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Journal of Inherited Metabolic Disease
|
July 1, 1997
Nerve cell lesions caused by 3-hydroxyglutaric acid: a possible mechanism for neurodegeneration in glutaric acidaemia I
B Flott-Rahmel, C Falter, P Schluff, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie
|
October 23, 1998
Ciprofibrate--racemate and enantiomers: effects of a four-week treatment on male inbred Fischer rats. A biochemical and morphological study
W Klinger, A Lupp, E Karge, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13
U Peters, G Senger, M Rählmann, et al.
Human Mutation
|
July 19, 2002
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia
S Sauter, B Miterski, S Klimpe, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene
J Seidel, S Streck, K Bellstedt, et al.
Psychological Medicine
|
June 26, 2013
Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia
C C Schultz, T W Mühleisen, I Nenadic, et al.
Neurology
|
October 13, 2006
High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia
C Beetz, A O H Nygren, J Schickel, et al.
Human Molecular Genetics
|
June 1, 1997
A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees
R L Robinson, N Monnier, W Wolz, et al.
Pediatric Research
|
February 1, 1997
A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evolutionary consideration
K Tanaka, N Gregersen, A Ribes, et al.
Human Molecular Genetics
|
March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
N Fonknechten, D Mavel, P Byrne, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
Journal of Inherited Metabolic Disease
|
July 1, 1997
Nerve cell lesions caused by 3-hydroxyglutaric acid: a possible mechanism for neurodegeneration in glutaric acidaemia I
B Flott-Rahmel, C Falter, P Schluff, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie
|
October 23, 1998
Ciprofibrate--racemate and enantiomers: effects of a four-week treatment on male inbred Fischer rats. A biochemical and morphological study
W Klinger, A Lupp, E Karge, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13
U Peters, G Senger, M Rählmann, et al.
Human Mutation
|
July 19, 2002
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia
S Sauter, B Miterski, S Klimpe, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene
J Seidel, S Streck, K Bellstedt, et al.
Psychological Medicine
|
June 26, 2013
Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia
C C Schultz, T W Mühleisen, I Nenadic, et al.
Neurology
|
October 13, 2006
High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia
C Beetz, A O H Nygren, J Schickel, et al.
Human Molecular Genetics
|
June 1, 1997
A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees
R L Robinson, N Monnier, W Wolz, et al.
Pediatric Research
|
February 1, 1997
A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evolutionary consideration
K Tanaka, N Gregersen, A Ribes, et al.
Human Molecular Genetics
|
March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
N Fonknechten, D Mavel, P Byrne, et al.
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of 8