Latest papers

Case reports: red scrotal syndrome: a localized phenotypical expression of erythromelalgia.

Nav1.7, its mutations, and the syndromes that they cause.

[Erythromelalgia: two case reports and literature review].

Treatment of familial erythromelalgia with venlafaxine.

A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity.

A case of primary erythermalgia, wintry hypothermia and encephalopathy.

[Hereditary erythermalgia: a model for understanding erythermalgia?].

[Case of erythromelalgia due to essential thrombocythemia].

A case of inherited erythromelalgia.

Mutation hotspots of SCN9A in primary erythermalgia.

Defining a treatable cause of erythromelalgia: acute adolescent autoimmune small-fiber axonopathy.

Characterization of a familial case with primary erythromelalgia from Taiwan.

Neurovascular instability syndrome: a unifying term to describe the coexistence of temperature-related vascular disorders in affected patients.

Hydroxyurea therapy: a rare cause of reversible azoospermia.

Temperature dependence of erythromelalgia mutation L858F in sodium channel Nav1.7.

Platelet-mediated erythromelalgic, cerebral, ocular and coronary microvascular ischemic and thrombotic manifestations in patients with essential thrombocythemia and polycythemia vera: a distinct aspirin-responsive and coumadin-resistant arterial thrombophilia.

Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.

Thermoregulatory sweat testing in patients with erythromelalgia.

Size matters: Erythromelalgia mutation S241T in Nav1.7 alters channel gating.

Inherited erythermalgia: limb pain from an S4 charge-neutral Na channelopathy.