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المؤلفون: Imen Ksiaa, Habib Besbes, Moncef Khairallah, Mohamed Ghachem, Slaheddine Chouchane, Sana Khochtali
المصدر: BMC Ophthalmology, Vol 20, Iss 1, Pp 1-4 (2020)
BMC Ophthalmologyمصطلحات موضوعية: medicine.medical_specialty, Fovea Centralis, genetic structures, Retina, 03 medical and health sciences, chemistry.chemical_compound, Retinal hemorrhages, 0302 clinical medicine, Optical coherence tomography, lcsh:Ophthalmology, Ophthalmology, Vitreoretinal interface, Case report, medicine, Humans, Shaken baby syndrome, medicine.diagnostic_test, business.industry, Optic disc pallor, Retinal traction, Internal limiting membrane, Infant, Retinal Hemorrhage, Retinal, General Medicine, medicine.disease, Retinal atrophy, eye diseases, Swept source optical coherence tomography, chemistry, lcsh:RE1-994, 030221 ophthalmology & optometry, Female, sense organs, business, 030217 neurology & neurosurgery, Tomography, Optical Coherence
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d1297b8a93862ce3f3ba3275505a7cTest
http://link.springer.com/article/10.1186/s12886-020-01666-9Test -
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المؤلفون: Ons, Fekih, Hamdi, Triki, Sonia, Triki, Fadoua, Neffati, Slaheddine, Chouchane, Mohamed Neji, Guediche, Mohamed Fadhel, Najjar
المصدر: Pediatric diabetes. 18(3)
مصطلحات موضوعية: Blood Glucose, Glycated Hemoglobin, Male, Tunisia, Adolescent, Osteoprotegerin, Reproducibility of Results, Enzyme-Linked Immunosorbent Assay, Comorbidity, Up-Regulation, Diabetes Mellitus, Type 1, Cardiovascular Diseases, Risk Factors, Case-Control Studies, Child, Preschool, Humans, Female, Cystatin C, Child, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::4ec78ab1fda4aa5bd10259a04007fb42Test
https://pubmed.ncbi.nlm.nih.gov/27111559Test -
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المؤلفون: Ons, Fekih, Sonia, Triki, Ilhem, Hellara, Fadoua, Neffati, Slaheddine, Chouchane, Mohamed, Neji Gueddiche, Mohamed, Fadhel Najjar
المصدر: Presse medicale (Paris, France : 1983). 44(5)
مصطلحات موضوعية: Adult, Glycated Hemoglobin, Male, Tunisia, Adolescent, Aryldialkylphosphatase, Young Adult, Diabetes Mellitus, Type 1, Cardiovascular Diseases, Risk Factors, Case-Control Studies, Child, Preschool, Humans, Female, Child, Biomarkers, Diabetic Angiopathies, Retrospective Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::db1af1b233e532269da7299f4af7820eTest
https://pubmed.ncbi.nlm.nih.gov/25769648Test -
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المؤلفون: Samir M'Rabet, Najoua Kahloul, Hassen Sboui, Sihem Trimech, N. Zouari, Felix G. Riepe, Mohamed Tahar Sfar, Fathi Amri, Saloua Makni, Abdelkarim Ayedi, Ali Saad, Ilhem Charfeddine, Eric Clauser, Paul-Martin Holterhus, Slaheddine Chouchane, Moez Gribaa, Hechmi Ben Hamouda
المصدر: Gene. 507(1)
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Tunisia, endocrine system diseases, Adolescent, Pseudogene, Population, Molecular Sequence Data, Single-nucleotide polymorphism, Steroid biosynthesis, Biology, urologic and male genital diseases, Polymorphism, Single Nucleotide, Genetics, medicine, Humans, Point Mutation, Congenital adrenal hyperplasia, Allele, education, Child, Gene, Alleles, Genetic Association Studies, education.field_of_study, Adrenal Hyperplasia, Congenital, Base Sequence, Point mutation, nutritional and metabolic diseases, Infant, General Medicine, Middle Aged, medicine.disease, Molecular biology, female genital diseases and pregnancy complications, Child, Preschool, Female, Steroid 21-Hydroxylase, Pseudogenes
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85eea49b042f7a19bb4c8932a2e55e59Test
https://pubmed.ncbi.nlm.nih.gov/22841790Test -
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المؤلفون: Saber Hamami, F. Amri, Wafa Ben Romdane, Gustavo Pérez de Nanclares, Donia Elhayek, Amel Haj Khelil, Nadia Leban, Mohamed Neji Gueddiche, Slaheddine Chouchane, Samir M'Rabet, Monia Troudi, Jemni Ben Chibani, Gema Ariceta, Luis Castaño, Adnene Mlika
المصدر: BMC Medical Genetics
Addi. Archivo Digital para la Docencia y la Investigación
instnameمصطلحات موضوعية: Male, Vacuolar Proton-Translocating ATPases, ATP6V0A4, Tunisia, Tunisian population, Hearing Loss, Sensorineural, Mutation, Missense, Black People, Biology, medicine.disease_cause, GENETICS AND HEREDITY, Frameshift mutation, Cohort Studies, Exon, Distal renal tubular acidosis, Anion Exchange Protein 1, Erythrocyte, medicine, Genetics, Missense mutation, Humans, Genetics(clinical), Frameshift Mutation, Gene, Genetics (clinical), Mutation, ATP6V1B1, Homozygote, Intron, Infant, Acidosis, Renal Tubular, Exons, medicine.disease, Child, Preschool, Sensorineural hearing loss, Female, Algorithm, Algorithms, Gene Deletion, Research Article
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9194b5f2301257c31892f0a0305f02Test
http://europepmc.org/articles/PMC4225572Test