1-8 of 8
P. Hillmen
Close
Sort by
Journal Articles

Defective Modification of Mannose Residues by Terminal Phosphoethanolamine Underlies Inherited GPI Deficiency.

A. M. Almeida, MD, P. Hillmen, MD, PhD, S. J. Richards, PhD, D. H. Crawford, PhD, A. Baker, MD, M. A. Ferguson, PhD, I. A. Roberts, MD, PhD, D. M. Layton, MD, PhD, A. Karadimitris, MD, PhD
Journal: Blood
Blood (2005) 106 (11): 128.
https://doi.org/10.1182/blood.V106.11.128.128
Published: 2005
Journal Articles

CD52 Expression Patterns in Normal and Neoplastic B-Cells: Myeloma Is an Unlikely Target for Single Agent Alemtuzumab Therapy.

A. C. Rawstron, G. Laycock-Brown, F. E. Davies, R. G. Owen, P. Hillmen, J. A. Child
Journal: Blood
Blood (2004) 104 (11): 4883.
https://doi.org/10.1182/blood.V104.11.4883.4883
Published: 2004
Journal Articles

International Standardized Approach to Molecular and Flow Cytometric Residual Disease Monitoring in CLL.

A. C. Rawstron, N. Villamor, J. L. Zehnder, P. Ghia, M. Ritgen, S. Bottcher, G. Lozanski, A. P. Mone, D. Colomer, C. Moreno, M. Geuna, P. A. Evans, M. Kneba, Y. Natkunam, S. E. Coutre, F. Caligaris-Cappio, M. J. Hallek, J. C. Byrd, E. Montserrat, P. Hillmen
Journal: Blood
Blood (2004) 104 (11): 15.
https://doi.org/10.1182/blood.V104.11.15.15
Published: 2004
Journal Articles

Both Paroxysmal Nocturnal Hemoglobinuria (PNH) Type II Cells and PNH Type III Cells Can Arise From Different Point Mutations Involving the Same Codon of the PIG-A Gene

S. Rollinson, S. Richards, D. Norfolk, K. Bibi, G. Morgan, P. Hillmen
Journal: Blood
Blood (1997) 89 (8): 3069.
https://doi.org/10.1182/blood.V89.8.3069
Published: 1997
Journal Articles

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type

K Nafa, PJ Mason, P Hillmen, L Luzzatto, M Bessler
Journal: Blood
Blood (1995) 86 (12): 4650–4655.
https://doi.org/10.1182/blood.V86.12.4650.bloodjournal86124650
Published: 1995
Journal Articles

Expression of recombinant transmembrane CD59 in paroxysmal nocturnal hemoglobinuria B cells confers resistance to human complement

RP Rother, SA Rollins, J Mennone, A Chodera, SA Fidel, M Bessler, P Hillmen, SP Squinto
Journal: Blood
Blood (1994) 84 (8): 2604–2611.
https://doi.org/10.1182/blood.V84.8.2604.2604
Published: 1994
Journal Articles

Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype

P Hillmen, M Bessler, DH Crawford, L Luzzatto
Journal: Blood
Blood (1993) 81 (1): 193–199.
https://doi.org/10.1182/blood.V81.1.193.193
Published: 1993
Journal Articles

Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuria [letter; comment]

M Bessler, P Hillmen, L Luzzatto
Journal: Blood
Blood (1992) 80 (3): 844–845.
https://doi.org/10.1182/blood.V80.3.844.844
Published: 1992