S. Pigullo

发表

No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients

P. Barone, U. Bonuccelli, G. Abbruzzese, 2001, Journal of Neural Transmission.

Inhibition of the Mr 70,000 S6 kinase pathway by rapamycin results in chromosome malsegregation in yeast and mammalian cells

R. Schiestl, A. Abbondandolo, A. Galli, 1998, Chromosoma.

Severe congenital neutropenia: a negative synergistic effect of multiple mutations of ELANE (ELA2) gene

G. Caridi, C. Rosano, C. Dufour, 2009, British journal of haematology.

A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci

P. Girlanda, A. Pizzuti, E. Bellone, 2002, Neuromuscular Disorders.

Does parkin play a role in the peripheral nervous system? A family report

G. Abbruzzese, R. Marchese, E. Bellone, 2004, Movement disorders : official journal of the Movement Disorder Society.

A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect

E. Bellone, A. Schenone, P. Balestra, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Essential tremor is not associated with alpha-synuclein gene haplotypes.

P. Barone, G. Abbruzzese, R. Marchese, 2003, Movement disorders : official journal of the Movement Disorder Society.

Analysis of telomeres in peripheral blood cells from patients with bone marrow failure

I. Dianzani, A. Aspesi, C. Dufour, 2009, Pediatric blood & cancer.

NOLA1 gene mutations in acquired aplastic anemia

I. Dianzani, J. Svahn, M. Pillon, 2009, Pediatric blood & cancer.

6DMAP inhibition of early cell cycle events and induction of mitotic abnormalities.

L. Ottaggio, G. Tavosanis, S. Bonatti, 1997, Mutagenesis.

Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements

M. Valsecchi, G. Basso, M. Luciani, 2005, Leukemia.

Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremor.

P. Barone, B. Dallapiccola, G. Abbruzzese, 2004, Parkinsonism & related disorders.

Clinical and genetic study of essential tremor in the Italian population

A. Berardelli, P. Barone, G. Abbruzzese, 2001, Neurological Sciences.

Induction of apoptosis and inhibition of signalling pathways by alkylated purines.

A. Abbondandolo, S. Bonatti, M. Simili, 2000, Mutagenesis.

Are genotypes of glutathione S-transferase superfamily a risk factor for childhood acute lymphoblastic leukemia? Results of an Italian case–control study

G. Basso, A. Biondi, R. Haupt, 2007, Leukemia.

Glutathione S-transferase polymorphisms and susceptibility to neuroblastoma

G. Tonini, L. Boni, R. Haupt, 2005, Pharmacogenetics and genomics.

Essential tremor is not associated with α‐synuclein gene haplotypes

P. Barone, G. Abbruzzese, R. Marchese, 2003 .

Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II.

A. Windebank, A. Pizzuti, E. Bellone, 1999, American journal of medical genetics.

Possible role of toll‐like receptor 9 polymorphism in chemotherapy‐related invasive mold infections in children with hematological malignancies

C. Dufour, E. Castagnola, S. Pigullo, 2008, Pediatric blood & cancer.

A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci

P. Girlanda, A. Pizzuti, E. Bellone, 2002, Neuromuscular Disorders.

Human Fanconi A cells are susceptible to TRAIL‐induced apoptosis

V. Pistoia, J. Svahn, G. Candiano, 2007, British journal of haematology.