Results 141 to 150 of about 10,460 (201)

Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis: A Case Report. [PDF]

Neurol Genet
Parmar JM, McNamara EL, Lamont PJ, Kumar KR, Rick A, Stoll M, Cheong PL, Ravenscroft G.   +7 more
europepmc   +1 more source

Radiological Changes in the Spinal Cord and Brain of Patients with HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP). [PDF]

Pathogens
Stack EH, Okar SV, Wu T, Stack M, Mina Y, Gaitán M, Azodi S, Frazier W, Ohayon J, Cortese ICM, Reich DS, Nair G, Jacobson S.   +12 more
europepmc   +1 more source

Progression of HTLV-1 Associated Myelopathy/Tropical Spastic Paraparesis after Pregnancy: A Case Series and Review of the Literature. [PDF]

Pathogens
Jacquerioz FA, La Rosa M, González-Lagos E, Alvarez C, Tipismana M, Luhmann K, Gotuzzo E.   +6 more
europepmc   +1 more source

Disseminated Cavernous Malformations Due to <i>KRIT1</i> Gene Mutation Causing Seizure and Spastic Paraparesis. [PDF]

Ann Indian Acad Neurol
Gomathy SB, Das A, Garg A, Srivastava AK.   +3 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. Neuropathological studies of the patients with hepatic myelopathy have demonstrated demyelination of the lateral corticospinal tracts with various degree of axonal loss ...
Ufuk Utku, Talip Asil, 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