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J C Turpin

Showing results (81-90 of 88) with videos related to

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American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Presse Medicale (Paris, France : 1983)|October 7, 1989
[Value of the early diagnosis of cerebral metastasis in non-small cell lung cancers]L Demange, L Tack, C Cossart, et al.
Neurology|January 1, 1990
Adult sphingomyelinase deficiency: report of 2 patients who initially presented with psychiatric disordersG Dubois, J M Mussini, M Auclair, et al.
Neurology|September 13, 2006
Late-onset metachromatic leukodystrophy: genotype strongly influences phenotypeH Rauschka, B Colsch, N Baumann, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
American Journal of Human Genetics|August 1, 1993
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophyJ Kreysing, W Bohne, C Bösenberg, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Presse Medicale (Paris, France : 1983)|October 7, 1989
[Value of the early diagnosis of cerebral metastasis in non-small cell lung cancers]L Demange, L Tack, C Cossart, et al.
Neurology|January 1, 1990
Adult sphingomyelinase deficiency: report of 2 patients who initially presented with psychiatric disordersG Dubois, J M Mussini, M Auclair, et al.
Neurology|September 13, 2006
Late-onset metachromatic leukodystrophy: genotype strongly influences phenotypeH Rauschka, B Colsch, N Baumann, et al.
Pageof 9