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BMJ Open Respiratory Research
|
December 6, 2014
Differential response to bacteria, and TOLLIP expression, in the human respiratory tract
Olga Lucia Moncayo-Nieto, Thomas S Wilkinson, Mairi Brittan, et al.
British Journal of Clinical Pharmacology
|
February 3, 2016
A model-based approach to assess the exposure-response relationship of Lorenzo's oil in adrenoleukodystrophy
Mariam A Ahmed, Reena V Kartha, Richard C Brundage, et al.
JAMA Neurology
|
March 14, 2017
Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy
Bela R Turk, Benjamin E Theisen, Christina L Nemeth, et al.
Molecular Genetics and Metabolism Reports
|
November 23, 2016
Diagnosis of a mild peroxisomal phenotype with next-generation sequencing
Meredith J Ventura, Dianna Wheaton, Mingchu Xu, et al.
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) method
Walter 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 oil
Hugo 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 trials
Hugo 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 feasible
Christiane Theda, Katy Gibbons, Todd E Defor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers
Michael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Molecular Genetics and Metabolism
|
July 26, 2017
Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots
Thais Armangue, Joseph J Orsini, Asako Takanohashi, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
BMJ Open Respiratory Research
|
December 6, 2014
Differential response to bacteria, and TOLLIP expression, in the human respiratory tract
Olga Lucia Moncayo-Nieto, Thomas S Wilkinson, Mairi Brittan, et al.
British Journal of Clinical Pharmacology
|
February 3, 2016
A model-based approach to assess the exposure-response relationship of Lorenzo's oil in adrenoleukodystrophy
Mariam A Ahmed, Reena V Kartha, Richard C Brundage, et al.
JAMA Neurology
|
March 14, 2017
Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy
Bela R Turk, Benjamin E Theisen, Christina L Nemeth, et al.
Molecular Genetics and Metabolism Reports
|
November 23, 2016
Diagnosis of a mild peroxisomal phenotype with next-generation sequencing
Meredith J Ventura, Dianna Wheaton, Mingchu Xu, et al.
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) method
Walter 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 oil
Hugo 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 trials
Hugo 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 feasible
Christiane Theda, Katy Gibbons, Todd E Defor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers
Michael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Molecular Genetics and Metabolism
|
July 26, 2017
Neonatal detection of Aicardi Goutières Syndrome by increased C26:0 lysophosphatidylcholine and interferon signature on newborn screening blood spots
Thais Armangue, Joseph J Orsini, Asako Takanohashi, et al.
Page
of 4