Academic literature on the topic 'Myoclonies'

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Dissertations / Theses on the topic "Myoclonies"

1

BEN, HADJALI BEN KHALIFA JAMEL. "Les myoclonies squelettiques." Lille 2, 1991. http://www.theses.fr/1991LIL2M234.

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2

Lantéri-Minet, Michel. "Traitement et pathogenie des myoclonies post-hypoxiques : etude prospective de l'effet du piracetam." Nice, 1991. http://www.theses.fr/1991NICE6829.

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3

GRANDSIRE, DIDIER. "Les myoclonies neonatales benignes du sommeil : un diagnostic differentiel des convulsions du nouveau-ne." Amiens, 1990. http://www.theses.fr/1990AMIEM082.

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4

Vellieux, Geoffroy. "Syndrome de Lance-Adams : étude translationnelle de l’homme à l’animal." Electronic Thesis or Diss., Sorbonne université, 2024. http://www.theses.fr/2024SORUS432.

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Le syndrome de Lance-Adams est une pathologie neurologie chronique très handicapante rencontrée chez les survivants d'anoxie cérébrale. Il est caractérisé essentiellement par des myoclonies positives, d'action, multifocales ou généralisées, et des myoclonies négatives. Les mécanismes sous-tendant les myoclonies de cette pathologie sont peu connus. De multiples hypothèses ont été proposées depuis la description initiale de ce syndrome. L'étude multimodale d'une large cohorte de patients avec un syndrome de Lance-Adams a montré que les myoclonies sont générées dans le cortex cérébral, en particu
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5

Carr, Jonathan. "Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy." Thesis, Stellenbosch : University of Stellenbosch, 2009. http://hdl.handle.net/10019.1/1201.

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Thesis (DMed (Medicine. Internal Medicine))--University of Stellenbosch, 2009.<br>ENGLISH ABSTRACT: Progressive Myoclonic Epilepsies (PME) are characterized by progressive neurological impairment with myoclonus, seizures and dementia. In contradistinction, Familial Adult Myoclonic Epilepsy (FAME) is characterized by a benign course with rare seizures and cortical tremor. Both conditions have neurophysiological features suggestive of a cortical origin for their myoclonus. This dissertation reports on a novel form of PME. Many of those who were affected had no or minimal progression of the
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6

Lafrenière, Ronald G. "Molecular and genetic studies of progressive myoclonus epilepsy type 1 (EPM1)." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0021/NQ36996.pdf.

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7

Waite, Adrian. "The molecular genetics of myoclonus-dystonia syndrome." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531805.

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8

Elmslie, Frances Veryan. "Molecular genetic analysis of juvenile myoclonic epilepsy." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299535.

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9

DASSO, MARTIN BRIGITTE. "Encephalopathie myoclonique precoce a bouffees electroencephalographiques periodiques : a propos de trois observations." Toulouse 3, 1988. http://www.theses.fr/1988TOU31062.

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10

VAUGIN-BOULANGER, VERONIQUE. "Effets indesirables des nouvelles quinolones." Clermont-Ferrand 1, 1989. http://www.theses.fr/1989CLF13005.

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