نتایج جستجو برای: paraplegia

تعداد نتایج: 4533  

2011
Yuko Wada Yo Nishimura Kimio Hashimoto

In this report, we describe the case of a patient with splenic marginal zone lymphoma (SMZL) who presented with spastic paraplegia as the initial symptom. A 42-year-old male developed progressive spastic paraplegia over 4 months. His neurologic examination revealed paraplegia with pyramidal syndrome, hypoesthesia below the T1 level, and anal hypotonia. Magnetic resonance imaging (MRI) of the sp...

Journal: :Archives of neurology 2007
Neviana Ivanova Kristl G Claeys Tine Deconinck Ivan Litvinenko Albena Jordanova Michaela Auer-Grumbach Jana Haberlova Ann Löfgren Gisele Smeyers Eva Nelis Rudy Mercelis Barbara Plecko Josef Priller Josef Zámecník Berten Ceulemans Anne Kjersti Erichsen Erik Björck Garth Nicholson Michael W Sereda Pavel Seeman Ivo Kremensky Vanio Mitev Peter De Jonghe

OBJECTIVE To study the frequency and distribution of mutations in SPG3A in a large cohort of patients with hereditary spastic paraplegia. DESIGN We screened a large cohort of 182 families and isolated cases with pure or complex hereditary spastic paraplegia phenotypes, which were negative for mutations in SPG4. RESULTS In 12 probands (6.6%), we identified 12 different SPG3A mutations (11 mi...

Journal: :Archives of physical medicine and rehabilitation 2007
John E Lewis Mark S Nash Larry F Hamm Shannon C Martins Suzanne L Groah

OBJECTIVE To examine the relationship between psychologic cues of somatic stress and physiologic responses to exercise in persons with paraplegia and tetraplegia. DESIGN Repeated measures with 2 comparison groups. SETTING Academic medical center. PARTICIPANTS Forty-two subjects between 18 and 69 years of age with motor-complete spinal cord injury (SCI) resulting in paraplegia or tetrapleg...

مدقق, باقر,

A thirteen years old girl was referred for back pain and right thoracic scoliosis, complete spastic paraplegia, bladder and bowel incontinence . The patient had history of back pain for a 4 year period eventually leading to scoliosis and neurological deficiency. Symptoms gradually worsened up to 4 months before admission converting to complete spastic paraplegia and bladder and bowel incontinen...

Journal: :Chest 1996
E Singas M Lesser A M Spungen W A Bauman P L Almenoff

Previously, we found that never-smokers with quadriplegia were hyperresponsive to aerosolized methacholine. To further explore the phenomenon, we compared responsiveness to methacholine in never-smokers with that of smokers and ex-smokers. We also evaluated responsiveness in subjects with high paraplegia (lesions at T-1 to T-6) or low paraplegia (lesions at T-7 and below). We found that smokers...

Journal: :Journal of rehabilitation research and development 2008
Limor Agam Amit Gefen

This study assessed the suitability of a new portable system that is based on Hertz's contact theory for evaluating internal gluteal muscle stresses under the ischial tuberosities of wheelchair users in real-time as a risk indicator for a deep tissue injury. Sitting in a wheelchair was monitored and processed with the portable system for six control subjects and five individuals with paraplegia...

Journal: :British Journal of Surgery 2021

Abstract Introduction Paraplegia post-thoracoabdominal aortic aneurysm (TAAA) repair remains both a devastating and poorly understood complication. We related temporal changes in cellular protein composition of cerebrospinal fluid (CSF) to neurological outcomes after TAAA gain mechanistic insights driving paraplegia. Method Patients undergoing (open or endovascular) with CSF drain were prospect...

2003
John K. Fink

T he hereditary spastic paraplegias (HSPs) are inherited neurologic disorders in which the primary symptom is insidiously progressive difficulty walking due to lower extremity weakness and spasticity. There have been great strides in our knowledge of this group of disabling disorders; 20 HSP loci and 9 HSP genes have been discovered. Insights into the molecular causes of HSPs are beginning to e...

Journal: :Cell 2005
Steven M. Claypool Carla M. Koehler

Defects in the mitochondrial AAA protease family member, paraplegin, result in an autosomal recessive form of hereditary spastic paraplegia (HSP). In this issue of Cell, Nolden et al. (2005) report a new molecular mechanism for HSP based on the requirement of paraplegin for the proteolysis of a specific mitochondrial ribosomal protein. The processing of this substrate is required for robust tra...

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