Teresa de Berardinis

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

Max A. Tischfield, Hagit Baris, Chen Wu et al. · Cell · 2010 · 589 citations · Full text

Axon Guidance, Protein Function, Molecular Biology +8

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

Koki Yamada, Caroline Andrews, Wai‐Man Chan et al. · Nature Genetics · 2003 · 260 citations

Extraocular Muscles, Congenital Fibrosis, Fibrosis +9

Possible risk factors for primary adult onset dystonia: a case-control investigation by the Italian Movement Disorders Study Group

Giovanni Defazio, Alfredo Berardelli, Giovanni Abbruzzese et al. · Journal of Neurology Neurosurgery & Psychiatry · 1998 · 126 citations · Full text

Identification of<i>KIF21A</i>Mutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3)

Koki Yamada, Wai‐Man Chan, Caroline Andrews et al. · Investigative Ophthalmology & Visual Science · 2004 · 95 citations · Full text

Risk factors for spread of primary adult onset blepharospasm: a multicentre investigation of the Italian movement disorders study group

Giovanni Defazio, Alfredo Berardelli, Giovanni Abbruzzese et al. · Journal of Neurology Neurosurgery & Psychiatry · 1999 · 71 citations · Full text