Results 81 to 90 of about 10,460 (201)

Epilepsia secundária a neurocisticercose: número de calcificações x tipos de crises [PDF]

open access: yes, 2001
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Newton, Fábio Antunes
core  

Mania associated with complicated hereditary spastic paraparesis

open access: yes, 2011
Hereditary spastic paraparesis (HSP) is an inherited group of neurological disorders with progressive lower limb spasticity. HSP can be clinically grouped into pure and complicated forms.
Raghavendra B Nayak   +3 more
core   +1 more source

Tropical spastic paraparesis.

open access: yesFolia neuropathologica, 2002
Human T-cell lymphotropic virus type I (HTLV-I) is the cause of endemic tropical spastic paraparesis (TSP) or HTLV-I-associated myelopathy (HAM). Because TSP/HAM is not a fatal disease, the neuropathology of this disease, albeit relatively well understood, is based on the examination of just a few incidental cases.
J, Buczyński   +10 more
openaire   +1 more source

Alzheimer's disease with spastic paraparesis and 'cotton wool' plaques: two pedigrees with PS-1 exon 9 deletions

open access: yes, 2003
Several pedigrees have recently been reported in which dominantly inherited familial Alzheimer’s disease is associated in some family members with spastic paraparesis and non-neuritic ‘cotton wool’ plaques.
Broe, G.   +8 more
core   +1 more source

ALDH18A1‐related hereditary spastic paraplegia and developmental and epileptic encephalopathy with spike‐wave activation in sleep: Expanding the clinical phenotype

open access: yesAnnals of the Child Neurology Society
Objective We present the cases of two sisters, both harboring the same ALDH18A1 gene mutations, who presented with a complex clinical phenotype characterized by spastic paraparesis with ataxia, epileptic encephalopathy, severe psychomotor deficits, and ...
Giusi Ferrara   +6 more
doaj   +1 more source

Overlapping Aicardi–Goutières and Singleton–Merten syndromes with a heterozygous gain-of-function mutation in IFIH1 mimicking juvenile idiopathic arthritis

open access: yesImmunological Medicine
Aicardi–Goutières syndrome (AGS) and Singleton–Merten syndrome (SMS) are associated with heterozygous gain-of-function mutations in the interferon induced with helicase C domain 1 (IFIH1) gene.
Susumu Yamazaki   +10 more
doaj   +1 more source

X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report

open access: yesJournal of International Medical Research
X-linked adrenoleukodystrophy is a rare peroxisomal disorder caused by mutations in ABCD1 , thereby resulting in impaired β-oxidation of very long-chain fatty acids.
Min Cheol Chang, Seoyon Yang
doaj   +1 more source

Tropical spastic paraparesis in Kerala, South India

open access: yes, 2003
Tropical Spastic Paraparesis (TSP) is an uncommon myeloneuropathy with an insular geographic distribution. In 1985, Human T-lymphotropic virus type I (HTLV-1) was reported to be a possible etiological factor.1 We did an epidemiological, clinical and ...
A. Oomman, M. Madhusoodanan
core   +2 more sources

Hepatic myelopathy neurological complication of chronic liver disease: two case reports

open access: yesJournal of Medical Case Reports
Background Hepatic myelopathy is a very rare neurological complication of chronic liver disease. Patients habitually present with progressive pure motor spastic paraparesis.
Mariem Mhiri   +12 more
doaj   +1 more source

The effect of progressive static stretching on treatment of spastic paraparesis in patients with cerebral palsy [PDF]

open access: yes, 2017
Title: The effect of progressive static stretching on treatment of spastic paraparesis in patients with cerebral palsy Objectives: The goal of this dissertation is to evaluate the effect of progressive static stretching on treatment of spastic ...
Prachařová, Eva
core  

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