Current issue n.3/2018

ORIGINAL ARTICLES

Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis

Prevalence of metabolic syndrome and non-alcoholic fatty liver disease in a cohort of Italian patients with spinal-bulbar muscular atrophy

Childhood onset limb-girdle muscular dystrophies in Aegean part of Turkey

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

CASE REPORT

Myotonic dystrophy type 1 and pulmonary embolism: successful thrombus resolution with dabigatran etexilate therapy

OBITUARY Professor Frank Lehmann-Horn (1948-2018) Reinhardt Rüdel

NEWS FROM AROUND THE WORLD

FORTHCOMING MEETINGS

go to issue n° 3/2018