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Marsha F Browning

Showing results (1-10 of 10) with videos related to

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Obstetrics and Gynecology|January 6, 2006
Fetal fatty acid oxidation defects and maternal liver disease in pregnancyMarsha F Browning, Harvey L Levy, Louise E Wilkins-Haug, et al.
Optometry (St. Louis, Mo.)|July 10, 2010
Ocular manifestations of Fabry disease within in a single kindredAlbert M Morier, John Minteer, Robert Tyszko, et al.
Pediatrics|September 15, 2010
Parents' decision-making in newborn screening: opinions, choices, and information needsEllen A Lipstein, Emara Nabi, James M Perrin, et al.
Journal of Cellular Physiology|November 4, 2009
Functional multimerization of mucolipin channel proteinsCyntia Curcio-Morelli, Peng Zhang, Bhuvarahamurthy Venugopal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 2009
Effect of sample collection on alpha-galactosidase A enzyme activity measurements in dried blood spots on filter paperPetra Olivova, Kristen van der Veen, Emmaline Cullen, et al.
American Journal of Human Genetics|October 10, 2007
Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IVBhuvarahamurthy Venugopal, Marsha F Browning, Cyntia Curcio-Morelli, et al.
Pediatrics|April 21, 2010
Systematic evidence review of newborn screening and treatment of severe combined immunodeficiencyEllen A Lipstein, Sienna Vorono, Marsha F Browning, et al.
Neurobiology of Disease|July 6, 2010
Macroautophagy is defective in mucolipin-1-deficient mouse neuronsCyntia Curcio-Morelli, Florie A Charles, Matthew C Micsenyi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2010
An evidence development process for newborn screeningJames M Perrin, Alixandra A Knapp, Marsha F Browning, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2010
Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delayBarbara Wiśniowiecka-Kowalnik, Monika Nesteruk, Sarika U Peters, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Obstetrics and Gynecology|January 6, 2006
Fetal fatty acid oxidation defects and maternal liver disease in pregnancyMarsha F Browning, Harvey L Levy, Louise E Wilkins-Haug, et al.
Optometry (St. Louis, Mo.)|July 10, 2010
Ocular manifestations of Fabry disease within in a single kindredAlbert M Morier, John Minteer, Robert Tyszko, et al.
Pediatrics|September 15, 2010
Parents' decision-making in newborn screening: opinions, choices, and information needsEllen A Lipstein, Emara Nabi, James M Perrin, et al.
Journal of Cellular Physiology|November 4, 2009
Functional multimerization of mucolipin channel proteinsCyntia Curcio-Morelli, Peng Zhang, Bhuvarahamurthy Venugopal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 2009
Effect of sample collection on alpha-galactosidase A enzyme activity measurements in dried blood spots on filter paperPetra Olivova, Kristen van der Veen, Emmaline Cullen, et al.
American Journal of Human Genetics|October 10, 2007
Neurologic, gastric, and opthalmologic pathologies in a murine model of mucolipidosis type IVBhuvarahamurthy Venugopal, Marsha F Browning, Cyntia Curcio-Morelli, et al.
Pediatrics|April 21, 2010
Systematic evidence review of newborn screening and treatment of severe combined immunodeficiencyEllen A Lipstein, Sienna Vorono, Marsha F Browning, et al.
Neurobiology of Disease|July 6, 2010
Macroautophagy is defective in mucolipin-1-deficient mouse neuronsCyntia Curcio-Morelli, Florie A Charles, Matthew C Micsenyi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2010
An evidence development process for newborn screeningJames M Perrin, Alixandra A Knapp, Marsha F Browning, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2010
Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delayBarbara Wiśniowiecka-Kowalnik, Monika Nesteruk, Sarika U Peters, et al.
Pageof 1