CNS involvement in CMTX1 caused by a novel connexin 32 mutation: a 6-year follow-up in neuroimaging and nerve conduction

Episodic neurological dysfunction in hereditary peripheral neuropathy

(2014) GirishBaburao Kulkarni et al.   Annals of Indian Academy of Neurology

A V139M Mutation Also Causes the Reversible CNS Phenotype in CMTX

(2014) Michelle Halbrich et al.   CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES

The Central Nervous System Phenotype of X-Linked Charcot-Marie-Tooth Disease

(2013) Majeed Al-Mateen et al.   JOURNAL OF CHILD NEUROLOGY

X-linked Charcot-Marie-Tooth disease predominates in a cohort of multiethnic Malaysian patients

(2013) Nortina Shahrizaila et al.   MUSCLE & NERVE

Recurrent central nervous system white matter changes in charcot-Marie-Tooth type X disease

(2013) Jennifer L. Mckinney et al.   MUSCLE & NERVE

How do mutations in GJB1 cause X-linked Charcot–Marie–Tooth disease?

(2012) Kleopas A. Kleopa et al.   BRAIN RESEARCH

Inflammatory demyelinating CNS disorder in a case of X-linked Charcot–Marie–Tooth disease: positive response to natalizumab

(2012) Jochen H. Weishaupt et al.   JOURNAL OF NEUROLOGY

Diffusion tensor imaging and magnetic resonance spectroscopy of transient cerebral white matter lesions in X-linked Charcot-Marie-Tooth disease

(2012) Kota Sato et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Clinical Reasoning: A young man with reversible paralysis, cerebral white matter lesions, and peripheral neuropathy

(2012) L. Zhong et al.   NEUROLOGY

MRI findings in X-linked Charcot–Marie–Tooth disease associated with a novel connexin 32 mutation

(2011) J.M. U-King-Im et al.   CLINICAL RADIOLOGY

A novel mutation of gap junction protein beta 1 gene in x-linked charcot-marie-tooth disease

(2011) Sheng Dong Chen et al.   MUSCLE & NERVE

Recurrent stroke-like episodes in X-linked Charcot-Marie-Tooth disease

(2011) A. Basu et al.   NEUROLOGY

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

(2010) H. Skre   CLINICAL GENETICS

X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode

(2010) GEETHA ANAND et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Transient Leukoencephalopathy Associated With X-Linked Charcot-Marie-Tooth Disease

(2010) Tena Rosser et al.   JOURNAL OF CHILD NEUROLOGY

Coexistent Central and Peripheral Nervous System Involvement in a Charcot-Marie-Tooth Syndrome X-linked Patient

(2010) Carlo Fusco et al.   JOURNAL OF CHILD NEUROLOGY

A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot–Marie–Tooth disease

(2010) Hideya Sakaguchi et al.   JOURNAL OF NEUROLOGY

A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese family

(2010) Pengfei Lin et al.   MUSCLE & NERVE

Persistent CNS dysfunction in a boy with CMT1X

(2009) Carly Siskind et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Diagnosis, natural history, and management of Charcot–Marie–Tooth disease

(2009) Davide Pareyson et al.   LANCET NEUROLOGY

Central Nervous System Signs in X-Linked Charcot-Marie-Tooth Disease After Hyperventilation

(2008) Jayasri Srinivasan et al.   PEDIATRIC NEUROLOGY