Literature DB >> 12397165

Myoclonic movement disorder associated with microdeletion of chromosome 22q11.

D Baralle, D Trump, C Ffrench-Constant, D J Dick.   

Abstract

Entities:  

Mesh：

Year:  2002        PMID： 12397165      PMCID： PMC1738101          DOI： 10.1136/jnnp.73.5.600

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


× No keyword cloud information.
  4 in total

1.  Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

Authors:  Vincent Strehlow; Marielle E M Swinkels; Rhys H Thomas; Nora Rapps; Steffen Syrbe; Thomas Dorn; Johannes R Lemke
Journal:  Mol Syndromol       Date:  2016-08-24

Review 2.  Neurological manifestation of 22q11.2 deletion syndrome.

Authors:  Michael Bayat; Allan Bayat
Journal:  Neurol Sci       Date:  2022-01-18       Impact factor: 3.307

Review 3.  22q11.2 Deletion Syndrome-Associated Parkinson's Disease.

Authors:  Erik Boot; Anne S Bassett; Connie Marras
Journal:  Mov Disord Clin Pract       Date:  2018-11-09

4.  Subcortical Myoclonus and Associated Dystonia in 22q11.2 Deletion Syndrome.

Authors:  Vincent Van Iseghem; Eavan McGovern; Emmanuelle Apartis; Boris Keren; Marie Vidailhet; Emmanuel Roze; Bertrand Degos
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2020-01-24
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.