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On a Hybrid Preamble/Soft-Output Demapper Approach for Time Synchronization for IEEE 802.15.6 Narrowband WBAN

China Communications 2015年第2期12卷 1-10页

作者： Imen Nasr leila najjar atallah Sofiane Cherif YANG Jianxiao WANG Kunlun Unité d'Informatique et d'Ingènierie des Systemes(U2IS) Ecole Nationale Supérieure de Techniques Avancées(ENSTA Paris Tech) Communication Signal and Image(COSIM) LaboratoryHigher School of Communications of Tunis(Sup'Com) Network Coding and Transmission Laboratory Shanghai Jiao Tong University

In this paper,we present a maximum likelihood(ML) based time synchronization algorithm for Wireless Body Area Networks(WBAN).The proposed technique takes advantage of soft information retrieved from the soft demapper for the time delay *** algorithm has a low complexity and is adapted to the frame structure specified by the IEEE 802.15.6standard[1]for the narrowband *** results have shown good performance which approach the theoretical mean square error limit bound represented by the Cramer Rao Bound(CRB).

关键词： WBAN IEEE 802.15.6 time synchronization ML estimation soft demapping

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Association of Fas/Apo1 gene promoter (-670 A/G) polymorphism in Tunisian patients with IBD

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World Journal of Gastroenterology 2009年第29期15卷 3643-3648页

作者： Walid Ben Aleya Imen Sfar leila Mouelhi Houda Aouadi Mouna Makhlouf Salwa Ayed-Jendoubi Samira Matri Azza Filali Taoufik najjar Taeib Ben Abdallah Khaled Ayed Yousr Gorgi Laboratory of Immunology EPS Charles Nicolle 1006 Bab Saadoun Tunis 1006 Tunisia Department of Gastroenterology EPS Charles Nicolle Tunis 1006 Tunisia Department of Gastroenterology La Rabta Tunis 1006 Tunisia

AIM： To detect a possible association between the polymorphism of the （-670 A/G） Fas/Apol gene promoter and susceptibility to Crohn＇s disease （CD） and ulcerative colitis （UC） in the Tunisian population. METHODS： The （-670 A/G） Fas polymorphism was analyzed in 105 patients with CD, 59 patients with UC, and 100 controls using the polymerase chain reaction restriction fragment length polymorphism method. RESULTS： Significantly lower frequencies of the Fas -670 A allele and A/A homozygous individuals were observed in CD and UC patients when compared with controls. Analysis of （-670 A/G） Fas polymorphism with respect to sex in CD and UC showed a significant difference in A/A genotypes between female patients and controls （P corrected = 0.004 ＂in CD patients＂ and P corrected = 0.02 ＂in UC patients＂, respectively）. Analysis also showed a statistically significant association between genotype AA of the （-670 A/G） polymorphism and the ileum localization of the lesions （P corrected = 0.048） and between genotype GG and the colon localization （P corrected = 0.009）. The analysis of IBD patients according to clinical behavior revealed no difference. CONCLUSION： Fas-670 polymorphism was associated with the development of CD and UC in the Tunisian population.

关键词： Fas/Apol Gene polymorphisms Inflammatory bowel disease Crohn's disease Ulcerative colitis

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Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia

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World Journal of Gastroenterology 2010年第4期16卷 479-483页

作者： Imen Sfar Walid Ben Aleya leila Mouelhi Houda Aouadi Thouraya Ben Rhomdhane Mouna Makhlouf Salwa Ayed-Jendoubi Houda Gargaoui Taoufik najjar Taieb Ben Abdallah Khaled Ayed Yousr Gorgi Laboratory of Immunology Charles Nicolle HospitalTunis 1006Tunisia Department of Gastroenterology Charles Nicolle HospitalTunis 1006Tunisia

AIM:To assess the possible association between PTPN22(R620W) gene polymorphism and inflammatory bowel disease(IBD).METHODS:One hundred and sixty-four patients with IBD 105 Crohn's disease(CD) and 59 ulcerative colitis(UC) and 100 healthy controls were *** of the PTPN22 gene 1858C→T polymorphism was performed by restriction fragment length polymorphism-polymerase chain reaction with Rsa Ⅰ ***:The genotypic and allelic frequencies of(R620W) PTPN22 gene polymorphism reveal a significant association of the PTPN22 620-W allele with IBD,compared to the healthy control group(OR:17.81,95% CI:4.18-21.86,P = 0.00001).Nevertheless,nodifference in this polymorphism was found between CD and UC *** significant association was found between the frequencies of genotypes of the PTPN22 gene with either the clinical features such as sex,age,age at disease onset,and extent of colitis,or the production of serological markers(anti-Saccharomyces cerevisiae antibody in CD and perinuclear anti-neutrophil cytoplasmic antibody in UC).CONCLUSION:These observations confirm the association of IBD susceptibility with the PTPN22 1858T(620-W) allele in Tunisian patients.

关键词： Inflammatory bowel disease PTPN22 Genetic polymorphism Genetic susceptibility

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