Novel Mutation in a Patient with Cholesterol Ester Storage Disease

Tekijä Lin, Patrick, Raikar, Sheela, Jimenez, Jennifer, Conard, Katrina, Furuya, Katryn N.
Julkaisussa Case Rep Genet (2015)

Acute severe hepatitis with coagulopathy: An unusual presentation of Kawasaki syndrome in association with Epstein-Barr virus

Tekijä Gordon, Michelle M, Silverman, Earl D, Kim, Jae Hong, Huber, Adam M, Furuya, Katryn
Julkaistu 2001

Diffuse Adenomatosis and Hepatocellular Carcinoma Treated with Liver Transplantation in an Adolescent Female with Kabuki Syndrome with a Novel KMT2D Gene Mutation

Tekijä Timothy, Leander D., Lehrke, Heidi D., Chandan, Vishal S., Kolbe, Amy B., Furuya, Katryn N.
Julkaisussa Case Rep Pediatr (2019)

Mesenchymal Hamartoma in Children: A Diagnostic Challenge

Tekijä Khan, Muhammad Rehan, Binkovitz, Larry A., Smyrk, Thomas C., Potter, D. Dean, Furuya, Katryn N.
Julkaisussa Case Rep Pediatr (2019)

A SIX-MONTH-OLD INFANT WITH LIVER STEATOSIS

Tekijä Stormon, Michael O., Cutz, Ernest, Furuya, Katryn, Bedford, Melanie, Yerkes, Laura, Tolan, Dean R., Feigenbaum, Annette
Julkaistu 2004

The SPLIT Research Agenda 2013

Tekijä Alonso, Estella M., Ng, Vicky L., Anand, Ravinder, Anderson, Christopher D., Ekong, Udeme D., Fredericks, Emily M., Furuya, Katryn N., Gupta, Nitika A., Lerret, Stacee, Sundaram, Shikha, Tiao, Greg
Julkaistu 2013

Early Life Predictive Markers of Liver Disease Outcome in an International, Multi-Center Cohort of Children with Alagille Syndrome

Tekijä Mouzaki, Marialena, Bass, Lee M., Sokol, Ronald J., Piccoli, David A., Quammie, Claudia, Loomes, Kathleen M., Heubi, James E., Hertel, Paula M., Scheenstra, Rene, Furuya, Katryn, Kutsch, Erika, Spinner, Nancy B., Robbins, Kristen N., Venkat, Veena, Rosenthal, Philip, Beyene, Joseph, Baker, Alastair, Kamath, Binita M.
Julkaisussa Liver Int (2015)

Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease

Tekijä Williams, Katie B, Brigatti, Karlla W, Puffenberger, Erik G, Gonzaga-Jauregui, Claudia, Griffin, Laurie B, Martinez, Erick D, Wenger, Olivia K, Yoder, Mark A, Kandula, Vinay V R, Fox, Michael D, Demczko, Matthew M, Poskitt, Laura, Furuya, Katryn N, Reid, Jeffrey G, Overton, John D, Baras, Aris, Miles, Lili, Radhakrishnan, Kadakkal, Carson, Vincent J, Antonellis, Anthony, Jinks, Robert N, Strauss, Kevin A
Julkaisussa Hum Mol Genet (2019)

Gamma Glutamyltransferase Reduction Is Associated With Favorable Outcomes in Pediatric Primary Sclerosing Cholangitis

Tekijä Deneau, Mark R., Mack, Cara, Abdou, Reham, Amin, Mansi, Amir, Achiya, Auth, Marcus, Bazerbachi, Fateh, Marie Broderick, Anne, Chan, Albert, DiGuglielmo, Matthew, El‐Matary, Wael, El‐Youssef, Mounif, Ferrari, Federica, Furuya, Katryn N., Gottrand, Frederic, Gupta, Nitika, Homan, Matjaž, Jensen, M.K., Kamath, Binita M., Mo Kim, Kyung, Kolho, Kaija‐Leena, Konidari, Anastasia, Koot, Bart, Iorio, Raffaele, Martinez, Mercedes, Mohan, Parvathi, Palle, Sirish, Papadopoulou, Alexandra, Ricciuto, Amanda, Saubermann, Lawrence, Sathya, Pushpa, Shteyer, Eyal, Smolka, Vratislav, Tanaka, Atsushi, Valentino, Pamela L., Varier, Raghu, Venkat, Veena, Vitola, Bernadette, Vos, Miriam B., Woynarowski, Marek, Yap, Jason, Miloh, Tamir
Julkaisussa Hepatol Commun (2018)