Results 141 to 150 of about 29,371 (197)

Imbalanced IL10/TGF-β production by regulatory T-lymphocytes in patients with HTLV-1-associated myelopathy/ tropical spastic paraparesis. [PDF]

BMC Infect Dis
Gois LL, Ribeiro-Soares B, Regis-Silva CG, Zanette DL, Lisboa R, Nascimento RS, Coutinho Junior R, Galvão-Castro B, Grassi MFR.   +8 more
europepmc   +1 more source

Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature. [PDF]

Neurogenetics
Cioffi E, Coppola G, Musumeci O, Gallone S, Silvestri G, Rossi S, Piemonte F, D'Amico J, Tessa A, Santorelli FM, Casali C.   +10 more
europepmc   +1 more source

Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability. [PDF]

Neurol Sci
Cioffi E, Gioiosa V, Tessa A, Petrucci A, Trovato R, Santorelli FM, Casali C.   +6 more
europepmc   +1 more source

Hepatic myelopathy with spastic paraparesis

Clinical Neurology and Neurosurgery, 2005
Progressive myelopathy is a rare neurological complication of chronic liver disease with portal hypertension and there is no special diagnostic tool for hepatic myelopathy.
Talip Asil, Yahya Çelik, Kemal Balcı
exaly   +5 more sources

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The neuropathology of hereditary spastic paraparesis

Clinical Neurology and Neurosurgery, 1992
Hereditary spastic paraparesis or Strümpell's disease is a genetically determined neurodegenerative disorder in which the signs and symptoms are predominant in the legs. Inheritance is usually autosomal dominant and in a minority recessive. Neuropathological study reveals a degeneration of the corticospinal tract decreasing from lower lumbar to ...
R P M Bruyn
exaly   +3 more sources

No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis

NeuroReport, 2007
Familial Alzheimer's disease due to presenilin 1 (PSEN1) mutations shows considerable phenotypic variability with differences in neuropathology and neurological symptoms. Spastic paraparesis is a common neurological phenotype associated with Alzheimer's disease arising from PSEN1 mutations.
Helena, Karlstrom, John B J, Kwok, Gillian C, Gregory, Marianne, Hallupp, William S, Brooks, Peter R, Schofield   +5 more
openaire   +2 more sources

Tropical spastic paraparesis

2023
A large number of causative agents can result in spinal cord disorders in the tropics including etiologies similar to those of temperate regions such as trauma, spinal bone and disc lesions, tumors, epidural abscess, and congenital malformations. Yet infectious and nutritional disorders differ in their higher prevalence in tropical regions including ...
openaire   +2 more sources

Tropical spastic paraparesis in an Aborigine

Medical Journal of Australia, 1993
To present the first documented case of human T-lymphotropic virus type I (HTLV-I) associated myelopathy/tropical spastic paraparesis in the Australian population.A 31-year-old Aboriginal man with an 18-month history of progressive weakness of the legs was found to have an upper motor neurone weakness of all limbs associated with sphincteric ...
N, Rajabalendaran, R, Burns, L C, Mollison, W, Blessing, M G, Kirubakaran, P, Lindschau   +5 more
openaire   +2 more sources

Hereditary spastic paraparesis

Clinical Neurology and Neurosurgery, 1993
R R Frants, R P M Bruyn, G W Padberg
exaly   +2 more sources