Treatment of Chylothorax complicating pulmonary resection with hypertonic glucose Pleurodesis

di Zhang, Kejian, Li, Changyuan, Zhang, Mingrui, Li, Yang
Pubblicato in J Cardiothorac Surg (2021)

X-linked lymphoproliferative syndromes: brothers or distant cousins?

di Filipovich, Alexandra H., Zhang, Kejian, Snow, Andrew L., Marsh, Rebecca A.
Pubblicazione 2010

Next generation sequencing technologies in medical genetics

di Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Pubblicazione 2013

Personalizing Drug Selection Using Advanced Clinical Decision Support

di Pestian, John, Spencer, Malik, Matykiewicz, Pawel, Zhang, Kejian, Vinks, Sander, Glauser, Tracy
Pubblicazione 2009

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

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

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

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

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

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

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

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

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

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

Analysis of gene mutations in children with cholestasis of undefined etiology

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Hereditary xerocytosis: Diagnostic considerations

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

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

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