Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Arzu SAGLAM"'
Publikováno v:
Türk Patoloji Dergisi, Vol 40, Iss 1, Pp 10-15 (2024)
Objective: The gold-standard method for assessment of autoimmune bullous disease is direct/indirect immunofluorescence (IF) examination applied to fresh frozen tissue. Since the sensitivity of IF is greatly reduced in formalin-fixed paraffin-embedded
Externí odkaz:
https://doaj.org/article/8495af1af567413aa337e21dca3658f7
Autor:
Tolga Yildirim, Rahmi Yilmaz, Arzu Saglam, Muge Uzerk-Kibar, Jabrayil Jabrayilov, Yunus Erdem
Publikováno v:
Nefrología, Vol 41, Iss 6, Pp 632-639 (2021)
Introduction and objectives: Canakinumab, an IL-1 blocking drug, decreases the frequency and severity of the attacks and decreases the proteinuria level in colchicine resistant/intolerant familial Mediterranean fever (FMF) patients. However, it is no
Externí odkaz:
https://doaj.org/article/554612b4b76f4a9d905e4f81cb25abd2
Publikováno v:
Nefrología, Vol 41, Iss 4, Pp 471-473 (2021)
Externí odkaz:
https://doaj.org/article/a54d7cced57b4d2d8fa7daba53c49b41
Autor:
Saliha Esenboga, Deniz Çagdas Ayvaz, Arzu Saglam Ayhan, Banu Peynircioglu, Ozden Sanal, Ilhan Tezcan
Publikováno v:
Case Reports in Immunology, Vol 2015 (2015)
Common variable immunodeficiency (CVID) is a frequent primary immune deficiency (PID), which consists of a heterogeneous group of disorders and can present with recurrent infections, chronic diarrhea, autoimmunity, chronic pulmonary and gastrointesti
Externí odkaz:
https://doaj.org/article/a2bc9d388d62422fb1ab3900d09fb503
Autor:
Ozbek, Deniz Aral, Koc, Sila Cankurtaran, Özkan, Nazlı Ezgi, Kablan, Sevilay Erdogan, Yet, Idil, Uner, Meral, Ozlu, Nurhan, Nemutlu, Emirhan, Lay, Incilay, Ayhan, Arzu Saglam, Yildirim, Tolga, Arici, Mustafa, Yilmaz, Seref Rahmi, Erdem, Yunus, Altun, Bulent
Publikováno v:
In Journal of Proteomics 20 February 2024 293
Publikováno v:
International Urology and Nephrology. 55:661-669
We aimed to investigate the immuno-histochemical expression of C4d, ADAM10 and WT1 in kidney biopsies of immunoglobulin A nephropathy (IgAN) patients and correlate the findings with clinical, laboratory and histopathologic features in the hope of def
Publikováno v:
Journal of Cutaneous Pathology. 49:971-977
Akademický článek
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Akademický článek
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Publikováno v:
Pediatric and Developmental Pathology. 25:339-344
Constitutional mismatch repair deficiency (CMMRD) syndrome is characterized by biallelic mutations in a mismatch repair gene and is associated with development of childhood cancers and symptoms resembling neurofibromatosis type 1, like café-au-lait