kw.\*:("Paraplejía espasmódica hereditaria Strümpell-Lorrain")
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Hereditary spastic paraplegiaDENNIS, S. C; GREEN, N. E.Journal of pediatric orthopedics. 1988, Vol 8, Num 4, pp 413-417, issn 0271-6798Article
Autosomal dominant familial spastic paraplegia : report of a large New England familyCOOLEY, W. C; RAWNSLEY, E; MELKONIAN, G et al.Clinical genetics. 1990, Vol 38, Num 1, pp 57-68, issn 0009-9163, 12 p.Article
Familial spastic paraglegiaKAMMANT PHANTHUMCHINDA; BOONCHOUY SOMREALVONGKUL.Chot Mai Het Thang Phaet. 1989, Vol 72, Num 2, pp 62-66, issn 0125-2208Article
Severe diaphragm weakness in spinocerebellar degenerationMIER, A; BROPHY, C; HAVARD, C. W et al.Thorax. 1988, Vol 43, Num 1, pp 78-79, issn 0040-6376Article
MASA syndrome : clinical variability and linkage analysisRIETSCHEL, M; FRIEDL, W; UHLHAAS, S et al.American journal of medical genetics. 1991, Vol 41, Num 1, pp 10-14, issn 0148-7299Article
Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegiaSOLOWSKA, Joanna M; GARBERN, James Y; BAAS, Peter W et al.Human molecular genetics (Print). 2010, Vol 19, Num 14, pp 2767-2779, issn 0964-6906, 13 p.Article
Hereditary spastic paraplegia caused by the PLP1 'rumpshaker mutation'SVENSTRUP, Kirsten; GIRAUD, Geneviève; HJERMIND, Lena E et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 6, pp 666-672, issn 0022-3050, 7 p.Article
Dementia in SPG4 hereditary spastic paraplegia: Clinical, genetic, and neuropathologic evidenceMURPHY, S; GORMAN, G; BEETZ, C et al.Neurology. 2009, Vol 73, Num 5, pp 378-384, issn 0028-3878, 7 p.Article
Hypomanic behaviour associated with familial spastic paraplegiaJANSEN, P. H. P; KEYSER, A; RAES, B. C. M et al.European archives of psychiatry and neurological sciences. 1988, Vol 238, Num 1, pp 28-30, issn 0175-758XArticle
The autosomal dominant form of pure familial spastic paraplegia: clinical findings and linkage analysis of a large pedigreeBOUSTANY, R-M. N; FLEISCHNICK, E; ALPER, C. A et al.Neurology. 1987, Vol 37, Num 6, pp 910-915, issn 0028-3878Article
Apport de l'imagerie par résonance magnétique dans les maladies dégénératives spino-cérébelleuses: à propos de 8 cas = NMR imaging findings in spinocerebellous degenerative diseases: 8 case reportsNICOLAU, A; DIARD, F; FONTAN, D et al.Pédiatrie (Marseille). 1987, Vol 42, Num 5, pp 359-365, issn 0031-4021Article
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamicsERRICO, Alessia; BALLABIO, Andrea; RUGARLI, Elena I et al.Human molecular genetics (Print). 2002, Vol 11, Num 2, pp 153-163, issn 0964-6906Article
Spastic paraplegia associated with brachydactyly and cone shaped epiphysesFITZSIMMONS, J. S; GUILBERT, P. R.Journal of medical genetics. 1987, Vol 24, Num 11, pp 702-705, issn 0022-2593Article
Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detectionNIELSEN, Jørgen E; KOEFOED, Pernille; KJAERGAARD, Susanne et al.Prenatal diagnosis. 2004, Vol 24, Num 5, pp 363-366, issn 0197-3851, 4 p.Article
Hereditary pure spastic paraplegia : a study of nine familiesPOLO, J. M; CALLEJA, J; COMBARROS, O et al.Journal of neurology, neurosurgery and psychiatry. 1993, Vol 56, Num 2, pp 175-181, issn 0022-3050Article
Familiäre spastische Spinalparalyse : Klinisches Spektrum und differentialdiagnostische Erwägungen = Familial spastic paraplegia: clinical spectrum and electrophysiological results in 5 familiesKLEMM, E; TACKMANN, W.Fortschritte der Neurologie, Psychiatrie. 1991, Vol 59, Num 5, pp 176-182, issn 0720-4299, 7 p.Article
Familial spasmodic paraplegia with coordination disorders and neurosensory deafnessBADALYAN, L. O; YADGAROV, I. S; TEMIN, P. A et al.Žurnal nevropatologii i psihiatrii im. S.S. Korsakova. 1990, Vol 90, Num 9, pp 94-97, issn 0044-4588, 4 p.Article
Amyotrophy of the hands and pyramidal features of predominantly the legs segregating within one large familyDE VISSER, M; ONGERBOER DE VISSER, B. W; VERJAAL, M et al.Journal of the neurological sciences. 1988, Vol 88, Num 1-3, pp 241-246, issn 0022-510XConference Paper
Clinical features of hereditary spastic paraplegia due to spastin mutationMCDERMOTT, C. J; BURNESS, C. E; SHAW, P. J et al.Neurology. 2006, Vol 67, Num 1, pp 45-51, issn 0028-3878, 7 p.Article
Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegiaFICHERA, M; LO GIUDICE, M; FALCO, M et al.Neurology. 2004, Vol 63, Num 6, pp 1108-1110, issn 0028-3878, 3 p.Article
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaCICCARELLI, Francesca D; PATTON, Michael A; MCKUSICK, Victor A et al.Nature genetics. 2002, Vol 31, Num 4, pp 347-348, issn 1061-4036Article
Primary lateral sclerosis : clinical features, neuropathology and diagnostic criteriaPRINGLE, C. E; HUDSON, A. J; MUNOZ, D. G et al.Brain. 1992, Vol 115, pp 495-520, issn 0006-8950, 2Article
Altered excitatory amino acid function and morphology of the cerebellum of the spastic Han-Wistar ratCOHEN, R. W; FISHER, R. S; TAIHUNG DUONG et al.Molecular brain research. 1991, Vol 11, Num 1, pp 27-36, issn 0169-328XArticle
Etiological heterogeneity in X-linked spastic paraplegiaKEPPEN, L. D; LEPPERT, M. F; O'CONNELL, P et al.American journal of human genetics. 1987, Vol 41, Num 5, pp 933-943, issn 0002-9297Article
Motor protein mutations cause a new form of hereditary spastic paraplegiaCABALLERO OTEYZA, Andrés; BATTALOGLU, Esra; BENDER, Benjamin et al.Neurology. 2014, Vol 82, Num 22, pp 2007-2016, issn 0028-3878, 10 p.Article