المؤلفون: Mohamed Amine Bekadja, Pierre Fenaux, Sabrina Akrouf, Redhouane Ahmed-Nacer, Rose-marie Hamladji, Amina Bouchakour, Souad Taoussi, Mohand Tahar Abad, Mohamed Bradai, Brahim Benzineb, Naima Mesli, M Cheritti, Z Zouaoui, Mohamed Benlazar, Soraya Bougherira, Fatiha Grifi, Hocine Ait-Ali, Malika allouda, Malika Djillali, Khadija Djouadi, Fatima Kherbache, Selma Hamdi, Hakim Hamouda, Imene Boumeida, Meriem Belhani, Nadia Boudjerra, Fatima Zohra Kaci, Soufi Osmani, Nabil Yafour, Soumia Barkat, Fatma Soltani, Razika Nacib, Mahdia Saidi, Laid Touati, Noureddine Lakhdari, Samira Zouani, Hadj Touhami, Djamel Saidi, Lamia Cherif Louazani, Mohamed Ramaoun, Cherifa Akkal, Nemra Mehalhal, Amina Krim, Noureddine Sidimansour, Zohra Ouchenane, Nadia Zidani, Salim Nekkal, Samia Barkat, Y Ouarlent, Mohamed Aberkane, Salah Eddine Belakehal, Aissa Bachiri, Samir Baghdad

المصدر: Asian Pacific Journal of Cancer Biology, Vol 8, Iss 1, Pp 21-29 (2023)

مصطلحات موضوعية: myelodysplastic syndrome, epidemiology, incidence, clinical features, overall survival, algerian population, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.waocp.com/journal/index.php/apjcb/article/view/1010; https://doaj.org/toc/2538-4635

URL الوصول: https://doaj.org/article/5a0d9fca78854b11a57eac59027b46af

المؤلفون: Rahma Mkaouar, Lamia Cherif Ben Abdallah, Chokri Naouali, Saida Lahbib, Zinet Turki, Sahar Elouej, Yosra Bouyacoub, Maali Somai, Kenneth Mcelreavey, Anu Bashamboo, Sonia Abdelhak, Olfa Messaoud

المصدر: Frontiers in Genetics, Vol 12 (2021)

مصطلحات موضوعية: hypogonadotropic hypogonadism, Kallmann syndrome, oligogenism, pathogenic combination, digenic score, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2021.665174/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/6da776bdce8e458aa2276521a5264d82

المؤلفون: Samir Baghdad, Aissa Bachiri, Salah Eddine Belakehal, Mohamed Aberkane, Y Ouarlent, Samia Barkat, Salim Nekkal, Nadia Zidani, Zohra Ouchenane, Noureddine Sidimansour, Amina Krim, Nemra Mehalhal, Cherifa Akkal, Mohamed Ramaoun, Lamia Cherif Louazani, Djamel Saidi, Hadj Touhami, Samira Zouani, Noureddine Lakhdari, Laid Touati, Mahdia Saidi, Razika Nacib, Fatma Soltani, Soumia Barkat, Nabil Yafour, Soufi Osmani, Fatima Zohra Kaci, Nadia Boudjerra, Meriem Belhani, Imene Boumeida, Hakim Hamouda, Selma Hamdi, Fatima Kherbache, Khadija Djouadi, Malika Djillali, Malika Allouda, Hocine Ait-Ali, Fatiha Grifi, Soraya Bougherira, Mohamed Benlazar, Z Zouaoui, M Cheritti, Naima Mesli, Brahim Benzineb, Mohamed Bradai, Mohand Tahar Abad, Souad Taoussi, Amina Bouchakour, Rose-marie Hamladji, Redhouane Ahmed-Nacer, Sabrina Akrouf, Pierre Fenaux, Mohamed Amine Bekadja

المصدر: Asian Pacific Journal of Cancer Biology. 8:21-29

مصطلحات موضوعية: Building and Construction, Electrical and Electronic Engineering

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::173facbc66bf607cb0fafbb64dacf1a5
https://doi.org/10.31557/apjcb.2023.8.1.21-29

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المؤلفون: Leila El Matri, A. Chaabouni, L. Largueche, Lamia Cherif, Kaouthar Derouiche, I. Chouchene, Sonia Abdelhak, Ahlem Amouri

المصدر: Genetic Testing and Molecular Biomarkers. 14:145-148

مصطلحات موضوعية: Genetics, Telecanthus, General Medicine, Consanguinity, Biology, medicine.disease, Blepharophimosis, Frameshift mutation, Exon, Forkhead box L2, Ptosis, Mutation (genetic algorithm), medicine, medicine.symptom, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c85aa8bd2bdf9c86d25ad84562b445c2
https://doi.org/10.1089/gtmb.2009.0091

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المؤلفون: Olfa Messaoud, Yosra Bouyacoub, Youssef Lakhoua, Zinet Turki, Karima Khiari, Sahar Elouej, Sonia Abdelhak, Lilia Romdhane, Majdi Nagara, Nejib Ben Abdallah, Lamia Cherif Ben Abdallah

المساهمون: Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Service d'Endocrinologie, Hôpital Charles Nicolle [Tunis], Institut National de Nutrition et de Technologie Alimentaire (Tunis) (INNTA)

المصدر: Hormone Research in Paediatrics
Hormone Research in Paediatrics, Karger, 2014, 82 (5), pp.338-43. ⟨10.1159/000365888⟩

مصطلحات موضوعية: Male, Candidate gene, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], MESH: RNA Splice Sites, Comorbidity, Bioinformatics, 0302 clinical medicine, Endocrinology, Eunuchism, Triple A syndrome, MESH: Nerve Tissue Proteins, 0303 health sciences, MESH: Esophageal Achalasia, Micropenis, 3. Good health, Gynecomastia, MESH: Adrenal Insufficiency, Mutation (genetic algorithm), Female, Congenital Hypogonadotropic Hypogonadism, MESH: Tunisia, medicine.medical_specialty, Tunisia, Allgrove Syndrome, Adolescent, Genetic counseling, Nerve Tissue Proteins, 030209 endocrinology & metabolism, Triple-A syndrome, 03 medical and health sciences, MESH: Eunuchism, Internal medicine, medicine, Humans, Point Mutation, Founder mutation, 030304 developmental biology, MESH: Point Mutation, Congenital hypogonadotropic hypogonadism, MESH: Adolescent, MESH: Humans, business.industry, medicine.disease, MESH: Male, Esophageal Achalasia, Nuclear Pore Complex Proteins, ALADIN, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Pediatrics, Perinatology and Child Health, RNA Splice Sites, business, MESH: Female, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Adrenal Insufficiency, MESH: Nuclear Pore Complex Proteins

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1e36ab07ed041877a515cbd9559a9ce
https://hal-riip.archives-ouvertes.fr/pasteur-01375104

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المساهمون: Lamia CHERIF

وصف الملف: JPG

الإتاحة: http://www.askzad.com/viewer?id=9be18ab6-7944-4ec2-b971-32102dd412ce&service=1&type=image&ref=eb

المساهمون: Lamia CHERIF

وصف الملف: JPG

الإتاحة: http://www.askzad.com/viewer?id=eb029fec-0f1a-41f2-b094-5939b82be17c&service=1&type=image&ref=eb