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Metabolic alkalosis with hypoelectrolytemia in infants with cystic fibrosis.
Pediatr Int. 2002 Jun;44(3):289-92. doi: 10.1046/j.1442-200x.2002.01563.x.
Pediatr Int. 2002.
PMID: 11982899
Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD).
Gucev ZS, Slaveska N, Laban N, Danilovski D, Tasic V, Pop-Jordanova N, Zatkova A.
Gucev ZS, et al. Among authors: slaveska n.
Prilozi. 2011;32(1):305-11.
Prilozi. 2011.
PMID: 21822197
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Nephrolithiasis in a child with glucose-galactose malabsorption.
Tasic V, Slaveska N, Blau N, Santer R.
Tasic V, et al. Among authors: slaveska n.
Pediatr Nephrol. 2004 Feb;19(2):244-6. doi: 10.1007/s00467-003-1327-6. Epub 2003 Dec 11.
Pediatr Nephrol. 2004.
PMID: 14673631
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