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Gerald V Raymond

Showing results (51-60 of 66) with videos related to

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Molecular Genetics and Metabolism|May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
Archives of Neurology|July 13, 2005
Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo's oilHugo W Moser, Gerald V Raymond, Shou-En Lu, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trialsHugo W Moser, Gerald V Raymond, Wolfgang Koehler, et al.
Molecular Genetics and Metabolism|November 26, 2013
Newborn screening for X-linked adrenoleukodystrophy: further evidence high throughput screening is feasibleChristiane Theda, Katy Gibbons, Todd E Defor, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|October 8, 2018
Survival and Functional Outcomes in Boys with Cerebral Adrenoleukodystrophy with and without Hematopoietic Stem Cell TransplantationGerald V Raymond, Patrick Aubourg, Asif Paker, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 12, 2019
Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot StudyCarlos Casasnovas, Montserrat Ruiz, Agatha Schlüter, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Neurology. Genetics|April 24, 2023
A Phase 1 Study of Oral Vitamin D<sub>3</sub> in Boys and Young Men With X-Linked AdrenoleukodystrophyKeith P Van Haren, Kristen Cunanan, Avni Awani, et al.
Chinese Medical Journal|April 12, 2012
ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian populationHong Wang, Jacqueline B Hetmanski, Ingo Ruczinski, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Molecular Genetics and Metabolism|May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
Archives of Neurology|July 13, 2005
Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo's oilHugo W Moser, Gerald V Raymond, Shou-En Lu, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trialsHugo W Moser, Gerald V Raymond, Wolfgang Koehler, et al.
Molecular Genetics and Metabolism|November 26, 2013
Newborn screening for X-linked adrenoleukodystrophy: further evidence high throughput screening is feasibleChristiane Theda, Katy Gibbons, Todd E Defor, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|October 8, 2018
Survival and Functional Outcomes in Boys with Cerebral Adrenoleukodystrophy with and without Hematopoietic Stem Cell TransplantationGerald V Raymond, Patrick Aubourg, Asif Paker, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 12, 2019
Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot StudyCarlos Casasnovas, Montserrat Ruiz, Agatha Schlüter, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Neurology. Genetics|April 24, 2023
A Phase 1 Study of Oral Vitamin D<sub>3</sub> in Boys and Young Men With X-Linked AdrenoleukodystrophyKeith P Van Haren, Kristen Cunanan, Avni Awani, et al.
Chinese Medical Journal|April 12, 2012
ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian populationHong Wang, Jacqueline B Hetmanski, Ingo Ruczinski, et al.
Pageof 7