Stefan Buk
Publications by Year
Research Areas
Ion channel regulation and function, Peptidase Inhibition and Analysis, Systemic Lupus Erythematosus Research, Muscle Physiology and Disorders, Glycosylation and Glycoproteins Research
Most-Cited Works
- → Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy(2012)279 cited
- → Pathology, histochemistry and immunocytochemistry of lesions in acute multiple sclerosis(1989)165 cited
- → Inflammatory vasculitis in multiple sclerosis(1985)139 cited
- → King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene(2011)114 cited
- → Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene(2010)90 cited
- → Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene(2013)61 cited
- → Infantile onset myofibrillar myopathy due to recessive CRYAB mutations(2010)60 cited
- → Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin(2010)53 cited
- → Simultaneous Demonstration of Connective Tissue elastica and Fibrin by a Combined Verhoeff's Elastic-Martius-Scarlet-Blue Trichrome Stain(1984)33 cited
- → PERLS‘ FERROCYANIDE TEST FOR IRON IN THE DIAGNOSIS OF VASCULITIC NEUROPATHY(1989)25 cited