A Pou-Serradell

Genetic spectrum of hereditary neuropathies with onset in the first year of life

Jonathan Baets, Tine Deconinck, Els De Vriendt et al. · Brain · 2011 · 132 citations · Full text

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Uwe Kornak, Inès Mademan, Marte Schinke et al. · Brain · 2014 · 105 citations · Full text

Peripheral Nerve Injury, Genetics, Atlastin Gtpase 3 +17

<i>SPTLC1</i> mutation in twin sisters with hereditary sensory neuropathy type I

K. Verhoeven, Katrien Coen, Els De Vriendt et al. · Neurology · 2004 · 40 citations

A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

Jan Meuleman, A Pou-Serradell, A. Löfgren et al. · Neuromuscular Disorders · 2001 · 29 citations

Molecular Neuroscience, Genetic Disorder, Medicine +8

A prospective study of atrial fibrillation and stroke.

L D'Olhaberriague, Alba Hernández-Vidal, L Molina et al. · Stroke · 1989 · 24 citations · Full text

Heart Failure, Cerebrovascular Disease, Acute Myocardial Infarction +20