Mellouli F - Search Results

1

Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients.

Ouederni M, Rouag H, Ben Fraj I, Rekaya S, Kouki R, Lamouchi T, Zaiter I, Mellouli F, Bejaoui M, Ben Khaled M. Ouederni M, et al. Among authors: mellouli f. Int Orthop. 2023 Dec;47(12):2941-2952. doi: 10.1007/s00264-023-05886-8. Epub 2023 Jul 15. Int Orthop. 2023. PMID: 37452863

2

[The hyper-IgM syndrome: 13 observations].

Bejaoui M, Mellouli F, Chouanine R, Dellagi K, Barbouche MR. Bejaoui M, et al. Among authors: mellouli f. Presse Med. 2003 Mar 29;32(12):544-9. Presse Med. 2003. PMID: 12714921 French.

3

Successful treatment of mycophenolate mofetil in a child with refractory Evans syndrome.

Guirat-Dhouib N, Mellouli F, Kouki R, Bejaoui M. Guirat-Dhouib N, et al. Among authors: mellouli f. J Pediatr Hematol Oncol. 2010 Aug;32(6):e244. doi: 10.1097/MPH.0b013e3181e40f45. J Pediatr Hematol Oncol. 2010. PMID: 20628320 No abstract available.

4

Hypocalcaemia due to hypoparathyroidism in β-thalassemia major. A study of a new case.

Dhouib N, Turki Z, Mellouli F, Ouederni M, Yahiaoui S, Nagi S, Kouki R, Ben Slama C, Bejaoui M. Dhouib N, et al. Among authors: mellouli f. Tunis Med. 2011 Mar;89(3):302-4. Tunis Med. 2011. PMID: 21387240 Free article.

5

Autoimmune polyglandular syndrome type II after bone marrow transplant: real transfer or acceleration of a programmed disease?

Mellouli F, Ksouri H, Lakhal A, Torjmen L, Ladeb S, Ben Othman T, Hmida S, Bejaoui M. Mellouli F, et al. Exp Clin Transplant. 2012 Feb;10(1):76-80. doi: 10.6002/ect.2011.0062. Exp Clin Transplant. 2012. PMID: 22309426 Free article.

6

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome).

Guirat-Dhouib N, Baccar Y, Mustapha IB, Ouederni M, Chouaibi S, El Fekih N, Barbouche MR, Fezaa B, Kouki R, Hmida S, Mellouli F, Bejaoui M. Guirat-Dhouib N, et al. Among authors: mellouli f. Clin Mol Allergy. 2012 Apr 23;10(1):6. doi: 10.1186/1476-7961-10-6. Clin Mol Allergy. 2012. PMID: 22524894 Free PMC article.

7

Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia.

Talmoudi F, Kammoun L, Benhalim N, Torjemane L, Ouederni M, Aissaoui L, Lakhal A, Mellouli F, Othmen TB, Bejaoui M, Abdelhak S, Meddeb M, Dellagi K, Hdiji S, Amouri A; Tunisian Fanconi Anemia Study Group. Talmoudi F, et al. Among authors: mellouli f. J Pediatr Hematol Oncol. 2013 Oct;35(7):547-50. doi: 10.1097/MPH.0b013e31827e56cb. J Pediatr Hematol Oncol. 2013. PMID: 23337544

8

[Effectiveness and acceptance of hydroxyurea in the treatment of severe forms of sickle cell disease: a prospective study of 65 cases].

Mellouli F, Chouaibi S, Dhouib N, Ouederni M, Ben Khaled M, Abbes S, Bejaoui M. Mellouli F, et al. Tunis Med. 2013 Aug-Sep;91(8-9):544-50. Tunis Med. 2013. PMID: 24227514 French.

9

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.

Amouri A, Talmoudi F, Messaoud O, d'Enghien CD, Rekaya MB, Allegui I, Azaiez H, Kefi R, Abdelhak A, Meseddi SH, Torjemane L, Ouederni M, Mellouli F, Abid HB, Aissaoui L, Bejaoui M, Othmen TB, Lyonnet DS, Soulier J, Hachicha M, Dellagi K, Abdelhak S, Fanconi T. Amouri A, et al. Among authors: mellouli f. Mol Genet Genomic Med. 2014 Mar;2(2):160-5. doi: 10.1002/mgg3.55. Epub 2014 Feb 5. Mol Genet Genomic Med. 2014. PMID: 24689079 Free PMC article.

10

Sequential asymptomatic enterovirus infections in a patient with major histocompatibility complex class II primary immunodeficiency.

Driss N, Mellouli F, Ben Yahia A, Touzi H, Barbouche MR, Triki H, Bejaoui M. Driss N, et al. Among authors: mellouli f. J Clin Microbiol. 2014 Sep;52(9):3486-9. doi: 10.1128/JCM.01122-14. Epub 2014 Jul 16. J Clin Microbiol. 2014. PMID: 25031436 Free PMC article.

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