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Case report: Neonatal diabetes mellitus with congenital hypothyroidism as a result of biallelic heterozygous mutations in GLIS3 gene.
Pediatr Diabetes. 2022 Sep;23(6):668-674. doi: 10.1111/pedi.13341. Epub 2022 Apr 24.
Pediatr Diabetes. 2022.
PMID: 35394098
The Ukrainian version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR).
Boyko Y, Hrytsiuk I, Consolaro A, Bovis F, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO).
Boyko Y, et al. Among authors: hrytsiuk i.
Rheumatol Int. 2018 Apr;38(Suppl 1):403-409. doi: 10.1007/s00296-018-3983-7. Epub 2018 Apr 7.
Rheumatol Int. 2018.
PMID: 29637352
Free PMC article.
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Starting dose of levothyroxine for the treatment of congenital hypothyroidism: a systematic review.
Hrytsiuk I, Gilbert R, Logan S, Pindoria S, Brook CG.
Hrytsiuk I, et al.
Arch Pediatr Adolesc Med. 2002 May;156(5):485-91. doi: 10.1001/archpedi.156.5.485.
Arch Pediatr Adolesc Med. 2002.
PMID: 11980555
Review.
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No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
Abo-Dalo B, Roes M, Canún S, Delatycki M, Gillessen-Kaesbach G, Hrytsiuk I, Jung C, Kerr B, Mowat D, Seemanova E, Steiner CE, Stewart H, Thierry P, van Buggenhout G, White S, Zenker M, Kutsche K.
Abo-Dalo B, et al. Among authors: hrytsiuk i.
Clin Dysmorphol. 2008 Jul;17(3):181-185. doi: 10.1097/MCD.0b013e3282f2514c.
Clin Dysmorphol. 2008.
PMID: 18541964
No abstract available.
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