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Abschlusseditorial.
Jilani H, Ehrmann U, Rathjen KI, Schilling I, Gerhardus A. Jilani H, et al. Z Evid Fortbild Qual Gesundhwes. 2022 Sep;173:106-107. doi: 10.1016/j.zefq.2022.07.005. Epub 2022 Aug 26. Z Evid Fortbild Qual Gesundhwes. 2022. PMID: 36031549 German. No abstract available.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K; ESCAPE Study group; GPN study group; Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium. Burgmaier K, et al. Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30. Kidney Int. 2021. PMID: 33940108
Genome Tunisia Project: paving the way for precision medicine in North Africa.
Hamdi Y, Trabelsi M, Ghedira K, Boujemaa M, Ben Ayed I, Charfeddine C, Souissi A, Rejeb I, Kammoun Rebai W, Hkimi C, Neifar F, Jandoubi N, Mkaouar R, Chaouch M, Bennour A, Kamoun S, Chaker Masmoudi H, Abid N, Mezghani Khemakhem M; GTCA Consortium; Masmoudi S, Saad A, BenJemaa L, BenKahla A, Boubaker S, Mrad R, Kamoun H, Abdelhak S, Gribaa M, Belguith N, Kharrat N, Hmida D, Rebai A. Hamdi Y, et al. Genome Med. 2024 Aug 27;16(1):104. doi: 10.1186/s13073-024-01365-w. Genome Med. 2024. PMID: 39187811 Free PMC article.
Barriers and facilitators to implementation of direct fruit and vegetables provision interventions in kindergartens and schools: a qualitative systematic review applying the consolidated framework for implementation research (CFIR).
Meshkovska B, Scheller DA, Wendt J, Jilani H, Scheidmeir M, Stratil JM, Lien N; PEN Consortium. Meshkovska B, et al. Among authors: jilani h. Int J Behav Nutr Phys Act. 2022 Jan 31;19(1):11. doi: 10.1186/s12966-022-01246-8. Int J Behav Nutr Phys Act. 2022. PMID: 35101084 Free PMC article. Review.
[Patient and public involvement in clinical research: An introduction].
Schilling I, Herbon C, Jilani H, Rathjen KI, Gerhardus A. Schilling I, et al. Among authors: jilani h. Z Evid Fortbild Qual Gesundhwes. 2020 Sep;155:56-63. doi: 10.1016/j.zefq.2020.06.007. Epub 2020 Aug 11. Z Evid Fortbild Qual Gesundhwes. 2020. PMID: 32798190 Review. German.
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Cammarata-Scalisi F, Matysiak U, Willoughby CE, Ruzaike G, Cárdenas Tadich A, Araya Castillo M, Zara-Chirinos C, Bracho A, Avendaño A, Jilani H, Callea M. Cammarata-Scalisi F, et al. Among authors: jilani h. J Pediatr Genet. 2021 Jul 26;12(4):339-341. doi: 10.1055/s-0041-1732474. eCollection 2023 Dec. J Pediatr Genet. 2021. PMID: 38162154 Free PMC article.
Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.
Sassi H, Elaribi Y, Jilani H, Rejeb I, Hizem S, Sebai M, Kasdallah N, Bouthour H, Hannachi S, Beygo J, Saad A, Buiting K, H'mida Ben-Brahim D, BenJemaa L. Sassi H, et al. Among authors: jilani h. Mol Genet Genomic Med. 2021 Oct;9(10):e1796. doi: 10.1002/mgg3.1796. Epub 2021 Sep 12. Mol Genet Genomic Med. 2021. PMID: 34510813 Free PMC article. Review.
Erratum: Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Cammarata-Scalisi F, Matysiak U, Willoughby CE, Ruzaike G, Cárdenas Tadich A, Araya Castillo M, Zara-Chirinos C, Bracho A, Avendaño A, Jilani H, Callea M. Cammarata-Scalisi F, et al. Among authors: jilani h. J Pediatr Genet. 2024 Jul 9;12(4):e1. doi: 10.1055/s-0044-1788343. eCollection 2023 Dec. J Pediatr Genet. 2024. PMID: 38993803 Free article.
44 results