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case report (2) 2
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Journal of Clinical and Analytical Medicine, ISSN 1309-0720, 09/2016, Volume 7, Issue 5, pp. 695 - 700
Aim: To evaluate demographic,clinical and laboratory characteristics, causes, MEFV gene mutations, and mortality rates of patients with secondary amyloidosis.... 
MEFV | AA amyloidosis | Familial mediterranean fever | AA Amyloidosis | Familial Mediterranean Fever
Journal Article
Renal Failure, ISSN 0886-022X, 10/2013, Volume 35, Issue 9, pp. 1285 - 1288
Abstract Gitelman's syndrome (GS) is a rare disease with autosomal recessive trait, characterized by hypokalemia, hypomagnesemia, metabolic alkalosis,... 
hypomagnesemia | hypokalemia | Gitelman's syndrome | Advanced age | chondrocalcinosis | Hypokalemia | Chondrocalcinosis | Hypomagnesemia | CLCNKB | HYPOKALEMIC ALKALOSIS | FORMS | BARTTER | CHLORIDE CHANNEL GENE | UROLOGY & NEPHROLOGY | MUTATIONS | EPLERENONE | Male | Chondrocalcinosis - etiology | Humans | Middle Aged | Gitelman Syndrome - complications | Gitelman Syndrome - diagnosis
Journal Article
Turkish Nephrology, Dialysis and Transplantation Journal, ISSN 1300-7718, 2013, Volume 22, Issue 1, pp. 16 - 29
Journal Article
Case Reports in Medicine, ISSN 1687-9627, 2013, Volume 2013, pp. 404710 - 4
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is responsible for 8-10% of patients with end-stage renal... 
Case studies | Complications and side effects | Care and treatment | Abnormalities | Diagnosis | Aorta, Thoracic | Polycystic kidney disease | Case Report
Journal Article
Renal Failure, ISSN 0886-022X, 10/2013, Volume 35, Issue 9, pp. 1285 - 1288
Journal Article
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