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581 documents classés par : 
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fulltext access Monoclonal antibodies to 65kDa glutamate decarboxylase induce epitope specific effects on motor and cognitive functions in rats.
Hampe C., Petrosini L., De Bartolo P., Caporali P., Cutuli D., Laricchiuta D., Foti F., Radtke J., Vidova V., Honnorat J. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 82 [inserm-00832792 - version 1]
fulltext access Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.
Ji Noh H., Ponting C. P., Boulding H. C., Meader S., Betancur C., Buxbaum J. D., Pinto D., Marshall C. R., Lionel A. C., Scherer S. W. et al
PLoS Genetics 9, 6 (2013) e1003523 [inserm-00834559 - version 1]
fulltext access Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
Milh M., Boutry-Kryza N., Sutera-Sardo J., Mignot C., Auvin S., Lacoste C., Villeneuve N., Roubertie A., Heron B., Carneiro M. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 80 [inserm-00829466 - version 1]
fulltext access Natural history of Barth syndrome: a national cohort study of 22 patients.
Rigaud C., Lebre A.-S., Touraine R., Beaupain B., Ottolenghi C., Chabli A., Ansquer H., Ozsahin H., Di Filippo S., De Lonlay P. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 70 [inserm-00823569 - version 1]
fulltext access Lupus enteritis: from clinical findings to therapeutic management.
Janssens P., Arnaud L., Galicier L., Mathian A., Hie M., Sene D., Haroche J., Veyssier-Belot C., Huynh-Charlier I., Grenier P. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 67 [inserm-00821479 - version 1]
fulltext access (Video-assisted surgery in children: Current progress and future perspectives).
Peycelon M., Parmentier B., Raquillet C., Louvet N., Audry G., Auber F.
Arch Pediatr 20, 5 (2013) 509-16 [inserm-00825077 - version 1]
fulltext access Clinicopathological study of glomerular diseases associated with sarcoidosis : A multicenter study.
Stehlé T., Joly D., Vanhille P., Boffa J.-J., Rémy P., Mesnard L., Hoffmann M., Grimbert P., Choukroun G., Vrtovsnik F. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 65 [inserm-00823377 - version 1]
fulltext access The dual effect of MSCs on tumour growth and tumour angiogenesis.
Kéramidas M., de Fraipont F., Karageorgis A., Moisan A., Persoons V., Richard M.-J., Coll J.-L., Rome C.
Stem Cell Research & Therapy 4, 2 (2013) 41 [inserm-00822004 - version 1]
restricted file access Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
Cattin M.-E., Bertrand A. T., Schlossarek S., Le Bihan M.-C., Skov Jensen S., Neuber C., Crocini C., Maron S., Lainé J., Mougenot N. et al
Human Molecular Genetics (2013) epub ahead of print [inserm-00826642 - version 1]
fulltext access Experimental designs for small randomised clinical trials: an algorithm for choice.
Cornu C., Kassai B., Fisch R., Chiron C., Alberti C., Guerrini R., Rosati A., Pons G., Tiddens H., Chabaud S. et al
Orphanet Journal of Rare Diseases 8, 1 (2013) 48 [inserm-00818031 - version 1]
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