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Une curieuse paraparésie = An uncommun paraparesiaBOUCHACOURT, P; HERVY, M.-P; FORETTE, F et al.Gazette médicale de France (1969). 1989, Vol 96, Num 36, pp 20-21, issn 0016-5557, 2 p.Article

HSP60 IS A RARE CAUSE OF HEREDITARY SPASTIC PARAPARESIS, BUT MAY ACT AS A GENETIC MODIFIERHEWAMADDUMA, C. A. A; KIRBY, J; KERSHAW, C et al.Neurology. 2008, Vol 70, Num 19, pp 1717-1718, issn 0028-3878, 2 p., 1Article

A 64-year-old woman with the abrupt onset of paraparesis after 10 months of of increasing episodic leg waeknessZERVAS, N. T; PILE-SPELLMAN, J.The New England journal of medicine. 1992, Vol 326, Num 12, pp 816-824, issn 0028-4793Article

Metastatic malignant struma ovarii presenting as paraparesis from a spinal metastasisMCDOUGALL, I. R; KRASNE, D; HANBERY, J. W et al.Journal of nuclear medicine. 1989, Vol 30, Num 3, pp 407-411, issn 0097-9058, 5 p.Article

Tropical spastic paraparesis and human T cell lymphotropic virus type 1 in the United KingdomCRUICKSHANK, J. K; RUDGE, P; DALGLEISH, A. G et al.Brain. 1989, Vol 112, Num 4, pp 1057-1090, issn 0006-8950, 34 p.Article

Clinical Reasoning: A case of slowly progressive painful paraparesisCORBETTO, Marzia; CAPONE, Fioravante; DENARO, Vincenzo et al.Neurology. 2014, Vol 82, Num 16, pp 1476-1479, issn 0028-3878, 4 p.Article

Paraparesis due to capsular hemorrhagesTAKAYA, Shigetoshi; HIROKI, Masahiko; SAWADA, Tsutomu et al.Neurology. 2004, Vol 62, Num 6, issn 0028-3878, p. 967Article

Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutationNICHOLAS, Anthony P; O'HEARN, Elizabeth; HOLMES, Susan E et al.Movement disorders. 2004, Vol 19, Num 6, pp 641-648, issn 0885-3185, 8 p.Article

Oculodentodigital dysplasia syndrome associated with anormal cerebral white matterGUTMANN, D. H; ZACKAI, E. H; MCDONALD-MCGINN, M et al.American journal of medical genetics. 1991, Vol 41, Num 1, pp 18-20, issn 0148-7299Article

Posterior fossa abnormalities in hereditary spastic paraparesis with spastin mutationsSCUDERI, C; FICHERA, M; CALABRESE, G et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 4, pp 440-443, issn 0022-3050, 4 p.Article

SPG11 compound mutations in spastic paraparesis with thin corpus callosumSAMARANCH, L; RIVEROL, M; MASDEU, J. C et al.Neurology. 2008, Vol 71, Num 5, pp 332-336, issn 0028-3878, 5 p.Article

Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformationWATERS, M. F; SHIELDS, D. C; MARTIN, N. A et al.Neurology. 2005, Vol 65, Num 6, pp 966-967, issn 0028-3878, 2 p.Article

Investigation of mitochondrial function in hereditary spastic paraparesisMCDERMOTT, C. J; TAYLOR, R. W; HAYES, C et al.Neuroreport (Oxford). 2003, Vol 14, Num 3, pp 485-488, issn 0959-4965, 4 p.Article

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15VANTAGGIATO, Chiara; CRIMELLA, Claudia; SANTORELLI, Filippo Maria et al.Brain. 2013, Vol 136, pp 3119-3139, issn 0006-8950, 21 p., 10Article

Serum concentration and genetic polymorphism in the 5'-untraslated region of VEGF is not associated with susceptibility to HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) in HTLV-I infected individualsSAITO, Mineki; USUKU, Koichiro; NOBUHARA, Yasuyuki et al.Journal of the neurological sciences. 2004, Vol 219, Num 1-2, pp 157-161, issn 0022-510X, 5 p.Article

Differentiation of Hereditary Spastic Paraparesis From Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron SyndromesBRUGMAN, Frans; VELDINK, Jan H; BRUYN, Richard P. M et al.Archives of neurology (Chicago). 2009, Vol 66, Num 4, pp 509-514, issn 0003-9942, 6 p.Article

Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene. CommentaryCHINNERY, P. F; KEERS, S. M; HOLDEN, M. J et al.Neurology. 2004, Vol 63, Num 4, pp 710-712, issn 0028-3878, 3 p.Article

Syndrome oculodentodigital révélé par une paraparésie spastique progressive = Progressive spastic paraplegia as a presentation of oculodentodigital syndromeNGUYEN, K; PHILIP, N; SUCHET, L et al.Revue neurologique (Paris). 2004, Vol 160, Num 1, pp 83-85, issn 0035-3787, 3 p.Article

HTLV seroepidemiology in a central African population with hight incidence of tropica spastic paraparesisGOUBAU, P; CARTON, H; KAZADI, K et al.Transactions of the Royal Society of Tropical Medicine and Hygiene. 1990, Vol 84, Num 4, pp 577-579, issn 0035-9203Article

Screening for prolonged incubation of HTLV-I infection in British and Jamaican relatives of British patients with tropical spastic paraparesisCRUICKSHANK, J. K; RICHARDSON, J. H; MORGAN, O. S. C et al.BMJ. British medical journal (International ed.). 1990, Vol 300, Num 6720, pp 300-304, issn 0959-8146Article

Spinocerebellar ataxia with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesisGEMIGNANI, F; WALTON, J.Journal of the neurological sciences. 1989, Vol 90, Num 3, pp 345-346, issn 0022-510X, 2 p.Article

Le concept de neuro-myélopathie tropicale = Tropical neuromyelopathy conceptDUMAS, M; GIORDANO, C; NDIAYE, I. P et al.Bulletin de la Société de pathologie exotique. 1988, Vol 81, Num 2, pp 183-188, issn 0037-9085Article

Skin infection and progressive paraparesisCARDENAS, Graciela; GUEVARA, Erik; DELGADO-HERNANDEZ, Rosa et al.Lancet. Infectious diseases (print). 2012, Vol 12, Num 5, issn 1473-3099, p. 422Article

Paraparésies des membres inférieursEL KHARRAS, A; DARBI, A; MINVIELLE, F et al.Feuillets de radiologie. 2008, Vol 48, Num 4, pp 260-263, issn 0181-9801, 4 p.Article

Severe resting clonus caused by thyrotoxicosis in a 16-year-old girl with hereditary spastic paraparesis: A case reportSANGER, Terence D.Movement disorders. 2004, Vol 19, Num 6, pp 712-713, issn 0885-3185, 2 p.Article

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