Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Mouna Mnif Feki"'
Autor:
Dhoha Ben Salah, Mouna Elleuch, Oumeyma Trimeche, Asma Zargni, Fakhri Kallabi, Salma Sakka, Fatma Mnif, Nabila Rekik, Nadia Charfi, Hassen Kamoun, Mouna Mnif Feki, Faten Hadj Kacem, Mohamed Abid
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 130-134 (2024)
Purpose Allgrove syndrome, also known as “triple A” syndrome, is characterized by adrenal insufficiency, achalasia, and alacrimia. When neurological signs are also present, the condition is referred to as “4 A” syndrome. Methods We conducted
Externí odkaz:
https://doaj.org/article/047022b12fb7477588ee364b1bf1b2b8
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 14-17 (2013)
Congenital adrenal hyperplasia (CAH) describes a group of autosomal recessive disorders where there is impairment of cortisol biosynthesis. CAH due to 21-hydroxylase deficiency accounts for 95% of cases and shows a wide range of clinical severity. Gl
Externí odkaz:
https://doaj.org/article/d37c1e5629eb4bdea2f33e7dcab39b5f
Autor:
Sofien Regaieg, Nadia Charfi, Mahdi Kamoun, Sameh Ghroubi, Haithem Rebai, Habib Elleuch, Mouna Mnif Feki, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 6, Pp 1040-1045 (2013)
Background: The prevalence of children obesity is rising alarmingly in both developed and developing countries. Developing effective exercise programs is a strategy for decreasing this prevalence and limiting obesity-associated long-term comorbiditie
Externí odkaz:
https://doaj.org/article/0ff9b3060474447e8c6ab93e1e1a2eac
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 4, Pp 543-544 (2013)
Externí odkaz:
https://doaj.org/article/2a30e05b18a4415aa7d1d77227be3107
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:
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:
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
Autor:
Mariam Moalla, N. Belguith, Wajdi Safi, H. Hadj Kacem, F. Mnif, M. Elleuch, Mouna Mnif-Feki, D H Ben Salah, Faten Hadjkacem, N. Charfi, H. Kammoun, Mohamed Abid, Noura Bougacha-Elleuch, Fatma Abdelhedi, Mongia Hachicha, Nabila Rekik, Thouraya Kammoun, G. Abid
Publikováno v:
Gynecological Endocrinology. 37:848-852
To explore unusual association between Turner Syndrome (TS) and Hypopituitarism in a Tunisian cohort.We reported 6 patients with TS associated to Hypopituitarism, including three familial cases except the fourth sister who showed only a TS phenotype.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6304b5d5b9f67567dacc119097934c6
https://doi.org/10.1080/09513590.2021.1939298
https://doi.org/10.1080/09513590.2021.1939298
Autor:
Baha Zantour, Mouna Tabebi, Mohammed Abid, Faiza Fakhfakh, Wajdi Safi, Rahma Felhi, Mouna Mnif Feki, Mohamed Habib Sfar, Houcem Mrabet
Publikováno v:
Open Journal of Genetics. 11:77-92
Mutations in the WFS1 gene have been reported in Wolfram syndrome (WFS), a rare and autosomal recessive disorder defined by early onset of diabetes mellitus and progressive optic and hearing impairment. Only few data are available concerning the asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1660e1ac62c51d26873a7bda584d59f
https://doi.org/10.4236/ojgen.2021.114008
https://doi.org/10.4236/ojgen.2021.114008