| IAS WEBSITE EDITORIAL BOARD |
 Editor-in-Chief |
Scott M. Grundy, MD, PhD
Dallas, TX, USA |
 Associate Editors |
Stefano Bellosta
Milan, Italy
Emanuela Folco
Milan, Italy
Ann Jackson
Houston, TX, USA |
 Website Editors |
Gianpaolo Bagnato
Milan, Italy
Annamaria Scimone
Milan, Italy
Mandi Wong
Dallas, TX, USA |
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What's New on the IAS Website
IAS Fellowship Award Winner
Congratulations to Tommaso Fasano, MD for winning the 2007 IAS Visiting Fellowship Award. Dr. Fasano was awarded a 6-month grant to study in the Research Laboratory of Dr. Anne Soutar in London.
About Dr. Fasano
RESEARCH INTERESTS
- Dr. Fasano wishes to extend his expertise in the field of molecular pathology of dyslipidemias and to acquire new tools to apply to the functional analysis of the putative loss of
function PCSK9 mutants.
- He is particularly interested in the study of genotype-phenotype correlations in monogenic dyslipidemias.
RECENT PUBLICATIONS OF DR. FASANO
- A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol.
Fasano T, Cefalu AB, Di Leo E, Noto D, Pollaccia D, Bocchi L, Valenti V, Bonardi R, Guardamagna O, Averna M, Tarugi P.
Arterioscler Thromb Vasc Biol. 2007 Mar;27(3):677-81. Epub 2006 Dec 14.
View Abstract
- Coding sequence and intron-exon junctions of the c-myb gene are intact in the chronic phase and blast crisis stages of chronic myeloid leukemia patients.
Bussolari R, Candini O, Colomer D, Corradini F, Guerzoni C, Mariani SA, Cattelani S, Silvestri C, Pecorari L, Iacobucci I, Soverini S, Fasano T, Martinelli G, Cervantes F, Calabretta B.
Leuk Res. 2007 Feb;31(2):163-7. Epub 2006 Jun 23.
View Abstract
- Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients.
Pisciotta L, Fasano T, Bellocchio A, Bocchi L, Sallo R, Fresa R, Colangeli I, Cantafora A, Calandra S, Bertolini S.
Atherosclerosis. 2006 Nov 29; [Epub ahead of print]
View Abstract
- Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency.
Fasano T, Bocchi L, Pisciotta L, Bertolini S, Calandra S.
J Lipid Res. 2005 Apr;46(4):817-22. Epub 2005 Feb 1.
View Abstract
- Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders.
Pisciotta L, Hamilton-Craig I, Tarugi P, Bellocchio A, Fasano T, Alessandrini P, Bon GB, Siepi D, Mannarino E, Cattin L, Averna M, Cefalu AB, Cantafora A, Calandra S, Bertolini S.
Atherosclerosis. 2004 Feb;172(2):309-20.
View Abstract
For more information about the IAS Fellowship, please visit:
http://www.athero.org
 Morocco - Moroccan Society of Atherosclerosis (SMA)
Members: 75
New Website: www.smamaroc.com
Officers
- President:
Cherif Abdelkhirane
- 1st Vice-President:
Ahmed Adlouni (Past President)
- 2nd Vice-President:
Aïcha Hafidi
- 3rd Vice-President:
El Mustapha Fatihi
- Secretary:
Mariame El Messal
Email: elmessal.m@smamaroc.com
- Adjoin Secretary:
Khalid Adnan
- Treasurer:
Rachid Saile
- Adjoin
Treasurer:
Noreddine Ghalim
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Assessors:
- Mohammed Abdellatifi
- Khalid Baghdadi
- Bouchra Benchekroun
- Abdelmajid Chraibi
- Abdelfettah Derouiche
- Anass Kettani
- Halima Lebrazi
- Ghislaine Medkouri
- Samya Moussamih
- Benyounes Ramdani
- Souad Safir
- Hassan Taki
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If your Member Society has an update, please send an email to: info@athero.org |
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