemia in Alzheimer diseaseMichael Linnebank, Anja Linnebank, Monika Jeub, et al.
The New England Journal of Medicine|April 4, 2008
Gene identification for the cblD defect of vitamin B12 metabolismDavid Coelho, Terttu Suormala, Martin Stucki, et al.
Pageof 14