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Journal of the Neurological Sciences|February 1, 1992
A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidenceN Augier, J Boucraut, J Léger, et al.
American Journal of Medical Genetics|October 23, 1997
Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chainB Chabrol, S Sigaudy, V Paquis, et al.
Acta Anaesthesiologica Scandinavica|August 19, 2004
Comparative analysis of in vitro contracture tests with ryanodine and a combination of ryanodine with either halothane or caffeine: a comparative investigation in malignant hyperthermiaD Bendahan, S Guis, N Monnier, et al.
Blood|July 1, 1984
Prolongation of sickle cell survival by dimethyl adipimidate is compromised by immune sensitizationM S Guis, W M Lande, N Mohandas, et al.
Epilepsia|March 1, 1994
Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsyP Tinuper, G Plazzi, L Monari, et al.
Pediatric Transplantation|March 24, 2000
Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failureA Delarue, O Paut, J M Guys, et al.
American Journal of Medical Genetics|February 27, 1995
Lafora disease is not linked to the Unverricht-Lundborg locusP Labauge, C Beck, H Bellet, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.
Arthritis and Rheumatism|March 27, 2001
Influence of shared epitope-negative HLA-DRB1 alleles on genetic susceptibility to rheumatoid arthritisD Reviron, A Perdriger, E Toussirot, et al.
Pediatric Hematology and Oncology|July 1, 1992
Cytogenetic studies in 45 pediatric brain tumorsA M Vagner-Capodano, J C Gentet, D Gambarelli, et al.
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