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Marvin R Natowicz

Showing results (11-20 of 46) with videos related to

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Annals of Neurology|September 1, 2005
Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutationIlka Warshawsky, Richard A Rudick, Susan M Staugaitis, et al.
Clinical Biochemistry|January 13, 2017
Investigations of blood ammonia analysis: Test matrices, storage, and stabilityBrittany N Goldstein, Jordan Wesler, Amy S Nowacki, et al.
Clinical Chemistry|January 30, 2007
Evaluation of the risk for Tay-Sachs disease in individuals of French Canadian ancestry living in new EnglandDianna C Martin, Brian L Mark, Barbara L Triggs-Raine, et al.
Frontiers in Neurology|November 30, 2023
Proteomic investigations of adult polyglucosan body disease: insights into the pathobiology of a neurodegenerative disorderJoseph R Abraham, Frederick M Allen, John Barnard, et al.
Genetic Testing|December 4, 2003
Rapid prenatal testing for human beta-glucuronidase deficiency (MPS VII)Marvin R Natowicz, Ferruh Isman, Elizabeth M Prence, et al.
Neurogenetics|February 18, 2010
Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxiaBeate Diehl, Michael S Lee, Janet R Reid, et al.
Plos One|September 18, 2012
Brain transcriptional and epigenetic associations with autismMatthew R Ginsberg, Robert A Rubin, Tatiana Falcone, et al.
Clinical Biochemistry|December 5, 2009
Serum chitotriosidase activity and Wegener's granulomatosisCurry L Koening, Carmen E Gota, Carol A Langford, et al.
Frontiers in Pediatrics|September 2, 2025
Adolescent to adult health care transition for persons with intellectual and developmental disability: current barriers, next stepsShwetha Ramachandran, Solveig Stensland, Julie H Corder, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 26, 2010
The C. elegans hyaluronidase: a developmentally significant enzyme with chondroitin-degrading activity at both acidic and neutral pHAllison Chatel, Rick Hemming, Judith Hobert, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Annals of Neurology|September 1, 2005
Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutationIlka Warshawsky, Richard A Rudick, Susan M Staugaitis, et al.
Clinical Biochemistry|January 13, 2017
Investigations of blood ammonia analysis: Test matrices, storage, and stabilityBrittany N Goldstein, Jordan Wesler, Amy S Nowacki, et al.
Clinical Chemistry|January 30, 2007
Evaluation of the risk for Tay-Sachs disease in individuals of French Canadian ancestry living in new EnglandDianna C Martin, Brian L Mark, Barbara L Triggs-Raine, et al.
Frontiers in Neurology|November 30, 2023
Proteomic investigations of adult polyglucosan body disease: insights into the pathobiology of a neurodegenerative disorderJoseph R Abraham, Frederick M Allen, John Barnard, et al.
Genetic Testing|December 4, 2003
Rapid prenatal testing for human beta-glucuronidase deficiency (MPS VII)Marvin R Natowicz, Ferruh Isman, Elizabeth M Prence, et al.
Neurogenetics|February 18, 2010
Atypical, perhaps under-recognized? An unusual phenotype of Friedreich ataxiaBeate Diehl, Michael S Lee, Janet R Reid, et al.
Plos One|September 18, 2012
Brain transcriptional and epigenetic associations with autismMatthew R Ginsberg, Robert A Rubin, Tatiana Falcone, et al.
Clinical Biochemistry|December 5, 2009
Serum chitotriosidase activity and Wegener's granulomatosisCurry L Koening, Carmen E Gota, Carol A Langford, et al.
Frontiers in Pediatrics|September 2, 2025
Adolescent to adult health care transition for persons with intellectual and developmental disability: current barriers, next stepsShwetha Ramachandran, Solveig Stensland, Julie H Corder, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 26, 2010
The C. elegans hyaluronidase: a developmentally significant enzyme with chondroitin-degrading activity at both acidic and neutral pHAllison Chatel, Rick Hemming, Judith Hobert, et al.
Pageof 5