Benign hereditary chorea related toNKX2.1: expansion of the genotypic and phenotypic spectrum

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

(2013) Kathryn J. Peall et al.   BRAIN

Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study

(2012) RUSSELL C DALE et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

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

(2012) Takashi Konishi et al.   JOURNAL OF NEUROLOGY

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in theTITF1/NKX2-1gene

(2012) Domitille Gras et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea

(2011) Katsuya Nakamura et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Benign hereditary chorea: An update

(2011) Rivka Inzelberg et al.   PARKINSONISM & RELATED DISORDERS

Benign hereditary chorea: Clinical and neuroimaging features in an Italian family

(2010) Elena Salvatore et al.   MOVEMENT DISORDERS

Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

(2009) A. Carre et al.   HUMAN MOLECULAR GENETICS

“Jerky” dystonia in children: Spectrum of phenotypes and genetic testing

(2009) Friedrich Asmus et al.   MOVEMENT DISORDERS

Psychosis, short stature in benign hereditary chorea: A novel thyroid transcription factor-1 mutation

(2008) Amir Glik et al.   MOVEMENT DISORDERS

A Novel NKX2.1 Mutation in a Family with Hypothyroidism and Benign Hereditary Chorea

(2008) Alfonso Massimiliano Ferrara et al.   THYROID