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The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes.
Published in:
2010
By:
- Touhami, Imed;
- Fattoum, Slaheddine;
- Bibi, Amina;
- Siala, Hajer;
- Messaoud, Taieb;
- Koubaa, Donia;
- Mankai, Rafik;
- Bartagi, Zakia;
- Le Gallais, Daniel
Publication type:
journal article
Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.
Published in:
Molecular Biology Reports, 2012, v. 39, n. 4, p. 4619, doi. 10.1007/s11033-011-1253-9
By:
- Jouini, Latifa;
- Bibi, Amina;
- Ouali, Faida;
- Hadj Fredj, Sondess;
- Ouennich, Fekria;
- Siala, Hajer;
- Messaoud, Taieb;
- Fattoum, Slaheddine
Publication type:
Article
Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population.
Published in:
Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 8, p. 1193, doi. 10.1515/cclm-2016-0253
By:
- Laouini, Naouel;
- Sahli, Chaima Abdelhafidh;
- Jouini, Latifa;
- Haloui, Sabrine;
- Fredj, Sondes Hadj;
- Daboubi, Rym;
- Siala, Hajer;
- Ouali, Faida;
- Becher, Meriam;
- Toumi, Nourelhouda;
- Bibi, Amina;
- Messsaoud, Taieb
Publication type:
Article
Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients.
Published in:
Journal of Genetics, 2016, v. 95, n. 1, p. 193, doi. 10.1007/s12041-015-0609-7
By:
- OUESLATI, SABRINE;
- HADJ FREDJ, SONDESS;
- SIALA, HAJER;
- BIBI, AMINA;
- ALOULOU, HAJER;
- BOUGHAMOURA, LAMIA;
- BOUSSETTA, KHADIJA;
- BARSAOUI, SIHEM;
- MESSAOUD, TAIEB
Publication type:
Article
New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient.
Published in:
Journal of Genetics, 2013, v. 92, n. 1, p. 81, doi. 10.1007/s12041-013-0208-4
By:
- FREDJ, SONDESS;
- BOUDAYA, MONIA;
- OUESLATI, SABRINE;
- SAHNOUN, SAFA;
- SAHLI, CHAIMA;
- SIALA, HAJER;
- BOUSSETTA, KHEDIJA;
- BIBI, AMINA;
- MESSAOUD, TAIEB
Publication type:
Article
Screening of three Mediterranean phenylketonuria mutations in Tunisian families.
Published in:
Journal of Genetics, 2012, v. 91, n. 1, p. 91, doi. 10.1007/s12041-012-0140-z
By:
- KHEMIR, SAMEH;
- SIALA, HAJER;
- TAIEB, SAMEH;
- CHERIF, WAFA;
- AZZOUZ, HATEM;
- KÉFI, RYM;
- ABDELHAK, SONIA;
- KHOUJA, NAZIHA;
- TEBIB, NEJI;
- MASSAOUD, TAIEB;
- DRIDI, MARIE;
- KAABACHI, NAZIHA
Publication type:
Article
Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification.
Published in:
Electrophoresis, 2017, v. 38, n. 17, p. 2210, doi. 10.1002/elps.201600423
By:
- Doggui, Radhouene;
- Abdelhafidh Sahli, Chaïma;
- Aissa, Wassef Lotfi;
- Hammami, Maroua;
- Ben Sedrine, Maha;
- Mahjoub, Rahma;
- Zouaoui, Khemais;
- Daboubi, Rim;
- Siala, Hajer;
- Messaoud, Taieb;
- Bibi, Amina
Publication type:
Article
Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).
Published in:
2016
By:
- Sahli, Chaima Abdelhafidh;
- Ben Salem, Ikbel;
- Jouini, Latifa;
- Laouini, Naouel;
- Dabboubi, Rym;
- Hadj Fredj, Sondes;
- Siala, Hajer;
- Othmeni, Rym;
- Dakhlaoui, Boutheina;
- Fattoum, Slaheddine;
- Bibi, Amina;
- Messaoud, Taieb
Publication type:
journal article
A lower-cost protocol for sickle cell disease neonatal screening in Tunisia.
Published in:
Annals of Saudi Medicine, 2012, v. 32, n. 1, p. 49, doi. 10.5144/0256-4947.2012.49
By:
- Hajer, Siala;
- Neila, Taboubi;
- Sondess, Hadj Fradj;
- Fekria, Ouenniche;
- Nabila, Aoun;
- Mahbouba, Khedhri;
- Melika, Douiri;
- Faida, Ouali;
- Amina, Bibi;
- Raja, Belhadj;
- Hedi, Rezigua;
- Sadok, Meriah;
- Naima, Krouf;
- Slaheddine, Fattoum;
- Taieb, Messaoud
Publication type:
Article
Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population.
Published in:
Neurochemical Research, 2014, v. 39, n. 2, p. 244, doi. 10.1007/s11064-013-1213-y
By:
- Achouri-Rassas, Afef;
- Hadj Fredj, Sondes;
- Mrabet Khiari, Hela;
- Bibi, Amina;
- Siala, Hajer;
- Mrabet, Amel;
- Messaoud, Taieb
Publication type:
Article
Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease.
Published in:
Journal of Neural Transmission, 2016, v. 123, n. 3, p. 317, doi. 10.1007/s00702-015-1468-3
By:
- Achouri-Rassas, Afef;
- Ali, Nadia;
- Cherif, Aroua;
- Fray, Saloua;
- Siala, Hajer;
- Zakraoui, Nouria;
- Hadj-Fredj, Sondes;
- Kechaou, Mariem;
- Anane, Nadia;
- Echebi, Slim;
- Messaoud, Taieb;
- Belal, Samir
Publication type:
Article
No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population.
Published in:
Journal of Neural Transmission, 2013, v. 120, n. 9, p. 1355, doi. 10.1007/s00702-013-0985-1
By:
- Rassas, Afef;
- Fredj, Sondess;
- Khiari, Hela;
- Sahnoun, Safa;
- Bibi, Amina;
- Siala, Hajer;
- Mrabet, Amel;
- Messaoud, Taieb
Publication type:
Article
First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients.
Published in:
2014
By:
- Sahli, Chaîma;
- Hadj Fredj, Sondess;
- Siala, Hajer;
- Bibi, Amina;
- Messaoud, Taieb
Publication type:
Letter to the Editor
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.
Published in:
Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 11, p. 2115, doi. 10.1515/cclm-2013-0354
By:
- Sahli, Chaima Abdelhafidh;
- Bibi, Amina;
- Ouali, Faida;
- Fredj, Sondess Hadj;
- Dakhlaoui, Boutheina;
- Othmani, Rym;
- Laouini, Naouel;
- Jouini, Latifa;
- Ouenniche, Fekria;
- Siala, Hajer;
- Touhami, Imed;
- Becher, Mariem;
- Fattoum, Slaheddine;
- Toumi, Nour El Houda;
- Messaoud, Taieb
Publication type:
Article
Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.
Published in:
Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1595, doi. 10.1515/cclm-2012-0842
By:
- Sahli, Chaima A.;
- Bibi, Amina;
- Ouali, Faida;
- Fredj, Sondess Hadj;
- Dakhlaoui, Boutheina;
- Othmani, Rym;
- Laaouini, Naouel;
- Jouini, Latifa;
- Ouenniche, Fekria;
- Siala, Hajer;
- Touhami, Imed;
- Becher, Mariem;
- Fattoum, Slaheddine;
- Toumi, Nour El Houda;
- Messaoud, Taieb
Publication type:
Article
δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients.
Published in:
Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 10, p. 1743, doi. 10.1515/cclm-2012-0102
By:
- Sahli, Chaima Abdelhafidh;
- Bibi, Amina;
- Ouali, Faida;
- Siala, Hajer;
- Fredj, Sondess Hadj;
- Othmani, Rym;
- Ouenniche, Fekria;
- Cheour, Mondher;
- Fitouri, Zohra;
- Becher, Saida Ben;
- Messaoud, Taieb
Publication type:
Article
Autism in Phenylketonuria Patients.
Published in:
Journal of Child Neurology, 2016, v. 31, n. 7, p. 843, doi. 10.1177/0883073815623636
By:
- Khemir, Sameh;
- Halayem, Soumeyya;
- Azzouz, Hatem;
- Siala, Hajer;
- Ferchichi, Maherzia;
- Guedria, Asma;
- Bedoui, Amel;
- Abdelhak, Sonia;
- Messaoud, Taieb;
- Tebib, Neji;
- Belhaj, Ahlem;
- Kaabachi, Naziha
Publication type:
Article
Association between angiotensin-converting enzyme gene polymorphism and competitive anxiety in Tunisian athlete.
Published in:
Sport Sciences for Health, 2016, v. 12, n. 2, p. 233, doi. 10.1007/s11332-016-0280-2
By:
- Znazen, Hela;
- Chtara, Mokhtar;
- Butovskaya, Marina;
- Siala, Hajer;
- Messaoud, Taieb;
- Souissi, Nizar
Publication type:
Article

Found: 18

The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes.

Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults.

Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients.

New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient.

Screening of three Mediterranean phenylketonuria mutations in Tunisian families.

Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA<sub>1c</sub> quantification.

Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).

A lower-cost protocol for sickle cell disease neonatal screening in Tunisia.

Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population.

Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease.

No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population.

First study of angiotensin converting enzyme in cystic fibrosis Tunisian patients.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.

δ<sup>0</sup>-Thalassemia in cis of β<sup>Knossos</sup> globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients.

Autism in Phenylketonuria Patients.

Association between angiotensin-converting enzyme gene polymorphism and competitive anxiety in Tunisian athlete.