Literature DB >> 22959176

Benign hereditary chorea: clinical features and long-term follow-up in a Spanish family.

Angel P Sempere, Silvia Aparicio, Santiago Mola, Jordi Pérez-Tur.   

Abstract

Entities:  

Mesh：

Year:  2012        PMID： 22959176     DOI： 10.1016/j.parkreldis.2012.08.006

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN： 1353-8020            Impact factor:   4.891


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  5 in total

1.  Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by NKX2-1 Mutations.

Authors:  Mered Parnes; Hassaan Bashir; Joseph Jankovic
Journal:  Mov Disord Clin Pract       Date:  2018-11-09

Review 2.  Benign Hereditary Chorea: An Update.

Authors:  Kathryn J Peall; Manju A Kurian
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-07-14

3.  NKX2-1 Is Required in the Embryonic Septum for Cholinergic System Development, Learning, and Memory.

Authors:  Lorenza Magno; Caswell Barry; Christoph Schmidt-Hieber; Polyvios Theodotou; Michael Häusser; Nicoletta Kessaris
Journal:  Cell Rep       Date:  2017-08-15       Impact factor: 9.423

4.  Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.

Authors:  Steffi Thust; Liana Veneziano; Michael H Parkinson; Kailash P Bhatia; Elide Mantuano; Cristina Gonzalez-Robles; Indran Davagnanam; Paola Giunti
Journal:  Neurogenetics       Date:  2022-01-25       Impact factor: 2.660

Review 5.  A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.

Authors:  Liana Veneziano; Michael H Parkinson; Elide Mantuano; Marina Frontali; Kailash P Bhatia; Paola Giunti
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847
  5 in total

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