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1دورية أكاديمية
المؤلفون: Ibtihel Benhaj Mbarek, Saoussen Mdimeg, Amira Moussa, Dorsaf Zellama, Hayat Kaarout, Jaouida Abdelmoula, Abdellatif Achour, Saoussen Abroug, Asma Omezzine, Ali Bouslama
المصدر: BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)
مصطلحات موضوعية: Primary hyperoxaluria type 1, Tunisian population, Urolithiasis, 33-34InsC mutation, Diseases of the genitourinary system. Urology, RC870-923
وصف الملف: electronic resource
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المؤلفون: Amira Moussa, Sana Samet, Ali Bouslama, Nourhene Khayati, Mariem Ammar, Omezzine Asma, Sana Ben Amor
المصدر: Revue Neurologique. 177:S89
مصطلحات موضوعية: Neurology, Neurology (clinical)
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المؤلفون: Hayet Kaarout, Jalel Chemli, Abdellatif Achour, Amira Moussa, Asma Omezzine, Saoussen Abroug, Ali Bouslama, Geneviéve Souche, Sabra Aloui, Saoussen M'dimegh, Ibtihel M'barek, Cécile Aquaviva-bourdain, Sameh Mabrouk
المصدر: Annals of Human Genetics. 81:1-10
مصطلحات موضوعية: 0301 basic medicine, Genetics, Mutation, Genetic heterogeneity, Haplotype, 030232 urology & nephrology, Gene mutation, Biology, medicine.disease, medicine.disease_cause, Primary hyperoxaluria, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, DNA Mutational Analysis, medicine, Restriction fragment length polymorphism, Allele frequency, Genetics (clinical)
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المؤلفون: Ons Fekih, Afifa Koubaa, Ibtihel B hajMbarek, Med-Fadhel Najjar, Haithem Hamdouni, Fadoua Neffati, Asma Omezzine, Marwa Ajmi, Sonia Triki, Ali Bouslama, Amira Moussa
المصدر: Clinical laboratory. 63(3)
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Angiotensin receptor, Genotype, Angiotensinogen, Peptidyl-Dipeptidase A, General Biochemistry, Genetics and Molecular Biology, Nephropathy, Diabetic nephropathy, Renin-Angiotensin System, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Internal medicine, parasitic diseases, Genetic predisposition, Medicine, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, Allele frequency, Polymorphism, Genetic, business.industry, Haplotype, Genetic Variation, medicine.disease, Genotype frequency, 030104 developmental biology, Endocrinology, 030220 oncology & carcinogenesis, Population study, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a079fe492eb005d49f47ae6c1231be8
https://pubmed.ncbi.nlm.nih.gov/28271690 -
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المؤلفون: Saoussen Mdimeg, Hayat Kaarout, Ali Bouslama, Abdellatif Achour, Asma Omezzine, Amira Moussa, Ibtihel M'barek, Jaouida Abdelmoula, Saoussen Abroug, Dorsaf Zellama
المصدر: BMC Nephrology
BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)مصطلحات موضوعية: 0301 basic medicine, Nephrology, Adult, Male, medicine.medical_specialty, Heterozygote, Tunisia, Adolescent, Tunisian population, 030232 urology & nephrology, Disease, lcsh:RC870-923, End stage renal disease, Primary hyperoxaluria, 03 medical and health sciences, Normal renal function, Young Adult, 0302 clinical medicine, Urolithiasis, Internal medicine, Primary hyperoxaluria type 1, medicine, Humans, 33-34InsC mutation, Child, Transaminases, Aged, Retrospective Studies, business.industry, Infant, Middle Aged, medicine.disease, lcsh:Diseases of the genitourinary system. Urology, Pedigree, 030104 developmental biology, Treatment Outcome, Child, Preschool, Mutation (genetic algorithm), Hyperoxaluria, Primary, Mutation, Female, Restriction fragment length polymorphism, Nephrocalcinosis, business, Research Article
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المؤلفون: Saoussen, M'dimegh, Asma, Omezzine, Ibtihel, M'barek, Amira, Moussa, Sameh, Mabrouk, Hayet, Kaarout, Geneviéve, Souche, Jalel, Chemli, Sabra, Aloui, Cécile, Aquaviva-Bourdain, Abdellatif, Achour, Saoussen, Abroug, Ali, Bouslama
المصدر: Annals of human genetics. 81(1)
مصطلحات موضوعية: Adult, Male, Adolescent, DNA Mutational Analysis, Mutation, Missense, Infant, Middle Aged, Consanguinity, Young Adult, Gene Frequency, Haplotypes, Child, Preschool, Hyperoxaluria, Primary, Humans, Female, Child, Genetic Association Studies, Transaminases, Aged
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المؤلفون: Kaouther Kchok, Naoufel Nabli, Nabila Ben Rejeb, R. Belkahla, Asma Omezzine, Lamia Rebhi, Ahmed Ben Abdelaziz, Essia Boughzala, Imen Boumaiza, Ali Bouslama, Ibtihel Ben HadjMbarek, Amira Moussa, Jihène Rejeb, Slim Kacem
المصدر: Molecular Biology Reports. 39:9893-9901
مصطلحات موضوعية: Male, medicine.medical_specialty, Tunisia, Genotype, Apolipoprotein B, Lipoproteins, Coronary Artery Disease, Biology, HindIII, Gastroenterology, Coronary artery disease, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Aged, Apolipoproteins B, Lipoprotein lipase, Polymorphism, Genetic, Apolipoprotein A-I, Haplotype, Coronary Stenosis, General Medicine, Middle Aged, medicine.disease, Lipids, Lipoprotein Lipase, Haplotypes, biology.protein, Female, lipids (amino acids, peptides, and proteins), Lipoprotein, Chylomicron
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المؤلفون: Benjamin Kuhar, Olga V. Savinova, Konstantinos Damiris, Maria M. Plummer, José Luis Millán, Daniel J Moussouros, Lawrence Markel, Amira Moussa, Afshan Tabassum, Matthew A. Cascio, Jes Kuruvilla, Slava Gitelman, JoseYnigo Villanueva, Ashna Mehra, Jennifer Behbodikhah, Alexander Ogden, Muhddesa Lakhana, Gregg D. Blumberg, Muhammad Ahsan
المصدر: Gastroenterology. 154:S-213
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Hepatology, Chemistry, Gastroenterology, medicine, Ischemic injury, Tissue-nonspecific Alkaline Phosphatase
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المؤلفون: Lobna Bouacida, Ali Bouslama, Ons Achour, Jihène Rejeb, Nabila Ben Rejeb, Dorsaf Zellama, Amira Moussa, Sahbi Elmtaoua, Abdellatif Achour, Asma Omezzine, Imene Boumaiza
المصدر: Journal of nephrology. 29(5)
مصطلحات موضوعية: Vitamin, Nephrology, Adult, Male, medicine.medical_specialty, Time Factors, Tunisia, Genotype, Pharmacogenomic Variants, medicine.medical_treatment, 030232 urology & nephrology, Hyperhomocysteinemia, Down-Regulation, 030204 cardiovascular system & hematology, Reductase, Gastroenterology, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Folic Acid, Renal Dialysis, Internal medicine, medicine, Humans, Vitamin B12, Cyanocobalamin, Homocysteine, Methylenetetrahydrofolate Reductase (NADPH2), biology, business.industry, Vitamins, Middle Aged, B vitamins, Vitamin B 12, Phenotype, Treatment Outcome, Biochemistry, chemistry, Pharmacogenetics, Methylenetetrahydrofolate reductase, Dietary Supplements, biology.protein, Female, Hemodialysis, business, Biomarkers
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المؤلفون: Asma Omezzine, Ahmed Ben Abdelaziz, Nabila Ben Rejeb, Amira Moussa, Lamia Rebhi, Essia Boughzala, Jihène Rejeb, Slim Kacem, Ali Bouslama, Imen Boumaiza
المصدر: Biochemical genetics. 52(5-6)
مصطلحات موضوعية: Hemoglobin binding, Male, medicine.medical_specialty, Tunisia, Genotype, Coronary Artery Disease, Biology, Biochemistry, Gastroenterology, Severity of Illness Index, Coronary artery disease, Diabetes mellitus, Internal medicine, Severity of illness, Genetics, medicine, Humans, Obesity, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Genetic Association Studies, Aged, Polymorphism, Genetic, Haptoglobins, Confounding, Haptoglobin, Smoking, Coronary Stenosis, General Medicine, Middle Aged, medicine.disease, Ferritin, Diabetes Mellitus, Type 2, biology.protein, Female