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Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1991
Improved synthesis of [1-14C]acyl-sphingosine-galactose-3-sulfate (sulfatide) for diagnosis of metachromatic leukodystrophy: usefulness of radioscanningM Masson, W X Li, A L Fluharty, et al.
Revue Neurologique|April 1, 2005
[Presentation of Niemann-Pick type C disease with psychiatric disturbance in an adult]L Tyvaert, T Stojkovic, J-M Cuisset, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from FranceG Lucotte, S Berriche, C Bathelier, et al.
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.
Rehabilitation Nursing : the Official Journal of the Association of Rehabilitation Nurses|May 31, 2002
A patient acuity and staffing tool for stroke rehabilitation inpatients based on the FIM instrumentJ C Gross, E A Faulkner, S W Goodrich, et al.
Clinical Nursing Research|March 8, 2002
Determining stroke rehabilitation inpatients' level of nursing careJ C Gross, S W Goodrich, M E Kain, 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.
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