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Michael J Bennett

Showing results (101-110 of 156) with videos related to

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Molecular Genetics and Metabolism|May 15, 2012
Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screeningLaura Vilarinho, Jorge Sales Marques, Hugo Rocha, et al.
The Journal of Pediatrics|November 1, 2002
Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutationsGeorgirene D Vladutiu, Elizabeth J Quackenbush, Bryan E Hainline, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 2, 2007
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndromeIna Knerr, K Michael Gibson, Jaya Ganesh, et al.
Muscle & Nerve|October 4, 2002
Phenotypic variability among first-degree relatives with carnitine palmitoyltransferase II deficiencyGeorgirene D Vladutiu, Michael J Bennett, Nadine M Fisher, et al.
JIMD Reports|February 28, 2016
ECHS1 Deficiency as a Cause of Severe Neonatal Lactic AcidosisRebecca D Ganetzky, Kaitlyn Bloom, Rebecca Ahrens-Nicklas, et al.
Pediatric Research|July 9, 2004
Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) MicePrem S Shekhawat, Han-Soo Yang, Michael J Bennett, et al.
Journal of Assisted Reproduction and Genetics|October 13, 2006
Power doppler ultrasound assessment of the relationship between age and ovarian perifollicular blood flow in women undergoing in vitro fertilization treatmentMichael F Costello, Sanu M Shrestha, Peter Sjoblom, et al.
Fertility and Sterility|April 12, 2005
Power Doppler ultrasound assessment of ovarian perifollicular blood flow in women with polycystic ovaries and normal ovaries during in vitro fertilization treatmentMichael F Costello, Sanu M Shrestha, Peter Sjoblom, et al.
American Journal of Human Genetics|October 18, 2008
Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10Eric A Sherman, Kevin A Strauss, Silvia Tortorelli, et al.
Journal of Inherited Metabolic Disease|February 25, 2011
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: the clinical relevance of an early diagnosis and report of four new casesEsmeralda Martins, M Luis Cardoso, Esmeralda Rodrigues, et al.
Pageof 16

Showing results (101-110 of 156) with videos related to

Sort By:
Pageof 16
Molecular Genetics and Metabolism|May 15, 2012
Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screeningLaura Vilarinho, Jorge Sales Marques, Hugo Rocha, et al.
The Journal of Pediatrics|November 1, 2002
Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutationsGeorgirene D Vladutiu, Elizabeth J Quackenbush, Bryan E Hainline, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 2, 2007
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndromeIna Knerr, K Michael Gibson, Jaya Ganesh, et al.
Muscle & Nerve|October 4, 2002
Phenotypic variability among first-degree relatives with carnitine palmitoyltransferase II deficiencyGeorgirene D Vladutiu, Michael J Bennett, Nadine M Fisher, et al.
JIMD Reports|February 28, 2016
ECHS1 Deficiency as a Cause of Severe Neonatal Lactic AcidosisRebecca D Ganetzky, Kaitlyn Bloom, Rebecca Ahrens-Nicklas, et al.
Pediatric Research|July 9, 2004
Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) MicePrem S Shekhawat, Han-Soo Yang, Michael J Bennett, et al.
Journal of Assisted Reproduction and Genetics|October 13, 2006
Power doppler ultrasound assessment of the relationship between age and ovarian perifollicular blood flow in women undergoing in vitro fertilization treatmentMichael F Costello, Sanu M Shrestha, Peter Sjoblom, et al.
Fertility and Sterility|April 12, 2005
Power Doppler ultrasound assessment of ovarian perifollicular blood flow in women with polycystic ovaries and normal ovaries during in vitro fertilization treatmentMichael F Costello, Sanu M Shrestha, Peter Sjoblom, et al.
American Journal of Human Genetics|October 18, 2008
Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10Eric A Sherman, Kevin A Strauss, Silvia Tortorelli, et al.
Journal of Inherited Metabolic Disease|February 25, 2011
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: the clinical relevance of an early diagnosis and report of four new casesEsmeralda Martins, M Luis Cardoso, Esmeralda Rodrigues, et al.
Pageof 16