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Showing results (31-40 of 40) with videos related to

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Neuroradiology|November 1, 1995
Leukoencephalopathy with swelling in children and adolescents: MRI patterns and differential diagnosisM S van der Knaap, J Valk, P G Barth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 21, 2013
A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 geneJ A Coebergh, D E Fransen van de Putte, I N Snoeck, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger syndrome in a preterm, small for gestational age infantJ F Samsom, C Jakobs, J van de Klei-van Moorsel, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
Monographs in Allergy|January 1, 1988
Junctional plasticity in hereditary myastheniaF G Jennekens, H Veldman, J H Wokke, et al.
Human Genetics|September 1, 1995
Molecular basis of phenotypic variation in patients with argininemiaT Uchino, S E Snyderman, M Lambert, et al.
The Journal of Clinical Investigation|August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamilA A Benders, J H Veerkamp, A Oosterhof, et al.
Pediatric Research|May 1, 1996
Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathyM Huizing, W Ruitenbeek, F P Thinnes, et al.
Annals of Neurology|July 1, 1997
Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalitiesM S van der Knaap, L M Smit, P G Barth, et al.
Human Genetics|March 10, 1999
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Neuroradiology|November 1, 1995
Leukoencephalopathy with swelling in children and adolescents: MRI patterns and differential diagnosisM S van der Knaap, J Valk, P G Barth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 21, 2013
A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 geneJ A Coebergh, D E Fransen van de Putte, I N Snoeck, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger syndrome in a preterm, small for gestational age infantJ F Samsom, C Jakobs, J van de Klei-van Moorsel, et al.
Human Genetics|March 1, 1996
A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familyE A Sistermans, I J de Wijs, R F de Coo, et al.
Monographs in Allergy|January 1, 1988
Junctional plasticity in hereditary myastheniaF G Jennekens, H Veldman, J H Wokke, et al.
Human Genetics|September 1, 1995
Molecular basis of phenotypic variation in patients with argininemiaT Uchino, S E Snyderman, M Lambert, et al.
The Journal of Clinical Investigation|August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamilA A Benders, J H Veerkamp, A Oosterhof, et al.
Pediatric Research|May 1, 1996
Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathyM Huizing, W Ruitenbeek, F P Thinnes, et al.
Annals of Neurology|July 1, 1997
Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalitiesM S van der Knaap, L M Smit, P G Barth, et al.
Human Genetics|March 10, 1999
Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyA B Van Kuilenburg, P Vreken, N G Abeling, et al.
Pageof 4