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Nicholas C P Cross

Showing results (41-50 of 221) with videos related to

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European Journal of Haematology|June 25, 2026
Adapting UK Clinical Practise in Chronic Myeloid Leukaemia in Chronic Phase to Contemporary Management Recommendations: The ADAPT 2.0 SurveyDragana Milojkovic, Nicholas C P Cross, Ketul Desai, et al.
American Journal of Hematology|July 7, 2015
Neutrophilic leukemoid reaction in multiple myelomaDragana Milojkovic, Ann Hunter, Linda Barton, et al.
Pediatric Blood & Cancer|November 23, 2011
Favorable outcome of allogeneic hematopoietic cell transplantation for 8p11 myeloproliferative syndrome associated with BCR-FGFR1 gene fusionMichelle Dolan, Adina Cioc, Nicholas C P Cross, et al.
Clinical Chemistry|April 1, 2006
Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndromeHelen E White, Victoria J Durston, John F Harvey, et al.
Acta Haematologica|September 13, 2021
Chronic Eosinophilic Leukaemia Associated with JAK2 Exon 13 Insertion/Deletion MutationsNicholas Lafferty, Matthew Salmon, Nicholas C P Cross, et al.
British Journal of Haematology|August 19, 2021
The use of genetic tests to diagnose and manage patients with myeloproliferative and myeloproliferative/myelodysplastic neoplasms, and related disordersNicholas C P Cross, Anna L Godfrey, Catherine Cargo, et al.
Leukemia|August 20, 2021
Clonal myelopoiesis promotes adverse outcomes in chronic kidney diseaseAhmed A Z Dawoud, Rodney D Gilbert, William J Tapper, et al.
Cell Cycle (Georgetown, Tex.)|January 12, 2011
Impact of BCR-ABL mutations on patients with chronic myeloid leukemiaAndreas Hochhaus, Paul La Rosée, Martin C Müller, et al.
British Journal of Haematology|March 16, 2017
Measurement of BCR-ABL1 by RT-qPCR in chronic myeloid leukaemia: findings from an International EQA ProgrammeStuart Scott, Debbie Travis, Liam Whitby, et al.
Journal of Pediatric Hematology/Oncology|December 14, 2005
Idiopathic hypereosinophilic syndrome in children: report of a 7-year-old boy with FIP1L1-PDGFRA rearrangementSusana Rives, Iñaki Alcorta, Teresa Toll, et al.
Pageof 23

Showing results (41-50 of 221) with videos related to

Sort By:
Pageof 23
European Journal of Haematology|June 25, 2026
Adapting UK Clinical Practise in Chronic Myeloid Leukaemia in Chronic Phase to Contemporary Management Recommendations: The ADAPT 2.0 SurveyDragana Milojkovic, Nicholas C P Cross, Ketul Desai, et al.
American Journal of Hematology|July 7, 2015
Neutrophilic leukemoid reaction in multiple myelomaDragana Milojkovic, Ann Hunter, Linda Barton, et al.
Pediatric Blood & Cancer|November 23, 2011
Favorable outcome of allogeneic hematopoietic cell transplantation for 8p11 myeloproliferative syndrome associated with BCR-FGFR1 gene fusionMichelle Dolan, Adina Cioc, Nicholas C P Cross, et al.
Clinical Chemistry|April 1, 2006
Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndromeHelen E White, Victoria J Durston, John F Harvey, et al.
Acta Haematologica|September 13, 2021
Chronic Eosinophilic Leukaemia Associated with JAK2 Exon 13 Insertion/Deletion MutationsNicholas Lafferty, Matthew Salmon, Nicholas C P Cross, et al.
British Journal of Haematology|August 19, 2021
The use of genetic tests to diagnose and manage patients with myeloproliferative and myeloproliferative/myelodysplastic neoplasms, and related disordersNicholas C P Cross, Anna L Godfrey, Catherine Cargo, et al.
Leukemia|August 20, 2021
Clonal myelopoiesis promotes adverse outcomes in chronic kidney diseaseAhmed A Z Dawoud, Rodney D Gilbert, William J Tapper, et al.
Cell Cycle (Georgetown, Tex.)|January 12, 2011
Impact of BCR-ABL mutations on patients with chronic myeloid leukemiaAndreas Hochhaus, Paul La Rosée, Martin C Müller, et al.
British Journal of Haematology|March 16, 2017
Measurement of BCR-ABL1 by RT-qPCR in chronic myeloid leukaemia: findings from an International EQA ProgrammeStuart Scott, Debbie Travis, Liam Whitby, et al.
Journal of Pediatric Hematology/Oncology|December 14, 2005
Idiopathic hypereosinophilic syndrome in children: report of a 7-year-old boy with FIP1L1-PDGFRA rearrangementSusana Rives, Iñaki Alcorta, Teresa Toll, et al.
Pageof 23