Zobrazeno 1 - 10
of 98
pro vyhledávání: '"S. Kmiha"'
Akademický článek
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Autor:
C. Bensignor, Yosra Halleb, A. Tej, A. Touati, A. Ben Ahmed, S. Kmiha, D. H’mida Ben Brahim, N. Mahdhaoui, Anisa Saad, Sonia Nouri, J. Mathlouthi
Publikováno v:
Archives de Pédiatrie. 26:102-107
Background and objectives Sanjad–Sakati syndrome (SSS; OMIM 241410) is a rare autosomal recessive disorder found almost exclusively in people of Arab origin. It is characterized by congenital hypoparathyroidism, severe prenatal and postnatal growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44ff8d7d0c12b176780f88632f2654f
https://doi.org/10.1016/j.arcped.2018.11.012
https://doi.org/10.1016/j.arcped.2018.11.012
Autor:
I. Jedidi, Ines Maaloul, L. Sfaihi, S. Kmiha, Thouraya Kamoun, O. Laaroussi, M. Hachicha, H. Aloulou
Publikováno v:
Transfusion Clinique et Biologique. 25:14-18
Resume But de l’etude Evaluer la prise en charge des patients atteints de beta-thalassemie majeure et preciser les differentes complications. Patients et methodes Une etude retrospective, colligeant 26 cas de beta-thalassemie majeure pris en charge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f721e60a94045154e088fc5db02d0e2a
https://doi.org/10.1016/j.tracli.2017.11.002
https://doi.org/10.1016/j.tracli.2017.11.002
Autor:
Hajer Aloulou, Meriem Amouri, Thouraya Kamoun, S. Kmiha, Emna Bahloul, R. Guirat, Lamia Sfaihi, Khadija Sellami, Hamida Turki, Mongia Hachicha, Madiha Mseddi
Publikováno v:
Indian Journal of Dermatology, Vol 63, Iss 1, Pp 62-65 (2018)
Indian Journal of Dermatology
Indian Journal of Dermatology
Background: Bacillus Calmette-Guerin (BCG) vaccine is a widely used vaccine. Management of local BCG complications differs between clinicians, and the optimal approach remains unclear. Aims: We aim to describe the epidemiological, clinical and therap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25b2572db98760ebcaf0f55f1b14a2e5
http://www.e-ijd.org/article.asp?issn=0019-5154
http://www.e-ijd.org/article.asp?issn=0019-5154
Autor:
Fatma Kamoun, Imen Chabchoub, S. Ben Ameur, M. Hachicha, Khaoula Aissa, S. Kmiha, Hatem Masmoudi, S. Feki, Hajer Aloulou
Publikováno v:
Revue Française d'Allergologie. 57:18-23
Resume L’allergie aux proteines du lait de vache (APLV) est la premiere allergie a apparaitre chez l’enfant. Son evolution naturelle se fait le plus souvent vers la guerison. Cependant, cette allergie peut persister apres l’âge de 3 ans. But E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79fc962f596f70a514ecbdb72bbe0a6d
https://doi.org/10.1016/j.reval.2016.09.009
https://doi.org/10.1016/j.reval.2016.09.009
Autor:
Sourour Yaich, Ines Maaloul, Mongia Hachicha, Hajer Aloulou, Jamel Damak, S. Kmiha, Kamoun Thouraya
Publikováno v:
The Pan African Medical Journal
Les accidents domestiques représentent un problème sérieux de santé publique en pédiatrie. Ils sont responsables d’une lourde morbidité et mortalité parmi la population pédiatrique. Nous avons mené une étude rétrospective colligeant 231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc23535fbf0f47542acf81624795ca47
http://europepmc.org/articles/PMC6711678
http://europepmc.org/articles/PMC6711678
Autor:
Imene Chabchoub, Aurélie Toussaint, S. Kmiha, Hajer Aloulou, Fatma Damak, Thouraya Kamoun, Ines Maaloul, Caroline Silve, Fatma Kamoun, Salma Ben Ameur, Lamia Sfaihi, Mongia Hachicha
Publikováno v:
Hormone Research in Paediatrics. 87:23-29
Background: Hereditary vitamin D-resistant rickets (HVDRR) is an autosomal recessive disorder characterized by the early onset of rickets and is caused by mutations in the vitamin D receptor (VDR) gene. Some HVDRR patients also have alopecia. Patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b1a6d688723986b1b257310b7f40a8
https://doi.org/10.1159/000452886
https://doi.org/10.1159/000452886
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hajer Aloulou, Moez Medhaffer, Choumous Kallel, Imen Krichen, Moez Elloumi, Sofien Alibi, S. Kmiha, Nacim Louhichi, Mongia Hachicha, Ines Maaloul, Faiza Fakhfakh
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 28(6)
Factor XIII deficiency is a rare autosomal recessive disorder of hemostasis characterized by a plasmatic factor XIII level less than 1% in homozygote and bleeding as of the youth. The aim of the study is to describe the clinical features and the outc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde67a179d6388a2cb6d30098d2e5147
https://pubmed.ncbi.nlm.nih.gov/28704210
https://pubmed.ncbi.nlm.nih.gov/28704210
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 25(1)
Our objectives were to assess the management of patients with major thalassemia and identify the various complications and monitoring means.A retrospective study was conducted on 26 β-thalassemic patients in the department of paediatrics, Hédi Chak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2368e2517078aa9e7732b825fdea4f0
https://pubmed.ncbi.nlm.nih.gov/29199112
https://pubmed.ncbi.nlm.nih.gov/29199112