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Health phenome of Parkinson's patients reveals prominent mood-sleep cluster.
Olsen A, Locascio J, Tuncali I, Laroussi N, Abatzis E, Kamenskaya P, Kuras Y, Yi T, Videnovic A, Hayes M, Ho G, Paulson J, Khurana V, Herrington T, Hyman B, Selkoe D, Growdon J, Gomperts S, Riise T, Schwarzschild M, Hung A, Wills A, Scherzer C. Olsen A, et al. Among authors: laroussi n. Res Sq [Preprint]. 2023 Dec 22:rs.3.rs-3683455. doi: 10.21203/rs.3.rs-3683455/v1. Res Sq. 2023. PMID: 38196602 Free PMC article. Preprint.
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis.
Charfeddine C, Laroussi N, Mkaouar R, Jouini R, Khayat O, Redissi A, Mosbah A, Dallali H, Chedly Debbiche A, Zaouak A, Fenniche S, Abdelhak S, Hammami-Ghorbel H. Charfeddine C, et al. Among authors: laroussi n. PLoS One. 2021 Oct 20;16(10):e0258777. doi: 10.1371/journal.pone.0258777. eCollection 2021. PLoS One. 2021. PMID: 34669720 Free PMC article.
A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
Sayeb M, Riahi Z, Laroussi N, Bonnet C, Romdhane L, Mkaouar R, Zaouak A, Marrakchi J, Abdessalem G, Messaoud O, Bouchniba O, Ghilane N, Mokni M, Besbes G, Yacoub-Youssef H, Petit C, Abdelhak S. Sayeb M, et al. Among authors: laroussi n. Int J Dermatol. 2019 Dec;58(12):1439-1443. doi: 10.1111/ijd.14452. Epub 2019 Apr 25. Int J Dermatol. 2019. PMID: 31020658
Genetic basis of dominant dystrophic epidermolysis bullosa in tunisian families and co-occurrence of dominant and recessive mutations.
Ben Brick AS, Laroussi N, Mesrati H, Kefi R, Ouragini H, Bchetnia M, Romdhane L, Marrakchi S, Boubaker MS, Castiglia D, Hovnanian A, Abdelhak S, Turki H, Kharfi M. Ben Brick AS, et al. Among authors: laroussi n. J Eur Acad Dermatol Venereol. 2016 Jan;30(1):155-7. doi: 10.1111/jdv.12645. Epub 2014 Aug 4. J Eur Acad Dermatol Venereol. 2016. PMID: 25088787 No abstract available.
Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C. Riahi Z, et al. Among authors: laroussi n. PLoS One. 2014 Jun 13;9(6):e99797. doi: 10.1371/journal.pone.0099797. eCollection 2014. PLoS One. 2014. PMID: 24926664 Free PMC article.
A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy.
Ben Rekaya M, Laroussi N, Messaoud O, Jones M, Jerbi M, Naouali C, Bouyacoub Y, Chargui M, Kefi R, Fazaa B, Boubaker MS, Boussen H, Mokni M, Abdelhak S, Zghal M, Khaled A, Yacoub-Youssef H. Ben Rekaya M, et al. Among authors: laroussi n. Biomed Res Int. 2014;2014:256245. doi: 10.1155/2014/256245. Epub 2014 May 4. Biomed Res Int. 2014. PMID: 24877075 Free PMC article. Clinical Trial.
The first Mal de Meleda case in Libya: identification of a SLURP1 mutation.
Bchetnia M, Bozgia M, Laroussi N, Ben Brick AS, Charfeddine C, Ben Halim N, Mokni M, Boubaker MS, Abdelhak S. Bchetnia M, et al. Among authors: laroussi n. Int J Dermatol. 2015 Dec;54(12):1426-8. doi: 10.1111/ijd.12373. Epub 2014 Apr 16. Int J Dermatol. 2015. PMID: 24738704 No abstract available.
17 results