Výsledky vyhledávání - "Nurdan Ciftci"

Akademický článek

A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene

Autor: Ismail Dundar, Emine Camtosun, Mustafa Dogan, Leman Kayas, Nurdan Ciftci, Aysehan Akinci

Publikováno v: Medicine Science, Vol 11, Iss 4, Pp 1731-3 (2022)

Familial hypocalciuric hypercalcemia (FHH) is a benign disease associated with heterozygous inactivating mutations in the calcium-sensing receptor (CaSR) gene. This article presents a girl with heterozygous p.Cys575Tyr variation in the CaSR gene. The

Externí odkaz: https://doaj.org/article/6afc545ffda94afa88bb8257f0092997

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Serum kisspeptin, neurokinin B and inhibin B levels can be used as alternative parameters to distinguish idiopathic CPP from premature thelarche in the early stages of puberty

Autor: Dogus Vuralli, Nurdan Ciftci, Huseyin Demirbilek

Publikováno v: Clinical Endocrinology. 98:788-795

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::97a7263d4528ea27faee6e2c005684d3
https://doi.org/10.1111/cen.14906

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Presentation, diagnosis and follow-up characteristics of 17α-hydroxylase deficiency cases with exon 1-6 deletion (founder mutation) in the CYP17A1 gene: 20-years single-center experience

Autor: Ismail Dundar, Aysehan Akinci, Emine Camtosun, Nurdan Ciftci, Leman Kayas

Publikováno v: Sexual Development.

Context: 17α-hydroxylase/17,20-lyase deficiency (17OHD) is characterized by decreased sex steroids and cortisol synthesis, as well as an increased mineralocorticoid effect. Aim: This study aimed to evaluate the clinical, biochemical, and molecular c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::391c21f2cc70899eaedcf81a1001019c
https://doi.org/10.1159/000529158

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Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis

Autor: Ismail Dundar, Nurdan Ciftci, Aysehan Akinci, Emine Camtosun, Leman Kayas, Ahmet Sigirci, Fatma Yagin

Publikováno v: Medicine Science | International Medical Journal. 11:1184

There is a scarcity of data concerning endocrine function and the effects of enzyme replacement therapy (ERT) on growth and other endocrine functions in patients with mucopolysaccharidosis (MPS). This study retrospectively evaluated height increase,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9395fad828d97bb5c3418869840347db
https://doi.org/10.5455/medscience.2022.03.053

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Investigation of the Levels of Serum Amyloid A, YKL‐40, and Pentraxin‐3 in Patients with Familial Mediterranean Fever

Autor: Hilmi Demirin, Muhammet Ramazan Yigitoglu, Pinar Atukeren, Fatmanur Hacievliyagil Kazanci, Mustafa Saygin Deniz, Sümeyye Gök, Sefa Ciftci, Huseyin Tugrul Celik, Nurdan Ciftci, Yasemin Coşkun Yavuz

Background Familial Mediterranean Fever (FMF) is an autosomal recessive form of recurrent episodes of fever and an autoinflammatory disease characterized by inflammation of the serous membranes. The clinical diagnosis is supported by the laboratory f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::332b82898a61377e4a796eed494c36cc
https://europepmc.org/articles/PMC6807204/

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Akademický článek

To use of triglyceride/hdl cholesterol ratio to predict insulin resistance and dysglycemia in overweight and obese children.

Autor: Ciftci, Nurdan¹ pediatrinurdan@gmail.com, Kayas, Leman²

Publikováno v: Annals of Medical of Research. Aug2023, Vol. 30 Issue 8, p920-923. 4p.

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