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  Behavioral neurobiology of Huntington's disease and Parkinson's disease

  Hoa Huu Phuc Nguyen, M. Angela Cenci, editors.

  Contents:
  Clinical Aspects of Huntington's Disease
  The Neuropathology of Huntington's Disease
  Neurobiology of Huntington's Disease
  Mouse Models of Huntington's Disease
  Transgenic Rat Models of Huntington's Disease
  Large Animal Models of Huntington's Disease
  Therapeutic Strategies for Huntington's Disease
  Clinical and Pathological Features of Parkinson's Disease
  Symptomatic Models of Parkinson?s Disease and L-DOPA-Induced Dyskinesia in Non-human Primates
  Neuroinflammation in Parkinson's Disease Animal Models: A Cell Stress Response or a Step in Neurodegeneration?
  Viral Vector-Based Models of Parkinson's Disease
  Transgenic Rodent Models to Study Alpha-Synuclein Pathogenesis, with a Focus on Cognitive Deficits
  Modeling LRRK2 Pathobiology in Parkinson's Disease: From Yeast to Rodents
  Models of Multiple System Atrophy.

  Digital Access Springer 2015
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• Article

  Trisomie 13qter par duplication en tandem 46,xx,dir dup 13(q21 leads to qter),9qh+. [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].

  de Grouchy J, Turleau C, Danis F, Kohout G, Briard ML.

  Ann Genet. 1978 Dec;21(4):247-51.

  A tandem translocation of chromosome 13-46,XXdup13(q21 leads to qter)--occurred de novo in a patient with the following features: normal birthweight; early feeding difficulties; mild psychomotor retardation; low set hairline on the forehead; thick eyebrows; long, upturned eyelashes; pointed nose; micrognathia; large, flat, posteriorly rotated ears; multiple hemangiomata; normal hematological status. The hypothesis of an unequal crossing-over is discussed, as well as the possibility of constructing a phenotypic map of chromosome 13.

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  PubMed