Yazar "Alp, Alper" için PubMed İndeksli Yayınlar Koleksiyonu listeleme
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Blue reflection of anemia
Alp, Alper; Pektaş, Gökhan; Gönül, Ercan; Gibyeli Genek, Dilek; Hüddam, Bülent (Blackwell Publishing Ltd., 2021) -
Immunological results of long-term use of mammalian target of rapamycin (Mtor) inhibitors and its effects on renal graft functions
Tanrısev, Mehmet; Ayna Kılıçaslan, Tülay; Çolak, Hülya; Ersan, Sibel; Yılmaz, Banu; Alp, Alper; Tuğmen, Cem; Engin Sevgili, Bahar (International Scientific Information, 2021)Background: Material/Methods: Results: Conclusions: Calcineurin inhibitor drugs (CNI), which are the basis of immunosuppression in kidney transplantation, contribute to renal graft loss, with increased morbidity and mortality ... -
In Reply to Dr Connors et al
Huddam, Bülent; Alp, Alper; Kırlı, İsmail; Yılmaz, Mehmet; Çağırtekin, Aytuğ; Allı, Hakan; Edebali, Sultan (Wilderness Medical Society, 2021) -
Medium Cut-Off Membrane Can Be a New Treatment Tool in Amanita phalloides Poisoning
Huddam, Bülent; Alp, Alper; Kırlı, İsmail; Yılmaz, Mehmet; Çağırtekin, Aytuğ; Allı, Hakan; Edebali, Sultan (Elsevier, 2021)Mushroom poisoning is a common health problem that can be seen seasonally and geographically. Most mushroom poisoning requiring treatment worldwide is due to Amanita phalloides. Although liver failure and kidney injury are ... -
An Old Enemy: Still Nephrotoxic
Özalp, Faruk Recep; Karadeniz, Tuğba; Alp, Alper (The College of Physician and Surgeons Pakistan, 2021)Tubulointerstitial nephritis (TIN) presents histopathologically as tubulitis and oedema/inflammation and fibrosis, affecting the renal tubules and interstitium with relative sparing of the glomeruli and vasculature. It can ... -
Screening Fabry's disease in chronic kidney disease patients not on dialysis: a multicenter study
Yeniçerioğlu, Yavuz; Akdam, Hakan; Dursun, Belda; Alp, Alper; Eyiler, Funda Sağlam; Akın, Davut; Okyay, Pınar; Huddam, Bülent; Gibyeli Genek, Dilek (Taylor & Francis Ltd, 2017)Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder, affecting multiple organs due to the deficient activity of a-galactosidase A (alpha-Gal A) enzyme. The prevalence has ...