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2010, 1, ISBN 9780195379099, xvii, 537
The study of anosognosia has witnessed an unprecedented increase in interest over the last 20 years. This has resulted in numerous empirical investigations as... 
Neurodegenerative Diseases | rehabilitation | psychology | Awareness | Nervous system | Hemiplegia | Degeneration | Anosognosia | Agnosia | Clinical & internal medicine | Rehabilitation | Internal medicine
Book
1995, International review of child neurology, ISBN 0781701635, xxiii, 216
Book
Book
2011, 1st, ISBN 9781908316400
This highly accessible guide describes how and why hemiplegia occurs, outlining the different approaches to therapy. It sets out guidance on how to support the... 
Hemiplegia
Web Resource
Toxicon, ISSN 0041-0101, 12/2018, Volume 156, p. S28
Journal Article
Case Report - Neurocysticercosis presenting as Weber’s syndrome: As short report, 12/2003
This case report describes a rare, non-epileptic manifestation of neurocysticercosis where a 22-year-old male presented with acute onset right 3rd nerve palsy... 
Cysticercosis, Hemiplegia
Journal
2004, ISBN 1560536047, xvi, 414
A great majority of people with neuromuscular diseases like muscular dystrophy, ALS, spinal muscular atrophy, myasthenia gravis and post-poliomyelitis continue... 
Neuromuscular Diseases | therapy | Respiratory Therapy
Book
by Panagiotakaki, Eleni and De Grandis, Elisa and Stagnaro, Michela and Heinzen, Erin L and Fons, Carmen and Sisodiya, Sanjay and De Vries, Boukje and Goubau, Christophe and Weckhuysen, Sarah and Kemlink, David and Scheffer, Ingrid and Lesca, Gaëtan and Rabilloud, Muriel and Klich, Amna and Ramirez-Camacho, Alia and Ulate-Campos, Adriana and Campistol, Jaume and Giannotta, Melania and Moutard, Marie-Laure and Doummar, Diane and Hubsch-Bonneaud, Cecile and Jaffer, Fatima and Cross, Helen and Gurrieri, Fiorella and Tiziano, Danilo and Nevsimalova, Sona and Nicole, Sophie and Neville, Brian and Van Den Maagdenberg, Arn M. J. M and Mikati, Mohamad and Goldstein, David B and Vavassori, Rosaria and Arzimanoglou, Alexis and Bassi, Maria Teresa and Borgatti, Renato and Cernetti, Roberta and Di Rosa, Gabriella and Franchini, Filippo and Gambardella, Antonio and Giacanelli, Manlio and Gobbi, Giuseppe and Granata, Tiziana and Guerrini, Renzo and Incorpora, Gemma and Nardocci, Nardo and Neri, Giovanni and Ragona, Francesca and Santucci, Margherita and Sartori, Stefano and Veneselli, Edvige and Vigevano, Federico and Zucca, Claudio and Aicardi, J and An, I and Arbues, A.S and Arzimanoglou, A and Bahi-Buisson, N and Barthez, M.-A and Billette de Villemeur, T and Bourgeois, M and Bru, M and Chabrol, B and Chaigne, D and Chaunu, M.P and Chaunu, C and Cournelle, A.M and Davoine, C.-S and De St Martin, A and Deny, B and Desguerres, I and Des Portes, V and Doummar, D and Dulac, O and Dusser, A and Gerard, M and Gitiaux, C and Godet Kiesel, I and Gokben, S and Goutieres, F and Guerrin, M.-H and Heron-Longe, B and Hubsch-Bonneaud, C and Hully, M and Husson, M and Husson, Ch and Kaminska, A and Laroche, C and Lazaro, L and Lepine, A and Magy, L and Marchal, C and Michel, J and Milh, M and Motte, J and Moutard, M.L and Napuri, S and Nassogne, M.C and Neau, J.P and Nicole, S and Panagiotakaki, Eleni and ... and IBAHC Consortium and French AHC Consortium and Int AHC Consortium and International AHC Consortium and Italian IBAHC Consortium and The French AHC Consortium and The Italian IBAHC Consortium and The International AHC Consortium
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 09/2015, Volume 10, Issue 1, p. 123
Journal Article
2011, Rehabilitation therapy in video
This video analyzes several everyday functions such as picking up a cup, standing up from a chair, walking with a cup, and sitting down in a chair. Analysis is... 
Treatment | Hemiplegia
Web Resource
Pediatric Neurology, ISSN 0887-8994, 2015, Volume 52, Issue 1, pp. 56 - 64
Abstract Background ATP1A3 mutations have now been recognized in infants and children presenting with a diverse group of neurological phenotypes, including... 
Pediatrics | Neurology | CAPOS syndrome | ataxia | rapid-onset dystonia-Parkinsonism | dystonia | ATP1A3 | hemiplegia | alternating hemiplegia of childhood | sodium potassium ATPases | FLUNARIZINE | CEREBRAL EDEMA | ALPHA-3 | MIGRAINE | CLINICAL NEUROLOGY | NA/K-ATPASE | DE-NOVO MUTATIONS | CLINICAL-MANIFESTATIONS | GENE | PEDIATRICS | CALCIUM-CHANNEL | Sodium-Potassium-Exchanging ATPase - genetics | Humans | Foot Deformities, Congenital - genetics | Hemiplegia - therapy | Cerebellar Ataxia - physiopathology | Hemiplegia - diagnosis | Hearing Loss, Sensorineural - diagnosis | Foot Deformities, Congenital - physiopathology | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hemiplegia - physiopathology | Child | Optic Atrophy - diagnosis | Optic Atrophy - genetics | Diagnosis, Differential | Dystonic Disorders - genetics | Optic Atrophy - physiopathology | Foot Deformities, Congenital - diagnosis | Foot Deformities, Congenital - therapy | Hearing Loss, Sensorineural - genetics | Reflex, Abnormal - genetics | Optic Atrophy - therapy | Phenotype | Animals | Cerebellar Ataxia - genetics | Cerebellar Ataxia - therapy | Dystonic Disorders - diagnosis | Hearing Loss, Sensorineural - therapy | Hemiplegia - genetics | Mutation | Cerebellar Ataxia - diagnosis | Hearing Loss, Sensorineural - physiopathology | Hemiplegia | Genetic aspects | Parkinson's disease | Dystonia
Journal Article
2011, ISBN 9781907655753, 174
Book
Intensive Care Medicine, ISSN 0342-4642, 11/2018, Volume 44, Issue 11, pp. 1957 - 1958
Journal Article
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