Katryn N. Furuya, M.D.

  1. Pediatric Gastroenterologist
  2. Pediatric Transplant Hepatologist
  3. Pediatrician

Publications

  1. Williams KB, Brigatti KW, Puffenberger EG, Gonzaga-Jauregui C, Griffin LB, Martinez ED, Wenger OK, Yoder MA, Kandula VVR, Fox MD, Demczko MM, Poskitt L, Furuya KN, Reid JG, Overton JD, Baras A, Miles L, Radhakrishnan K, Carson VJ, Antonellis A, Jinks RN, Strauss KA. Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease. Hum Mol Genet. 2019 Feb 15; 28 (4):525-538
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  2. Timothy LD, Lehrke HD, Chandan VS, Kolbe AB, Furuya KN. Diffuse Adenomatosis and Hepatocellular Carcinoma Treated with Liver Transplantation in an Adolescent Female with Kabuki Syndrome with a Novel KMT2D Gene Mutation. Case Rep Pediatr. 2019; 2019:7983824 Epub 2019 Apr 24
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  3. Deneau MR, Mack C, Abdou R, Amin M, Amir A, Auth M, Bazerbachi F, Marie Broderick A, Chan A, DiGuglielmo M, El-Matary W, El-Youssef M, Ferrari F, Furuya KN, Gottrand F, Gupta N, Homan M, Jensen MK, Kamath BM, Mo Kim K, Kolho KL, Konidari A, Koot B, Iorio R, Martinez M, Mohan P, Palle S, Papadopoulou A, Ricciuto A, Saubermann L, Sathya P, Shteyer E, Smolka V, Tanaka A, Valentino PL, Varier R, Venkat V, Vitola B, Vos MB, Woynarowski M, Yap J, Miloh T. Gamma Glutamyltransferase Reduction Is Associated With Favorable Outcomes in Pediatric Primary Sclerosing Cholangitis. Hepatol Commun. 2018 Nov; 2 (11):1369-1378 Epub 2018 Sept 25
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  4. Lurz E, Quammie C, Englesbe M, Alonso EM, Lin HC, Hsu EK, Furuya KN, Gupta NA, Venkat VL, Daniel JF, Leonis MA, Miloh T, Telega GW, Yap J, Menendez J, Book LS, Himes RW, Sundaram SS, Parekh R, Sonnenday C, Bucuvalas J, Ng VL, Kamath BM. Frailty in Children with Liver Disease: A Prospective Multicenter Study. J Pediatr. 2018 Mar; 194:109-115.e4
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  5. Deneau MR, El-Matary W, Valentino PL, Abdou R, Alqoaer K, Amin M, Amir AZ, Auth M, Bazerbachi F, Broderick A, Chan A, Cotter J, Doan S, El-Youssef M, Ferrari F, Furuya KN, Gottrand M, Gottrand F, Gupta N, Homan M, Kamath BM, Kim KM, Kolho KL, Konidari A, Koot B, Iorio R, Ledder O, Mack C, Martinez M, Miloh T, Mohan P, O'Cathain N, Papadopoulou A, Ricciuto A, Saubermann L, Sathya P, Shteyer E, Smolka V, Tanaka A, Varier R, Venkat V, Vitola B, Vos MB, Woynarowski M, Yap J, Jensen MK. The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration. Hepatology. 2017 Aug; 66 (2):518-527 Epub 2017 June 26
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  6. Mouzaki M, Bass LM, Sokol RJ, Piccoli DA, Quammie C, Loomes KM, Heubi JE, Hertel PM, Scheenstra R, Furuya K, Kutsch E, Spinner NB, Robbins KN, Venkat V, Rosenthal P, Beyene J, Baker A, Kamath BM. Early life predictive markers of liver disease outcome in an International, Multicentre Cohort of children with Alagille syndrome. Liver Int. 2016 May; 36: (5)755-60.
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  7. Uppal V, Mansoor S, Furuya KN. Pediatric Non-alcoholic Fatty Liver Disease. Curr Gastroenterol Rep. 2016 May; 18: (5)24.
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  8. Burton BK, Balwani M, Feillet F, Baric I, Burrow TA, Camarena Grande C, Coker M, Consuelo-Sanchez A, Deegan P, Di Rocco M, Enns GM, Erbe R, Ezgu F, Ficicioglu C, Furuya KN, Kane J, Laukaitis C, Mengel E, Neilan EG, Nightingale S, Peters H, Scarpa M, Schwab KO, Smolka V, Valayannopoulos V, Wood M, Goodman Z, Yang Y, Eckert S, Rojas-Caro S, Quinn AG. A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency. N Engl J Med. 2015 Sep 10; 373: (11)1010-20.
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  9. Lin P, Raikar S, Jimenez J, Conard K, Furuya KN. Novel mutation in a patient with cholesterol ester storage disease. Case Rep Genet. 2015; 2015:347342.
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  10. Alonso EM, Ng VL, Anand R, Anderson CD, Ekong UD, Fredericks EM, Furuya KN, Gupta NA, Lerret SM, Sundaram S, Tiao G, Studies of Pediatric Liver Transplantation (SPLIT) Research Group. The SPLIT research agenda 2013. Pediatr Transplant. 2013 Aug; 17: (5)412-22.
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  11. Kutsch E, Kreiger P, Consolini D, Furuya KN. Colonic perforation after rituximab treatment for posttransplant lymphoproliferative disorder. J Pediatr Gastroenterol Nutr. 2013 Jun; 56: (6)e41.
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  12. Brennan SO, Davis RL, Conard K, Savo A, Furuya KN. Novel fibrinogen mutation gamma314Thr-->Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia. Liver Int. 2010 Nov; 30: (10)1541-7.
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  13. Mouzaki M, Nichter C, Qureshi M, Rountree B, Furuya KN. Idiopathic intracranial hypertension in two patients with Alagille syndrome. J Child Neurol. 2010 Aug; 25: (8)1006-8.
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  14. Mager DR, McGee PL, Furuya KN, Roberts EA. Prevalence of vitamin K deficiency in children with mild to moderate chronic liver disease. J Pediatr Gastroenterol Nutr. 2006 Jan; 42: (1)71-6.
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  15. Stormon MO, Cutz E, Furuya K, Bedford M, Yerkes L, Tolan DR, Feigenbaum A. A six-month-old infant with liver steatosis. J Pediatr. 2004 Feb; 144: (2)258-63.
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  16. Chen L, Goryachev A, Sun J, Kim P, Zhang H, Phillips MJ, Macgregor P, Lebel S, Edwards AM, Cao Q, Furuya KN. Altered expression of genes involved in hepatic morphogenesis and fibrogenesis are identified by cDNA microarray analysis in biliary atresia. Hepatology. 2003 Sep; 38: (3)567-76.
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  17. Lebel S, Nakamachi Y, Hemming A, Verjee Z, Phillips MJ, Furuya KN. Glycine conjugation of para-aminobenzoic acid (PABA): a pilot study of a novel prognostic test in acute liver failure in children. J Pediatr Gastroenterol Nutr. 2003 Jan; 36: (1)62-71.
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  18. Yasuda K, Lan LB, Sanglard D, Furuya K, Schuetz JD, Schuetz EG. Interaction of cytochrome P450 3A inhibitors with P-glycoprotein. J Pharmacol Exp Ther. 2002 Oct; 303: (1)323-32.
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  19. Stormon M, Friedman J, King S, Cutz E, Furuya KN. An unusual case of diarrhea in schimke immuno-osseous dysplasia. J Pediatr Gastroenterol Nutr. 2002 Sep; 35: (3)369-71.
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  20. Emadi-Konjin HP, Zhang H, Anandan V, Sun D, Schuetz J, Furuya KN. Isolation of a genomic clone containing the promoter region of the human ATP binding cassette (ABC) transporter, ABCB6. Biochim Biophys Acta. 2002 Mar 19; 1574: (2)117-30.
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  21. Gordon MM, Silverman ED, Kim JH, Huber AM, Furuya K. Acute severe hepatitis with coagulopathy: An unusual presentation of Kawasaki syndrome in association with Epstein-Barr virus. Paediatr Child Health. 2001 Nov; 6: (9)627-30.
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  22. Hemming AW, Gallinger S, Greig PD, Cattral MS, Langer B, Taylor BR, Verjee Z, Giesbrecht E, Nakamachi Y, Furuya KN. The hippurate ratio as an indicator of functional hepatic reserve for resection of hepatocellular carcinoma in cirrhotic patients. J Gastrointest Surg. 2001 May-Jun; 5 (3):316-21
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  23. Furuya KN, Bradley G, Sun D, Schuetz EG, Schuetz JD. Identification of a new P-glycoprotein-like ATP-binding cassette transporter gene that is overexpressed during hepatocarcinogenesis. Cancer Res. 1997 Sep 01; 57 (17):3708-16
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  24. Furuya KN, Thottassery JV, Schuetz EG, Sharif M, Schuetz JD. Bromocriptine transcriptionally activates the multidrug resistance gene (pgp2/mdr1b) by a novel pathway. J Biol Chem. 1997 Apr 25; 272 (17):11518-25
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  25. Schuetz EG, Furuya KN, Schuetz JD. Interindividual variation in expression of P-glycoprotein in normal human liver and secondary hepatic neoplasms. J Pharmacol Exp Ther. 1995 Nov; 275 (2):1011-8
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  26. Furuya KN, Durie PR, Roberts EA, Soldin SJ, Verjee Z, Yung-Jato L, Giesbrecht E, Ellis L. Glycine conjugation of para-aminobenzoic acid (PABA): a quantitative test of liver function. Clin Biochem. 1995 Oct; 28 (5):531-40
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  27. Schuetz JD, Silverman JA, Thottassery JV, Furuya KN, Schuetz EG. Divergent regulation of the class II P-glycoprotein gene in primary cultures of hepatocytes versus H35 hepatoma by glucocorticoids. Cell Growth Differ. 1995 Oct; 6 (10):1321-32
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  28. Furuya KN, Gebhardt R, Schuetz EG, Schuetz JD. Isolation of rat pgp3 cDNA: evidence for gender and zonal regulation of expression in the liver. Biochim Biophys Acta. 1994 Nov 22; 1219 (3):636-44
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  29. Roberts EA, Furuya KN, Tang BK, Kalow W. Caffeine biotransformation in human hepatocyte lines derived from normal liver tissue. Biochem Biophys Res Commun. 1994 Jun 15; 201 (2):559-66
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  30. Furuya KN, Burrows PE, Phillips MJ, Roberts EA. Transjugular liver biopsy in children. Hepatology. 1992 Jun; 15: (6)1036-42.
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  31. Furuya KN, Roberts EA, Canny GJ, Phillips MJ. Neonatal hepatitis syndrome with paucity of interlobular bile ducts in cystic fibrosis. J Pediatr Gastroenterol Nutr. 1991 Jan; 12: (1)127-30.
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PST-20308451