achille iolascon
achille iolascon
Affiliazione Dept of Molecular Medicine and Medical Biotechnology
Verified email at unina.it
TitleCited byYear
Subgroup-specific structural variation across 1,000 medulloblastoma genomes
PA Northcott, DJH Shih, J Peacock, L Garzia, AS Morrissy, T Zichner, ...
Nature 488 (7409), 49, 2012
5602012
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, CN Lo, GM Ghiggeri, ...
Nature genetics 26 (1), 103-105, 2000
3392000
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single …
M Seri, A Pecci, F Di Bari, R Cusano, M Savino, E Panza, A Nigro, P Noris, ...
Medicine 82 (3), 203-215, 2003
3112003
Guidelines for the diagnosis and management of hereditary spherocytosis
PHB Bolton‐Maggs, RF Stevens, NJ Dodd, G Lamont, P Tittensor, ...
British journal of haematology 126 (4), 455-474, 2004
2932004
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
C Camaschella, A Campanella, L De Falco, L Boschetto, R Merlini, ...
Blood 110 (4), 1353-1358, 2007
2892007
MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastoma
L Garzia, I Andolfo, E Cusanelli, N Marino, G Petrosino, D De Martino, ...
PloS one 4 (3), e4998, 2009
2802009
Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia …
J Donadieu, T Leblanc, BB Meunier, M Barkaoui, O Fenneteau, ...
haematologica 90 (1), 45-53, 2005
279*2005
Guidelines for the diagnosis and management of hereditary spherocytosis–2011 update
PHB Bolton‐Maggs, JC Langer, A Iolascon, P Tittensor, MJ King
British journal of haematology 156 (1), 37-49, 2012
2372012
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
K Wang, SJ Diskin, H Zhang, EF Attiyeh, C Winter, C Hou, RW Schnepp, ...
Nature 469 (7329), 216, 2011
2242011
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
K Schwarz, A Iolascon, F Verissimo, NS Trede, W Horsley, W Chen, ...
Nature genetics 41 (8), 936, 2009
2112009
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
SJ Diskin, M Capasso, RW Schnepp, KA Cole, EF Attiyeh, C Hou, ...
Nature genetics 44 (10), 1126, 2012
1762012
Position of nonmuscle myosin heavy chain IIA (NMMHC‐IIA) mutations predicts the natural history of MYH9‐related disease
A Pecci, E Panza, N Pujol‐Moix, C Klersy, F Di Bari, V Bozzi, P Gresele, ...
Human mutation 29 (3), 409-417, 2008
1742008
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome
A Savoia, CL Balduini, M Savino, P Noris, M Del Vecchio, S Perrotta, ...
Blood 97 (5), 1330-1335, 2001
1712001
Coinheritance of Gilbert Syndrome Increases the Risk for Developing Gallstones in Patients With Hereditary Spherocytosis: Presented in part at the 40th Annual Meeting of the …
EM del Giudice, S Perrotta, B Nobili, C Specchia, G d’Urzo, A Iolascon
Blood 94 (7), 2259-2262, 1999
1681999
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
I Andolfo, SL Alper, L De Franceschi, C Auriemma, R Russo, L De Falco, ...
Blood 121 (19), 3925-3935, 2013
1632013
Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus–related chronic hepatitis: insulin resistance and response to antiviral therapy
M Persico, M Capasso, E Persico, M Svelto, R Russo, D Spano, L Crocè, ...
Hepatology 46 (4), 1009-1015, 2007
1612007
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1
LJ Bruce, HC Robinson, H Guizouarn, F Borgese, P Harrison, MJ King, ...
Nature genetics 37 (11), 1258, 2005
1562005
Involvement of SNAP-23 and syntaxin 6 in human neutrophil exocytosis
B Martın-Martın, SM Nabokina, J Blasi, PA Lazo, F Mollinedo
Blood 96 (7), 2574-2583, 2000
1532000
Inherited thrombocytopenias: from genes to therapy
CL Balduini, A Iolascon, A Savoia
haematologica 87 (8), 860-880, 2002
1492002
MiR-34a targeting of Notch ligand delta-like 1 impairs CD15+/CD133+ tumor-propagating cells and supports neural differentiation in medulloblastoma
P de Antonellis, C Medaglia, E Cusanelli, I Andolfo, L Liguori, G De Vita, ...
PloS one 6 (9), e24584, 2011
1472011
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