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Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases.
Gedikbasi A, Toksoy G, Karaca M, Gulec C, Balci MC, Gunes D, Gunes S, Aslanger AD, Unverengil G, Karaman B, Basaran S, Demirkol M, Gokcay GF, Uyguner ZO. Gedikbasi A, et al. Among authors: karaca m. Front Genet. 2023 Jun 12;14:1191159. doi: 10.3389/fgene.2023.1191159. eCollection 2023. Front Genet. 2023. PMID: 37377599 Free PMC article.
Levodopa-refractory hyperprolactinemia and pituitary findings in inherited disorders of biogenic amine metabolism.
Yıldız Y, Kuseyri Hübschmann O, Akgöz Karaosmanoğlu A, Manti F, Karaca M, Schwartz IVD, Pons R, López-Laso E, Palacios NAJ, Porta F, Kavecan I, Balcı MC, Dy-Hollins ME, Wong SN, Oppebøen M, Medeiros LS, de Paula LCP, García-Cazorla A, Hoffmann GF, Jeltsch K, Leuzzi V, Gökçay G, Hübschmann D, Harting I, Özön ZA, Sivri S, Opladen T. Yıldız Y, et al. Among authors: karaca m. J Inherit Metab Dis. 2024 May;47(3):431-446. doi: 10.1002/jimd.12658. Epub 2023 Jul 24. J Inherit Metab Dis. 2024. PMID: 37452721
A different perspective into clinical symptoms in CPT I deficiency.
Balci MC, Karaca M, Selamioglu A, Korbeyli HK, Durmus A, Ak B, Kozanoglu T, Gokcay GF. Balci MC, et al. Among authors: karaca m. Mol Genet Metab Rep. 2023 Nov 30;38:101032. doi: 10.1016/j.ymgmr.2023.101032. eCollection 2024 Mar. Mol Genet Metab Rep. 2023. PMID: 38090675 Free PMC article.
Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study.
Bozkaya-Yilmaz S, Karadag-Oncel E, Olgac-Dundar N, Gencpinar P, Sarioglu B, Arican P, Ersen A, Yilmaz-Ciftdoğan D, Yuksel MF, Bektas O, Teber S, Kilic B, Calik M, Karaca M, Canpolat M, Kumandas S, Per H, Gumus H, Ozturk S, Okuyaz C, Komur M, Ipek R, Ozbudak P, Arhan E, Ince H, Gurbuz G, Mert GG, Ozcan N, Turker AO, Gazeteci-Tekin H, Kırık S, Günbey C, Çarman KB, Yarar C, Çavuşoğlu D. Bozkaya-Yilmaz S, et al. Among authors: karaca m. Eur J Pediatr. 2022 Jan;181(1):383-391. doi: 10.1007/s00431-021-04219-4. Epub 2021 Aug 5. Eur J Pediatr. 2022. PMID: 34355277
A rare urea cycle disorder in a neonate: N-acetylglutamate synthetase deficiency.
Olgac A, Kasapkara ÇS, Kilic M, Emine Derinkuyu B, Azapagasi E, Kesici S, Biberoğlu G, Ozyazici A, Karaca M, Haberle J. Olgac A, et al. Among authors: karaca m. Arch Argent Pediatr. 2020 Dec;118(6):e545-e548. doi: 10.5546/aap.2020.eng.e545. Arch Argent Pediatr. 2020. PMID: 33231058 Free article. English, Spanish.
334 results