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Using comprehensive genomic and functional analyses for resolving genotype-phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study.
Hamideh D, Das A, Bianchi V, Chung J, Negm L, Levine A, Basbous M, Sanchez-Ramirez S, Mikael L, Jabado N, Atweh L, Lteif M, Mahfouz R, Tarek N, Abboud M, Muwakkit S, Hawkins C, Tabori U, Saab R; International Replication Repair Deficiency Consortium (IRRDC). Hamideh D, et al. Among authors: tarek n. Hum Genet. 2023 Apr;142(4):563-576. doi: 10.1007/s00439-023-02530-8. Epub 2023 Feb 15. Hum Genet. 2023. PMID: 36790526
Genetic polymorphisms in candidate genes are not associated with increased vincristine-related peripheral neuropathy in Arab children treated for acute childhood leukemia: a single institution study.
Zgheib NK, Ghanem KM, Tamim H, Aridi C, Shahine R, Tarek N, Saab R, Abboud MR, El-Solh H, Muwakkit SA. Zgheib NK, et al. Among authors: tarek n. Pharmacogenet Genomics. 2018 Aug;28(8):189-195. doi: 10.1097/FPC.0000000000000345. Pharmacogenet Genomics. 2018. PMID: 30119132
Treatment-induced cerebral sinus venous thrombosis in childhood acute lymphoblastic malignancies: New risk factors to consider.
El-Khoury H, Saifi O, Haddad S, Chahrour M, Ghanem KM, Mubarak Y, Tamim H, Makki M, Zakka C, Chan AK, Mahfouz R, Tarek N, El-Solh H, Abboud MR, Saab R, Muwakkit SA. El-Khoury H, et al. Among authors: tarek n. Pediatr Blood Cancer. 2021 Nov;68(11):e29210. doi: 10.1002/pbc.29210. Epub 2021 Jul 29. Pediatr Blood Cancer. 2021. PMID: 34327817
38 results