Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Hereditary spastic paraplegia")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 244

  • Page / 10
Export

Selection :

  • and

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 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

FAMILIAL SPASTIC PARAPLEGIA CLINICAL AND PATHOLOGIC STUDIES IN A LARGE KINDREDSACK GH JR; HUETHER CA; GARG N et al.1978; JOHNS HOPKINS MED. J.; USA; DA. 1978; VOL. 143; NO 4; PP. 117-121; BIBL. 36 REF.Article

THE LATE FORM OF PURE FAMILIAL SPASTIC PARAPLEGIAVERNEA J; SYMINGTON GR.1977; PROC. AUSTRAL. ASS. NEUROLOGISTS; AUS; DA. 1977 PUBL. 1978; VOL. 14; PP. 37-41; BIBL. 11 REF.Article

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegiaMAGARIELLO, Angela; MUGLIA, Maria; GAMBARDELLA, Antonio et al.Journal of the neurological sciences. 2010, Vol 288, Num 1-2, pp 96-100, issn 0022-510X, 5 p.Article

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

ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegiaTOLSTRUP NIELSEN, Troels; SVENSTRUP, Kirsten; BUDTZ JØRARGENSEN, Esben et al.Journal of the neurological sciences. 2012, Vol 321, Num 1-2, pp 100-102, issn 0022-510X, 3 p.Article

Novel compound heterozygous mutations of the SPG11 gene in Korean families with hereditary spastic paraplegia with thin corpus callosumKIM, Sung-Min; LEE, Jeong-Seon; KIM, Suhyun et al.Journal of neurology. 2009, Vol 256, Num 10, pp 1714-1718, issn 0340-5354, 5 p.Article

Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegiaSVENSTRUP, Kirsten; BROSS, Peter; NIELSEN, Jørgen E et al.Journal of the neurological sciences. 2009, Vol 284, Num 1-2, pp 90-95, issn 0022-510X, 6 p.Article

Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspotsBEETZ, Christian; SCHÜLE, Rebecca; DEUFEL, Thomas et al.Journal of the neurological sciences. 2008, Vol 268, Num 1-2, pp 131-135, issn 0022-510X, 5 p.Article

Spastin related hereditary spastic paraplegia with dysplastic corpus callosumALBER, Burkhard; PERNAUER, Magdalena; DULLINGER, Jörn et al.Journal of the neurological sciences. 2005, Vol 236, Num 1-2, pp 9-12, issn 0022-510X, 4 p.Article

THE SPINAL CANAL IN FAMILIAL SPASTIC PARAPLEGIAVASSILOPOULOS D; SPENGOS M; ZOUMBOU V et al.1981; EUR. NEUROL.; ISSN 0014-3022; CHE; DA. 1981; VOL. 20; NO 2; PP. 110-114; BIBL. 7 REF.Article

LA PARAPLEGIE SPASMODIQUE FAMILIALE (MALADIE DE STRUMPELL-LORRAIN). A PROPOS DE 11 GENEALOGIES.GRASSIN DY.1975; LYON; ASSOC. CORP. ETUD. MED.; DA. 1975; PP. 1-48; BIBL. 4 P.; (THESE DOCT. MED.; CLAUDE BERNARD-LYON)Thesis

AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY.BOUCHARD JP; BARBEAU A; BOUCHARD R et al.1978; CANAD. J. NEUROL. SCI.; CANADA; DA. 1978; VOL. 5; NO 1; PP. 61-69; ABS. FR.; BIBL. 38 REF.Article

STRUMPELL'S PURE FAMILIAL SPASTIC PARAPLEGIA: CASE STUDY AND REVIEW OF THE LITERATURE.HOLMES GL; SHAYWITZ BA.1977; J. NEUROL. NEUROSURG. PSYCHIATRY; G.B.; DA. 1977; VOL. 40; NO 10; PP. 1003-1008; BIBL. 31 REF.Article

PATTERN VISUAL EVOKED RESPONSES IN HEREDITARY SPASTIC PARAPLEGIALIVINGSTONE IR; MASTAGLIA FL; EDIS R et al.1981; J. NEUROL. NEUROSURG. PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1981; VOL. 44; NO 2; PP. 176-178; BIBL. 13 REF.Article

PERIPHERAL NERVE INVOLVEMENT IN FAMILIAL SPASTIC PARAPLEGIATREDICI G; MINOLI G.1979; ARCH. NEUROL.; USA; DA. 1979; VOL. 36; NO 4; PP. 236-239; BIBL. 12 REF.Article

LA PARAPLESIE SPASMODIQUE FAMILIALE DE STRUMPELL-LORRAIN (P.S.F.): UNE NOUVELLE OBSERVATION ANATOMO-CLINIQUEBUGE A; ESCOUROLLE R; RANCUREL G et al.1979; REV. NEUROL.; FRA; DA. 1979; VOL. 135; NO 4; PP. 329-337; ABS. ENG; BIBL. 24 REF.Article

ELECTROPHYSIOLOGICAL AND PATHOLOGICAL STUDIES IN SPINOCEREBELLAR DEGENERATIONS.MCLEOD JG; MORGAN JA.1976; PROC. AUSTRAL. ASS. NEUROLOGISTS; AUSTRAL.; DA. 1976; VOL. 13; PP. 113-117; BIBL. 9 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

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

Cognitive Profile in Spastic Paraplegia with Thin Corpus Callosum and Mutations in SPG11SIRI, L; BATTAGLIA, F. M; TESSA, A et al.Neuropediatrics. 2010, Vol 41, Num 1, pp 35-38, issn 0174-304X, 4 p.Article

  • Page / 10