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Can untreated PKU patients escape from intellectual disability? A systematic review.
van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Blau N, Bulut FD, Casas K, Didycz B, Djordjevic M, Federico A, Feillet F, Gizewska M, Gramer G, Hertecant JL, Hollak CEM, Jørgensen JV, Karall D, Landau Y, Leuzzi V, Mathisen P, Moseley K, Mungan NÖ, Nardecchia F, Õunap K, Powell KK, Ramachandran R, Rutsch F, Setoodeh A, Stojiljkovic M, Trefz FK, Usurelu N, Wilson C, van Karnebeek CD, Hanley WB, van Spronsen FJ. van Vliet D, et al. Among authors: bulut fd. Orphanet J Rare Dis. 2018 Aug 29;13(1):149. doi: 10.1186/s13023-018-0890-7. Orphanet J Rare Dis. 2018. PMID: 30157945 Free PMC article.
Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations.
Kör D, Şeker-Yılmaz B, Bulut FD, Kılavuz S, Öktem M, Ceylaner S, Yıldızdaş D, Önenli-Mungan N. Kör D, et al. Among authors: bulut fd. Turk J Pediatr. 2019;61(3):330-336. doi: 10.24953/turkjped.2019.03.003. Turk J Pediatr. 2019. PMID: 31916709 Free article.
Kor D, Seker-Yilmaz B, Bulut FD, Kilavuz S, Oktem M, Ceylaner S, Yildizdas D, Onenli-Mungan N. ...
Kor D, Seker-Yilmaz B, Bulut FD, Kilavuz S, Oktem M, Ceylaner S, Yildizdas D, Onenli-Mungan N. ...
26 results