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J Steinberg

Showing results (291-300 of 323) with videos related to

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Canadian Prosthetics & Orthotics Journal|September 4, 2025
Using a novel psychosocial group intervention to improve adaption, coping and mental health outcomes following dysvascular limb amputations: A feasibility studyR J Steinberg, L R Robinson, O Kachmarchuk, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Stem Cell Research & Therapy|August 31, 2015
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalitiesXiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
The Journal of Biological Chemistry|May 1, 2002
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recyclingStephanie J Mihalik, Steven J Steinberg, Zhengtong Pei, et al.
Brain Injury|January 3, 2025
Identifying mild traumatic brain injury in the post-acute polytrauma setting: a scoping review of diagnostic approaches and screening toolsMatthew J Burke, Yomna E Ahmed, Zoe Li, et al.
Molecular Genetics and Metabolism|January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelinesNancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Clinical Genetics|March 7, 2014
Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1J M van de Kamp, A Errami, M Howidi, et al.
Journal of Inherited Metabolic Disease|January 8, 2009
A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblastsS J Steinberg, A Snowden, N E Braverman, 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) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
The Oncologist|March 29, 2025
Tri-Ad5 vaccine plus bintrafusp alfa for newly diagnosed, advanced-stage head and neck cancer not associated with human papillomavirus infectionJason M Redman, Renee N Donahue, Seth J Steinberg, et al.
Pageof 33

Showing results (291-300 of 323) with videos related to

Sort By:
Pageof 33
Canadian Prosthetics & Orthotics Journal|September 4, 2025
Using a novel psychosocial group intervention to improve adaption, coping and mental health outcomes following dysvascular limb amputations: A feasibility studyR J Steinberg, L R Robinson, O Kachmarchuk, et al.
Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.
Stem Cell Research & Therapy|August 31, 2015
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalitiesXiao-Ming Wang, Wing Yan Yik, Peilin Zhang, et al.
The Journal of Biological Chemistry|May 1, 2002
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recyclingStephanie J Mihalik, Steven J Steinberg, Zhengtong Pei, et al.
Brain Injury|January 3, 2025
Identifying mild traumatic brain injury in the post-acute polytrauma setting: a scoping review of diagnostic approaches and screening toolsMatthew J Burke, Yomna E Ahmed, Zoe Li, et al.
Molecular Genetics and Metabolism|January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelinesNancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Clinical Genetics|March 7, 2014
Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1J M van de Kamp, A Errami, M Howidi, et al.
Journal of Inherited Metabolic Disease|January 8, 2009
A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblastsS J Steinberg, A Snowden, N E Braverman, 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) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
The Oncologist|March 29, 2025
Tri-Ad5 vaccine plus bintrafusp alfa for newly diagnosed, advanced-stage head and neck cancer not associated with human papillomavirus infectionJason M Redman, Renee N Donahue, Seth J Steinberg, et al.
Pageof 33