Zobrazeno 1 - 4
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pro vyhledávání: '"Nida Gulderen Kalay"'
Autor:
Selcen Bozkurt, Ayse Merve Usta, Nafiye Urganci, Nida Gulderen Kalay, Gulsen Kose, Evrim Ozmen
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene.
Externí odkaz:
https://doaj.org/article/ded3f46f8c144650a60677018b66dfb9
Autor:
Selcen Bozkurt, Ayse Merve Usta, Nafiye Urganci, Nida Gulderen Kalay, Gulsen Kose, Evrim Ozmen
Publikováno v:
BMC pediatrics. 22(1)
Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene. Besides r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1e5b00654ec9e3b95b4214212bf41f4
https://pubmed.ncbi.nlm.nih.gov/35260125
https://pubmed.ncbi.nlm.nih.gov/35260125
Publikováno v:
Hormone research in paediatrics. 94(9-10)
Objective: Spexin (SPX) is a novel peptide implicated in food intake and satiety. SPX levels are reduced in obese patients. Aim: This study aimed to compare serum SPX levels in obese adolescents versus healthy controls and to assess the associations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b453dc3d7e1eb0364e7fb34c22f04cf6
https://pubmed.ncbi.nlm.nih.gov/34839286
https://pubmed.ncbi.nlm.nih.gov/34839286
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