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Blood|June 1, 1993
An AML1/ETO fusion transcript is consistently detected by RNA-based polymerase chain reaction in acute myelogenous leukemia containing the (8;21)(q22;q22) translocationJ R Downing, D R Head, A M Curcio-Brint, et al.
Journal of Alzheimer'S Disease : JAD|April 14, 2009
AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesionsLivia Bernardi, Silvana Geracitano, Rosanna Colao, et al.
The American Journal of Pathology|November 1, 1993
Detection of the (11;22)(q24;q12) translocation of Ewing's sarcoma and peripheral neuroectodermal tumor by reverse transcription polymerase chain reactionJ R Downing, D R Head, D M Parham, et al.
Cell Death & Disease|December 21, 2012
Effects of long-term treatment with pioglitazone on cognition and glucose metabolism of PS1-KI, 3xTg-AD, and wild-type miceF Masciopinto, N Di Pietro, C Corona, et al.
Journal of Neurology|July 26, 2002
A large Calabrian kindred segregating frontotemporal dementiaS A M Curcio, T Kawarai, A D Paterson, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2009
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementiaMaura Gallo, Carmine Tomaino, Gianfranco Puccio, et al.
Archives of Neurology|August 18, 2004
Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutationAmalia C Bruni, Junko Takahashi-Fujigasaki, Francesca Maltecca, et al.
Neurobiology of Aging|March 4, 2008
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementiaLivia Bernardi, Carmine Tomaino, Maria Anfossi, et al.
Journal of Alzheimer'S Disease : JAD|February 8, 2011
PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotypeLivia Bernardi, Maria Anfossi, Maura Gallo, et al.
Journal of Alzheimer'S Disease : JAD|June 25, 2013
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutationLivia Bernardi, Maura Gallo, Maria Anfossi, et al.
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