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Page 1
Molecular basis of mild hyperphenylalaninaemia in Turkey.
Yilmaz E, Cali F, Roman V, Ozalp I, Coşkun T, Tokatli A, Kalkanoğlu HS, Ozgüç M. Yilmaz E, et al. Among authors: kalkanoglu hs. J Inherit Metab Dis. 2000 Jul;23(5):523-5. doi: 10.1023/a:1005628717813. J Inherit Metab Dis. 2000. PMID: 10947211 No abstract available.
Maple syrup urine disease: mutation analysis in Turkish patients.
Dursun A, Henneke M, Ozgül K, Gartner J, Coşkun T, Tokatli A, Kalkanoğlu HS, Demirkol M, Wendel U, Ozalp I. Dursun A, et al. Among authors: kalkanoglu hs. J Inherit Metab Dis. 2002 May;25(2):89-97. doi: 10.1023/a:1015668425004. J Inherit Metab Dis. 2002. PMID: 12118532
Phenylketonuria and cystic fibrosis in the same patient.
Kalkanoğlu HS, Anadol D, Yilmaz E, Coşkun T. Kalkanoğlu HS, et al. Pediatr Int. 2000 Feb;42(1):92-3. doi: 10.1046/j.1442-200x.2000.01160.x. Pediatr Int. 2000. PMID: 10703245 No abstract available.
A boy with spastic paraparesis and dyspnea.
Kalkanoğlu HS, Dursun A, Tokatli A, Coşkun T, Karasimav D, Topaloğlu H. Kalkanoğlu HS, et al. J Child Neurol. 2004 May;19(5):397-8. doi: 10.1177/088307380401900517. J Child Neurol. 2004. PMID: 15224716
20 results