Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bourane, Kamoun"'
Autor:
Franz P. W. Radner, Slaheddine Marrakchi, Peter Kirchmeier, Gwang-Jin Kim, Florence Ribierre, Bourane Kamoun, Leila Abid, Michael Leipoldt, Hamida Turki, Werner Schempp, Roland Heilig, Mark Lathrop, Judith Fischer
Publikováno v:
PLoS Genetics, Vol 9, Iss 6 (2013)
Externí odkaz:
https://doaj.org/article/a4dfe7cb25674ce28820d9c2acb3da8b
Autor:
Franz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, Gwang-Jin Kim, Florence Ribierre, Bourane Kamoun, Leila Abid, Michael Leipoldt, Hamida Turki, Werner Schempp, Roland Heilig, Mark Lathrop, Judith Fischer
Publikováno v:
PLoS Genetics, Vol 9, Iss 6, p e1003536 (2013)
Autosomal recessive congenital ichthyosis (ARCI) is a rare genetic disorder of the skin characterized by abnormal desquamation over the whole body. In this study we report four patients from three consanguineous Tunisian families with skin, eye, hear
Externí odkaz:
https://doaj.org/article/eb205806975848f0bae15868d1c06749
Autor:
Jamel Feki, Madiha Mseddi, Hamida Turki, Imène Sayadi, Abdelmagid Zahaf, Bourane Kamoun, Héla Khlif
Publikováno v:
La Presse Médicale. 35:779-783
Resume Introduction Le pseudoxanthome elastique (PXE) est une affection hereditaire caracterisee par une atteinte cutanee, oculaire et cardiovasculaire. Nous avons analyse les atteintes oculaires des cas de PXE observes dans notre hopital. Methodes O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df2e5084f13f3502abfd68aba323730a
https://doi.org/10.1016/s0755-4982(06)74689-9
https://doi.org/10.1016/s0755-4982(06)74689-9
Autor:
Gwang-Jin Kim, Leila Abid, Werner Schempp, Franz P.W. Radner, Judith Fischer, Slaheddine Marrakchi, Hamida Turki, Peter Kirchmeier, Florence Ribierre, Roland Heilig, Mark Lathrop, Bourane Kamoun, Michael Leipoldt
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 9, Iss 6 (2013)
PLoS Genetics, Vol 9, Iss 6 (2013)
The following information was missing from the Funding section: "This work has been supported in part by grants to M. Lathrop from Genome Quebec, le Ministere de l'Enseignement superieur, de la Recherche, de la Science et de la Technologie (MESRST) Q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80ae4cdced08f9b9795c008a4f963719
https://doi.org/10.1371/annotation/df5af830-8e1d-495a-a206-f881ed85e7fe
https://doi.org/10.1371/annotation/df5af830-8e1d-495a-a206-f881ed85e7fe
Publikováno v:
La Tunisie medicale. 84(2)
A restrospective study was carried in order to evaluate the efficacy and safety of retrobulbar anaesthesia during keratoplasty.Of 250 consecutive keratoplasty, 30 (12%) were performed under retrobulbar anaesthesia. Patients received a mean volume of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26cdbf5cfc8c0fe48eee551a9fa44ade
https://pubmed.ncbi.nlm.nih.gov/16755971
https://pubmed.ncbi.nlm.nih.gov/16755971
Autor:
Bourane, Kamoun, Héla, Khlif, Madiha, Mseddi, Imène, Sayadi, Hamida, Turki, Abdelmagid, Zahaf, Jamel, Feki
Publikováno v:
Presse medicale (Paris, France : 1983). 35(5 Pt 1)
Pseudoxanthoma elasticum (PXE) is a hereditary disease characterized by skin, ocular, and cardiovascular lesions. Its prognosis depends mainly on the ocular and vascular lesions.This study included 11 patients with PXE. All patients had an ophthalmol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b07b2cc895b900c3e1e91e2972eb442f
https://pubmed.ncbi.nlm.nih.gov/16710145
https://pubmed.ncbi.nlm.nih.gov/16710145
Autor:
Bourane, Kamoun, Héla, Khlif, Dorra, Sellami, Ines, Ghorbel, Yassine, Aloulou, Amira, Trigui, Zineb, Benzina, Jamel, Feki
Publikováno v:
La Tunisie medicale. 83(3)
Strabismus surgery is underwent with general anaesthesia since it's a paediatric surgery in the majority of cases. The aim of our study is to analyse the safety and tolerance of peribulbar anaesthesia for strabismus surgery.sixty two patients underwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f292edd626b984dd7db3fddc39fd770
https://pubmed.ncbi.nlm.nih.gov/15929441
https://pubmed.ncbi.nlm.nih.gov/15929441
Publikováno v:
La Tunisie medicale. 81(5)
The congenital impermeability of see lacrymal is frequent affection of new born. Whimpering is the master symptom. We propose a retrospective study with 492 cases of congenital imperforations treated in our ophthalmology department in Sfax, between 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e485dcdf9438ecc9f07c104a51396b45
https://pubmed.ncbi.nlm.nih.gov/12934448
https://pubmed.ncbi.nlm.nih.gov/12934448
Autor:
Bourane Kamoun, Michael Leipoldt, Leila Abid, Werner Schempp, Slaheddine Marrakchi, Gwang-Jin Kim, Florence Ribierre, Roland Heilig, Peter Kirchmeier, Judith Fischer, Franz P.W. Radner, Hamida Turki, Mark Lathrop
Publikováno v:
PLoS Genetics, Vol 9, Iss 6, p e1003536 (2013)
PLoS Genetics
PLoS Genetics
Autosomal recessive congenital ichthyosis (ARCI) is a rare genetic disorder of the skin characterized by abnormal desquamation over the whole body. In this study we report four patients from three consanguineous Tunisian families with skin, eye, hear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763ed9cb67f3a2b74eb7bb146dad34a2
https://doi.org/10.1371/journal.pgen.1003536
https://doi.org/10.1371/journal.pgen.1003536