Zobrazeno 1 - 10
of 55
pro vyhledávání: '"F. Maazoun"'
Autor:
F. Maazoun, M. Bouassida, F. Mejdoub, Y. Lajmi, I. Boujelbene, I. Ben Ayed, R. Kammoun, Fatma Abdelhedi, Hassen Kamoun, S. Guidara, N. Gharbi
Publikováno v:
Annales d'Endocrinologie. 82:460
Introduction Le syndrome du triple X est une anomalie chromosomique frequente, due a la presence d’un chromosome X surnumeraire chez des individus de sexe feminin. Dans certains cas, ce syndrome peut etre revele par une amenorrhee primaire ou secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00a952a0663993bff3a660d6ae50d9b0
https://doi.org/10.1016/j.ando.2021.08.602
https://doi.org/10.1016/j.ando.2021.08.602
Autor:
S. Guidara, Fatma Abdelhedi, F. Maazoun, Y. Lajmi, Thouraya Kammoun, Hassen Kamoun, I. Ben Ayed, I. Boujelbene
Publikováno v:
Annales d'Endocrinologie. 82:328
Le marqueur chromosomique surnumeraire (MCS) est un chromosome additionnel de structure anormale dont l’origine et la composition ne peuvent etre caracterises que par des techniques de cytogenetique moleculaire. Il peut deriver de tous les chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02a5079fc2534b323229db2e2f8e3a02
https://doi.org/10.1016/j.ando.2021.08.200
https://doi.org/10.1016/j.ando.2021.08.200
Autor:
S. Guidara, Mohamed Abid, Fatma Abdelhedi, Mouna Mnif, Hassen Kamoun, F. Mejdoub, F. Maazoun, I. Boujelbene, F. Mnif, I. Ben Ayed
Publikováno v:
Annales d'Endocrinologie. 82:414
L’objectif de ce travail est d’etudier les pathologies endocriniennes auto-immunes qui peuvent etre observees chez des patientes ayant le syndrome de Turner (ST) avec un variant cytogenetique du chromosome X, a savoir l’isochromosome du bras lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1feea785d5ffd2051b0ddef065abde44
https://doi.org/10.1016/j.ando.2021.08.463
https://doi.org/10.1016/j.ando.2021.08.463
Autor:
S. Pissard, J.-L. Lagrange, Dora Bachir, K. Debbache, Pablo Bartolucci, Alain Rahmouni, Frédéric Galactéros, Anoosha Habibi, J. Gellen Dautremer, F. Maazoun, A. Boutekadjirt, Marc Michel
Publikováno v:
La Revue de Médecine Interne. 37:5-12
Resume Introduction L’hematopoiese extra-medullaire (HE) symptomatique par compression des organes adjacents est une complication rare mais potentiellement severe des β-thalassemies. Son traitement est mal codifie. Methodes Etude descriptive retro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a578a3d9460fa762658af523a4ce9e5
https://doi.org/10.1016/j.revmed.2015.07.005
https://doi.org/10.1016/j.revmed.2015.07.005
Autor:
Mahamed Nabil Mhiri, Zouhir Bahloul, Jawaher Masmoudi, Faten Frikha, Raida Ben Salah, Mouna Snoussi, F. Maazoun
Publikováno v:
La Presse Médicale. 40:e521-e527
Summary Objective The aim of this study is to assess sexual functioning in a group of married women with rheumatoid arthritis using a self-questionnaire. Methods This is a horizontal study for descriptive and analytical purposes. (between October and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edf83534f529d690d3742aaf5ada4f47
https://doi.org/10.1016/j.lpm.2011.04.015
https://doi.org/10.1016/j.lpm.2011.04.015
Autor:
F, Maazoun, J, Gellen Dautremer, A, Boutekadjirt, S, Pissard, A, Habibi, D, Bachir, A, Rahmouni, P, Bartolucci, K, Debbache, J-L, Lagrange, M, Michel, F, Galacteros
Publikováno v:
La Revue de medecine interne. 37(1)
Symptomatic extramedullary hematopoiesis (EH) is a rare but potentially severe phenomenon which occurs in β-thalassemia. There are no treatment guidelines.Retrospective single centre study including the cases of symptomatic EH encountered between 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54a2c244d62d9aaeea46295fa26630c8
https://pubmed.ncbi.nlm.nih.gov/26410419
https://pubmed.ncbi.nlm.nih.gov/26410419
Publikováno v:
La Presse Médicale. 41:669-671
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73d7edf87d4c80cf7e3773670855a1df
https://doi.org/10.1016/j.lpm.2011.07.021
https://doi.org/10.1016/j.lpm.2011.07.021
Publikováno v:
La Revue de medecine interne. 36(11)
Hyper-reactive malarial splenomegaly is a rare and severe form of chronic malaria. This condition is a common cause of splenomegaly in endemic areas. The pathophysiology of hyper-reactive malarial splenomegaly involves an intense immune reaction (pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc02e08135b8691ece723f3d6f8cb03b
https://pubmed.ncbi.nlm.nih.gov/26119345
https://pubmed.ncbi.nlm.nih.gov/26119345
Publikováno v:
Clinics and Practice, Vol 1, Iss 4 (2011)
Clinics and Practice; Volume 1; Issue 4; Pages: e89
Clinics and Practice
Clinics and Practice; Volume 1; Issue 4; Pages: e89
Clinics and Practice
The incidence of myositis in patients with systemic lupus erythematosus (SLE) is low among different series. Here we attempt to describe the main features of SLE/myositis overlap syndrome. We retrospectively reviewed the medical records of 174 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46f375ef6d5e41b0f1311183ac10ac02
https://www.clinicsandpractice.org/index.php/cp/article/view/217
https://www.clinicsandpractice.org/index.php/cp/article/view/217
Autor:
H. Hriz, N. Saidi, F. Maazoun, M. Frigui, F. Frikha, Neila Kaddour, Mouna Snoussi, Zouhir Bahloul, R. Ben Salah, Sameh Marzouk
Publikováno v:
La Revue de Médecine Interne. 32:S410-S411
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcdf574a4b9bef71b0ff009948295707
https://doi.org/10.1016/j.revmed.2011.10.222
https://doi.org/10.1016/j.revmed.2011.10.222