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No. 20 (2020): October / December 2020
No. 20 (2020): October / December 2020
Published:
2020-12-31
Review Article
Diagnosis and management of childhood idiopathic nephrotic syndrome: what's new?
S Mabrouk, S Nouir, F Majdoub, S Abroug (Author)
7-11
PDF (French)
Original Article
Bronchiolitis in preterm children: A study of 52 cases
F Safi, D Kamoun, I Moalla, A Ben Ahmed, O Ayanleh, M Hsairi, L Gargouri, S Ben Ameur, A Mahfoudh (Author)
12-17
PDF (French)
La Tuberculose multi-focale chez l'enfant : aspects cliniques et évolutifs
F Khalsi, S Kbaier, I Trabelsi, M Ben Romdhane, I Brini, I Belhadj, S Hamouda, K Bousetta (Author)
18-22
PDF (French)
Convulsive status epilepticus in children: prognostic factors
S Haddad, S Benhassine, F Mezghani, E Jebabli, S Rhayem, F Ben mansour, F Fdhila-ayed, M Khemiri (Author)
23-29
PDF (French)
Screening for nutritional risk in hospitalized children under the age of five: Predictors of high nutritional risk
R Ben Rabeh, S Mazigh Mrad, N Missaoui, A Babay, S Atitallah, S Yahyaoui, S Boukhtir (Author)
30-40
PDF (French)
Case Report
Contributions and limits of pancreatectomy in hyperinsulinism
J Ben Hfaiedh, A Ben Chehida, S Ben Mrad, H Boudabous, R Ben Abdallah, R Ben Abdelaziz, H Azzouz, H Ben Turkia, R Ben Malek, N Kaabar, MS Abdelmoula, N Tebib (Author)
41-46
PDF (French)
Antenatal diagnosis of complete agenesis of the corpus callosum: study of two cases
S Smida, J Methlouthi, B Bannour, M Bellaleh, I Bannour, O Mghirbi, M Bibi, S Nouri, L Lassoued, N Mahdhaoui (Author)
47-49
PDF (French)
Deficiency of the seventh component of complement in an eight-year-old girl
A Werdani, A Ben Mabrouk, I Ayadi, N Jemmali, A Rassas, M Kallel Sellami, B Mahjoub (Author)
50-51
PDF (French)
Prenatal diagnosis of cleft lip associated with bilateral choanal atresia: therapeutic challenge in a newborn
J Ben Hfaiedh, S Blibech, I Ayadi, H Kammoun, H Ben Salem, N Kasdalla, H Brahem, M Daiiki, R Ben Mhemmed, I Labbene, M Douagi (Author)
52-55
PDF (French)
Phenotypical diversity in three family members with LEOPARD syndrome caused by Tyr279Cys mutation in PTPN11 gene
R Ben Aziza, F Mezghani, E Jbebli, L Kraoua, S Rhayem, F Fedhila, R Mrad, S Haddad, M Khemiri (Author)
56-59
PDF (French)
Congenital tourniquet syndrome is also possible! About two premature infants
J Hafaiedh, S Blibech, N Kasdallah, H Ben Salem, M Douagi (Author)
60-63
PDF (French)
Case of the Day
A persistent hip pain in a 7-year-old child: what is your diagnosis?
E Sfar, C Chouchane, R Hadj Salem, H Besbes, F Thabet, T Ghédira, S Chouchane (Author)
66-70
PDF (French)
Reading Notes
Procalcitonin, C-reactive protein, and erythrocyte sedimentation rate for the diagnosis of acute pyelonephritis in children
L Sfaihi, R Kolsi, T Kamoun (Author)
64-65
PDF (French)
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