Items where Creator is "Walker, Claire"

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Number of items: 11.

Article

Hong, Ying, Capitani, Melania, Walker, Claire, Pandey, Sumeet, Cavounidis, Athena, Takeshita, Haruo, Nanthapisal, Sira, Yasuda, Toshihiro, Bader-Meunier, Brigitte, McCreary, Dara, Omoyinmi, Ebun, Rao, Anupama, Booth, Claire, Gilmour, Kimberly, Sebire, Neil, Shah, Neil, Klein, Nigel, Bullock, Alex N., Eleftheriou, Despina, Uhlig, Holm H. and Brogan, Paul (2020) Janus kinase inhibition for autoinflammation in patients with DNASE2 deficiency. Journal of Allergy and Clinical Immunology, 145 (2). 701-705.e8.

Wang, Junwen, Omoyinmi, Ebun, Standing, Ariane, Keylock, Annette, Price-Kuehne, Fiona, Melo Gomes, Sonia, Rowczenio, Dorota, Nanthapisal, Sira, Cullup, Thomas, Nyanhete, Rodney, Ashton, Emma, Walker, Claire, Clarke, Megan, Ahlfors, Helena, Jenkins, Lucy, Gilmour, Kimberly, Eleftheriou, Despina, Lachmann, Helen J., Hawkins, Philip N., Klein, Nigel and Brogan, Paul A. (2017) Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis. PLOS ONE, 12 (7). e0181874.

Nanthapisal, Sira, Walker, Claire, Omoyinmi, Ebun, Hong, Ying, Standing, Ariane, Berg, Stefan, Ekelund, Maria, Jolles, Stephen, Harper, Lorraine, Youngstein, Taryn, Gilmour, Kimberly, Klein, Nigel J., Eleftheriou, Despina and Brogan, Paul A. (2016) Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases. Arthritis & Rheumatology, 68 (9). pp. 2314-2322.

Nanthapisal, Sira, Walker, Claire, Omoyinmi, Ebun, Hong, Ying, Standing, Ariane, Berg, Stefan, Ekelund, Maria, Jolles, Stephen, Harper, Lorraine, Youngstein, Taryn, Gilmour, Kimberly, Klein, Nigel J., Eleftheriou, Despina and Brogan, Paul A. (2016) Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases. Arthritis & Rheumatology, 68 (9). pp. 2314-2322.

Nanthapisal, Sira, Omoyinmi, Ebun, Walker, Claire, Standing, Ariane, Eisenhut, Michael, Eleftheriou, Despina and Brogan, Paul A. (2016) Early-Onset Juvenile SLE Associated With a Novel Mutation in Protein Kinase C δ. Pediatrics, 139 (1). e20160781.

Walker, Claire, Nanthapisal, Sira, Gilmour, Kimberly, Laurent, Sue, D'Arco, Felice, Hemingway, Cheryl, Brogan, Paul and Eleftheriou, Despina (2016) Progressive neurologic disorder: Initial manifestation of hemophagocytic lymphohistiocytosis. Neurology, 86 (22). pp. 2109-2111.

Walker, Claire, Nanthapisal, Sira, Gilmour, Kimberly, Laurent, Sue, D'Arco, Felice, Hemingway, Cheryl, Brogan, Paul and Eleftheriou, Despina (2016) Progressive neurologic disorder: Initial manifestation of hemophagocytic lymphohistiocytosis. Neurology, 86 (22). pp. 2109-2111.

Gomes, Sonia Melo, Arostegui, Joan, Omonyinmi, Ebun, Gonzalez-Roca, Eva, Standing, Ariane, Rowczenio, Dorota, Nathanpisal, Sira, Walker, Claire, Elephteriou, Despina, Klein, Nigel, Hawkins, Philip, Lachmann, Helen and Brogan, Paul (2014) The role of somatic NLRP3 mosaicism and new gene discovery in mutation negative cryopyrin-associated periodic syndrome patients. Pediatric Rheumatology, 12 (S1).

De Benedetti, F., Anton, J., Gattorno, M., Lachmann, H., Kone-Paut, I., Ozen, S., Frenkel, J., ...., , Walker, Claire and et al., Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one.

Conference or Workshop contribution

Walker, Claire (2018) Gene-edited allogeneic CAR19 T cells (UCART19) induce molecular remission ahead of allo-SCT in high risk pediatric patients with CD19+ relapsed/refractory B-cell acute lymphoblastic leukemia. In: Bone Marrow Transplantation.

Walker, Claire (2017) Preliminary Results of UCART19, an Allogeneic Anti-CD19 CAR T-Cell Product in a First-in-Human Trial (PALL) in Pediatric Patients with CD19+ Relapsed/Refractory B-Cell Acute Lymphoblastic Leukemia. In: UNSPECIFIED.

This list was generated on Wed Feb 24 14:43:46 2021 GMT.