Triki CC - Search Results

1

Treatment of seizures in the neonate: Guidelines and consensus-based recommendations-Special report from the ILAE Task Force on Neonatal Seizures.

Pressler RM, Abend NS, Auvin S, Boylan G, Brigo F, Cilio MR, De Vries LS, Elia M, Espeche A, Hahn CD, Inder T, Jette N, Kakooza-Mwesige A, Mader S, Mizrahi EM, Moshé SL, Nagarajan L, Noyman I, Nunes ML, Samia P, Shany E, Shellhaas RA, Subota A, Triki CC, Tsuchida T, Vinayan KP, Wilmshurst JM, Yozawitz EG, Hartmann H. Pressler RM, et al. Among authors: triki cc. Epilepsia. 2023 Oct;64(10):2550-2570. doi: 10.1111/epi.17745. Epub 2023 Sep 1. Epilepsia. 2023. PMID: 37655702

2

Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.

Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A. Elghezal H, et al. Eur J Med Genet. 2007 Nov-Dec;50(6):441-5. doi: 10.1016/j.ejmg.2007.07.002. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17851150

3

[DNET underlying focal central epilepsy].

Hsairi-Guidara I, Fourati H, Gargouri MA, Kamoun I, Mnif Z, Triki C. Hsairi-Guidara I, et al. Arch Pediatr. 2016 Apr;23(4):411-3. doi: 10.1016/j.arcped.2016.01.013. Epub 2016 Mar 9. Arch Pediatr. 2016. PMID: 26971136 French. No abstract available.

4

Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies.

Hadj Salem I, Kamoun F, Louhichi N, Rouis S, Mziou M, Fendri-Kriaa N, Makni-Ayadi F, Triki C, Fakhfakh F. Hadj Salem I, et al. Biosci Rep. 2011 Apr;31(2):125-35. doi: 10.1042/BSR20100026. Biosci Rep. 2011. PMID: 20477750

5

[Schimmelpenning-Feuerstein-Mims syndrome: a case report].

Bahloul E, Abid I, Masmoudi A, Makni S, Kamoun F, Boudawara T, Triki C, Turki H. Bahloul E, et al. Arch Pediatr. 2015 Nov;22(11):1157-62. doi: 10.1016/j.arcped.2015.07.013. Epub 2015 Aug 29. Arch Pediatr. 2015. PMID: 26320679 French.

6

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.

Triki C, Louhichi N, Méziou M, Choyakh F, Kéchaou MS, Jlidi R, Mhiri C, Fakhfakh F, Ayadi H. Triki C, et al. Neuromuscul Disord. 2003 Jan;13(1):4-12. doi: 10.1016/s0960-8966(02)00188-8. Neuromuscul Disord. 2003. PMID: 12467726

7

[Importance of electromyography in the diagnosis of botulism].

Zouari N, Choyakh F, Triki C, Mhiri C. Zouari N, et al. Neurophysiol Clin. 1997 Jun;27(3):220-6. doi: 10.1016/s0987-7053(97)83778-1. Neurophysiol Clin. 1997. PMID: 9304049 French.

8

Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.

Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F. Mkaouar-Rebai E, et al. Biosci Rep. 2010 Dec;30(6):405-11. doi: 10.1042/BSR20090120. Biosci Rep. 2010. PMID: 20055758

9

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.

Louhichi N, Triki C, Quijano-Roy S, Richard P, Makri S, Méziou M, Estournet B, Mrad S, Romero NB, Ayadi H, Guicheney P, Fakhfakh F. Louhichi N, et al. Neurogenetics. 2004 Feb;5(1):27-34. doi: 10.1007/s10048-003-0165-9. Epub 2003 Dec 2. Neurogenetics. 2004. PMID: 14652796 Free PMC article.

10

LAMA2 mRNA processing alterations generate a complete deficiency of laminin-alpha2 protein and a severe congenital muscular dystrophy.

Siala O, Louhichi N, Triki C, Morinière M, Fakhfakh F, Baklouti F. Siala O, et al. Neuromuscul Disord. 2008 Feb;18(2):137-45. doi: 10.1016/j.nmd.2007.09.003. Epub 2007 Nov 28. Neuromuscul Disord. 2008. PMID: 18053718

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