Treatment of Chylothorax complicating pulmonary resection with hypertonic glucose Pleurodesis

od Zhang, Kejian, Li, Changyuan, Zhang, Mingrui, Li, Yang
izdano v J Cardiothorac Surg (2021)

X-linked lymphoproliferative syndromes: brothers or distant cousins?

od Filipovich, Alexandra H., Zhang, Kejian, Snow, Andrew L., Marsh, Rebecca A.
Izdano 2010

Next generation sequencing technologies in medical genetics

od Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Izdano 2013

Personalizing Drug Selection Using Advanced Clinical Decision Support

od Pestian, John, Spencer, Malik, Matykiewicz, Pawel, Zhang, Kejian, Vinks, Sander, Glauser, Tracy
Izdano 2009

Mediastinal small cell cancer associated with Lambert-Eaton myasthenic syndrome: A case report

od ZHANG, KEJIAN, LIU, WEI, LI, YANG, ZHANG, KEWEI, GAO, XINLIANG, WANG, JING
izdano v Exp Ther Med (2015)

LINC00210 plays oncogenic roles in non-small cell lung cancer by sponging microRNA-328-5p

od Liu, Zhengjia, Xu, Lei, Zhang, Kejian, Guo, Bo, Cui, Zhi, Gao, Nan
izdano v Exp Ther Med (2020)

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

od Lindsley, Andrew W., Qian, Yaping, Valencia, C. Alexander, Shah, Kara, Zhang, Kejian, Assa’ad, Amal
izdano v J Clin Immunol (2014)

Novel Mutation in Syntaxin-Binding Protein 2 (STXBP2) Prevents IL-2-induced Natural Killer Cell Cytotoxicity

od Saltzman, Rushani W., Monaco-Shawver, Linda, Zhang, Kejian, Sullivan, Kathleen E., Filipovich, Alexandra H., Orange, Jordan S.
Izdano 2012

Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH

od Rubin, Tamar S., Zhang, Kejian, Gifford, Carrie, Lane, Adam, Choo, Sharon, Bleesing, Jack J., Marsh, Rebecca A.
izdano v Blood (2017)

Analysis of gene mutations in children with cholestasis of undefined etiology

od Matte, Ursula, Mourya, Reena, Miethke, Alexander, Liu, Cong, Kauffmann, Gregory, Moyer, Katie, Zhang, Kejian, Bezerra, Jorge A.
Izdano 2010

Genetics of pain perception, COMT and postoperative pain management in children

od Sadhasivam, Senthilkumar, Chidambaran, Vidya, Olbrecht, Vanessa A, Esslinger, Hope R, Zhang, Kejian, Zhang, Xue, Martin, Lisa J
Izdano 2014

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

od Sumegi, Janos, Nestheide, Shawnagay V., Barnes, Michael G., Villanueva, Joyce, Zhang, Kejian, Grom, Alexei A., Filipovich, Alexandra H.
Izdano 2013

Novel UNC13D intronic variant disrupting a NFκB enhancer in a patient with recurrent macrophage activation syndrome and systemic juvenile idiopathic arthritis

od Schulert, Grant S., Zhang, Mingce, Husami, Ammar, Fall, Ndate, Brunner, Hermine, Zhang, Kejian, Cron, Randy Q., Grom, Alexei A.
izdano v Arthritis Rheumatol (2018)

Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis

od Zhang, Kejian, Chandrakasan, Shanmuganathan, Chapman, Heather, Valencia, C. Alexander, Husami, Ammar, Kissell, Diane, Johnson, Judith A., Filipovich, Alexandra H.
Izdano 2014

Accuracy of flow cytometric perforin screening for detecting patients with FHL due to PRF1 mutations

od Abdalgani, Manar, Filipovich, Alexandra H., Choo, Sharon, Zhang, Kejian, Gifford, Carrie, Villanueva, Joyce, Bleesing, Jack J., Marsh, Rebecca A.
izdano v Blood (2015)

Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders

od Gadoury-Levesque, Vanessa, Dong, Lei, Su, Rui, Chen, Jianjun, Zhang, Kejian, Risma, Kimberly A., Marsh, Rebecca A., Sun, Miao
izdano v Blood Adv (2020)

Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis

od Goldschmidt, Monique L., Mourya, Reena, Connor, Jessica, Dexheimer, Phillip, Karns, Rebekah, Miethke, Alexander, Sheridan, Rachel, Zhang, Kejian, Bezerra, Jorge A.
izdano v Hepatol Res (2015)

Elevated Granzyme B in Cytotoxic Lymphocytes is a Signature of Immune Activation in Hemophagocytic Lymphohistiocytosis

od Mellor-Heineke, Sabine, Villanueva, Joyce, Jordan, Michael B., Marsh, Rebecca, Zhang, Kejian, Bleesing, Jack J., Filipovich, Alexandra H., Risma, Kimberly A.
Izdano 2013

Hereditary xerocytosis: Diagnostic considerations

od Risinger, Mary, Glogowska, Edyta, Chonat, Satheesh, Zhang, Kejian, Dagaonkar, Neha, Joiner, Clinton H., Quinn, Charles T., Kalfa, Theodosia A., Gallagher, Patrick G.
izdano v Am J Hematol (2017)

Macrophage Activation Syndrome in Systemic Juvenile Idiopathic Arthritis is Associated With MUNC13-4 Gene Polymorphisms

od Zhang, Kejian, Biroschak, Jennifer, Glass, David N., Thompson, Susan, Finkel, Terri, Passo, Murray H., Binstadt, Bryce A., Filipovich, Alexandra, Grom, Alexei A.
Izdano 2008