Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Soumaya, Gaigi"'
Publikováno v:
Indian Journal of Dermatology, Vol 54, Iss 4, Pp 357-360 (2009)
Background: Mammalian pigmentation results from the synthesis and accumulation of photo protective epidermal melanin. Melanin was formed from the amino acid precursor L-tyrosine within specialized cells, the melanocytes. Oxidative stress has been sug
Externí odkaz:
https://doaj.org/article/b18ae06a899548cc879cf8f50f7cd4c5
Publikováno v:
Indian Journal of Dermatology, Vol 54, Iss 4, Pp 330-333 (2009)
Background: Vitiligo is an important skin disease that can alter individual self-image and thus have major impact on the quality of life. Aims: The objective of this study was to translate and to test the reliability and validity of the 10-item Derma
Externí odkaz:
https://doaj.org/article/9ec184d4688947c8ad2beeafb5cda9e1
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 3 (2010)
We report a case of sirenomelia sequence observed in an incident of preterm labor during the 29th gestational week. According to some authors, this syndrome should be classified separately from caudal regression syndrome and is likely to be the resul
Externí odkaz:
https://doaj.org/article/58bf42fbd279402f872c6eed6a9d45ce
Autor:
Myriam Chaabouni, Moez Ben Saad, Fatma Bchir, Soumaya Gaigi, Hela Mssaed, Badis Chanoufi, Béchir Zouaoui, Dalenda Chelli, Kaouther Dimassi, Hela Chelli, Ezzeddine Sfar
Publikováno v:
Cahiers de Santé. 18:199-203
La trisomie 21 (T21) ou syndrome de Down est l’anomalie chromosomique congenitale la plus frequente chez l’homme. Les signes cliniques sont actuellement bien connus. Les moyens de depistage antenatal de la T21 se sont nettement ameliores depuis u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adb8a1b25b73f2af5294cbdcb9fe9d94
https://doi.org/10.1684/san.2008.0127
https://doi.org/10.1684/san.2008.0127
Autor:
Dalenda, Chelli, Kaouther, Dimassi, Mouna, Bouaziz, Aida, Masmoudi, Nadia, Ben Jemaa, Béchir, Zouaoui, Ezzeddine, Sfar, Héla, Chelli, Mohamed Badis, Channoufi, Soumaya, Gaigi
Publikováno v:
La Tunisie medicale. 86(4)
To analyze the contribution of prenatal ultrasound in the diagnosis of arthrogryposis multiplex congenital according to its type and antenatal expression.Retrospective study led between January 1993 and November 2007. We studied the cases of arthrogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5166015837b219b5b9f189c0f0463a3f
https://pubmed.ncbi.nlm.nih.gov/19476133
https://pubmed.ncbi.nlm.nih.gov/19476133
Autor:
Dalenda, Chelli, Kaouther, Dimassi, Souhir, Jallouli-Bouzguenda, Essia, Ebdellah, Feten, Hermi, Bechir, Zouaoui, Ezzeddine, Sfar, Tania, Kitova, Hela, Chelli, Mohamed Badis, Channoufi, Soumaya, Gaigi
Publikováno v:
La Tunisie medicale. 86(2)
Ectopia cordis is a rare and impressive malformation presenting as an isolated lesion or as part of the Cantrell's pentology syndrom. It is defined as an anomaly in which the fetal heart lies outside the thoracic cavity. THE AIM of the study is to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2919be9dbe44d7ad8069603e8dabbe3
https://pubmed.ncbi.nlm.nih.gov/18444537
https://pubmed.ncbi.nlm.nih.gov/18444537
Autor:
Seddik, Oueslati, Hela, Louati, Rym, Dhiab, Saadia, Kchaou, Aida, Masmoudi, Chiraz, Fkih, Jilani, Nsiri, Soumaya, Gaigi, Nebil B, Zineb, Mounira, Chaabane
Publikováno v:
La Tunisie medicale. 85(5)
Multicystic dysplastic of the kidney (UCDK) in the most common cause of an abdominal man in the new born period and is the most common cystic malformation of the kidney in infancy. The increasingly widespread use of prenatal diagnostic techniques has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f678939ac79ceac2b41a327b641dac09
https://pubmed.ncbi.nlm.nih.gov/17657924
https://pubmed.ncbi.nlm.nih.gov/17657924
Autor:
Radhouane, Rachdi, Mahdi, Kaabi, Hichem, M'Hamdi, Ines, Chtioui, Mohamed, Basly, Fethi, Messaoudi, Houcine, Zayene, Lotfi, Messaoudi, Mounir, Chibani, Soumaya, Gaigi
Publikováno v:
La Tunisie medicale. 82(7)
Potter's reno-facial syndrome is a rare innate abnormality. We bring 4 observations repertoried at the maternity of military hospital of Tunis over a period of 6 years (1997 - 2002). The purpose of our work is to determine after a review of the liter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa9d58c88b92c173458bb00c123db6f1
https://pubmed.ncbi.nlm.nih.gov/15552029
https://pubmed.ncbi.nlm.nih.gov/15552029