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Clinical Characterization and Underlying Genetic Findings in Brazilian Patients with Syndromic Microcephaly Associated with Neurodevelopmental Disorders.
Tolezano GC, Bastos GC, da Costa SS, Scliar MO, de Souza CFM, Van Der Linden H Jr, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AAL, Bertola DR, Krepischi ACV. Tolezano GC, et al. Among authors: haddad la. Mol Neurobiol. 2024 Jan 5. doi: 10.1007/s12035-023-03894-8. Online ahead of print. Mol Neurobiol. 2024. PMID: 38180615
A Cell Junctional Protein Network Associated with Connexin-26.
Batissoco AC, Salazar-Silva R, Oiticica J, Bento RF, Mingroni-Netto RC, Haddad LA. Batissoco AC, et al. Among authors: haddad la. Int J Mol Sci. 2018 Aug 27;19(9):2535. doi: 10.3390/ijms19092535. Int J Mol Sci. 2018. PMID: 30150563 Free PMC article.
A dermatological assessment of pediatric patients with tuberous sclerosis complex (TSC).
Nunes BA, Romano AKFG, Pasa Morgan MA, Gonçalves AA, Cardozo LFM, de Almeida LGD, Haddad LA, Crippa ACS, Antoniuk SA, Abagge KT. Nunes BA, et al. Among authors: haddad la. An Bras Dermatol. 2024 Apr 23:S0365-0596(24)00058-8. doi: 10.1016/j.abd.2023.11.004. Online ahead of print. An Bras Dermatol. 2024. PMID: 38658236 Free article.
FMRP ribonucleoprotein complexes and RNA homeostasis.
Suardi GAM, Haddad LA. Suardi GAM, et al. Among authors: haddad la. Adv Genet. 2020;105:95-136. doi: 10.1016/bs.adgen.2020.01.001. Epub 2020 Feb 6. Adv Genet. 2020. PMID: 32560791 Review.
32 results