Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M N, Guediche"'
Publikováno v:
Case Reports in Medicine, Vol 2013 (2013)
Major histocompatibility complex class II expression deficiency is an autosomal recessive primary combined immunodeficiency. The prevalence of this deficiency is the highest in Mediterranean areas, especially North Africa. Early diagnosis is essentia
Externí odkaz:
https://doaj.org/article/4380e7474c0b4230b576b757c53cf057
Publikováno v:
Case Reports in Nephrology, Vol 2011 (2011)
Nephrotic syndrome (NS) is a renal disorder characterized by heavy proteinuria, hypoalbuninemia, edema and hypercholesterolemia. Nephrotic syndrome in children is known to be associated with an hypercoagulable state and thromboembolic complications.
Externí odkaz:
https://doaj.org/article/28ea71a8515a478e80ac926a8d5bf7c8
Publikováno v:
La Tunisie medicale. 92(4)
In Tunisia, few studies have an interest to the assessment of medication errors and the implementation of preventive measures. The aim of this study was to evaluate the barriers existing in hospital pharmacies in order to prevent medication errors an
Autor:
H, Belhadjali, M, Amri, S, Chouchene, C, Chouchene, H, Khorchani, B, Seket, K, Monastiri, M, Youssef, M-N, Guediche, J, Zili
Publikováno v:
Annales de dermatologie et de venereologie. 133(6-7)
Autor:
F, Thabet, S, Tilouche, B, Tabarki, F, Amri, M-N, Guediche, M-T, Sfar, A, Harbi, M, Yacoub, A-S, Essoussi
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 14(4)
Despite advances in antibiotic therapy strategies and pediatric intensive care, prognosis of Streptococcus pneumoniae meningitis remains very poor. To determine the factors associated with hospital mortality of children with pneumococcal meningitis.W
Autor:
A. Laadjimi, Cherine Charfeddine, Sonia Abdelhak, Neji Tebib, M.F. Ben Dridi, M. Keirallah, M. N. Guediche, M. Nilges, Kamel Monastiri, Mohamed Ridha Kamoun, Samir Boubaker, A. Ben Osman, Selma Kassar, Mourad Mokni, Naziha Kaabachi, O. Perin
Publikováno v:
Molecular Genetics and Metabolism
Molecular Genetics and Metabolism, Elsevier, 2006, 88 (2), pp.184--91. ⟨10.1016/j.ymgme.2006.02.006⟩
Molecular Genetics and Metabolism, 2006, 88 (2), pp.184--91. ⟨10.1016/j.ymgme.2006.02.006⟩
Molecular Genetics and Metabolism, Elsevier, 2006, 88 (2), pp.184--91. ⟨10.1016/j.ymgme.2006.02.006⟩
Molecular Genetics and Metabolism, 2006, 88 (2), pp.184--91. ⟨10.1016/j.ymgme.2006.02.006⟩
International audience; Tyrosinemia type II or Richner-Hanhart Syndrome (RHS) is an autosomal recessive disorder characterized by keratitis, palmoplantar keratosis, mental retardation, and elevated blood tyrosine levels. The disease is due to a defic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f79db4a591047f21bedec11b54c7ed
https://hal.archives-ouvertes.fr/hal-01974010
https://hal.archives-ouvertes.fr/hal-01974010
Autor:
S, Chouchane, H, Fehri, C, Chouchane, Z, Merchaoui, B, Seket, S, Haddad, C, Ben Meriem, K, Monastiri, M N, Guediche
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 12(12)
The hypernatremic dehydration defined by a serum sodium concentrationor = to 150 mmol/l, is a particular form of acute dehydration and constitutes a medical emergency requiring a prompt and adequate diagnosis and management.To precise the epidemiolog
Autor:
C, Ben Meriem, S, Nouri, C, Chouchane, S, Chouchane, M, Said, L, Ghédira, A, Moussa, M, Boubtane, M N, Guediche
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 13(1)
Langerhans cell histiocytose is a rare condition in childhood. It presents in different ways ranging from a single bony disease to a multisystemic disease involving vital organs.We report a case of single bone involvement revealed by torticollis in a
Autor:
H, Jaïdane, C, Chouchane, J, Gharbi, S, Chouchane, Z, Merchaoui, C, Ben Meriem, M, Aouni, M N, Guediche
Publikováno v:
Medecine et maladies infectieuses. 35(1)
Non-polio enteroviruses are the most common identified cause of viral neuromeningeal infections following the introduction of the mumps and polio vaccines.The aim of this study was to describe the epidemiology, clinical presentation, and the outcome
Autor:
S, Chouchane, C H, Chouchane, C H, Ben Meriem, B, Seket, S, Hammami, S, Nouri, K, Monastiri, M N, Guediche
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 11(11)
The first problem to face in prolonged fever is its etiologic diagnosis. Its incidence varies between 0,5 to 3% of all paediatric hospital-stay. Precise diagnosis need an extensive questionnary, complete physical examination and an algorithm of compl