Literature DB >> 15986422

Alterations of striatal neurons in benign hereditary chorea.

Galit Kleiner-Fisman1, Noel Y Calingasan, Mary Putt, June Chen, M Flint Beal, Anthony E Lang.   

Abstract

Benign hereditary chorea (BHC) recently has been associated with mutations in TITF-1 gene, although a pathological study of an individual with BHC and a TITF-1 mutation revealed no significant gross or microscopic abnormalities using standard methods. Immunohistochemical staining of striatal tissue from a BHC-affected postmortem brain was performed using antibodies against neurotransmitters of interneurons whose tangential migration is mediated by TITF-1. There was a loss of most TITF-1-mediated striatal interneurons in the BHC specimen compared to four matched control brains. Copyright (c) 2005 Movement Disorder Society.

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Year:  2005        PMID: 15986422     DOI: 10.1002/mds.20577

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  11 in total

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Authors:  Kurt A Jellinger
Journal:  J Neural Transm (Vienna)       Date:  2019-06-24       Impact factor: 3.575

2.  Benign hereditary chorea: dopaminergic brain imaging in patients with a novel intronic NKX2.1 gene mutation.

Authors:  Takashi Konishi; Satoshi Kono; Masaya Fujimoto; Tatsuhiro Terada; Kozo Matsushita; Yasuomi Ouchi; Hiroaki Miyajima
Journal:  J Neurol       Date:  2012-07-24       Impact factor: 4.849

3.  Update on the Non-Huntington's Disease Choreas with Comments on the Current Nomenclature.

Authors:  Ruth H Walker
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2012-01-30

4.  The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.

Authors:  Davide Martino; Maria Stamelou; Kailash P Bhatia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2012-09-19       Impact factor: 10.154

Review 5.  Benign Hereditary Chorea: An Update.

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

Review 6.  Functional neuroimaging and chorea: a systematic review.

Authors:  Debra J Ehrlich; Ruth H Walker
Journal:  J Clin Mov Disord       Date:  2017-06-21

7.  The Movement Disorder of Brain-Lung-Thyroid Syndrome Can be Responsive to Methylphenidate.

Authors:  Laurence Gauquelin; Luan T Tran; Sylvain Chouinard; Geneviève Bernard
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2017-10-26

8.  Chiari Malformation Type I in a Patient with a Novel NKX2-1 Mutation.

Authors:  Daniel Gonçalves; Lara Lourenço; Micaela Guardiano; Cintia Castro-Correia; Mafalda Sampaio; Miguel Leão
Journal:  J Pediatr Neurosci       Date:  2019-09-27

9.  Striatal disorders dissociate mechanisms of enhanced and impaired response selection - Evidence from cognitive neurophysiology and computational modelling.

Authors:  Christian Beste; Mark Humphries; Carsten Saft
Journal:  Neuroimage Clin       Date:  2014-04-12       Impact factor: 4.881

Review 10.  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

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