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1دورية أكاديمية
المؤلفون: Ines Cherif, Ghassen Kharroubi, Imen Darragi, Soumaya El Benna, Adel Gharbi, Amor Baccouche, Cyrine Souissi, Olfa Bahri, Melika Ben Ahmed, Jihene Bettaieb
المصدر: Libyan Journal of Medicine, Vol 19, Iss 1 (2024)
مصطلحات موضوعية: Kinetics, antibodies, COVID-19, Health Personnel, Tunisia, Medicine
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Nawel Trabelsi, Ghada Bouguerra, Faten Haddad, Monia Ouederni, Imen Darragi, Imen Boudrigua, Dorra Chaouachi, Mbarka Barmat, Chaker Fouzai, Mohamed Bejaoui, Samia Menif, Imen Kraiem, Salem Abbes
المصدر: Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
مصطلحات موضوعية: Physiology, QP1-981, Biochemistry, QD415-436
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Leila Chaouch, Miniar Kalai, Manel Ben Jbara, Arij Ben Chaabene, Imen Darragi, Dorra Chaouachi, Fethi Mallouli, Raouf Hafsia, Abderraouf Ghanem, Salem Abbes
المصدر: Biomedical Papers, Vol 159, Iss 1, Pp 145-149 (2015)
مصطلحات موضوعية: sickle cell anemia, bmp6 polymorphisms, osteonecrosis, Medicine
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Mouna, Jaouani, Nadia, Hamdi, Leila, Chaouch, Miniar, Kalai, Fethi, Mellouli, Imen, Darragi, Imen, Boudriga, Dorra, Chaouachi, Mohamed, Bejaoui, Salem, Abbes
المصدر: In Egyptian Journal of Medical Human Genetics July 2016 17(3):265-270
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المؤلفون: Mohamed Bejaoui, Samia Menif, Mbarka Barmat, Salem Abbes, Imen Boudrigua, Imen Darragi, Imen Kraiem, Nawel Trabelsi, Dorra Chaouachi, Monia Ouederni, Faten Haddad, Ghada Bouguerra, Chaker Fouzai
المصدر: Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
مصطلحات موضوعية: Hemolytic anemia, Adult, Male, Proteomics, medicine.medical_specialty, Tunisia, Adolescent, Physiology, Physical examination, Spherocytosis, Hereditary, Gastroenterology, lcsh:Physiology, Hereditary spherocytosis, lcsh:Biochemistry, Internal medicine, medicine, Humans, lcsh:QD415-436, Family history, Child, Band 3, biology, medicine.diagnostic_test, lcsh:QP1-981, business.industry, Erythrocyte Membrane, Erythrocyte fragility, Infant, Membrane Proteins, Gel electrophoresis of proteins, medicine.disease, Flow Cytometry, Osmotic Fragility, Membrane protein, Child, Preschool, biology.protein, Eosine Yellowish-(YS), Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b3c518fb926b1127e15a7e77018cf9
https://pubmed.ncbi.nlm.nih.gov/33667330 -
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المؤلفون: Houssem Sellami, Imen Darragi, Samia Mnif, Dorra Chaouachi, Leila Chaouch, Miniar Kalai, Imen Boudrigua, Salem Abbes
المصدر: Journal of pediatric hematology/oncology. 42(1)
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, HBG1, Cell, Disease, Anemia, Sickle Cell, Response Elements, law.invention, 03 medical and health sciences, 0302 clinical medicine, law, hemic and lymphatic diseases, Fetal hemoglobin, medicine, Humans, Binding site, Gene, Transcription factor, Polymerase chain reaction, Fetal Hemoglobin, Retrospective Studies, Sequence Deletion, Base Sequence, business.industry, Hematology, Molecular biology, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, Pediatrics, Perinatology and Child Health, Female, business, 030215 immunology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37848dc001c29eeb5464935a43f6a4da
https://pubmed.ncbi.nlm.nih.gov/31688634 -
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المؤلفون: Nawel Trabelsi, Aminetou Abba, Mohamed Lemine Ould Salem, Sidi M. Ghaber, Faten Haddad, Salem Abbes, Imen Darragi
المصدر: Hemoglobin. 42:7-10
مصطلحات موضوعية: Anemia, Hemolytic, Globin genes, Hemoglobins, Abnormal, Point mutation, Biochemistry (medical), Clinical Biochemistry, Mauritania, Mutation, Missense, De novo mutation, Sequence Analysis, DNA, beta-Globins, Hematology, Biology, Molecular biology, 03 medical and health sciences, 0302 clinical medicine, Chronic hemolytic anemia, hemic and lymphatic diseases, 030220 oncology & carcinogenesis, Humans, Point Mutation, Female, Genetics (clinical), Unstable hemoglobin, 030215 immunology
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المؤلفون: Imen Darragi, Salem Abbes, Imen Boudrigua, Miniar Kalai, Houyem Ouragini, Mouna Ben Sassi, Raouf Hafsia, Leila Chaouch, Imen Moumni, Dorra Chaouachi
المصدر: Acta Haematologica Polonica. 47:242-247
مصطلحات موضوعية: medicine.medical_treatment, Single-nucleotide polymorphism, Hematology, Disease, Biology, medicine.disease, IGF1R Gene, Phenotype, Sickle cell anemia, 03 medical and health sciences, Insulin-like growth factor, 0302 clinical medicine, Oncology, 030220 oncology & carcinogenesis, Immunology, Genotype, medicine, 030215 immunology, Cause of death
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::706def2ca8b8575c97ae2fd0edec4602
https://doi.org/10.1016/j.achaem.2016.10.004 -
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المؤلفون: Emna Barkaoui, Imen Boudrigua, Faten Haddad, Nawel Trabelsi, Samia Menif, Salem Abbes, Dorra Chaouachi, Imen Darragi, Leila Chaouch, Mouna Jaouani
المصدر: European Journal of Medical Genetics. 64:104139
مصطلحات موضوعية: Adult, Male, Gilbert Syndrome, Adolescent, Crigler–Najjar syndrome, Biology, medicine.disease_cause, digestive system, symbols.namesake, chemistry.chemical_compound, Exon, microRNA, Genetics, medicine, Humans, Glucuronosyltransferase, Child, Genetics (clinical), Crigler-Najjar Syndrome, Unconjugated hyperbilirubinemia, Sanger sequencing, Mutation, General Medicine, Middle Aged, medicine.disease, Molecular biology, chemistry, Child, Preschool, symbols, Female, DNA