Bibliografías temáticas / Hereditary neuropathy with pressure palsies

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Literatura académica sobre el tema "Hereditary neuropathy with pressure palsies"

Autor: Grafiati
Publicado: 7 de junio de 2025
Última modificación: 2 de agosto de 2025

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Artículos de revistas sobre el tema "Hereditary neuropathy with pressure palsies"

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Choi, Hyoung Won, and Nancy L. Kuntz. "Hereditary Neuropathy with Liability to Pressure Palsies." Pediatric Neurology Briefs 29, no. 11 (2015): 83. http://dx.doi.org/10.15844/pedneurbriefs-29-11-2.

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Harada, Yohei, Araya Puwanant, and David N. Herrmann. "Hereditary Neuropathy With Liability to Pressure Palsies." Journal of Clinical Neuromuscular Disease 18, no. 2 (2016): 79–83. http://dx.doi.org/10.1097/cnd.0000000000000136.

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Jafarnia, Kourosh, Michael J. Sullivan, and David H. Hildreth. "Hereditary Neuropathy With Liability to Pressure Palsies." Clinical Orthopaedics and Related Research 385 (April 2001): 253–55. http://dx.doi.org/10.1097/00003086-200104000-00036.

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Attarian, Shahram, Farzad Fatehi, Yusuf A. Rajabally, and Davide Pareyson. "Hereditary neuropathy with liability to pressure palsies." Journal of Neurology 267, no. 8 (2019): 2198–206. http://dx.doi.org/10.1007/s00415-019-09319-8.

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Smith, Greg N., and Thomas S. Higgins. "Hereditary neuropathy with liability to pressure palsies." Journal of Hand Surgery 27, no. 2 (2002): 362–63. http://dx.doi.org/10.1053/jhsu.2002.30364.

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Dharmakeerthi, D. M. W., and D. Sirisena. "Hereditary neuropathy with liability to pressure palsies." Sri Lanka Journal of Neurology 5, no. 1 (2018): 24. http://dx.doi.org/10.4038/sljon.v5i1.65.

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Grishina, D. A., and N. A. Suponeva. "Neurophysiological differential diagnostic markers in hereditary neuropathy with liability to pressure palsies and chronic inflammatory demyelinating polyradiculoneuropathy." Neuromuscular Diseases 13, no. 1 (2023): 52–67. http://dx.doi.org/10.17650/2222-8721-2023-13-1-52-67.

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Background. Today, the issues of differential diagnosis of chronic hereditary and acquired demyelinating neuropathies are still relevant. The variety of phenotypic variants of chronic inflammatory demyelinating polyradiculoneuropathy and hereditary neuropathy with liability to pressure palsies, their remitting course and the non-specificity of neurophysiological changes necessitate the identification of clear markers that can help in the differential diagnosis of the neuropathies under discussion already at the stage of the analysis of the electroneuromyographic study data.Aim. To determine ne
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Pareyson, D. "Hereditary Neuropathy with liability to Pressure Palsies (HNPP)." Electroencephalography and Clinical Neurophysiology 103, no. 1 (1997): 12. http://dx.doi.org/10.1016/s0013-4694(97)87955-6.

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Topakian, R., S. Wimmer, B. Pischinger, and R. Pichler. "Hereditary neuropathy with liability to pressure palsies presenting with sciatic neuropathy." Case Reports 2014, oct17 1 (2014): bcr2014206883. http://dx.doi.org/10.1136/bcr-2014-206883.

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Lane, Joshua E., Guy D. Foulkes, Thomas D. Hope, Vladimir I. Mayorov, and Linda Adkison. "Hereditary neuropathy with liability to pressure palsies mimicking multifocal compression neuropathy." Journal of Hand Surgery 26, no. 4 (2001): 670–74. http://dx.doi.org/10.1053/jhsu.2001.26029.

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Tesis sobre el tema "Hereditary neuropathy with pressure palsies"

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Carballo, Sebastian. "Hereditary neuropathy with liability to pressure palsies : an electrophysiological and genetic study /." Genève : [s.n.], 2002. http://www.unige.ch/cyberdocuments/theses2002/CarballoS/these.pdf.

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Granat, Heidi Pauliina [Verfasser], Michael Werner [Akademischer Betreuer] Sereda, Michael Werner [Gutachter] Sereda, and Michael [Gutachter] Müller. "Experimental therapy with progesterone on a mouse model for hereditary neuropathy with liability to pressure palsies (HNPP) / Heidi Pauliina Granat ; Gutachter: Michael Werner Sereda, Michael Müller ; Betreuer: Michael Werner Sereda." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://d-nb.info/1206731699/34.

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Lima, Diogo Afonso Figueiredo de. "Envolvimento do sistema nervoso central em “Hereditary Neuropathy with liability to Pressure Palsies”." Master's thesis, 2020. http://hdl.handle.net/10451/46715.

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Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2020<br>“Hereditary Neuropathy with liability to Pressure Palsies” (HNPP) é uma doença genética de expressão autossómica dominante, causada por mutações do gene “Peripheral Myelin Protein 22 (PMP22)”. Nesta condição clínica, os nervos periféricos são lesados quando sujeitos a compressões ligeiras, causando períodos transitórios e recorrentes de sintomas focais motores e/ou sensitivos no território dos nervos periféricos afetados. Apesar de HNPP ter uma clara expressão no sistema nervoso p
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Kuo, Hung-Chang, and 郭弘昌. "Molecular Diagnosis of Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy with Liability to Pressure Palsies by Real-time Quantitative PCR using SYBR Green I dye." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/58998911227186265443.

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碩士<br>高雄醫學大學<br>醫學研究所<br>97<br>Charcot-Marie-Tooth disease (CMT) is one of the most common inherited peripheral neuropathies. According to the hereditary pattern, clinical manifestations and electrophysiologic findings, CMT could be divided into many subgroups. CMT type 1 is an autosomal dominant demyelinating motor and sensory neuropathy. The most common subtype of CMT type 1 is CMT1A, which is caused by the duplication of a 1.5 Mb region containing the peripheral myelin protein 22 (PMP22) gene on chromosome 17p11.2-12. Hereditary neuropathy with liability to pressure palsies (HNPP), another
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Libros sobre el tema "Hereditary neuropathy with pressure palsies"

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Parker, James N., and Philip M. Parker. Hereditary neuropathy with liability to pressure palsies: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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Donaghy, Michael. Focal peripheral neuropathy. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0487.

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Some causes of focal peripheral nerve damage are self-evident, such as involvement at sites of trauma, tissue necrosis, infiltration by tumour, or damage by radiotherapy. Focal compressive and entrapment neuropathies are particularly valuable to identify in civilian practice, since recovery may follow relief of the compression. Leprosy is a common global cause of focal neuropathy, which involves prominent loss of pain sensation with secondary acromutilation, and requires early antibiotic treatment. Mononeuritis multiplex due to vasculitis requires prompt diagnosis and immunosuppressive treatme
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Mills, Kerry R. Disorders of single nerves, roots, and plexuses. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0021.

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The role of electromyography (EMG) and nerve conduction studies in disorders of single nerve, root, and plexus lesions are discussed. The motor and sensory anatomy underpinning diagnosis is described and a scheme presented showing the key muscles to be examined using EMG to differentiate nerve, plexus, and root lesions. The main causes of mononeuritis multiplex, of either axonal degeneration or demyelinative pathology, are covered, including diabetic neuropathy, vasculitic neuropathy, multifocal motor neuropathy with block, and the Lewis–Sumner syndrome. The confirmatory role of EMG and nerve
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Capítulos de libros sobre el tema "Hereditary neuropathy with pressure palsies"

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Angelini, Corrado. "Hereditary Neuropathy with Pressure Palsies." In Genetic Neuromuscular Disorders. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56454-8_97.

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Angelini, Corrado. "Hereditary Neuropathy with Pressure Palsies." In Genetic Neuromuscular Disorders. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07500-6_77.

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Metze, Dieter, Vanessa F. Cury, Ricardo S. Gomez, et al. "Hereditary Neuropathy with Liability to Pressure Palsies." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7957.

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Khadilkar, Satish V., Rakhil S. Yadav, and Bhagyadhan A. Patel. "Hereditary Liability to Pressure Palsies." In Neuromuscular Disorders. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-5361-0_35.

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Khadilkar, Satish V., Rakhil S. Yadav, and Bhagyadhan A. Patel. "Hereditary Neuropathy with Pressure Palsy (HNPP)." In Neuromuscular Disorders. Springer Nature Singapore, 2024. https://doi.org/10.1007/978-981-97-9010-4_43.

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Ellezam, Benjamin. "Hereditary neuropathy with liability to pressure palsy." In Peripheral nerve disorders. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118618424.ch15.

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Nelis, E., P. De Jonghe, and V. Timmerman. "Charcot-Marie-Tooth disease type 1 (CMT1) and hereditary neuropathy with liability to pressure palsy (HNPP)." In Hereditary Peripheral Neuropathies. Steinkopff, 2005. http://dx.doi.org/10.1007/3-7985-1586-7_6.

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Attarian, Shahram. "Hereditary Neuropathy With Liability to Pressure Palsies." In Reference Module in Neuroscience and Biobehavioral Psychology. Elsevier, 2024. http://dx.doi.org/10.1016/b978-0-323-95702-1.00236-0.

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Kumar, Kishore R., Carolyn M. Sue, Alexander Münchau, and Christine Klein. "Hereditary Neuropathy with Liability to Pressure Palsies." In Neurogenetics. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199383894.003.0019.

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"Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)." In Encyclopedia of Pain. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-28753-4_100914.

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Actas de conferencias sobre el tema "Hereditary neuropathy with pressure palsies"

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Carroll, Mitch, Ciaran McAuley, Mustafa Al-Musawi, and Abhishek Malhotra. "2354 Hereditary neuropathy with liability to pressure palsies (HNPP): two cases highlight the electrophysiological variability and associated diagnostic conundrum." In ANZAN Annual Scientific Meeting 2022 Abstracts. BMJ Publishing Group Ltd, 2022. http://dx.doi.org/10.1136/bmjno-2022-anzan.120.

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Šeparović, Iva, M. Kukuruzović, and M. Malenica. "392 Hereditary Neuropathy with Liability to Pressure Palsy." In 10th Europaediatrics Congress, Zagreb, Croatia, 7–9 October 2021. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2021. http://dx.doi.org/10.1136/archdischild-2021-europaediatrics.392.

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