Suchergebnisse - "Pilotto, Andrea"

PubPharm (313)

301

Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy

enthalten in: Neurological sciences | 2011

von Borroni, B. | Pilotto, A. | Bonvicini, C. | +5

302

Role of cytochrome P4502D6 functional polymorphisms in the efficacy of donepezil in patients with Alzheimer's disease

enthalten in: Pharmacogenetics and genomics | 2011

von Seripa, D. | Bizzarro, A. | Pilotto, A. | +10

303

Pharmacogenetics of cytochrome P450 (CYP) in the elderly

enthalten in: Ageing research reviews | 2010

von Seripa, D. | Pilotto, A. | Panza, F. | +2

304

The shortness of Pygmies is associated with severe under-expression of the growth hormone receptor

enthalten in: Molecular genetics and metabolism | 2009

von Bozzola, M. | Travaglino, P. | Marziliano, N. | +10

305

Effect of a CYP2D6 polymorphism on the efficacy of donepezil in patients with Alzheimer disease

enthalten in: Neurology | 2009

von Pilotto, A. | Franceschi, M. | D'Onofrio, G. | +11

306

Novel human pathological mutations. Gene symbol : LMNA. Disease: cardiomyopathy, dilated with conduction defects

enthalten in: Human genetics | 2009

von Arbustini, E. | Pilotto, A. | Grasso, M. | +7

307

Letter by Maurizia Grasso et al. regarding article, "Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutation"

enthalten in: International journal of cardiology | 2008

von Grasso, M. | Pilotto, A. | Marziliano, N. | +2

CommentOn: Int J Cardiol. 2007 Apr 25;117(2):244-53. - PMID 16890305

308

Long-term outcome and risk stratification in dilated cardiolaminopathies

enthalten in: Journal of the American College of Cardiology | 2008

von Pasotti, M. | Klersy, C. | Pilotto, A. | +18

CommentIn: J Am Coll Cardiol. 2008 Oct 7;52(15):1261-2. - PMID 18926330

309

Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies

enthalten in: Journal of human genetics | 2007

von Olivieri, C. | Pagella, F. | Semino, L. | +8

310

Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies

enthalten in: Human mutation | 2005

von Arbustini, E. | Grasso, M. | Ansaldi, S. | +19