Treatment of Chylothorax complicating pulmonary resection with hypertonic glucose Pleurodesis

per Zhang, Kejian, Li, Changyuan, Zhang, Mingrui, Li, Yang
Publicat a J Cardiothorac Surg (2021)

X-linked lymphoproliferative syndromes: brothers or distant cousins?

per Filipovich, Alexandra H., Zhang, Kejian, Snow, Andrew L., Marsh, Rebecca A.
Publicat 2010

Next generation sequencing technologies in medical genetics

per Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Publicat 2013

Personalizing Drug Selection Using Advanced Clinical Decision Support

per Pestian, John, Spencer, Malik, Matykiewicz, Pawel, Zhang, Kejian, Vinks, Sander, Glauser, Tracy
Publicat 2009

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

per ZHANG, KEJIAN, LIU, WEI, LI, YANG, ZHANG, KEWEI, GAO, XINLIANG, WANG, JING
Publicat a Exp Ther Med (2015)

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

per Liu, Zhengjia, Xu, Lei, Zhang, Kejian, Guo, Bo, Cui, Zhi, Gao, Nan
Publicat a Exp Ther Med (2020)

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

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

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

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

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

per Rubin, Tamar S., Zhang, Kejian, Gifford, Carrie, Lane, Adam, Choo, Sharon, Bleesing, Jack J., Marsh, Rebecca A.
Publicat a Blood (2017)

Analysis of gene mutations in children with cholestasis of undefined etiology

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Hereditary xerocytosis: Diagnostic considerations

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

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

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