Literature DB >> 19553144

Gaucher disease in Tunisia: High frequency of the most common mutations.

Wafa Cherif, Hadhami Ben Turkia, Faten Ben Rhouma, Imene Riahi, Jalel Chemli, Rym Kefi, Habib Messai, Olga Amaral, Maria Clara Sá Miranda, Catherine Caillaud, Neji Tebib, Marie Françoise Ben Dridi, Sonia Abdelhak.   

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Year:  2009        PMID： 19553144     DOI： 10.1016/j.bcmd.2009.05.004

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN： 1079-9796            Impact factor:   3.039


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  5 in total

1.  A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report.

Authors:  Houweyda Jilani; Faten Hsoumi; Imen Rejeb; Yasmina Elaribi; Syrine Hizem; Molka Sebai; Arndt Rolfs; Lamia Benjemaa
Journal:  Clin Case Rep       Date:  2022-05-12

2.  Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa.

Authors:  Kenya Nishioka; Carles Vilariño-Güell; Stephanie A Cobb; Jennifer M Kachergus; Owen A Ross; Christian Wider; Rachel A Gibson; Faycal Hentati; Matthew J Farrer
Journal:  Neurosci Lett       Date:  2009-11-27       Impact factor: 3.046

3.  Adult Gaucher disease in southern Tunisia: report of three cases.

Authors:  Faten Ben Rhouma; Faten Kallel; Rym Kefi; Wafa Cherif; Majdi Nagara; Hela Azaiez; Ines Jedidi; Moez Elloumi; Sonia Abdelhak; Sondes Mseddi
Journal:  Diagn Pathol       Date:  2012-01-10       Impact factor: 2.644

4.  Genetics and genomic medicine in Tunisia.

Authors:  Houda Elloumi-Zghal; Habiba Chaabouni Bouhamed
Journal:  Mol Genet Genomic Med       Date:  2018-03       Impact factor: 2.183

5.  Twenty- five years of biochemical diagnosis of Gaucher disease: the Egyptian experience.

Authors:  Ekram Fateen; Zeinab Y Abdallah
Journal:  Heliyon       Date:  2019-11-01
  5 in total

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