Results 21 to 30 of about 485 (123)

Neuromuscular Diseases and Rehabilitation [PDF]

, 2017
Neuromuscular diseases (NMDs) are a heterogeneous group of diseases that are inherited or acquired, resulting from an abnormality in the anterior horn motor cells, peripheral nerves, neuromuscular junctions, or ...
Demir, Yasemin Parlak
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구척수근위축증에서 감각신경병의 단면적 및 종적 연구 [PDF]

, 2014
Objectives: Bulbo-spinal muscular atrophy (BSMA) is an inherited motor neuronopathy, but it is known that subclinical sensory neuropathy can be found.
김승민, 선우일남
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Central excitability contributes to supramaximal volitional contractions in human incomplete spinal cord injury [PDF]

, 2011
Individuals with a motor incomplete spinal cord injury (SCI) present clinically with partial control of muscles below the site of the injury, but experience profound weakness which can limit the ability to perform functional tasks such as walking ...
Hornby, T George, Jayaraman, Arun, Lewek, Michael D, Thompson, Christopher K   +3 more
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Kennedy Disease Showing Prominent Remyelinating Features of Sural Nerve [PDF]

, 2010
We report a 55-year-old man with chronic weakness of both legs with recently experienced nasal voice. Despite the absence of sensory symptoms, electrophysiologic studies revealed the presence of sensorimotor polyneuropathy.
김승민, 김태승, 선우일남
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Ultrasound-guided percutaneous nerve stimulation in post-stroke spasticity: A case report [PDF]

Introduction: Post-stroke spasticity (PSS) significantly impacts the quality of life for stroke survivors. While various treatments exist, options for refractory cases are limited.
Picañol, Javier, Puig-Diví, Albert, Sartori, Francesco   +2 more
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The seminal vesicles : anatomy, comparative anatomy and development. [PDF]

, 2020
There are many reasons which induced me to choose this subject for a thesis. I would like to mentioned only the most important one. Between 1942 and 1945, while in the South African Medical Corps, I was posted to the Wynberg Military Hospital.
Retief, Peter John Mitford
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The cranial nerves [PDF]

, 2020
With the exception of the olfactory and optic nerves, all cranial nerves enter or leave the brain stem. Three of the cranial nerves are purely sensory (I, II and VIII), five are motor (III, IV, VI, XI and XII) and the remaining nerves (V, VII, IX and X ...
A Brodal, A Brodal, A Brodal, A Faurion, A Gavalas, A Gavalas, A Hafferl, A Jean, A King, A Leblanc, A Lumsden, A Strassman, A Zwergal, AD Craig, AD Craig, AJ Miller, AK Moschovakis, AK Moschovakis, AK Moschovakis, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AKE Horn, AM Graybiel, B Coiner, B Skarf, BO Genc, BW Ongerboer de Visser, BW Ongerboer de Visser, BW Peterson, C Evinger, C Fernandez, C Fernandez, C Fernandez, C Helmchen, C Pieh, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Pierrot-Deseilligny, C Suárez, C van Buskirk, C Watson, C Watson, CH Hockman, CS Konen, D Bowsher, DA McRitchie, DH Zald, DH Zald, DM Small, DM Small, DM Small, E Keshner, E Tarlov, E Tarlov, EC Engle, EC Engle, EC Engle, EC Engle, EC Ngwa, EM Carpenter, ET Rolls, ET Rolls, ET Rolls, ET Rolls, F Marín, F Müller, F van der Werf, FA Lenz, FL Wuyts, G Cascino, G Cruccu, G Heidary, G Hirose, G Holstege, G Holstege, G Holstege, G Paxinos, G Paxinos, G Ugolini, GR Holstein, H Ogawa, H Ogawa, HF Schuknecht, HGJM Kuypers, HGJM Kuypers, HGJM Kuypers, HJ Steiger, HJ ten Donkelaar, HJ ten Donkelaar, HJ ten Donkelaar, HJ ten Donkelaar, HJ ten Donkelaar, HJ ten Donkelaar, HM Duvernoy, HN Kim, I Dehaene, I Törk, I Vieille-Grosjean, IS Curthoys, J Baker, J Bogousslavsky, J Goldberg, J Jen, J Jen, J Lang, J Nageotte, J Olszewski, J Olszewski, J O’Doherty, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JA Büttner-Ennever, JC Rucker, JD Porter, JD Porter, JG McElligott, JG Osis, JH Allum, JI Lane, JI Lane, JR Guy, K Fukushima, K Onoda, K Sadjadpour, K Schmidtke, L Puelles, L Tomás-Roca, LM Luxon, M Aramideh, M Aramideh, M Brödel, M Dieterich, M Dieterich, M Dieterich, M Dieterich, M Dieterich, M Dieterich, M Imagawa, M Imagawa, M Kalia, M Kwon, M Pasqualetti, M Prosiegel, M Rossel, M Uemura, M Yamashita, M-M Mesulam, MA Barry, MA Tischfield, MB Carpenter, MB Carpenter, MB Carpenter, MG Hotchkiss, MG Veldhuizen, MJ Morrow, N Goto, N Mizuno, NJ Gutowski, NL Sicotte, NP Williams, NR Miller, O Combarros, O Meienberg, OJ Grüsser, OJ Grüsser, P Smith, P Vuilleumier, PH Schiller, PJ Jannetta, PJ Ranalli, PP Urban, PP Urban, PP Urban, PP Urban, PT Fox, R Baker, R Baloh, R Gunny, R Norgren, R O’Rahilly, R Perlia, R Warwick, RA Fay, RA Fay, RA Fay, RA McCrea, RA McCrea, RA McCrea, RE McMasters, RF Gasser, RJ Leigh, RJ Maciewicz, RJ Morecraft, RM Beckstead, RM Beckstead, RM Benjamin, RM Benjamin, RM Müri, RM Müri, RW Doty, S Akbarian, S Frey, S Guthrie, S Ito, S Love, S Rivaud, SB Eickhoff, SC Cannon, SC Carleton, SC Carleton, SE Thurston, SH Graham, SP Cordes, ST Carmichael, ST Carmichael, T Brandt, T Brandt, T Brandt, T Hirai, T Kobayakawa, T Kobayakawa, T Kokkoroyannis, T Miyazaki, T Satoda, TC Pritchard, TC Pritchard, TC Pritchard, TC Pritchard, TC Pritchard, TH Schwartz, TM Bosley, TM Bosley, TP Langer, TP Langer, V Henn, VJ Wilson, VJ Wilson, W Graf, W Guldin, W Lang, W Penfield, W Wurst, WJ Atkinson, WO Guldin, Y Nakajima, Y Suzuki, Y Uesaka, Á Esteban   +269 more
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The role of non-invasive camera technology for gait analysis in patients with vestibular disorders [PDF]

, 2017
Purpose of the study Current balance assessments performed in clinical settings do not provide objective measurements of gait. Further, objective gait analysis typically requires expensive, large and dedicated laboratory facilities.
Dimitriadis, Panagiotis, Dunn, Marcus, Ray, Jaydip   +2 more
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Characterizing Molecular Modifiers of Pathogenesis in Spinobulbar Muscular Atrophy. [PDF]

, 2015
Spinobulbar muscular atrophy (SBMA), or Kennedy’s disease, is an inherited neuromuscular disorder caused by a polyglutamine (polyQ) tract expansion in the androgen receptor (AR).
Carreon Chua, Jason P.
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Mucopolissacaridose e fossa posterior : achados de imagem por estudo de ressonância magnética [PDF]

, 2018
Introdução: Mucopolissacaridose (MPS) é uma doença multissistêmica hereditária integrante do grupo das desordens de depósito lisossomais. O sistema nervoso central é frequentemente acometido em pacientes com MPS, e exame de ressonância magnética (RM) é o
Reichert, Roberta
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