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Molecular Genetics and Metabolism
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November 28, 2020
The variability conundrum in neurometabolic degenerative diseases
Clara D M van Karnebeek, Phillip A Richmond, Frans van der Kloet, et al.
Molecular Neurodegeneration
|
November 20, 2024
Stearoyl-CoA desaturase-1: a potential therapeutic target for neurological disorders
Melanie Loix, Sam Vanherle, Marta Turri, et al.
Histochemistry and Cell Biology
|
March 31, 2019
Peroxisomes: new insights into protein sorting, dynamics, quality control, signalling and roles in health and disease
Joseph L Costello, Einat Zalckvar, Stephan Kemp, et al.
Clinical Neurology and Neurosurgery
|
September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"
Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
Molecular Genetics and Metabolism
|
January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy
Stephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Experimental Cell Research
|
August 9, 2005
Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastoma
Annemieke J M de Ruijter, Rutger J Meinsma, Peter Bosma, et al.
Brain : a Journal of Neurology
|
December 12, 2018
Progression of myelopathy in males with adrenoleukodystrophy: towards clinical trial readiness
Irene C Huffnagel, Wouter J C van Ballegoij, Björn M van Geel, et al.
Orphanet Journal of Rare Diseases
|
August 15, 2012
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
Marc Engelen, Stephan Kemp, Marianne de Visser, et al.
Molecular Genetics and Metabolism
|
July 12, 2003
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry
Fredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, et al.
American Journal of Medical Genetics. Part A
|
April 5, 2013
Intellectual disability and hemizygous GPD2 mutation
Daniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 107) with videos related to
Sort By:
Page
of 11
Molecular Genetics and Metabolism
|
November 28, 2020
The variability conundrum in neurometabolic degenerative diseases
Clara D M van Karnebeek, Phillip A Richmond, Frans van der Kloet, et al.
Molecular Neurodegeneration
|
November 20, 2024
Stearoyl-CoA desaturase-1: a potential therapeutic target for neurological disorders
Melanie Loix, Sam Vanherle, Marta Turri, et al.
Histochemistry and Cell Biology
|
March 31, 2019
Peroxisomes: new insights into protein sorting, dynamics, quality control, signalling and roles in health and disease
Joseph L Costello, Einat Zalckvar, Stephan Kemp, et al.
Clinical Neurology and Neurosurgery
|
September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"
Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
Molecular Genetics and Metabolism
|
January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy
Stephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Experimental Cell Research
|
August 9, 2005
Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastoma
Annemieke J M de Ruijter, Rutger J Meinsma, Peter Bosma, et al.
Brain : a Journal of Neurology
|
December 12, 2018
Progression of myelopathy in males with adrenoleukodystrophy: towards clinical trial readiness
Irene C Huffnagel, Wouter J C van Ballegoij, Björn M van Geel, et al.
Orphanet Journal of Rare Diseases
|
August 15, 2012
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
Marc Engelen, Stephan Kemp, Marianne de Visser, et al.
Molecular Genetics and Metabolism
|
July 12, 2003
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry
Fredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, et al.
American Journal of Medical Genetics. Part A
|
April 5, 2013
Intellectual disability and hemizygous GPD2 mutation
Daniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Page
of 11