Adolf Pou Serradell

Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic)

Claire Donger, Éric Krejci, Adolf Pou Serradell et al. · The American Journal of Human Genetics · 1998 · 160 citations · Full text

Mendelian Disorder, Connective Tissue Disease, Genetic Disorder +9

Comparison of three different volumes of mepivacaine in axillary plexus block using multiple nerve stimulation †

Adolf Pou Serradell, Rocío López-Herrero, J.A. Villanueva et al. · British Journal of Anaesthesia · 2003 · 44 citations

Stimulation Device, Axillary Plexus Block, Neurophysiology +9

[3 cases of rare peripheral neuropathies associated with primary Gougerot-Sjögren syndrome].

Adolf Pou Serradell, Jaume Gayà · PubMed · 1993 · 21 citations

The cuff method: a pilot study of a new method of monitoring neuromuscular function

J. Rodiera, Adolf Pou Serradell, José Antonio Álvarez Gómez et al. · Acta Anaesthesiologica Scandinavica · 2005 · 18 citations

[Acute posterior cord lesions in multiple sclerosis. An MRI study of the clinical course in 20 cases].

Adolf Pou Serradell, Jaume Roquer, X. Perich Alsina · PubMed · 2000 · 13 citations