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Ann B Moser

Showing results (1-10 of 77) with videos related to

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JAMA Neurology|June 28, 2018
Newborn Screening and Emerging Therapies for X-Linked AdrenoleukodystrophyAnn B Moser, Ali Fatemi
Biochimica Et Biophysica Acta|May 26, 2012
Functions of plasmalogen lipids in health and diseaseNancy E Braverman, Ann B Moser
Wiener Medizinische Wochenschrift (1946)|May 12, 2017
Therapeutic strategies in adrenoleukodystrophyBela R Turk, Ann B Moser, Ali Fatemi
International Journal of Neonatal Screening|February 28, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Past, Present, and FutureAnn B Moser, Elisa Seeger, Gerald V Raymond
Molecular Diagnosis & Therapy|December 15, 2007
Newborn screening for adrenoleukodystrophy: implications for therapyGerald V Raymond, Richard O Jones, Ann B Moser
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|November 29, 2019
X-linked Adrenoleukodystrophy: Pathology, Pathophysiology, Diagnostic Testing, Newborn Screening, and TherapiesBela R Turk, Christiane Theda, Ali Fatemi, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 8, 2020
X-linked adrenoleukodystrophy: Pathology, pathophysiology, diagnostic testing, newborn screening and therapiesBela R Turk, Christiane Theda, Ali Fatemi, et al.
Molecular Genetics and Metabolism|July 11, 2006
Combined liquid chromatography-tandem mass spectrometry as an analytical method for high throughput screening for X-linked adrenoleukodystrophy and other peroxisomal disorders: preliminary findingsWalter C Hubbard, Ann B Moser, Silvia Tortorelli, et al.
Journal of Molecular Neuroscience : MN|September 29, 2007
"Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacyHugo W Moser, Ann B Moser, Kim Hollandsworth, et al.
Human Mutation|December 24, 2008
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disordersWing Yan Yik, Steven J Steinberg, Ann B Moser, et al.
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
JAMA Neurology|June 28, 2018
Newborn Screening and Emerging Therapies for X-Linked AdrenoleukodystrophyAnn B Moser, Ali Fatemi
Biochimica Et Biophysica Acta|May 26, 2012
Functions of plasmalogen lipids in health and diseaseNancy E Braverman, Ann B Moser
Wiener Medizinische Wochenschrift (1946)|May 12, 2017
Therapeutic strategies in adrenoleukodystrophyBela R Turk, Ann B Moser, Ali Fatemi
International Journal of Neonatal Screening|February 28, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Past, Present, and FutureAnn B Moser, Elisa Seeger, Gerald V Raymond
Molecular Diagnosis & Therapy|December 15, 2007
Newborn screening for adrenoleukodystrophy: implications for therapyGerald V Raymond, Richard O Jones, Ann B Moser
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|November 29, 2019
X-linked Adrenoleukodystrophy: Pathology, Pathophysiology, Diagnostic Testing, Newborn Screening, and TherapiesBela R Turk, Christiane Theda, Ali Fatemi, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 8, 2020
X-linked adrenoleukodystrophy: Pathology, pathophysiology, diagnostic testing, newborn screening and therapiesBela R Turk, Christiane Theda, Ali Fatemi, et al.
Molecular Genetics and Metabolism|July 11, 2006
Combined liquid chromatography-tandem mass spectrometry as an analytical method for high throughput screening for X-linked adrenoleukodystrophy and other peroxisomal disorders: preliminary findingsWalter C Hubbard, Ann B Moser, Silvia Tortorelli, et al.
Journal of Molecular Neuroscience : MN|September 29, 2007
"Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacyHugo W Moser, Ann B Moser, Kim Hollandsworth, et al.
Human Mutation|December 24, 2008
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disordersWing Yan Yik, Steven J Steinberg, Ann B Moser, et al.
Pageof 8