Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mohamed Ridha, Barbouch"'
Autor:
Sonia, Halioui-Louhaichi, Ons, Azzabi, Nadia, Mattoussi, Hasna, Labiadh, Khadija, Bousseta, Neji, Tebib, Taher, Gargah, Sayda, Ben Becher, Mohamed Ridha, Barbouch, Mohamed, Bejaoui, Ahmed, Maherzi
Publikováno v:
La Tunisie medicale. 94(4)
Background Primary immunodeficiencies (PID) are a group of heterogeneous and relatively rare diseases. Aim to determine the clinical characteristics, outcome and genetic data of primary immunodeficiencies in pediatrics patients. Methods A retrospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b2b67837078594811a8cf6099ff7d33
https://pubmed.ncbi.nlm.nih.gov/27704518
https://pubmed.ncbi.nlm.nih.gov/27704518
Autor:
Lamia, Sfaihi, Dominique, Stoppa Lyonnet, Salma, Ben Ameur, Catherine, Dubois D'enghien, Thouraya, Kamoun, Mohamed Ridha, Barbouch, Mongia, Hachicha
Publikováno v:
La Tunisie medicale. 93(8-9)
Ataxia-telangiectasia (A-T) is a multisystem disorder characterized by progressive neurologic impairment, variable immunodeficiency, impaired organ maturation, X-ray hypersensitivity, oculocutaneous telangiectasia, and a predisposition to malignancy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::514f3797563f7b4739d16e5f682ba0df
https://pubmed.ncbi.nlm.nih.gov/26815515
https://pubmed.ncbi.nlm.nih.gov/26815515
Autor:
Neji Tebib, KH Bousetta, S. Halioui-Louhaichi, H. Labiadb, S. Ben Becher, Ahmed Maherzi, S. Abdelkefi, T. Gargah, N. Mattoussi, Mohamed Bejaoui, Mohamed Ridha Barbouch
Publikováno v:
Archives de Pédiatrie. 22:293
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92c092d14fe282543871b52a9916c190
https://doi.org/10.1016/s0929-693x(15)30416-4
https://doi.org/10.1016/s0929-693x(15)30416-4
Autor:
Sonia, Halioui-Louhaichi, Mongi, Ben Hariz, Mohamed, Fathallah Dahmani, Mohamed Ridha, Barbouch, Jouhaïna, Mahmoudi, Mohamed, Bejaoui, Alain, Fischer, Kossay, Dellagi, Bachra, Ben Ammar, Ahmed, Maherzi
Publikováno v:
La Tunisie medicale. 84(7)
Leukocyte adhesion deficiency (LAD) is a rare primary immunodeficiency inherited as an autosomal recessive genetic disorder. LAD was suspected in a four days old girl. She was born from healthy first cousins. A family history of a boy who died from o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e941ed20957cc701f4551dd1211dc954
https://pubmed.ncbi.nlm.nih.gov/17039742
https://pubmed.ncbi.nlm.nih.gov/17039742