يعرض 1 - 10 نتائج من 10 نتيجة بحث عن '"Hadj Fredj, Sondes"', وقت الاستعلام: 0.99s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A gain-of-function mutation in zinc cluster transcription factor Rob1 Drives Candida albicans adaptive growth in the cystic fibrosis lung environment.

    المؤلفون: Gnaien, Mayssa, Maufrais, Corinne, Rebai, Yasmine, Kallel, Aicha, Ma, Laurence, Hamouda, Samia, Khalsi, Fatma, Meftah, Khaoula, Smaoui, Hanen, Khemiri, Monia, Hadj Fredj, Sondes, Bachellier-Bassi, Sophie, Najjar, Imène, Messaoud, Taieb, Boussetta, Khadija, Kallel, Kalthoum, Mardassi, Helmi, d'Enfert, Christophe, Bougnoux, Marie-Elisabeth, Znaidi, Sadri

    المصدر: PLoS Pathogens; 4/11/2024, Vol. 20 Issue 4, p1-37, 37p

    مصطلحات موضوعية: GAIN-of-function mutations, CYSTIC fibrosis, CANDIDA albicans, QUORUM sensing, PULMONARY fibrosis, CHILD patients

    Find this article in full text from ProQuest Full Text Finder
    أضف إلى المفضلة
  2. 2
    دورية أكاديمية
    Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease

    المؤلفون: Achouri-Rassas, Afef, Ali, Nadia Ben, Cherif, Aroua, Fray, Saloua, Siala, Hajer, Zakraoui, Nouria Oudiaa, Hadj-Fredj, Sondes, Kechaou, Mariem, Anane, Nadia, Echebi, Slim, Messaoud, Taieb, Belal, Samir

    المصدر: Journal of Neural Transmission: Translational Neuroscience, Neurology and Preclinical Neurological Studies, Psychiatry and Preclinical Psychiatric Studies. March 2016 123(3):317-321

    Find this article in full text from Springer Verlag. Full Text Finder
    أضف إلى المفضلة
  3. 3
    دورية أكاديمية
    Association Between Alzheimer Disease and the −491T Allele of Regulatory Region Polymorphism of Apolipoprotein E in a Tunisian Population

    المؤلفون: Achouri-Rassas, Afef, Hadj Fredj, Sondes, Mrabet Khiari, Hela, Bibi, Amina, Siala, Hajer, Mrabet, Amel, Messaoud, Taieb

    المصدر: Neurochemical Research. February 2014 39(2):244-247

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest Full Text Finder
    أضف إلى المفضلة
  4. 4
    دورية أكاديمية
    Association between H2 haplotype of microtubule associated protein tau gene (deletion / insertion) with Alzheimer Disease in Tunisian patients.

    المؤلفون: Fray, Saloua, Achouri-Rassas, Afef Achouri, Hadj Fredj, Sondes, Messaoud, Taieb, Belal, Samir

    المصدر: Neurological Research; Sep2022, Vol. 44 Issue 9, p814-818, 5p

    مصطلحات موضوعية: TAU proteins, TUBULINS, HAPLOTYPES, ALZHEIMER'S disease, AMYLOID plaque, PEPTIDES, APOLIPOPROTEIN E4

    PDF full text from Publisher
    أضف إلى المفضلة
  5. 5
    دورية أكاديمية
    High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population

    المؤلفون: Rassas, Afef Achouri, Mrabet Khiari, Hela, Hadj Fredj, Sondes, Sahnoun, Safa, Batti, Hend, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Anane, Nadia, Ben Ali, Nadia, Messaoud, Taieb, Mrabet, Amel

    المصدر: Neurological Sciences: Official Journal of the Italian Neurological Society. February 2012 33(1):33-37

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest Full Text Finder
    أضف إلى المفضلة
  6. 6
    دورية أكاديمية
    Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).

    المؤلفون: 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

    المصدر: Journal of Clinical Laboratory Analysis; Sep2016, Vol. 30 Issue 5, p392-398, 7p

    أضف إلى المفضلة
  7. 7
    دورية أكاديمية
    Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease

    المؤلفون: Achouri-Rassas, Afef, Ben Ali, Nadia, Fray, Saloua, Hadj Fredj, Sondes, Kechaou, Meriem, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Chabbi, Slim, Anane, Nadia, Messaoud, Taieb, Gouider, Riadh, Belal, Samir

    المصدر: In Neurobiology of Aging October 2015 36(10):2904-2904

    View record from ScienceDirect Full Text via ClinicalKey Full Text Finder
    أضف إلى المفضلة
  8. 8
    مؤتمر
    Molecular characterization of Mycobacterium tuberculosis strains resistant to isoniazid

    المؤلفون: Smaoui, Salma, Siala, Mariem, Hadj Fredj, Sondes, Kammoun, Sana, Marouane, Chema, Hachicha, Salma, Ghorbel, Asma, Gdoura, Radhouane, Slim, Leila, Ben Messaoud, Taieb, Messadi, Férièle

    المصدر: In International Journal of Mycobacteriology December 2016 5 Supplement 1:S151-S151

    View record from ScienceDirect Full Text Finder
    أضف إلى المفضلة
  9. 9
    دورية
    Molecular characterization of Mycobacterium tuberculosisstrains resistant to isoniazid

    المؤلفون: Smaoui, Salma, Siala, Mariem, Hadj Fredj, Sondes, Kammoun, Sana, Marouane, Chema, Hachicha, Salma, Ghorbel, Asma, Gdoura, Radhouane, Slim, Leila, Ben Messaoud, Taieb, Messadi, Férièle

    المصدر: International Journal of Mycobacteriology; December 2016, Vol. 5 Issue: 1, Number 1 Supplement 1 pS151-S151, 1p

    View record from ScienceDirect Full Text Finder
    أضف إلى المفضلة
  10. 10
    دورية أكاديمية
    Pseudo-Bartter syndrome as the sole manifestation of cystic fibrosis in a child with 711+G>T/IVS8-5T mutation: a new face of an old disease.

    المؤلفون: Tinsa F; Department of pediatrics B, children's Hospital Bechir Hamza, Tunis, Tunisia, University of medicine, Tunis El Manar, Tunisia, Laboratory of biomedical genomics and oncogenetics LR11IPT05, University of Tunis El Manar, Pasteur Institut of Tunis, Tunis, Tunisia., Hadj Fredj S; Biochemistry laboratory, Children's hospital, Research laboratory 'Haemoglobinopathies and Cystic fibrosis, LR00SP03', Tunis, Tunisia., Bel Hadj I; Department of pediatrics B, children's Hospital Bechir Hamza, Tunis, Tunisia, University of medicine, Tunis El Manar, Tunisia., Khalsi F; Department of pediatrics B, children's Hospital Bechir Hamza, Tunis, Tunisia, University of medicine, Tunis El Manar, Tunisia., Abdelhak S; Laboratory of biomedical genomics and oncogenetics LR11IPT05, University of Tunis El Manar, Pasteur Institut of Tunis, Tunis, Tunisia., Boussetta K; Department of pediatrics B, children's Hospital Bechir Hamza, Tunis, Tunisia, University of medicine, Tunis El Manar, Tunisia., Messaoud T; Biochemistry laboratory, Children's hospital, Research laboratory 'Haemoglobinopathies and Cystic fibrosis, LR00SP03', Tunis, Tunisia.

    المصدر: Annales de biologie clinique [Ann Biol Clin (Paris)] 2017 Aug 01; Vol. 75 (4), pp. 466-473.

    نوع المنشور: Case Reports; Journal Article

    بيانات الدورية: Publisher: John Libbey Eurotext Country of Publication: France NLM ID: 2984690R Publication Model: Print Cited Medium: Internet ISSN: 1950-6112 (Electronic) Linking ISSN: 00033898 NLM ISO Abbreviation: Ann Biol Clin (Paris) Subsets: MEDLINE

    مواضيع طبية MeSH: Mutation*, Bartter Syndrome/*diagnosis , Cystic Fibrosis/*diagnosis , Cystic Fibrosis/*genetics , Cystic Fibrosis Transmembrane Conductance Regulator/*genetics, Bartter Syndrome/genetics ; Child, Preschool ; Cystic Fibrosis/complications ; Diagnosis, Differential ; Humans ; Male ; Polymorphism, Genetic

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS – أرسل هذا البحث بالبريد الإلكتروني – حفظ البحث – جدول التنبيهات: لا شيء