Severe case and literature review of primary erythromelalgia: Novel SCN9A gene mutation

Eritromelalgia primária: relato de caso

(2011) Lígia Guedes Morais de Albuquerque et al.   ANAIS BRASILEIROS DE DERMATOLOGIA

A new Nav1.7 sodium channel mutation I234T in a child with severe pain

(2010) Hye-Sook Ahn et al.   EUROPEAN JOURNAL OF PAIN

Can robots patch-clamp as well as humans? Characterization of a novel sodium channel mutation

(2010) M. Estacion et al.   JOURNAL OF PHYSIOLOGY-LONDON

Chronic non-paroxysmal neuropathic pain — Novel phenotype of mutation in the sodium channel SCN9A gene

(2010) Ron Dabby et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Mutations at opposite Ends of the DIII/S4-S5 Linker of Sodium Channel NaV1.7 Produce Distinct Pain Disorders

(2010) Xiaoyang Cheng et al.   Molecular Pain

A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia

(2009) Tanya Z. Fischer et al.   ANNALS OF NEUROLOGY

Erythromelalgia mutation L823R shifts activation and inactivation of threshold sodium channel Nav1.7 to hyperpolarized potentials

(2009) Angelika Lampert et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Early- and late-onset inherited erythromelalgia: genotype–phenotype correlation

(2009) Chongyang Han et al.   BRAIN

Mexiletine-responsive erythromelalgia due to a new Nav1.7 mutation showing use-dependent current fall-off

(2009) Jin-Sung Choi et al.   EXPERIMENTAL NEUROLOGY

NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders

(2008) M. Estacion et al.   JOURNAL OF NEUROSCIENCE

Incidence of erythromelalgia: a population-based study in Olmsted County, Minnesota

(2008) KB Reed et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY