Latest papers

Inherited disorders of the neuromuscular junction.

In vivo and in vitro functional characterization of Andersen's syndrome mutations.

The contribution of Dr. Mary Walker towards myasthenia gravis and periodic paralysis whilst working in poor law hospitals in London.

Thyrotoxic periodic paralysis after allogeneic haematopoietic stem cell transplantation.

Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family.

[Anesthesia in hereditary peripheral muscular disease].

Thyrotoxic periodic paralysis in a Maori patient.

[The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis].

Patient page. Attacks of immobility caused by diet or exercise? The mystery of periodic paralyses.

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

Treatment in myotonia and periodic paralysis.

Andersen syndrome: the newest variant of the hereditary-familial long QT syndrome.

Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation.

Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis.

Index of suspicion.

Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.

Electrocardiographic manifestations in patients with thyrotoxic periodic paralysis.

[Thyreotoxic periodic paralysis. A cause of pseudo-paralysing hypokalemia that should not be ignored in Caucasians].

Thyrotoxic periodic paralysis in western countries.

An unrecognized cause of paralysis in ED: Thyrotoxic normokalemic periodic paralysis