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124 results

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Page 1
Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3.
Hizem S, Maamouri R, Zaouak A, Rejeb I, Karoui S, Sebai M, Jilani H, Elaribi Y, Fenniche S, Cheour M, Bilan F, Ben Jemaa L. Hizem S, et al. Among authors: zaouak a. Ophthalmic Genet. 2024 Feb;45(1):84-94. doi: 10.1080/13816810.2023.2206891. Epub 2023 May 9. Ophthalmic Genet. 2024. PMID: 37158316
Proliferative fasciitis in the abdominal region.
Zaraa I, Zaouak A, El Euch D, Chelly I, Haouet S, Mokni M, Ben Osman A. Zaraa I, et al. Among authors: zaouak a. Skinmed. 2014 Mar-Apr;12(2):111-2. Skinmed. 2014. PMID: 24933852
Association between scalp psoriasis and alopecia areata.
Khaled A, Hawilo A, Zaouak A, Zeglaoui F, Kharfi M, Kamoun MR. Khaled A, et al. Among authors: zaouak a. Tunis Med. 2012 Apr;90(4):344. Tunis Med. 2012. PMID: 22535354 Free article. No abstract available.
H syndrome: Clinical, histological and genetic investigation in Tunisian patients.
Jaouadi H, Zaouak A, Sellami K, Messaoud O, Chargui M, Hammami H, Jones M, Jouini R, Chadli Debbiche A, Chraiet K, Fenniche S, Mrad R, Mokni M, Turki H, Benkhalifa R, Abdelhak S. Jaouadi H, et al. Among authors: zaouak a. J Dermatol. 2018 Aug;45(8):978-985. doi: 10.1111/1346-8138.14359. Epub 2018 May 29. J Dermatol. 2018. PMID: 29808591
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: zaouak a. 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 tale of subcutaneous nodules of the hands.
Chamli A, Massaoudi C, Frioui R, Ben Brahim E, Debbiche A, Fenniche S, Hammami H, Zaouak A. Chamli A, et al. Among authors: zaouak a. Scand J Rheumatol. 2023 Jul;52(4):434-435. doi: 10.1080/03009742.2022.2152586. Epub 2022 Dec 22. Scand J Rheumatol. 2023. PMID: 36546640 No abstract available.
Keloid scar after herpes zoster ophthalmicus.
Maamouri R, Zaouak A, Ali A, Frioui R, Cheour M. Maamouri R, et al. Among authors: zaouak a. J Cosmet Dermatol. 2023 May;22(5):1704-1705. doi: 10.1111/jocd.15636. Epub 2023 Jan 31. J Cosmet Dermatol. 2023. PMID: 36718842 No abstract available.
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: zaouak a. Int J Dermatol. 2019 Dec;58(12):1439-1443. doi: 10.1111/ijd.14452. Epub 2019 Apr 25. Int J Dermatol. 2019. PMID: 31020658
An unusual presentation of celiac disease in adult patient.
Frioui R, Zaouak A, Chamli A, Jouini R, Fenniche S, Hammami H. Frioui R, et al. Among authors: zaouak a. Clin Case Rep. 2022 Oct 8;10(10):e6437. doi: 10.1002/ccr3.6437. eCollection 2022 Oct. Clin Case Rep. 2022. PMID: 36245465 Free PMC article.
124 results