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Human Molecular Genetics|January 1, 1993
Ten novel mutations in the HEXA gene in non-Jewish Tay-Sachs patientsS Akli, J C Chomel, J M Lacorte, et al.
Acta Physiologica (Oxford, England)|December 18, 2007
Combined effects of hypoxia and endurance training on lipid metabolism in rat skeletal muscleO Galbès, L Goret, C Caillaud, et al.
Molecular Genetics and Metabolism|January 29, 2010
Cognitive and neuroradiological improvement in three patients with attenuated MPS I treated by laronidaseV Valayannopoulos, N Boddaert, V Barbier, et al.
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1997
[Beta mannosidosis: a new case]E Gourrier, M P Thomas, A Munnich, et al.
Gene Therapy|September 1, 1996
Restoration of hexosaminidase A activity in human Tay-Sachs fibroblasts via adenoviral vector-mediated gene transferS Akli, J E Guidotti, E Vigne, et al.
Scandinavian Journal of Rheumatology|December 17, 2009
Bone and joint involvement in Fabry diseaseK Sacre, Olivier Lidove, B Giroux Leprieur, et al.
Oecologia|February 20, 2014
Coexistence in space and time of sexual and asexual populations of the cereal aphid Sitobion avenaeCharles-Antoine Dedryver, Maurice Hullé, Jean-François Le Gallic, et al.
Medicine and Science in Sports and Exercise|February 1, 1996
Influence of post-surgery time after cardiac transplantation on exercise responsesJ Mercier, N Ville, P Wintrebert, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
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