Treatment of Chylothorax complicating pulmonary resection with hypertonic glucose Pleurodesis

door Zhang, Kejian, Li, Changyuan, Zhang, Mingrui, Li, Yang
Gepubliceerd in J Cardiothorac Surg (2021)

X-linked lymphoproliferative syndromes: brothers or distant cousins?

door Filipovich, Alexandra H., Zhang, Kejian, Snow, Andrew L., Marsh, Rebecca A.
Gepubliceerd in 2010

Next generation sequencing technologies in medical genetics

door Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Gepubliceerd in 2013

Personalizing Drug Selection Using Advanced Clinical Decision Support

door Pestian, John, Spencer, Malik, Matykiewicz, Pawel, Zhang, Kejian, Vinks, Sander, Glauser, Tracy
Gepubliceerd in 2009

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

door ZHANG, KEJIAN, LIU, WEI, LI, YANG, ZHANG, KEWEI, GAO, XINLIANG, WANG, JING
Gepubliceerd in Exp Ther Med (2015)

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

door Liu, Zhengjia, Xu, Lei, Zhang, Kejian, Guo, Bo, Cui, Zhi, Gao, Nan
Gepubliceerd in Exp Ther Med (2020)

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

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

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

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

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

door Rubin, Tamar S., Zhang, Kejian, Gifford, Carrie, Lane, Adam, Choo, Sharon, Bleesing, Jack J., Marsh, Rebecca A.
Gepubliceerd in Blood (2017)

Analysis of gene mutations in children with cholestasis of undefined etiology

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

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

door Sadhasivam, Senthilkumar, Chidambaran, Vidya, Olbrecht, Vanessa A, Esslinger, Hope R, Zhang, Kejian, Zhang, Xue, Martin, Lisa J
Gepubliceerd in 2014

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Hereditary xerocytosis: Diagnostic considerations

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

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

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