Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Mouna Feki"'
Publikováno v:
Forests, Vol 15, Iss 3, p 539 (2024)
The concept of integrated forest management offers a framework for understanding how forest ecosystem services interact with efforts to conserve natural resources. Forests face various disturbances stemming from human activities, management approache
Externí odkaz:
https://doaj.org/article/c4733dabebf1474bbfd8cedcf5e5b159
Publikováno v:
Soil and Water Research, Vol 15, Iss 3, Pp 135-147 (2020)
In this study, different methods were compared in order to determine the soil hydraulic conductivity at the saturation (Ks) of two heavily anthropized soils in northern Italy: an irrigated field and a landfill cover. In situ, laboratory measurements
Externí odkaz:
https://doaj.org/article/f7617843a95d46a19186f2684f34b4dd
Publikováno v:
Forests, Vol 12, Iss 12, p 1794 (2021)
In this paper, the FEST-FOREST model is presented. A FOREST module is written in the FORTRAN-90 programming language, and was included in the FEST-WB distributed hydrological model delivering the FEST-FOREST model. FEST-FOREST is a process-based dyna
Externí odkaz:
https://doaj.org/article/5805ab7b026f4c34865cbbac07c84576
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
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:
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:
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