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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: atweh l. Hum Genet. 2023 Apr;142(4):563-576. doi: 10.1007/s00439-023-02530-8. Epub 2023 Feb 15. Hum Genet. 2023. PMID: 36790526
A rare case of pelvic bone duplication.
Atweh LA, Jurjus A, Farah N, Nassar L. Atweh LA, et al. Skeletal Radiol. 2018 Aug;47(8):1171-1175. doi: 10.1007/s00256-017-2869-1. Epub 2018 Feb 14. Skeletal Radiol. 2018. PMID: 29445931
Acute soft head syndrome in a sickle cell disease patient.
Zadeh C, Rameh V, Atweh LA. Zadeh C, et al. Among authors: atweh la. J Radiol Case Rep. 2021 Apr 30;15(4):1-6. doi: 10.3941/jrcr.v15i4.4026. eCollection 2021 Apr. J Radiol Case Rep. 2021. PMID: 34276870 Free PMC article.
Emergency abdominal radiology: the acute abdomen.
Birjawi GA, Nassar LJ, Atweh LA, Akel S, Haddad MC. Birjawi GA, et al. J Med Liban. 2009 Jul-Sep;57(3):178-212. J Med Liban. 2009. PMID: 19938402 No abstract available.
20 results