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Relevant bibliographies by topics / Paraparesie

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Academic literature on the topic 'Paraparesie'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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Journal articles on the topic "Paraparesie"

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Aljaafari, Danah, and Noman Ishaque. "Paraparetic Variant of Guillain-Barré Syndrome in First 24 Hours of Postpartum Period: A case report." Sultan Qaboos University Medical Journal [SQUMJ] 20, no. 2 (2020): 227. http://dx.doi.org/10.18295/squmj.2020.20.02.015.

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Guillain-Barré syndrome (GBS) is a heterogeneous disorder with a diverse clinical presentation ranging from weakness of certain body regions to tetraparesis with autonomic dysfunction and respiratory failure. Paraparetic GBS is a variant of GBS which is characterised by weakness limited to the lower limbs only. It is crucial to identify such topographical presentations, as a delay in diagnosis can lead to delayed initiation of specific treatment, which can negatively impact the outcome. We report a 29-year-old female patient who presented to the King Fahd Hospital of the University, Al Khobar,

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Marco Orsini, Marco Orsini, Marcos RG de Feitas, Mariana P. Mello, et al. "Hidroterapia no gerenciamento da espasticidade nas paraparesias espásticas de várias etiologias." Revista Neurociências 18, no. 1 (2001): 81–86. http://dx.doi.org/10.34024/rnc.2010.v18.8507.

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A espasticidade é uma manifestação clínica comum resultante da lesão do neurônio motor superior no sistema nervoso central. É uma condição que afeta adultos e crianças com uma grande variedade de patologias agudas e crônicas, sendo a característica predominante de diversas condições. Um dos aspectos mais incapacitantes das doenças que cursam com paraparesia espástica refere-se ao comprometimento progressivo da marcha, podendo levar aos indivíduos a permanecerem confinados a cadeira de rodas. A hidroterapia, por suas propriedades de suporte, assistência e resistência, constitui uma alternativa

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Hassan, Anhar, Shivam Om Mittal, William T. Hu, Keith A. Josephs, Eric J. Sorenson, and J. Eric Ahlskog. "Natural History of “Pure” Primary Lateral Sclerosis." Neurology 96, no. 17 (2021): e2231-e2238. http://dx.doi.org/10.1212/wnl.0000000000011771.

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ObjectiveTo assess whether primary lateral sclerosis (PLS), classified as pure when the EMG is normal, converts to amyotrophic lateral sclerosis (ALS) after longitudinal follow-up.MethodsRetrospective chart review was performed of patients with pure PLS at Mayo Clinic in Rochester, MN (1990–2016). Inclusion criteria required a normal EMG during the first 4 years of symptoms.ResultsForty-three patients had pure PLS (25 female, 58%) with a median onset age of 50 years (range 38–78 years) and median follow-up at 9 years’ disease duration (range 4–36 years). The ascending paraparesis phenotype (n

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Carletti, Beatrice Enrica, Irene Espadas, and Daniel Sanchez-Masian. "Thoracic vertebral canal stenosis due to articular process hypertrophy in two cats treated by hemilaminectomy with partial osteotomy of the spinous process." Journal of Feline Medicine and Surgery Open Reports 5, no. 2 (2019): 205511691986317. http://dx.doi.org/10.1177/2055116919863176.

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Case summary A 9-year-old neutered female British Shorthair cat (case 1) and a 13-year-old neutered male domestic shorthair cat (case 2) showed signs of chronic T3–L3 myelopathy, which progressed over 6 and 12 months, respectively. On presentation, case 1 had moderate pelvic limb proprioceptive ataxia and ambulatory paraparesis, and case 2 was non-ambulatory paraparetic and had urinary incontinence. Bilateral enlargement of the articular process joints at T11–T12 in case 1 and T3–T4 in case 2 causing dorsolateral extradural spinal cord compression was shown on MRI. Surgical decompression by a

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Chaudhuri, Arunima, SamirK Hazra, AmitK Bandopadhyay, and Soma Datta. "Postspinal paraparesis." Journal of Obstetric Anaesthesia and Critical Care 2, no. 1 (2012): 54. http://dx.doi.org/10.4103/2249-4472.99333.

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Tribus, Clifford B. "Transient Paraparesis." Spine 26, no. 9 (2001): 1086–89. http://dx.doi.org/10.1097/00007632-200105010-00021.

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Fattahi, Arash, Seyed Mohammad Reza Mohajeri, Abdolhadi Daneshi, and Ardeshir Shahivand. "Hyperextension thoracic spine fracture with complete neurological recovery after surgical fixation: A case report." Surgical Neurology International 11 (May 30, 2020): 137. http://dx.doi.org/10.25259/sni_226_2020.

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Background: Hyperextension thoracic spine fractures (HTSFs) typically involve the anterior ligamentous complex of the spine. These patients often present with paraplegia and warrant early surgical reduction/fixation even though few deficits resolve. Here, we present the unusual case of a 40-year-old male whose paraparetic deficit resolved following reduction/fixation of a T7-T8 HTSF. Case Description: A 40-year-old male presented with a thoracic computed tomography (CT) documented T7- T8 HTSF following a motor vehicle accident. His neurological examination revealed severe paraparesis, but with

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Crowe, Yvette C., Georgina Child, Richard Lam, and Ross McGregor. "Congenital block vertebrae and intervertebral disc protrusion in a young cat." Journal of Feline Medicine and Surgery Open Reports 5, no. 2 (2019): 205511691986803. http://dx.doi.org/10.1177/2055116919868037.

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Case summaryA 6-month-old domestic shorthair cat was evaluated for proprioceptive ataxia of the pelvic limbs. Over 2 months, the cat became poorly ambulatory, paraparetic with proprioceptive ataxia and developed a firm, distended bladder with intermittent overflow urinary incontinence. Block vertebrae (T1–3, T4–5 and T10–11) and lordosis were identified on radiographs of the vertebral column. MRI revealed T3/4 intervertebral disc protrusion with severe extradural compression, secondary syringohydromyelia caudal to the protrusion and generalised intervertebral disc disease throughout the cervic

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Raj, Anil K., Peter D. Neuhaus, Adrien M. Moucheboeuf, Jerryll H. Noorden, and David V. Lecoutre. "Mina: A Sensorimotor Robotic Orthosis for Mobility Assistance." Journal of Robotics 2011 (2011): 1–8. http://dx.doi.org/10.1155/2011/284352.

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While most mobility options for persons with paraplegia or paraparesis employ wheeled solutions, significant adverse health, psychological, and social consequences result from wheelchair confinement. Modern robotic exoskeleton devices for gait assistance and rehabilitation, however, can support legged locomotion systems for those with lower extremity weakness or paralysis. The Florida Institute for Human and Machine Cognition (IHMC) has developed the Mina, a prototype sensorimotor robotic orthosis for mobility assistance that provides mobility capability for paraplegic and paraparetic users. T

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Ferreira, Adelmo, Bonfim Alves Silva Jr, F. Menezes Braga, Núbia M. Noschese Gargiulo, and J. Norberto Stávale. "Paraparesia por gota." Arquivos de Neuro-Psiquiatria 47, no. 4 (1989): 479–83. http://dx.doi.org/10.1590/s0004-282x1989000400017.

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Os autores apresentam um caso de bloqueio de canal raquidiano por tofo em paciente de 23 anos de idade com gota tofácea crônica e artrite gotosa, que desenvolveu paraparesia crural. Submetido a laminectomia, com exérese de acúmulos de cristais junto ao ligamento amarelo, não houve melhora do déficit motor. A revisão da literatura mostrou 9 casos previamente relatados.

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Dissertations / Theses on the topic "Paraparesie"

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Erhart, Camille. "Embolies de cholesterol : une etiologie rare d'une paraparesie chez un sujet age." Université Louis Pasteur (Strasbourg) (1971-2008), 1992. http://www.theses.fr/1992STR1M050.

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CHBICHEB, MOHAMMED. "Contribution a l'etude des paraparesies spastiques progressives et isolees de l'adulte." Angers, 1993. http://www.theses.fr/1993ANGE1066.

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Gessain, Antoine. "Virus HTLV-1 et paraparesie spastique tropicale. Un rétrovirus leucemogene associe a une maladie neurologique : épidémiologie, caractérisation des isolats viraux associes et aspects moléculaires." Paris 7, 1992. http://www.theses.fr/1992PA077309.

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Le virus htlv-i retrovirus isole chez l'homme en 1980 est endemique au japon, dans la region caraibe, en amerique du sud et en afrique intertropicale. Dans ces regions 1 a 30% de la population generale a des anticorps seriques anti-htlv-i. Ce virus est l'agent etiologique de la leucemie t de l'adulte (atl) et d'une neuromyelopathie chronique denommee paraparesie spastique tropicale/myelopathie associee a l'htlv-i (tsp/ham). Ce travail realise entre 1983 et 1991 comporte quatre etapes successives. 1) dans un travail initial d'epidemiologie clinique et de terrain, j'ai participe a la decouverte

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Almeida, Camila de. "Aplicabilidade, validação e reprodutibilidade do Spinal Cord Independence Measure version III (SCIM III) nos pacientes com paraparesia espástica." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/17/17142/tde-29052015-101117/.

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Objetivo: verificar a aplicabilidade, reprodutibilidade e validade do SCIM III nos pacientes com paraparesia espástica. Método: estudo transversal incluindo 30 sujeitos (66% mulheres; 41,5±14,7 anos) com paraparesia espástica de etiologia genética, infecciosa ou a esclarecer que foram avaliados pela análise computadorizada da marcha, versão brasileira da SCIM III (0-100 pontos), MIF (18-126 pontos), por 2 examinadores (A e B) no mesmo dia e 1 semana depois (A). Resultados: o coeficiente de correlação intraclasse (CCI) para o uso da SCIM III indicou boa reprodutibilidade intra e inter-examinado

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Silva, Felipe von Glehn 1978. "Espectro da neuromielite óptica : estudo clínico, imunológico e de neuroimagem." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/310332.

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Orientadores: Leonilda Maria Barbosa dos Santos, Benito Pereira Damasceno<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-22T19:26:19Z (GMT). No. of bitstreams: 1 Silva_FelipevonGlehn_D.pdf: 6687964 bytes, checksum: 5e92607a118fbc6e4c8085aa93b540a0 (MD5) Previous issue date: 2013<br>Resumo: A Neuromielite óptica (NMO) é uma doença inflamatória e desmielinizante do SNC, de natureza autoimune, caracterizada por surtos graves de neurite óptica e mielite transversa, de evolução mais freqüente na forma recidivante-remit

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Aulitzky, Anna [Verfasser]. "Klinische Phänotypisierung und genetische Aufarbeitung von Patienten mit Sporadischer Spastischer Paraparese und Familien mit Hereditärer Spastischer Paraparese / Anna Aulitzky." Ulm : Universität Ulm, 2017. http://d-nb.info/112490266X/34.

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Coelho, Juliana Nogueira. "A funcionalidade dos indivíduos com lesão medular de etiologia não-traumática - uma proposta para o uso da Classificação Internacional de Funcionalidade, Incapacidade e Saúde." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/17/17142/tde-20072016-113108/.

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Objetivo: Construir e testar a aplicabilidade de um instrumento baseado no Core Set resumido da CIF para lesão medular em indivíduos com etiologia não-traumática. Métodos: Foi realizada uma revisão sistemática para identificarmos as escalas de avaliação funcional que tenham sido aplicadas em indivíduos com paraparesia espástica. Para o desenvolvimento do instrumento utilizamos as descrição das categorias selecionadas para o Core Set resumido de lesão medular traumática crônica e elaboramos perguntas de fácil compreensão e alternativas de respostas descritos com detalhes que satisfizessem os se

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Tauil, Carlos Bernardo. ""Ensaio clínico controlado randomizado aberto com metil-prednisolona em portadores de mielopatia associada ao HTLV-1 paraparesia espástica tropical"." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-13092006-121302/.

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Estudamos a avaliação clínica de longo termo da resposta de pacientes com diagnóstico precoce de HAM/TSP ao tratamento com metil-prednisolona. Objetivamos pesquisar em relação ao tempo de evolução e apresentação da doença a eficácia deste tratamento. Realizamos o acompanhamento dos pacientes utilizando como parâmetros as escalas de critérios clínicos de Osame e Kurtzke e comparamos com um grupo controle que não recebeu este tipo de tratamento.Os pacientes do grupo experimental e do grupo controle que realizaram fisioterapia mantiveram-se estáveis ou obtiveram melhora de alguns sintomas da doen

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Nishimura, Paula Lumi Goulart. "Diretrizes para o design de dispositivo para animais com problemas de locomoção com uso da prototipagem rápida." Universidade Estadual Paulista (UNESP), 2018. http://hdl.handle.net/11449/154153.

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Submitted by Paula Lumi Goulart Nishimura (lumi.paula@gmail.com) on 2018-06-04T19:58:13Z No. of bitstreams: 1 Nishimura_Paula_diretrizes_design_cadeirasderodas.pdf: 8095797 bytes, checksum: 1357536835458a473e7ca38e94c32e9f (MD5)<br>Approved for entry into archive by Lucilene Cordeiro da Silva Messias null (lubiblio@bauru.unesp.br) on 2018-06-05T12:45:18Z (GMT) No. of bitstreams: 1 nishimura_plg_me_bauru.pdf: 7973597 bytes, checksum: d53a2fda1c6589b14cd407d952d45b81 (MD5)<br>Made available in DSpace on 2018-06-05T12:45:18Z (GMT). No. of bitstreams: 1 nishimura_plg_me_bauru.pdf: 7973597 byte

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Verkkoniemi, Auli. "Variant Alzheimerś disease with spastic paraparesis : clinical, neuropathological and molcecular genetic characterization." Helsinki : University of Helsinki, 2001. http://ethesis.helsinki.fi/julkaisut/laa/kliin/vk/verkkoniemi/.

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Books on the topic "Paraparesie"

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Parker, James N., and Philip M. Parker. The official patient's sourcebook on tropical spastic paraparesis. Edited by Icon Group International Inc. Icon Health Publications, 2002.

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Alleyne, Cargill Herley. Clinical and seroepidemiological case-control study of tropical spastic paraparesis and multiple sclerosis in Barbados. s.n.], 1991.

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Mckhann, Guy Mead. Isolation and characterization of human T-cell lymphotropic virus type-1 from patients with tropical spastic paraparesis. s.n.], 1990.

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Current issues in clinical neurovirology: Pathogenesis, diagnosis and treatment. Saunders, 2008.

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Publications, ICON Health. The Official Patient's Sourcebook on Tropical Spastic Paraparesis. Icon Health Publications, 2002.

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Harbourne, George. Genetic linkage studies of autosomal dominant hereditary spastic paraparesis. 1995.

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Miller, Aaron E., and Teresa M. DeAngelis. HTLV Myelopathy. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199732920.003.0009.

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Infection due to the human T-lymphocytic 1 (HTLV-1) virus can result in a myelopathy involving the thoracolumbar spinal cord, which typically manifests clinically as a spastic paraparesis—hence its alternative moniker tropical spastic paraparesis. In this chapter, we summarize the diagnostic approach to a patient with a spastic paraparesis and the key points, which assist in narrowing down the lengthy differential diagnosis to HTLV-1.

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Provan, Drew, Trevor Baglin, Inderjeet Dokal, and Johannes de Vos. Haematological emergencies. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0013.

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Septic shock/neutropenic fever - Acute transfusion reactions - Delayed transfusion reaction - Post-transfusion purpura - Hypercalcaemia - Hyperviscosity - Disseminated intravascular coagulation - Overdosage of thrombolytic therapy - Heparin overdosage - Heparin-induced thrombocytopenia - Warfarin overdosage - Massive blood transfusion - Paraparesis/spinal collapse - Leucostasis - Thrombotic thrombocytopenic purpura - Sickle crisis

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Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos, and Hassan Al-Sader. Haematological emergencies. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0013_update_001.

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Septic shock/neutropenic fever - Acute transfusion reactions - Delayed transfusion reaction - Post-transfusion purpura - Hypercalcaemia - Hyperviscosity - Disseminated intravascular coagulation - Overdosage of thrombolytic therapy - Heparin overdosage - Heparin-induced thrombocytopenia - Warfarin overdosage - Massive blood transfusion - Paraparesis/spinal collapse - Leucostasis - Thrombotic thrombocytopenic purpura - Sickle crisis

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Araujo, Abelardo Q.-C. Neurological Manifestations of the Human T-lymphotropic Virus Type 1. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0161.

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The human T cell lymphotropic virus type 1 (HTLV-1) is a retrovirus that infects about 20 million individuals worldwide. Its typical neurological presentation is of a chronic, slowly progressive myelopathy named “HTLV-1-associated myelopathy/tropical spastic paraparesis” (HAM/TSP). HAM/TSP emerges as the tip of the iceberg among numerous other neurological clinical syndromes caused by this virus, such as inflammatory myopathies, polyneuropathies, ALS-like syndromes, dysautonomia, etc. HAM/TSP designates a spastic paraparesis with neurogenic bladder, and minor sensory signs. Pathologically, HAM

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Book chapters on the topic "Paraparesie"

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Poeck, Klaus. "Chronisch-progrediente Paraparese." In Diagnostische Entscheidungen in der Neurologie. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-06601-0_15.

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Angelini, Corrado. "Spastic Paraparesis Type 4." In Genetic Neuromuscular Disorders. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56454-8_102.

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Angelini, Corrado. "Spastic Paraparesis Type 7." In Genetic Neuromuscular Disorders. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56454-8_103.

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Angelini, Corrado. "Spastic Paraparesis Type 4." In Genetic Neuromuscular Disorders. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07500-6_81.

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Angelini, Corrado. "Spastic Paraparesis Type 7." In Genetic Neuromuscular Disorders. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07500-6_82.

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Poeck, Klaus. "Chronisch-progrediente zentrale Paraparese." In Diagnostische Entscheidungen in der Neurologie. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-662-21782-5_15.

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Marsden, Jon, Lisa Bunn, Amanda Denton, and Krishnan Padmakumari Sivaraman Nair. "Hereditary Spastic Paraparesis and Other Hereditary Myelopathies." In Neurological Rehabilitation. CRC Press, 2018. http://dx.doi.org/10.1201/9781315374369-9.

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Karlstrom, Helena, William S. Brooks, John B. J. Kwok, Jillian J. Kril, Glenda M. Halliday, and Peter R. Schofield. "Variable Phenotype of Alzheimer's Disease with Spastic Paraparesis." In Genotype — Proteotype — Phenotype Relationships in Neurodegenerative Diseases. Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/3-540-26522-8_7.

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Rowan, Aileen G., and Charles R. M. Bangham. "The Pathogenesis of HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis." In Neurotropic Viral Infections. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33189-8_1.

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Schönbach, Christian. "Human T-Lymphotropic Virus Type-I-associated Myelopathytropical Spastic Paraparesis." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_753.

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Conference papers on the topic "Paraparesie"

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Fragio-Gil, Jorge Juan, Roxana Gonzalez Mazario, Jose Ivorra Cortés, et al. "AB0900 ACUTE PARAPARESIS AS CLINICAL PRESENTATION OF VERTEBRAL OSTEOMYELITIS." In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.6662.

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Hasenöhrl, T., W. Mayr, M. Dimitrijevic, S. Palma, C. Ambrozy, and R. Crevenna. "Neuromuskuläre Elektrostimulation verbessert das Gangbild einer Patientin mit spastischer Paraparese – ein Fallbericht." In Jahrestagung 2018 der Österreichischen Gesellschaft für Physikalische Medizin und Rehabilitation. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1673269.

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Paiva, Lohanna, Alexandre Zuquete Guarato, Vinicius Sousa, and Felipe Chagas Rodrigues de Souza. "DESENVOLVIMENTO DE UMA CADEIRA DE RODAS REGULÁVEL E DE BAIXO CUSTO PARA CÃES COM PARAPARESIA USANDO IMPRESSÃO 3D." In XXVI Congresso Nacional de Estudantes de Engenharia Mecânica. ABCM, 2019. http://dx.doi.org/10.26678/abcm.creem2019.cre2019-0214.

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Leitão, Juliana Rodrigues, Marcelo Candido Portilho Gouveia, Bruno Watanabe Minto, and Luis Gustavo Gosuen Gonçalves Dias. "RUPTURA DE BEXIGA URINÁRIA E FRATURA VERTEBRAL EM L5 DECORRENTES DE TRAUMA EM CÃO: RELATO DE CASO." In I Congresso On-line Nacional de Clínica Veterinária de Pequenos Animais. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1825.

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Introdução: As fraturas da coluna vertebral são causas potenciais de injúrias da medula espinhal em pequenos animais. Frequentemente, o paciente com trauma toracolombar têm lesões associadas em outros órgãos. Objetivos: Objetivou-se relatar um caso de ruptura da bexiga urinária e fratura completa oblíqua na 5° vértebra lombar e descrever as técnicas cirúrgicas utilizadas. Materiais e métodos: Uma cadela, Shih Tzu, com 5 anos de idade, 5 kg, foi atendido com histórico de trauma há 4 horas pela queda de um botijão de gás cheio na região toracolombar. Paraparesia, disúria, hematúria e dor abdomin

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Ju, Wei, Meili Zhang, Bonita R. Bryant, et al. "Abstract 2526: CP690550 inhibits interleukin-2 (IL-2), IL-9 and IL-15 mediated JAK3 activation and proliferation of T cells obtained from patients with HTLV-1-associated adult T cell leukemia (ATL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP)." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-2526.

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Gopan, Gayatri, Geetha Narayanan, Sreejith G. Nair, et al. "Outcome of Treatment in Elderly Myeloma—A Single-Centre Experience." In Annual Conference of Indian Society of Medical and Paediatric Oncology (ISMPO). Thieme Medical and Scientific Publishers Pvt. Ltd., 2021. http://dx.doi.org/10.1055/s-0041-1735368.

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Abstract Introduction Multiple myeloma (MM) accounts for approximately 1% of all cancers and 10% of all hematologic malignancies. In our institution, we see around 200 patients with myeloma every year. We present our experience with multiple myeloma in the patients aged more than 60 years. Objectives This is a retrospective study of 300 newly diagnosed multiple myeloma patients above 60 years of age treated in the Department of Medical Oncology, Regional Cancer Center, Thiruvananthapuram, Kerala, India, during the period between 2014 and 2017. The medical records of the patients were studied a

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