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Nucleosides, Nucleotides & Nucleic Acids Volume 39, 2020 - Issue 10-12
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Conference Proceedings

Modified forearm ischemic test in hypouricemic patients

Ivan SebestaDepartment of Pediatrics and Adolescent Medicine, Institute of Medical Biochemistry and Laboratory Diagnostics, Charles University First Faculty of Medicine, Prague, Czech Republic; Correspondence[email protected]
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Daisuke MiyamotoDepartment of Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan; View further author information
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Blanka StiburkovaDepartment of Pediatrics and Adolescent Medicine, Institute of Rheumatology, Charles University First Faculty of Medicine, Prague, Czech Republic; ORCID Iconhttp://orcid.org/0000-0003-2465-1476View further author information
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Sarka BlahovaDepartment of Pediatrics and Adolescent Medicine, Charles University First Faculty of Medicine, Prague, Czech Republic; View further author information
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Nana SatoDepartment of Applied Biological Chemistry, The University of Tokyo Graduate School of Agricultural and Life Sciences Faculty of Agriculture, Bunkyo-ku, Japan; View further author information
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Koji NagataDepartment of Applied Biological Chemistry, The University of Tokyo Graduate School of Agricultural and Life Sciences Faculty of Agriculture, Bunkyo-ku, Japan; View further author information
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Ken OkamotoDepartment of Applied Biological Chemistry, The University of Tokyo Graduate School of Agricultural and Life Sciences Faculty of Agriculture, Bunkyo-ku, Japan; View further author information
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Shuichi TsuruokaDepartment of Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan; View further author information
&
Kimiyoshi IchidaDivision of Kidney and Hypertension, Department of Pathophysiology, Jikei University School of Medicine, Tokyo University of Pharmacy and Life Sciences, Tokyo, JapanView further author information
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Pages 1432-1439 | Received 20 Dec 2019, Accepted 30 Mar 2020, Published online: 20 Apr 2020

References

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  • Bierau, J.; Seta, I. Pyrimidine Disorders (Chapter 41). In Physician´s Guide to the Diagnosis,Treatment, and Follow-Up of Inherited Metabolic Diseases. Blau, N., Duran, M., Gibson, K.M., Dionisi-Vici, C. Eds.; Springer-Verlag: Berlin, 2014; pp. 641–660.
  • Coleman, R. A.; Stajich, J. M.; Pact, V. W.; Pericak-Vance, M. A. The Ischemic Exercise Test in Normal Adults and in Patients with Weakness and Cramps. Muscle Nerve 1986, 9, 216–221. DOI: 10.1002/mus.880090305.
  • Stiburkova, B.; Stekrova, J.; Nakamura, M.; Ichida, K. Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease. Am. J. Med. Sci. 2015, 350, 268–271. DOI: 10.1097/MAJ.0000000000000550.
  • Mancikova, A.; Krylov, V.; Hurba, O.; Sebesta, I.; Nakamura, M.; Ichida, K.; Stiburkova, B. Functional Analysis of Novel Allelic Variants in URAT1 and GLUT9 Causing Renal Hypouricemia Type 1 and 2. Clin. Exp. Nephrol. 2016, 20, 578–584. DOI: 10.1007/s10157-015-1186-z.
  • Iwai, N.; Mino, Y.; Hosoyamada, M.; Tago, N.; Kokubo, Y.; Endou, H. A High Prevalence of Renal Hypouricemia Caused by Inactive SLC22A12 in Japanese. Kidney Int. 2004, 66, 935–944. DOI: 10.1111/j.1523-1755.2004.00839.x.
  • Stiburkova, B.; Krijt, J.; Vyletal, P.; Bartl, J.; Gerhatova, E.; Korinek, M.; Sebesta, I. Novel Mutations in Xanthine Dehydrogenase/Oxidase Cause Severe Hypouricemia: biochemical and Molecular Genetic Analysis in Two Czech Families with Xanthinuria Type I. Clin. Chim. Acta 2012, 413, 93–99. DOI: 10.1016/j.cca.2011.08.038.
  • Mraz, M.; Hurba, O.; Bartl, J.; Dolezel, Z.; Marinaki, A.; Fairbanks, L.; Stiburkova, B. Modern Diagnostic Approach to Hereditary Xanthinuria. Urolithiasis 2015, 43, 61–67. DOI: 10.1007/s00240-014-0734-4.
  • Tanaka, Y.; Hlsatome, I.; Klnugawa, T.; Tanaka, H.; Tomikura, Y.; Ando, F.; Matsuura, T.; Igawa, G.; Matsubara, K.; Yamamoto, Y.; et al. Exessive Purine Degradation during Semi-Ischemic Forearm Test in Patients with Diabetes Mellitus. Intern. Med. 2003, 42, 788–792. DOI: 10.2169/internalmedicine.42.788.
  • Lee, J. H.; Choi, H. J.; Lee, B. H.; Kang, H. K.; Chin, H. J.; Yoon, H. J.; Ha, I. S.; Kim, S.; Choi, Y.; Cheong, H. I. Prevalence of Hypouricaemia and SLC22A12 Mutations in Healthy Korean Subjects. Nephrology 2008, 13, 661–666. DOI: 10.1111/j.1440-1797.2008.01029.x.
  • Stiburkova, B.; Gabrikova, D.; Čepek, P.; Šimek, P.; Kristian, P.; Cordoba-Lanus, E.; Claverie-Martin, F. Prevalence of URAT1 Allelic Variants in the Roma Population. Nucleosides Nucleotides Nucleic Acids 2016, 35, 529–535. DOI: 10.1080/15257770.2016.1168839.

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