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Les amyotrophies spinales de l'adulte: à propos d'un cas = Spinal amyotrophy in adults: case reportLABENNE, M; REIS, J; WASSER, P et al.Journal de médecine de Strasbourg. 1986, Vol 17, Num 4, pp 201-203, issn 0021-7905Article

Spinal monomelic amyotrophySERRATRICE, G.Advances in neurology. 1991, Vol 56, pp 169-173, issn 0091-3952Article

Amyotrophie spinale progressive distale et asymétrique des membres inférieurs à caractère familial = Assymetrical, familial chronic spinal muscular atrophy involving the lower limbsNEDELEC, C; DUBAS, F; TRUELLE, J. L et al.Revue neurologique (Paris). 1987, Vol 143, Num 11, pp 765-767, issn 0035-3787Article

Static spinal muscular atrophy causing temporomandibular joint dysfunctionBAILEY, R. O; RADIN, A. B.Journal of oral and maxillofacial surgery. 1987, Vol 45, Num 2, pp 182-184, issn 0278-2391Article

A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophyJANSEN, P. H. P; JOOSTEN, E. M. G; JASPAR, H. H. J et al.Annals of neurology. 1986, Vol 20, Num 4, pp 538-540, issn 0364-5134Article

Population data on acute infantilej and chronic childhood spinal muscular atrophy in WarsawSPIEGLER, A. W. J; HAUSMANOWA-PETRUSEWICZ, I; BORKOWSKA, J et al.Human genetics. 1990, Vol 85, Num 2, pp 211-214, issn 0340-6717Article

Therapeutic benefits of cardiotrophin-1 gene transfer in a mouse model of spinal muscular atrophyLESBORDES, Jeanne-Claire; CIFUENTES-DIAZ, Carmen; MIROGLIO, Audrey et al.Human molecular genetics (Print). 2003, Vol 12, Num 11, pp 1233-1239, issn 0964-6906, 7 p.Article

Electromyographic and computed tomographic findings in five patients with monomelic spinal muscular atrophyDE VISSER, M; ONGERBOER DE VISSER, B. W; VERBEETEN, B. JR et al.European neurology. 1988, Vol 28, Num 3, pp 135-138, issn 0014-3022Article

A propos d'un cas féminin de syndrome de la colonne raide = Report of a case of rigid spine syndrom in femaleBEN HAMIDA, M; HENTATI, F; BEN HAMIDA, C et al.Tunisie médicale. 1986, Vol 64, Num 6-7, pp 645-648, issn 0041-4131Article

Observational study of spinal muscular atrophy type I and implications for clinical trialsFINKEL, Richard S; McDERMOTT, Michael P; OSKOUI, Maryam et al.Neurology. 2014, Vol 83, Num 9, pp 810-817, issn 0028-3878, 8 p.Article

Corticomotoneuronal Integrity and Adaptation in Spinal Muscular AtrophyFARRAR, Michelle A; VUCIC, Steve; JOHNSTON, Heather M et al.Archives of neurology (Chicago). 2012, Vol 69, Num 4, pp 467-473, issn 0003-9942, 7 p.Article

Observational Study of Spinal Muscular Atrophy Type 2 and 3: Functional Outcomes Over 1 YearKAUFMANN, Petra; MCDERMOTT, Michael P; TAWIL, Rabi et al.Archives of neurology (Chicago). 2011, Vol 68, Num 6, pp 779-786, issn 0003-9942, 8 p.Article

The spinal muscular atrophy disease protein SMN is linked to the rho-kinase pathway via profilinNÖLLE, Anna; ZEUG, Andre; JABLONKA, Sibylle et al.Human molecular genetics (Print). 2011, Vol 20, Num 24, pp 4865-4878, issn 0964-6906, 14 p.Article

Stem Cell Model of Spinal Muscular AtrophyEBERT, Allison D; SVENDSEN, Clive N.Archives of neurology (Chicago). 2010, Vol 67, Num 6, pp 665-669, issn 0003-9942, 5 p.Article

The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestorBERNAL, S; ALIAS, L; BORREGO, S et al.Journal of medical genetics. 2010, Vol 47, Num 9, pp 640-642, issn 0022-2593, 3 p.Article

A Positive Modifier of Spinal Muscular Atrophy in the SMN2 GenePRIOR, Thomas W; KRAINER, Adrian R; YIMIN HUA et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 408-413, issn 0002-9297, 6 p.Article

Motor neuron degeneration in a 20-week male fetus : Spinal muscular atrophy type 0SARNAT, Harvey B; TREVENEN, Cynthia L.Canadian journal of neurological sciences. 2007, Vol 34, Num 2, pp 215-220, issn 0317-1671, 6 p.Article

Spine deformity in Spinal muscular atrophySUCATO, Daniel J.Journal of bone and joint surgery. American volume. 2007, Vol 89A, pp 148-154, issn 0021-9355, 7 p., SUP1Conference Paper

In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproateBRICHTA, Lars; HOLKER, Irmgard; HAUG, Karsten et al.Annals of neurology. 2006, Vol 59, Num 6, pp 970-975, issn 0364-5134, 6 p.Article

Evidence of reduced frequency of spinal muscular atrophy type I in the cuban populationZALDIVAR, T; MONTEJO, Y; ACEVEDO, A. M et al.Neurology. 2005, Vol 65, Num 4, pp 636-638, issn 0028-3878, 3 p.Article

Bone mineral density in a paediatric spinal muscular atrophy populationKINALI, M; BANKS, L. M; MERCURI, E et al.Neuropediatrics. 2004, Vol 35, Num 6, pp 325-328, issn 0174-304X, 4 p.Article

Phenotypic variability in siblings with type III spinal muscular atrophyMUQIT, M. M. K; MOSS, J; SEWRY, C et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 12, pp 1762-1764, issn 0022-3050, 3 p.Article

Amyotrophies spinales progressives = Progressive spinal amyotrophySERRATRICE, G.La Presse médicale (1983). 1998, Vol 27, Num 6, pp 269-272, issn 0755-4982Article

Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron geneGAMBARDELLA, A; MAZZEI, R; AGUGLIA, U et al.Annals of neurology. 1998, Vol 44, Num 5, pp 836-839, issn 0364-5134Article

Spinal muscular atrophy : A clinicopathologic analysisRADHAKRISHNAN, V. V; NAIR, M. D; KURUVILLA, A et al.Indian journal of pediatrics. 1997, Vol 64, Num 5, pp 687-691, issn 0019-5456Article

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