TY  - JOUR
T1  - Sistinüri (iki kardeşte tespit edilen herediter sistinüri vakası nedeni ile)
TT  - Cystinuria (A Case Report of Two Siblings Diagnosed with Hereditary Cystinuria)
AU  - Akgün, Güneş
PY  - 1970
DA  - December
JF  - Ankara Üniversitesi Tıp Fakültesi Mecmuası
PB  - Ankara University
WT  - DergiPark
SN  - 0365-8104
SP  - 1763
EP  - 1768
VL  - 23
IS  - 6
LA  - en
AB  - In this paper, two brothers who were diagnosed with cystinuria with the manifestations of repetitive nephrolithiasis and hematuria have been presented. Taking the opportunity of these cases, the subject of cystinuria has been reviewed.
KW  - Cystinuria
KW  - hereditary metabolic disease
KW  - nephrolithiasis
KW  - kidney stone
KW  - dibasic amino acids
KW  - cystine crystals
N2  - Tekrar eden taş düşürme ve hematüri şikayetleri ile kliniğimizde incelenen iki sistinürili kardeş takdim edilmiştir. Bu vesileyle sistinüriye ait literatür gözden geçirilmiştir.
CR  - Harrison, T. Principles of Internal Medicine, 5th ed., McGraw-Hill Comp., New York, Toronto, London, 1966.
CR  - Nelson, W. Textbook of Pediatrics, 8th ed., Saunders Comp., Philadelphia, London, 1966.
CR  - Baitter, F. “Cystinuria”, Ann. Intern. Med., 62:796, 1965.
CR  - Huth, E. Kidney Stones, A Medical Approach to Diagnosis, Med. Clin. N. Amer., 47:959, 1963.
CR  - Editorial: “A New Look at Cystinuria”, New Engl. J. Med., 273:613, 1965.
CR  - Rosenberg, L., Crawhall, J., Segal, S. “Intestinal Transport of Cystine and Cystine in Man”, J. Clin. Invest., 46:1, 1967.
CR  - Thier, S., Segal, S. “Cystinuria, Defective Intestinal Transport of Dibasic Amino Acids and Cystine”, J. Clin. Invest., 44:442, 1965.
CR  - McCarthy, C., Barland, J., Lynch, H. “Defective Uptake of Basic Amino Acids and L-Cystine by Intestinal Mucosa of Patients with Cystinuria”, J. Clin. Invest., 43:1518, 1964.
UR  - https://dergipark.org.tr/en/pub/autfm/issue//1737664
L1  - https://dergipark.org.tr/en/download/article-file/5035365
ER  -