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kw.\*:("PARAPLEGIE SPASMODIQUE HEREDITAIRE STRUMPELL LORRAIN")

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HEREDITARY "PURE" SPASTIC PARAPLEGIA: A CLINICAL AND GENETIC STUDY OF 22 FAMILIESHARDING AE.1981; J. NEUROL. NEUROSURG. PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1981; VOL. 44; NO 10; PP. 871-883; BIBL. 58 REF.Article

PARALISI SPINALE SPASTICA PURA AD ESCORDIO PRECOCE. STUDIO DI UN CEPO FAMILIAREPASCOTTO A; MORIERI A; SALVATI G et al.1975; NEUROPSICHIATR. INFANT.; ITAL.; DA. 1975; NO 166-167; PP. 247-260; ABS. ANGL.; BIBL. 18 REF.Article

HEEL DEFORMITY IN HEREDITARY SPASTIC PARAPLEGIAROTHSCHILD H; SHOJI H; MCCORMICK D et al.1981; CLIN. ORTHOP. RELAT. RES.; ISSN 0009-921X; USA; DA. 1981; NO 160; PP. 48-51; BIBL. 7 REF.Article

Hereditary spastic paraplegiaDENNIS, S. C; GREEN, N. E.Journal of pediatric orthopedics. 1988, Vol 8, Num 4, pp 413-417, issn 0271-6798Article

OSTEOPETROSIS ASSOCIATED WITH FAMILIAL PARAPLEGIA: REPORT OF A FAMILY = OSTEOPETROSE ASSOCIEE A UNE PARAPLEGIE FAMILIALE. PRESENTATION D'UNE FAMILLEJACQUES S; GARNER JT; JOHNSON D et al.1975; PARAPLEGIA; G.B.; DA. 1975; VOL. 13; NO 3; PP. 143-152; ABS. FR. ALLEM.; BIBL. 1 P.Article

HEREDOFAMILIAL SYNDROME OF SPASTIC PARAPLEGIA, DYSARTHRIA AND CUTANEOUS LESIONS IN FIVE SIBLINGSBAHEMUKA M; BROWN JD.1982; DEV. MED. CHILD NEUROL.; ISSN 0012-1622; GBR; DA. 1982; VOL. 24; NO 4; PP. 519-524; ABS. FRE/GER/SPA; BIBL. 16 REF.Article

VISUAL, AUDITORY AND SOMATOSENSORY PATHWAY INVOLVEMENT IN HEREDITARY CEREBELLAR ATAXIA, FRIEDREICH'S ATAXIA AND FAMILIAL SPASTIC PARAPLEGIAPEDERSEN L; TROJABORG W.1981; ELECTROENCEPHALOGR. CLIN. NEUROPHYSIOL.; ISSN 0013-4694; NLD; DA. 1981; VOL. 52; NO 4; PP. 283-297; ABS. FRE; BIBL. 2 P.Article

FAMILIAL SPASTIC PARAPLEGIA WITH KALLMANN'S SYNDROMETUCK RR; O'NEILL BP; GHARIB H et al.1983; JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1983; VOL. 46; NO 7; PP. 671-674; BIBL. 36 REF.Article

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 paraplegia, mental retardation, and precocious pubertyRAPHAELSON, M. I; STEVENS, J. C; ELDERS, J et al.Archives of neurology (Chicago). 1983, Vol 40, Num 13, pp 809-810, issn 0003-9942Article

THE ACUTE EFFECT OF THE GABA-AGONIST, THIP, ON PROPRIOCEPTIVE AND FLEXOR REFLEXES IN SPASTIC PATIENTSMONDRUP K; PEDERSEN E.1983; ACTA NEUROLOGICA SCANDINAVICA; ISSN 0001-6314; DNK; DA. 1983; VOL. 67; NO 1; PP. 48-54; BIBL. 17 REF.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

THE NASOLOGY OF GENETIC PERIPHERAL NEUROPATHIES IN SWEDISH CHILDRENHAGBERG B; WESTERBERG B.1983; DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; ISSN 0012-1622; GBR; DA. 1983; VOL. 25; NO 1; PP. 3-18; ABS. FRE/GER/SPA; BIBL. 1 P.Article

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

Cerebellar degeneration in dominantly inherited spastic paraplegiaSCHOLTZ, C. L; SWASH, M.Journal of neurology, neurosurgery and psychiatry. 1985, Vol 48, Num 2, pp 145-149, issn 0022-3050Article

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

Comparative study of visual evoked potentials in spinocerebellar ataxias and multiple sclerosisGHEZZI, A; MONTANINI, R.Acta neurologica scandinavica. 1985, Vol 71, Num 3, pp 252-256, issn 0001-6314Article

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

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