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1دورية أكاديمية
المؤلفون: Imen Ksiaa, Mohamed Ghachem, Habib Besbes, Sana Khochtali, Slaheddine Chouchane, Moncef Khairallah
المصدر: BMC Ophthalmology, Vol 20, Iss 1, Pp 1-4 (2020)
مصطلحات موضوعية: Shaken baby syndrome, Swept source optical coherence tomography, Retinal hemorrhages, Vitreoretinal interface, Case report, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s12886-020-01666-9Test; https://doaj.org/toc/1471-2415Test
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2دورية أكاديمية
المؤلفون: Guediche Pierre Pothier, Nabil Sakly, Slaheddine Chouchane, Mohamed Neji, Khira Sdiri-loulizi Mouna Hassine
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
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3دورية أكاديمية
المؤلفون: Sabeur, Hammami, Chebil, B. Meriem, Karim, B. Ameur, Samir, Hadded, Leila, Ghédira, Chiraz, Hafsa, Slaheddine, Chouchane, Néji, Guediche Mohamed
المصدر: Joint Bone Spine ; volume 76, issue 5, page 565-566 ; ISSN 1297-319X
مصطلحات موضوعية: Rheumatology
الإتاحة: https://doi.org/10.1016/j.jbspin.2009.01.014Test
https://api.elsevier.com/content/article/PII:S1297319X09001389?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1297319X09001389?httpAccept=text/plainTest -
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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