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S Seneca

Showing results (31-40 of 60) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
Journal of Medical Genetics|February 6, 2004
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12L De Meirleir, S Seneca, W Lissens, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 13, 2004
Intractable ulcerative colitis of infancy in a child with mitochondrial respiratory chain disorderM Vanderborght, M C Nassogne, D Hermans, et al.
Cancer Health Disparities|November 29, 2019
Mortality disparities: A comparison with the Haudenosaunee in New York StateRodney C Haring, Melissa A Jim, Deborah Erwin, et al.
American Journal of Public Health|April 24, 2014
Racial misclassification of American Indians and Alaska Natives by Indian Health Service Contract Health Service Delivery AreaMelissa A Jim, Elizabeth Arias, Dean S Seneca, et al.
Human Reproduction (Oxford, England)|December 1, 1996
Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entitiesW Lissens, B Mercier, H Tournaye, et al.
Acta Gastro-Enterologica Belgica|November 12, 2009
Abdominal pain and vomiting as first sign of mitochondrial diseaseS Van Biervliet, P Verloo, S Vande Veldel, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase deficiency in a female due to a 4 base pair deletion in exon 10 of the E1 alpha geneW Lissens, I Desguerre, C Benelli, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Molecular Human Reproduction|September 11, 1998
Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)K Sermon, A De Vos, H Van de Velde, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1996
A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophyW Lissens, R Vervoort, N Van Regemorter, et al.
Journal of Medical Genetics|February 6, 2004
Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12L De Meirleir, S Seneca, W Lissens, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 13, 2004
Intractable ulcerative colitis of infancy in a child with mitochondrial respiratory chain disorderM Vanderborght, M C Nassogne, D Hermans, et al.
Cancer Health Disparities|November 29, 2019
Mortality disparities: A comparison with the Haudenosaunee in New York StateRodney C Haring, Melissa A Jim, Deborah Erwin, et al.
American Journal of Public Health|April 24, 2014
Racial misclassification of American Indians and Alaska Natives by Indian Health Service Contract Health Service Delivery AreaMelissa A Jim, Elizabeth Arias, Dean S Seneca, et al.
Human Reproduction (Oxford, England)|December 1, 1996
Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entitiesW Lissens, B Mercier, H Tournaye, et al.
Acta Gastro-Enterologica Belgica|November 12, 2009
Abdominal pain and vomiting as first sign of mitochondrial diseaseS Van Biervliet, P Verloo, S Vande Veldel, et al.
Human Molecular Genetics|February 1, 1995
Pyruvate dehydrogenase deficiency in a female due to a 4 base pair deletion in exon 10 of the E1 alpha geneW Lissens, I Desguerre, C Benelli, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Molecular Human Reproduction|September 11, 1998
Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)K Sermon, A De Vos, H Van de Velde, et al.
Pageof 6