Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Mahdi, Kamoun"'
Autor:
Mahdi Kamoun, Mouna Feki Mnif, Nadia Charfi, Basma Ben Naceur, Fatma Mnif, Nabila Rekik, Zainab Mnif, Mohamed Habib Sfar, Mohamed Tahar Sfar, Mongia Hachicha, Azza Ben Salem, Leila Ammar Keskes, Mohamed Abid
Publikováno v:
Middle East Fertility Society Journal, Vol 19, Iss 2, Pp 89-95 (2014)
Objective: To investigate fertility in a sample of Tunisian patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Design: Tunisian bicentric prospective study. Setting: Endocrinology department, Hedi Chaker Hospital, Sf
Externí odkaz:
https://doaj.org/article/7ede3c2240314239aea23584d9604d9a
Autor:
Faten Hadj Kacem, Nadia Charfi, Mouna Feki Mnif, Mahdi Kamoun, Faouzi Akid, Fatma Mnif, Basma Ben Naceur, Nabila Rekik, Zainab Mnif, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 107-110 (2013)
We report a 22-year-old woman who presented with asthenia, weight loss and hypotension in which extensive pituitary and adrenal investigations were diagnostic of isolated adrenocorticotropic hormone deficiency (IAD) of pituitary origin. Magnetic reso
Externí odkaz:
https://doaj.org/article/d0c44f12b9044777a66a1f4ce1d7e073
Autor:
Mouna Feki Mnif, Mahdi Kamoun, Faten Hadj Kacem, Zainab Bouaziz, Nadia Charfi, Fatma Mnif, Basma Ben Naceur, Nabila Rekik, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 3, Pp 442-445 (2013)
Diabetes mellitus has a number of long-term effects on the genitourinary system. These effects predispose to bacterial urinary tract infections (UTIs) in the patient with diabetes mellitus. Complicated UTIs are also common and potentially life-threat
Externí odkaz:
https://doaj.org/article/9b964f7bc275459393d3c1288e6cd45a
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:
Mouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, Nadia Charfi, Nozha Kallel, Nabila Rekik, Basma Ben Naceur, Hela Fourati, Emna Daoud, Zainab Mnif, Mohamed Habib Sfar, Samia Younes-Mhenni, Mohamed Tahar Sfar, Mongia Hachicha, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 1, Pp 121-127 (2013)
Background: Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis. The enzymes most commonly affected are 21-hydroxylase. Past reports suggested brain magnetic resonance imaging (MRI) abnormalities in CAH
Externí odkaz:
https://doaj.org/article/3fa499640002449e8efeaed951b32800
Autor:
Mouna Feki Mnif, Mahdi Kamoun, Faten Hadj Kacem, Fatma Mnif, Nadia Charfi, Basma Ben Naceur, Nabila Rekik, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 5, Pp 790-793 (2013)
Fertility in women with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) appears to be reduced, especially in women with the classic salt-wasting type. Several factors have been suggested to contribute to this subfertili
Externí odkaz:
https://doaj.org/article/3683a90bc5f045fbabf7a3a75e4b66c5
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
Autor:
Sahbi Kebaili, Kais Chaabane, Mouna Feki Mnif, Mahdi Kamoun, Faten Hadj Kacem, Nouha Guesmi, Hichem Gassara, Abdallah Dammak, Doulira Louati, Habib Amouri, Mohamed Guermazi
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 3, Pp 505-508 (2013)
Mayer-Rokitansky-Kuster-Hauser (MRKH) is a characteristic syndrome in which the Mullerian structures are absent or rudimentary. It is also associated with anomalies of the genitourinary and skeletal systems. Its association with gonadal dysgenesis is
Externí odkaz:
https://doaj.org/article/950fe13803064318b907c69a12f5e7e2
Autor:
Sonia Grine, Nadia Charfi, Mahdi Kamoun, Fatma Mnif, Basma Ben Naceur, Nabila Rekik, Mouna Mnif, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 6, Pp 1104-1107 (2013)
Several disorders of coagulation and fibrinolysis have been widely reported in patients with hyperthyroidism. Most reports have focused on only the venous thromboembolism risk, and few of them have studied specifically the association between hyperth
Externí odkaz:
https://doaj.org/article/90cb983ddb1b4f94ac0e62624030de55
Autor:
Mouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, Nadia Charfi, Basma Ben Naceur, Nozha Kallel, Nabila Rekik, Zainab Mnif, Mohamed Habib Sfar, Mohamed Tahar Sfar, Mongia Hachicha, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 6, Pp 939-946 (2012)
Background: In congenital adrenal hyperplasia (CAH), long-term glucocorticoid treatment coupled with increased androgens may lead to undesirable metabolic effects. The aim of our report was to determine the prevalence of metabolic abnormalities and c
Externí odkaz:
https://doaj.org/article/f00ef0004d8d4e8abca091ad18851ad0