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Page 1
[Use of recombinant factor VII in Glanzmann thrombasthenia: a case report].
Chabchoub Ben Abdallah R, Trabelsi L, Ben Ameur S, Kammoun F, Boukédi A, Ben Salah M, Ben Hlima N, Mahfoudh A. Chabchoub Ben Abdallah R, et al. Among authors: trabelsi l. Arch Pediatr. 2010 Jul;17(7):1062-4. doi: 10.1016/j.arcped.2010.04.006. Epub 2010 Jun 8. Arch Pediatr. 2010. PMID: 20570498 French.
[Multiple cerebral cavernomatosis in a 1-year-old child].
Chabbchoub Ben Abdallah R, Kammoun F, Ayedi M, Trabelsi L, Ben Salah M, Ben Hlima N, Mahfoudh A. Chabbchoub Ben Abdallah R, et al. Among authors: trabelsi l. Arch Pediatr. 2010 Aug;17(8):1156-8. doi: 10.1016/j.arcped.2010.05.002. Epub 2010 Jun 9. Arch Pediatr. 2010. PMID: 20542671 French.
[Septic cavernous sinus thrombosis following ethmoiditis: a case report].
Ben Abdallah Chabchoub R, Kmiha S, Turki F, Trabelsi L, Maalej B, Ben Salah M, Abdelhédi Gargouri L, Boukédi A, Ben Halima N, Mahfoudh A. Ben Abdallah Chabchoub R, et al. Among authors: trabelsi l. Arch Pediatr. 2014 Jan;21(1):66-9. doi: 10.1016/j.arcped.2013.10.012. Epub 2013 Nov 26. Arch Pediatr. 2014. PMID: 24290188 French.
[Pituitary tuberculosis: a case report].
Trabelsi L, Majdoub-Rekik N, Bouaziz H, Mnif-Feki M, Hammemi B, Maaloul I, Ben Jmaa M, Abid M. Trabelsi L, et al. Ann Endocrinol (Paris). 2005 Sep;66(4):340-6. doi: 10.1016/s0003-4266(05)81791-3. Ann Endocrinol (Paris). 2005. PMID: 16392184 French.
[Hematidrosis in a child].
Ben Abdallah Chabchoub R, Safi F, Trabelsi L, Maalej B, Gargouri L, Turki F, Amouri M, Ben Halima N, Turki H, Mahfoud A. Ben Abdallah Chabchoub R, et al. Among authors: trabelsi l. Arch Pediatr. 2013 May;20(5):563-4. doi: 10.1016/j.arcped.2013.02.068. Epub 2013 Apr 3. Arch Pediatr. 2013. PMID: 23562314 French. No abstract available.
[Myasthenia gravis and hyperthyroidism: two cases].
Trabelsi L, Charfi N, Triki Ch, Mnif M, Rekik N, Mhiri Ch, Abid M. Trabelsi L, et al. Ann Endocrinol (Paris). 2006 Jun;67(3):265-9. doi: 10.1016/s0003-4266(06)72597-5. Ann Endocrinol (Paris). 2006. PMID: 16840920 French.
Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene.
Louhichi N, Bahloul E, Marrakchi S, Othman HB, Triki C, Aloulou K, Trabelsi L, Mahfouth N, Ayadi-Mnif Z, Keskes L, Fakhfakh F, Turki H. Louhichi N, et al. Among authors: trabelsi l. Orphanet J Rare Dis. 2019 May 22;14(1):112. doi: 10.1186/s13023-019-1095-4. Orphanet J Rare Dis. 2019. PMID: 31118107 Free PMC article.
28 results