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2001 1
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20 results

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Page 1
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.
Exploring Health-Related Quality of Life in Children With Hypertrophic Cardiomyopathy and Relationship to Physical Activity.
Wagner MJ, Jeewa A, Pidborochynski T, Lemaire-Paquette S, Khoury M, Cunningham C, Dhillon S, Laroussi NA, Vaujois L, Dallaire F, Schantz D, Armstrong K, Mawad W, Bradley TJ, Conway J. Wagner MJ, et al. Among authors: laroussi na. J Am Heart Assoc. 2024 Jun 18;13(12):e033968. doi: 10.1161/JAHA.123.033968. Epub 2024 Jun 15. J Am Heart Assoc. 2024. PMID: 38879453 Free PMC article.
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.
Riahi Z, Zainine R, Mellouli Y, Hannachi R, Bouyacoub Y, Laroussi N, Beltaief N, Kefi R, Romdhane L, Bonnet C, Abdelhak S, Besbes G. Riahi Z, et al. Among authors: laroussi n. Int J Pediatr Otorhinolaryngol. 2013 Sep;77(9):1481-4. doi: 10.1016/j.ijporl.2013.06.013. Epub 2013 Jul 12. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23856378 Review.
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.
Assessing Cardiovascular Health in Paediatric Hypertrophic Cardiomyopathy Using the CANHEART Health Index.
Srbely V, Jeewa A, Pidborochynski T, Lemaire-Paquette S, Khoury M, Cunningham C, Dhillon S, Laroussi NA, Vaujois L, Dallaire F, Schantz D, Armstrong K, Mawad W, Bradley T, Conway J. Srbely V, et al. Among authors: laroussi na. CJC Pediatr Congenit Heart Dis. 2024 Jul 8;3(5):183-190. doi: 10.1016/j.cjcpc.2024.06.002. eCollection 2024 Oct. CJC Pediatr Congenit Heart Dis. 2024. PMID: 39619007 Free PMC article.
Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.
Ben Brick AS, Laroussi N, Mesrati H, Kefi R, Bchetnia M, Lasram K, Ben Halim N, Romdhane L, Ouragini H, Marrakchi S, Boubaker MS, Meddeb Cherif M, Castiglia D, Hovnanian A, Abdelhak S, Turki H. Ben Brick AS, et al. Among authors: laroussi n. Arch Dermatol Res. 2014 May;306(4):405-11. doi: 10.1007/s00403-013-1421-y. Epub 2013 Oct 30. Arch Dermatol Res. 2014. PMID: 24170138
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.
Modifiable Health Behaviours in Children with HCM: Lessons from the Heart Health Survey.
Wagner MJ, Jeewa A, Pidborochynski T, Lemaire-Paquette S, Khoury M, Cunningham C, Dhillon S, Laroussi NA, Vaujois L, Dallaire F, Schantz D, Armstrong K, Mawad W, Bradley TJ, Conway J. Wagner MJ, et al. Among authors: laroussi na. Pediatr Cardiol. 2025 Jan 8. doi: 10.1007/s00246-024-03746-9. Online ahead of print. Pediatr Cardiol. 2025. PMID: 39774709
20 results