Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Wajdi, Safi"'
Autor:
Hassen Hadj Kacem, Mariam Moalla, Faten Hadj Kacem, Oumeyma Trimeche, Wajdi Safi, Mouna Mnif-Feki, Mohamed Abid
Publikováno v:
Endocrine and Metabolic Science, Vol 14, Iss , Pp 100160- (2024)
Background: Turner syndrome (TS) is a genetic disorder found only in females who are completely or partially missing an X chromosome. It is rarely inherited from parent to offspring and is not reported to be associated with any causal gene. In additi
Externí odkaz:
https://doaj.org/article/22a456da4b9d4fb087dbb6546bac6a30
Autor:
Mariam Moalla, Wajdi Safi, Maab Babiker Mansour, Mohamed Hadj Kacem, Mona Mahfood, Mohamed Abid, Thouraya Kammoun, Mongia Hachicha, Mouna Mnif-Feki, Faten Hadj Kacem, Hassen Hadj Kacem
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Introduction/AimsMaturity-Onset Diabetes of the Young (MODY) is a monogenic non-autoimmune diabetes with 14 different genetic forms. MODY-related mutations are rarely found in the Tunisian population. Here, we explored MODY related genes sequences am
Externí odkaz:
https://doaj.org/article/ab669c4e4fe347acb48a9a60ead0b4ee
Autor:
Mouna Tabebi, Wajdi Safi, Rahma Felhi, Olfa Alila Fersi, Leila Keskes, Mohamed Abid, Mouna Mnif, Faiza Fakhfakh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Mitochondrial diabetes (MD) is a rare monogenic form of diabetes and divided into type l and type 2. It is characterized by a strong familial clustering of diabetes with the presence of maternal transmission in conjunction with bi
Externí odkaz:
https://doaj.org/article/8c8a1057c14b4cd1bd474c4e605bf461
Autor:
Marwa Ammar, Wajdi Safi, Abdelaziz Tlili, Olfa Alila‐Fersi, Fakher Frikha, Jihen Chouchen, Fatma Mnif, Marwa Kharrat, Marwa Maalej, Rahma Felhi, Mohamed Abid, Mouna Mnif‐Feki, Faten Hadj Kacem, Faiza Fakhfakh, Emna Mkaouar‐Rebai
Publikováno v:
International Journal of Developmental Neuroscience. 82:626-638
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE; OMIM 603041) is a rare inherited metabolic disorder mostly caused by mutations in TYMP gene encoding thymidine phosphorylase (TP) protein that affects the mitochondrial nucleotide metaboli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58d9fb9f57db145e78a91ba53c83985
https://doi.org/10.1002/jdn.10215
https://doi.org/10.1002/jdn.10215
Autor:
Kacem Akid Faten Haj, Wafa Belabed, Missaoui Abdel Mouhaymen, Wajdi Safi, Salah Dhoha Ben, Fatma Mnif, Nabila Mejdoub, Mouna Mnif, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4293b93c140d2ed698d467b3d069a333
https://doi.org/10.1530/endoabs.90.p711
https://doi.org/10.1530/endoabs.90.p711
Autor:
Kacem Akid Faten Haj, Wafa Belabed, Missaoui Abdel Mouhaymen, Wajdi Safi, Mouna Elleuch, Nadia Charfi, Fatma Mnif, Nabila Mejdoub, Mouna Mnif, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::155d2ba94e1f3aeda6888e22abf5688e
https://doi.org/10.1530/endoabs.90.ep877
https://doi.org/10.1530/endoabs.90.ep877
Autor:
Faten Haj Kacem Akid, Abdel Mouhaymen Missaoui, Wafa Belabed, Wajdi Safi, Nadia Charfi, Fatma Mnif, Dhoha Ben Salah, Nabila Mejdoub, Mouna Mnif, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2972f97f558c9460ceaaf52ce8a0cdc8
https://doi.org/10.1530/endoabs.90.ep736
https://doi.org/10.1530/endoabs.90.ep736
Predictive clinical factors of stature gain in congenital growth hormone deficiency treated patients
Autor:
Kacem Akid Faten Haj, Wafa Belabed, Abdel Mouhaymen Missaoui, Wajdi Safi, Mouna Elleuch, Fatma Mnif, Dhoha Ben Salah, Nabila Mejdoub, Mouna Mnif, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1070bdfed7b0520470c21300a98ddbf
https://doi.org/10.1530/endoabs.90.ep735
https://doi.org/10.1530/endoabs.90.ep735
Autor:
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 24; Pages: 7525
Background: Non-syndromic combined pituitary hormone deficiency (CPHD) occurs due to defects in transcription factors that govern early pituitary development and the specification of hormone-producing cells. The most common mutations are in the Proph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db8876fca3642dbdf452ec7e31a46856
Autor:
Mariam, Moalla, Mouna, Mnif-Feki, Wajdi, Safi, Nadia, Charfi, Nabila, Mejdoub-Rekik, Mohamed, Abid, Faten, Hadj Kacem, Hassen, Hadj Kacem
Publikováno v:
Journal of clinical medicine. 11(24)
Non-syndromic combined pituitary hormone deficiency (CPHD) occurs due to defects in transcription factors that govern early pituitary development and the specification of hormone-producing cells. The most common mutations are in the Prophet of Pit-1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ddb01e043d19cec35c6a94db1c5bf39
https://pubmed.ncbi.nlm.nih.gov/36556141
https://pubmed.ncbi.nlm.nih.gov/36556141