Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Burcu Guven"'
Autor:
Gulcin Aytac, Burcu Guven, Ilyas Aydin, Ezgi Topyildiz, Ayca Aykut, Asude Durmaz, Neslihan Edeer Karaca, Guzide Aksu, Necil Kutukculer
Publikováno v:
Case Reports in Immunology, Vol 2023 (2023)
Background. APECED is a syndrome characterized by autoimmune polyendocrinopathy, candidiasis, and ectodermal dystrophy. The most observed clinical findings are chronic mucocutaneous candidiasis, hypoparathyroidism, and autoimmune adrenal insufficienc
Externí odkaz:
https://doaj.org/article/706171607f8842c598cc5dff4b77131b
Autor:
Murat Cakir, Elif Sag, Burcu Guven, Ulas Emre Akbulut, Fatma Issi, Alper Han Cebi, Thomas Müller, Denise Aldrian, Andreas R. Janecke
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 6, Pp 612-619 (2021)
Background: Congenital diarrheal disorders (CDDs) are a rare group of enteropathies that typically present in the early few months of life and pose a diagnostic challenge. We aimed to analyze the clinical findings and outcome of infants with CDDs and
Externí odkaz:
https://doaj.org/article/4f1f67007e0342319775497790907672
Autor:
Necil Kutukculer, Ezgi Topyildiz, Afig Berdeli, Burcu Guven Bilgin, Ayca Aykut, Asude Durmaz, Ozgur Cogulu, Guzide Aksu, Neslihan Edeer Karaca
Publikováno v:
Clinical Case Reports, Vol 9, Iss 4, Pp 2023-2031 (2021)
Abstract We suggest PLAID, APLAID, and FCAS3 have to be considered as different aspects of the same underlying condition, because of our long‐term clinical and genetical experiences. Some CVID patients have the same disease‐causing mutations in P
Externí odkaz:
https://doaj.org/article/ba0b3403cfbd40dda11f638b3d0b7a7e
Publikováno v:
Medicine Science, Vol 7, Iss 4, Pp 956-8 (2018)
Background: Ganglioneuromas are rare, benign, slow-growing tumors arising from the neural crest. They are most commonly in posterior mediastinum, retroperitoneum, adrenal medulla and neck. They are very rare in presacral region. Case Report: A 15 yea
Externí odkaz:
https://doaj.org/article/a4aa4b9041c64d64916b0f3d61795f20
Autor:
Emine Kubra Tayyarcan, Esra Acar-Soykut, Serap Durakli-Velioglu, Sefika Evran, Ismail Hakki Boyaci, Burcu Guven
Publikováno v:
Canadian Journal of Microbiology. 68:55-65
Resistance to antibiotics is one of the most critical health problems in the world. Therefore, finding new treatment methods to be used as alternatives to antibiotics has become a priority for researchers. Similar to phages, certain products containi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2712fccce95ad2523af11ead03375b
https://doi.org/10.1139/cjm-2021-0211
https://doi.org/10.1139/cjm-2021-0211
Publikováno v:
Acta Reumatológica Portuguesa, Vol 2021, Iss 2, Pp 134-139 (2021)
Introduction: Generalized joint hypermobility is a clinical feature that is associated with excessive joint laxity, which can occur alone or with various inherited disorders. The term of benign joint hypermobility or joint hypermobility is used when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::ab07c9843932cafa8a3028f542d32ad8
http://www.actareumatologica.com/files/article/1340_prevalence_of_celiac_disease_in_children_with_joint_hypermobility_file.pdf
http://www.actareumatologica.com/files/article/1340_prevalence_of_celiac_disease_in_children_with_joint_hypermobility_file.pdf
Autor:
Afig Berdeli, Guzide Aksu, Neslihan Edeer Karaca, Necil Kutukculer, Burcu Guven Bilgin, Asude Durmaz, Ozgur Cogulu, Ayca Aykut, Ezgi Topyildiz
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 4, Pp 2023-2031 (2021)
Clinical Case Reports, Vol 9, Iss 4, Pp 2023-2031 (2021)
We suggest PLAID, APLAID, and FCAS3 have to be considered as different aspects of the same underlying condition, because of our long-term clinical and genetical experiences. Some CVID patients have the same disease-causing mutations in PLCG2 gene, so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9f14eaafc93d6f3b4a450a7e0ea21d
https://doi.org/10.1002/ccr3.3934
https://doi.org/10.1002/ccr3.3934
Autor:
Gulcin Aytac, Burcu Guven, Ilyas Aydın, Ezgi Topyildiz, Ayca Aykut, Guzide Aksu, Asude Durmaz, Neslihan Edeer Karaca, Necil Kutukculer
Background: APACED is a syndrome characterized by autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy. The most often observed clinical findings are chronic mucucutaneous candidiasis, hypoparatiroidism and autoimmune adrenal insuffici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23f931d1313a91eab568e74e50ccc81f
https://doi.org/10.21203/rs.3.rs-1473397/v1
https://doi.org/10.21203/rs.3.rs-1473397/v1
Publikováno v:
Turkish Journal of Medical Sciences
Taiwan-Turkey Science Summit on Translation of Cells, Nanomaterials and Signaling Molecules into Regenerative Medicine -- APR 01-03, 2018 -- Ankara, TURKEY /0000-0002-5463-8355; Akcan, Ramazan/0000-0002-4100-9488; Tamer, Ugur/0000-0001-9989-6123; Yil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23ae0286183b473200e968748cd22ca1
https://doi.org/10.3906/sag-1912-196
https://doi.org/10.3906/sag-1912-196
Publikováno v:
Pediatric gastroenterology, hepatologynutrition. 25(5)
At the beginning of the Coronavirus disease (COVID-19) epidemic, physicians paid close attention to children with chronic diseases to prevent transmission or a severe course of infection. We aimed to measure the severe acute respiratory syndrome coro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f04d80ea918681a6b515a0b4c85abfa4
https://pubmed.ncbi.nlm.nih.gov/36148294
https://pubmed.ncbi.nlm.nih.gov/36148294