au.\*:("LEROY, Jean Paul")
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Vitamine A et défense immunitaireCLOT, Jacques; LEROY, Jean-Paul.La Revue du praticien. Médecine générale. 2008, Num 805, pp 678-683, issn 0989-2737, 6 p.Article
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferationAURE, Karine; FAYET, Guillemette; LEROY, Jean Paul et al.Brain. 2006, Vol 129, pp 1249-1259, issn 0006-8950, 11 p., 5Article
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesiaROMERO, Norma Beatriz; MONNIER, Nicole; VIOLLET, Louis et al.Brain. 2003, Vol 126, pp 2341-2349, issn 0006-8950, 9 p., 11Article
Association myosite à inclusions et sarcoïdose : à propos de trois cas = Inclusion body myositis associated with sacroidosis : a report of 3 casesBOUILLOT, Sandrine; COQUET, Michelle; FERRER, Xavier et al.Annales de pathologie (Paris). 2001, Vol 21, Num 4, pp 334-336, issn 0242-6498Article
LA PRATIQUE SPORTIVE DANS L'HABITAT SOCIAL. RECHERCHE SUR LES CONDITIONS SOCIOLOGIQUES, INSTITUTIONNELLES ET TECHNIQUE D'UN MEILLEUR USAGE POUR LES SPORTS DES ESPACES ET EQUIPEMENTS COLLECTIFS DANS L'HABITAT SOCIALLEROY JEAN PAUL; DEVE FLORENCE; FIANT MICHEL et al.1978; ; FRA; DA. 1978; DGRST/77 7 0810; 117 P.; 30 CM; BIBL. 30 REF.; ACTION CONCERTEE: SPORTSReport
The origin of tubular aggregates in human myopathiesCHEVESSIER, Frédéric; BAUCHE-GODARD, Stéphanie; LEROY, Jean-Paul et al.Journal of pathology. 2005, Vol 207, Num 3, pp 313-323, issn 0022-3417, 11 p.Article
Phosphonocationic lipids in protein delivery to mice lungsGUILLAUME, Christine; DELEPINE, Pascal; MERCIER, Bernard et al.Journal of pharmaceutical sciences. 2000, Vol 89, Num 5, pp 639-645, issn 0022-3549Conference Paper
Localisation temporale d'un lymphome = Lymphoma involving the temporal arteryPOTARD, Mireille; ANSART, Séverine; HUTIN, Pascal et al.Annales de médecine interne (Paris). 2000, Vol 151, Num 6, pp 513-515, issn 0003-410XArticle
Abnormal distribution of calcium-handling proteins : A novel distinctive marker in core myopathiesHERASSE, Muriel; PARAIN, Karine; MARTY, Isabelle et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 1, pp 57-65, issn 0022-3069, 9 p.Article
Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: Reassessing the nosology of early-onset myopathiesFERREIRO, Ana; QUIJANO-ROY, Susana; ROMERO, Norma B et al.American journal of human genetics. 2002, Vol 71, Num 4, pp 739-749, issn 0002-9297, 11 p.Article
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 geneFERREIRO, Ana; MONNIER, Nicole; LEMAINQUE, Arnaud et al.Annals of neurology. 2002, Vol 51, Num 6, pp 750-759, issn 0364-5134Article
MUSK, a new target for mutations causing congenital myasthenic syndromeCHEVESSIER, Frédéric; FARAUT, Brice; AZULAY, Jean-Philippe et al.Human molecular genetics (Print). 2004, Vol 13, Num 24, pp 3229-3240, issn 0964-6906, 12 p.Article
Caractérisation physiopathologique des syndromes myasthéniques congénitaux : l'exemple de mutations dans le gène MUSK = Pathophysiological characterization of congenital myasthenic syndromes : the example of mutations in the MUSK geneCHEVESSIER, Frédéric; FARAUT, Brice; AZULAY, Jean-Philippe et al.Journal de la Société de biologie. 2005, Vol 199, Num 1, pp 61-77, issn 1295-0661, 17 p.Conference Paper