Zobrazeno 1 - 10
of 80
pro vyhledávání: '"herediter"'
Autor:
Mehmet Bankir, Güzin Özden
Publikováno v:
Family Practice and Palliative Care, Vol 6, Iss 3, Pp 135-144 (2021)
Introduction: The study aims to determine the depression and anxiety levels of patients with hereditary angioedema using the Beck depression inventory(BDI), Beck anxiety inventory (BAI) and to compare the results with the patients' demographic charac
Externí odkaz:
https://doaj.org/article/b5aa463aee554cf6983ad9245b49b01f
Publikováno v:
Sakarya Tıp Dergisi, Vol 11, Iss 3, Pp 647-653 (2021)
Amaç: Meme kanseri kadınlarda en sık teşhis edilen kanserdir. Sporadik meme kanserlerinden sonra en sık ailesel ardından herediter meme kanserleri gelir. Çalışmamızda herediter ve ailesel meme kanserlerinin klinikopatolojik özelliklerini k
Externí odkaz:
https://doaj.org/article/906d69af221b462d8fc9685e04a03e25
Publikováno v:
Cukurova Medical Journal, Vol 47, Iss 1, Pp 463-465 (2022)
Pseudohypoparathyroidism is a rare inherited metabolic disorder that associated with parathormone resistance. Low serum calcium, high phosphates and raised parathormone levels suggesting parathormone resistance are biochemical characteristic features
Externí odkaz:
https://doaj.org/article/655cc71406ef4aac9707ba9dd7412c4f
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 6, Pp 924-926 (2021)
Hereditary methemoglobinemia is one of the rare causes of hypoxemia. Mutations in the CYB5R3 gene cause autosomal recessive hereditary methemoglobinemia. Mostly, symptoms such as shortness of breath, bruise and and fatique occur. It may not display a
Externí odkaz:
https://doaj.org/article/d950ed03eebd430b93bc400eff116ca4
Publikováno v:
Sakarya Tıp Dergisi, Vol 10, Iss 3, Pp 528-535 (2020)
Herediter adenomatöz polipozis sendromları; Familyal Adenomatöz Polipozis (FAP), Atenüe Familyal Adenomatöz Polipozis (AFAP), MUTHY ilişkili Adenomatöz Polipozis (MAP) ve Polimeraz Proofreading Sendrom (PPS) olarak tanımlanan farklı hastalı
Externí odkaz:
https://doaj.org/article/19597d50cd1e4c74813256bce3139353
Autor:
Öner Özdemir
Publikováno v:
Sakarya Tıp Dergisi, Vol 10, Iss 1, Pp 152-161 (2020)
Herediter anjioödem (HAÖ) nadir görülen, genelde C1 inhibitör (C1-INH) eksikliğine bağlı, tekrarlayan anjioödem ataklarıyla bilinen ölümcül olabilen otozomla dominant geçişli bir hastalıktır. Anjioödem atakları aniden oluşur, sık
Externí odkaz:
https://doaj.org/article/c0695715c2994edda1c7666ce509da6b
Autor:
Öner Özdemir
Publikováno v:
Southern Clinics of Istanbul Eurasia, Vol 30, Iss 4, Pp 355-361 (2019)
Hereditary angioedema (HAE) is a rare, inherited disease mostly associated with mutations in the SERPING1 gene (serpin family G member 1), which encodes the C1 inhibitor (C1-INH) protein. Regulation can lead to plasma deficiency and ensuing repeated
Externí odkaz:
https://doaj.org/article/1a2d23fbe4ea48c2a60b7a4e87770875
Autor:
Osman Emre Aycan
Publikováno v:
Acta Medica Alanya, Vol 3, Iss 3, Pp 287-292 (2019)
Aim: In this study, we sought to evaluate the complications of Hereditary Multiple Exostosis (HME) particularly the presence of pain, and its effects on pediatric and adolescent groups.Patients and Methods: 72 (37male/32female) patients aging between
Externí odkaz:
https://doaj.org/article/d7e8bed5d4c44222a704fb69d7babcb9
Publikováno v:
Selcuk Dental Journal, Vol 6, Iss 2, Pp 190-195 (2019)
Herediter anjio ödem (HAÖ), C1 esteraz inhibitör proteininin konjenital eksikliğine bağlı olarak meydana gelen, nadir gözlenen, otozomal dominant bir hastalıktır. HAÖ atakları, spontan veya bir travmaya bağlı olarak, ekstremitelerde, yü
Externí odkaz:
https://doaj.org/article/b32cd8469f764b398cf5945f447784e0
Publikováno v:
Jurnal Matematika Integratif, Vol 15, Iss 1, Pp 63-68 (2019)
Misalkan E suatu graf berarah dan K lapangan. Aljabar lintasan Leavitt LK(E) adalah K-aljabar lintasan diperluas yang berasosiasi dengan graf E modulo relasi tertentu. Dalam tulisan ini, diselidiki sifat keherediteran modul atas aljabar lintasan Leav
Externí odkaz:
https://doaj.org/article/58132f973f9440108fbb00b595e88dac