Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Banu Küçükemre-Aydın"'
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 303-307 (2020)
Increased intestinal permeability (IIP) precedes several autoimmune disorders. Although Hashimoto’s thyroiditis (HT) is the most common autoimmune disorder, the role of IIP in its pathogenesis had received little attention. Zonulin plays a critical
Externí odkaz:
https://doaj.org/article/8a35c617ea4945f2bb44ce79fa29a833
Autor:
Alper Gezdirici, Gizem Ersoy, Banu Küçükemre-Aydın, Gonul Aydogan, Tuba Nur Tahtakesen, Işık Odaman-Al, Hasan Önal, Zafer Salcioglu, Melek Yildiz
Publikováno v:
The Turkish journal of pediatrics. 61(2)
Odaman-Al I, Gezdirici A, Yildiz M, Ersoy G, Aydogan G, Salcioglu Z, Tahtakesen TN, Onal H, Kucukemre-Aydin B. A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome. Turk J Pediatr 2019; 61: 257
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d72ef8e4a0e64719c6006a58bc62da
https://pubmed.ncbi.nlm.nih.gov/31951336
https://pubmed.ncbi.nlm.nih.gov/31951336
Autor:
Zeynep Tamay, Rüveyde Bundak, Ayşe Süleyman, Banu Küçükemre Aydın, Esen Özkaya, Feyza Darendeliler, Nermin Guler, Nurçin Saka, Gürkan Kılıç, Firdevs Baş
Publikováno v:
Pediatric Dermatology. 31:90-94
Netherton syndrome (NS) is a rare autosomal recessive disorder characterized by ichthyosiform scaling, hair abnormalities, and variable atopic features. Mutations in the serine protease inhibitor Kazal type 5 (SPINK5) gene leading to lymphoepithelial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b4532125aa36f32f4de1ec9da5c01b
https://doi.org/10.1111/pde.12220
https://doi.org/10.1111/pde.12220
Autor:
Banu, Küçükemre-Aydın, Özlem, Öğrendil-Yanar, Ilmay, Bilge, Firdevs, Baş, Şükran, Poyrazoğlu, Alev, Yılmaz, Sevinç, Emre, Rüveyde, Bundak, Nurçin, Saka, Feyza, Darendeliler
Publikováno v:
The Turkish journal of pediatrics. 57(3)
The CYP17A1 gene encodes the enzyme P450c17, which mediates both 17α-hydroxylase and 17,20-lyase activities and is essential for production of cortisol and sex steroids. Loss-of-function mutations of this gene cause 17α-hydroxylase/17,20-lyase defi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::822066db14948705ca50dd2b76507441
https://pubmed.ncbi.nlm.nih.gov/26701948
https://pubmed.ncbi.nlm.nih.gov/26701948
Autor:
Banu Küçükemre, Aydın, Demet, Demirkol, Firdevs, Baş, Umit, Türkoğlu, Alkın, Kumral, Metin, Karaböcüoğlu, Agop, Cıtak, Feyza, Darendeliler
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 56(3)
Although studied widely in adulthood, little is known about endocrinological disorders during critical illnesses in childhood. The aims of this study were to define the endocrinological changes in patients admitted to pediatric intensive care unit (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c322f0b273c845e749b62fa024731a4
https://pubmed.ncbi.nlm.nih.gov/24299000
https://pubmed.ncbi.nlm.nih.gov/24299000
Autor:
Aydın, Banu Küçükemre1 bkucukemre@yahoo.com, Yıldız, Melek1, Akgün, Abdurrahman1, Topal, Neval1, Adal, Erdal2, Önal, Hasan1
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. Sep2020, Vol. 12 Issue 3, p303-307. 5p.
Autor:
Aygün, Fatih1 (AUTHOR), Ekici, Barış2 (AUTHOR) ekicibaris@istanbul.edu.tr, Aydınlı, Nur2 (AUTHOR), Aydın, Banu Küçükemre3 (AUTHOR), Baş, Firdevs3 (AUTHOR), Tatlı, Burak2 (AUTHOR)
Publikováno v:
International Journal of Neuroscience. Feb2012, Vol. 122 Issue 2, p69-73. 5p.
Autor:
Sari, Erkan, Bereket, Abdullah, Yeşilkaya, Ediz, Baş, Firdevs, Bundak, Rüveyde, Aydın, Banu Küçükemre, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat
Publikováno v:
American Journal of Medical Genetics. Part A; Apr2016, Vol. 170A Issue 4, p942-948, 7p
Autor:
Aydın, Banu Küçükemre, Demirkol, Demet, Baş, Firdevs, Türkoğlu, Ümit, Kumral, Alkın, Karaböcüoğlu, Metin, Çıtak, Agop, Darendeliler, Feyza
Publikováno v:
Pediatrics International; Jun2014, Vol. 56 Issue 3, p349-353, 5p, 2 Charts, 1 Graph