Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant

Familial Hemiplegic Migraines and Baseline Neuropsychological Testing: A Case Report

(2019) Elizabeth M. Trahan et al.   HEADACHE

Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant

(2018) Chloé Angelini et al.   European Journal of Medical Genetics

The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature

(2018) E. Indelicato et al.   EUROPEAN JOURNAL OF NEUROLOGY

Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia

(2017) Cèlia Sintas et al.   Scientific Reports

Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation

(2016) Luca Pradotto et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Migraine Mutations Impair Hippocampal Learning Despite Enhanced Long-Term Potentiation

(2015) E. Dilekoz et al.   JOURNAL OF NEUROSCIENCE

Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature

(2014) Wolfgang Nachbauer et al.   JOURNAL OF NEUROLOGY

The International Classification of Headache Disorders, 3rd edition (beta version)

(2013)   CEPHALALGIA

A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation

(2010) R. Romaniello et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

(2010) F. Riant et al.   NEUROLOGY

CaV2.1 channelopathies

(2010) Daniela Pietrobon   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY