Zobrazeno 1 - 10
of 73
pro vyhledávání: '"D. H'mida"'
Publikováno v:
Journal of Investigative Dermatology. 142:S234
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b4d4e70b369c3f8a0af2560b510cec
https://doi.org/10.1016/j.jid.2022.09.326
https://doi.org/10.1016/j.jid.2022.09.326
Autor:
H. Chouk, S. Mokni, N. Litaiem, H. Hammami, M. Mokni, B. Sriha, A. Saad, A. Hovnanian, M. Denguezli, D. H’Mida
Publikováno v:
Journal of Investigative Dermatology. 142:S216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed7b4ad8ac56b091a6f8c309e2786f94
https://doi.org/10.1016/j.jid.2022.09.224
https://doi.org/10.1016/j.jid.2022.09.224
Autor:
C. Bensignor, Yosra Halleb, A. Tej, A. Touati, A. Ben Ahmed, S. Kmiha, D. H’mida Ben Brahim, N. Mahdhaoui, Anisa Saad, Sonia Nouri, J. Mathlouthi
Publikováno v:
Archives de Pédiatrie. 26:102-107
Background and objectives Sanjad–Sakati syndrome (SSS; OMIM 241410) is a rare autosomal recessive disorder found almost exclusively in people of Arab origin. It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44ff8d7d0c12b176780f88632f2654f
https://doi.org/10.1016/j.arcped.2018.11.012
https://doi.org/10.1016/j.arcped.2018.11.012
Akademický článek
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Akademický článek
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Autor:
Fayçal Hentati, Meriem Tazir, F. Ferrat, Dominique Stoppa-Lyonnet, C. Thibaut, Mathieu Anheim, Karine Nguyen, Michel Koenig, Yosr Bouhlal, Filippo M. Santorelli, Lamia Alipacha, R. Amouri, Nathalie Drouot, Mirna Assoum, Malika Chaouch, Abdelmadjid Hamri, J. Poujet, Traki Benhassine, Fabiana Fattori, D. H’mida-Ben Brahim, A. M’zahem, Y. Sifi, Clotilde Lagier-Tourenne
Publikováno v:
Journal of Neurology. 258:56-67
The diagnosis of rare inherited diseases is becoming more and more complex as an increasing number of clinical conditions appear to be genetically heterogeneous. Multigenic inheritance also applies to the autosomal recessive progressive cerebellar at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de125cd3a0a01ae31a78369bf07894cc
https://doi.org/10.1007/s00415-010-5682-5
https://doi.org/10.1007/s00415-010-5682-5
Akademický článek
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Publikováno v:
Placenta. 29:454-460
Placental mesenchymal dysplasia (PMD) is a distinct placental disorder that may coexist with a normal fetus. In one-third of cases, the fetus exhibits Beckwith-Wiedemann Syndrome (BWS). In the present study, we report a case of PMD changes associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42bb1885cf1a076a3c851d93951c2c02
https://doi.org/10.1016/j.placenta.2008.01.001
https://doi.org/10.1016/j.placenta.2008.01.001
Autor:
Kalthoum Tlili, N. Karmeni, Nadia Mama, Ali Saad, Mohamed Tahar Yacoubi, Saoussen Trabelsi, H. Krifa, M. Mokni, M. Haddaji Mastouri, Marwa Chourabi, Mohamed Ladib, D. H’mida Ben Brahim
Publikováno v:
Clinicaltranslational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico. 18(4)
The MGMT gene encodes a DNA repair enzyme that counteracts with chemotherapy efficiency, specifically with alkylating agents such as temozolomide (TMZ). It is well established that MGMT methylation should be screened as a predictive marker for TMZ in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7368e99052d16a3b3168863a2936fe8d
https://pubmed.ncbi.nlm.nih.gov/26289551
https://pubmed.ncbi.nlm.nih.gov/26289551
Autor:
Tahar Yacoubi, D. H’mida Ben Brahim, Saoussen Trabelsi, Ali Saad, Chris Jones, Kalthoum Tlili, Nadia Mama, M. Mokni, H. Krifa, Sergey Popov, Anna Burford, Marileila Varella-Garcia, Mohamed Ladib
Publikováno v:
Neuro-Chirurgie. 61(6)
Background PA is a grade I glial tumor that mostly occurs in children. However, although apparently similar to paediatric PA, adult PA presents a different clinical follow-up that could arise from specific molecular alterations. A variety of genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9197d03ed948380ddd6218a44a14df21
https://pubmed.ncbi.nlm.nih.gov/26597605
https://pubmed.ncbi.nlm.nih.gov/26597605