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Artykuły w czasopismach na temat "Nodding syndrome"

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Dowell, Scott F., James J. Sejvar, Lul Riek, et al. "Nodding Syndrome." Emerging Infectious Diseases 19, no. 9 (2013): 1374–73. http://dx.doi.org/10.3201/eid1909.130401.

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Abd-Elfarag, Gasim, and Michaël Boele van Hensbroek. "Nodding Syndrome." Pediatric Infectious Disease Journal 38 (June 2019): S67—S71. http://dx.doi.org/10.1097/inf.0000000000002327.

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Bhwana, Dan, Bruno Mmbando, An Hotterbeekx, and Robert Colebunders. "Nodding Syndrome." Pediatric Infectious Disease Journal 38, no. 11 (2019): e313. http://dx.doi.org/10.1097/inf.0000000000002442.

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Imma, Ferraiuolo. "Nodding syndrome." Journal of the Neurological Sciences 455 (December 2023): 121272. http://dx.doi.org/10.1016/j.jns.2023.121272.

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Spencer, P. S., R. Mazumder, V. S. Palmer, and M. S. Pollanen. "Nodding syndrome phenotypes." Revue Neurologique 175, no. 10 (2019): 679–85. http://dx.doi.org/10.1016/j.neurol.2019.09.005.

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Johnson, Tory P., James Sejvar, Thomas B. Nutman, and Avindra Nath. "The Pathogenesis of Nodding Syndrome." Annual Review of Pathology: Mechanisms of Disease 15, no. 1 (2020): 395–417. http://dx.doi.org/10.1146/annurev-pathmechdis-012419-032748.

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Nodding syndrome is a rare, enigmatic form of pediatric epilepsy that has occurred in an epidemic fashion beginning in the early 2000s in geographically distinct regions of Africa. Despite extensive investigation, the etiology of nodding syndrome remains unclear, although much progress has been made in understanding the pathogenesis of the disease, as well as in treatment and prevention. Nodding syndrome is recognized as a defined disease entity, but it is likely one manifestation along a continuum of Onchocerca volvulus–associated neurological complications. This review examines the epidemiol
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Vieri, Melissa Krizia, Adam Hendy, John L. Mokili, and Robert Colebunders. "Nodding syndrome research revisited." International Journal of Infectious Diseases 104 (March 2021): 739–41. http://dx.doi.org/10.1016/j.ijid.2021.02.006.

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Arndts, Kathrin, Josua Kegele, Alain S. Massarani, et al. "Epilepsy and nodding syndrome in association with an Onchocerca volvulus infection drive distinct immune profile patterns." PLOS Neglected Tropical Diseases 17, no. 8 (2023): e0011503. http://dx.doi.org/10.1371/journal.pntd.0011503.

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Previous studies have described the association of onchocerciasis (caused by Onchocerca volvulus) with epilepsy, including nodding syndrome, although a clear etiological link is still missing. Cases are found in different African countries (Tanzania, South Sudan, Uganda, Democratic Republic of the Congo, Central African Republic and Cameroon). In our study we investigated immunological parameters (cytokine, chemokine, immunoglobulin levels) in individuals from the Mahenge area, Tanzania, presenting with either epilepsy or nodding syndrome with or without O. volvulus infection and compared them
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Kaiser, Christoph, Walter Kipp, Ephraim Tukesiga, George Asaba, and Tom Rubaale. "Nodding Syndrome, Western Uganda, 1994." American Journal of Tropical Medicine and Hygiene 93, no. 1 (2015): 198–202. http://dx.doi.org/10.4269/ajtmh.14-0838.

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Abd-Elfarag, Gasim Omer Elkhalifa, Arthur Wouter Dante Edridge, René Spijker, Mohamed Boy Sebit, and Michaël B. van Hensbroek. "Nodding Syndrome: A Scoping Review." Tropical Medicine and Infectious Disease 6, no. 4 (2021): 211. http://dx.doi.org/10.3390/tropicalmed6040211.

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Nodding syndrome (NS) is a debilitating yet often neglected neurological disease affecting thousands of children in several sub-Saharan African countries. The cause of NS remains unknown, and effective treatment options are lacking. Moreover, knowledge regarding NS is scarce and is based on a limited number of publications, with no comprehensive overview published to date. Therefore, the aim of this scoping review was to summarise the current evidence and identify existing knowledge gaps in order to help clinicians, scientists, and policymakers develop guidelines for prioritising this severe c
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Rozprawy doktorskie na temat "Nodding syndrome"

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Miehle, Kathrin [Verfasser], Bernhard [Akademischer Betreuer] Hemmer, Bernhard [Gutachter] Hemmer, and Jan S. [Gutachter] Kirschke. "Comprehensive analysis of current knowledge of Nodding Syndrome / Kathrin Miehle ; Gutachter: Bernhard Hemmer, Jan S. Kirschke ; Betreuer: Bernhard Hemmer." München : Universitätsbibliothek der TU München, 2019. http://d-nb.info/1186889314/34.

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Kegele, Josua [Verfasser], and Holger [Akademischer Betreuer] Lerche. "Genetische Ursachen des Nodding Syndroms und familiärer Epilepsien in Subsahara-Afrika / Josua Kegele ; Betreuer: Holger Lerche." Tübingen : Universitätsbibliothek Tübingen, 2019. http://d-nb.info/120488076X/34.

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Książki na temat "Nodding syndrome"

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Shorter, Edward, and Max Fink. Kidnapped! Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190881191.003.0006.

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Catatonia remained a subtype of schizophrenia for the next hundred years because a “Praetorian guard” around Kraepelin relentlessly flacked their teacher’s diagnoses. There was, to be sure, some initial support for Kahlbaum’s diagnosis as a separate entity, yet Kraepelin’s “textbook,” in its various editions, carried the day. Psychosis became the hallmark of schizophrenia, and catatonic patients who became psychotic simply had their diagnoses changed. In a world dominated by “schizophrenia,” catatonia was only of nodding interest. By the end of the Second World War, the term “schizophrenia” ha
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Części książek na temat "Nodding syndrome"

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Ongaya, Kizito, Paul Ssemalullu, Benedict Oyo, Gilbert Maiga, and Augustus Aturinde. "Towards a Spatial-Temporal Model of Prevalence of Nodding Syndrome and Epilepsy." In Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-16042-5_7.

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Lagoro Kitara, David, Denis Anywar Arony, and Suzanne Gazda. "Nodding Syndrome and Autism Spectrum Disorder." In Autism Spectrum Disorders - Advances at the End of the Second Decade of the 21st Century. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.83530.

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Robertson, Mary M., and Andrea E. Cavanna. "What is Tourette syndrome?" In Tourette Syndrome. Oxford University PressOxford, 2008. http://dx.doi.org/10.1093/oso/9780199298198.003.0002.

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Abstract TS begins in early life, usually between 5 and 7 years of age and consists of many tics. The syndrome includes motor tics or twitches and vocal tics or noises, which must have been present for a year although not necessarily together. These tics can be simple or complex. Vocal tics are often called phonic tics, as many of the noises made by patients with TS do not use the vocal cords. Common motor tics are blinking, head nodding, face grimacing, and nose twitching, and common phonic tics are sniffing, throat clearing, and coughing. The swearing tic (coprolalia) receives a lot of media
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Shibasaki, Hiroshi, Mark Hallett, Kailash P. Bhatia, Stephen G. Reich, and Bettina Balint. "Dyskinesia, Motor Stereotypies, and Tics." In Involuntary Movements. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190865047.003.0006.

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Dyskinesia is characterized by complex, irregular involuntary movements involving lips, tongue, extremities, and/or trunk. The term “dyskinesia” is often used to encompass complex involuntary movements that do not fit into another category of involuntary movements. Focal dyskinesia is commonly seen in the lips and tongue (orolingual dyskinesia or oral dyskinesia). Drug side effects are the most common cause of generalized dyskinesia, usually those that influence dopamine such as L-dopa and neuroleptics (drug-induced dyskinesia, tardive dyskinesia). Motor stereotypies are repetitive occurrences
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Streszczenia konferencji na temat "Nodding syndrome"

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"Beauvericin in Sorghum Proximate to Nodding Syndrome." In International Conference on Chemical, Agricultural and Medical Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2013. http://dx.doi.org/10.15242/iicbe.c1213069.

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