Decreased C3b receptors (CR1) on erythrocytes from patients with systemic lupus erythematosus.

E Holme, Alistair I. Fyfe, Asad Zoma, +3

PubMed

C3b ReceptorsImmunologyGenetic EpidemiologyPathologyImmune-related Gene Polymorphism +18

Progressive Encephalopathy and Complex I Deficiency Associated with Mutations in <i>MTND1</i>

Ali-Reza Moslemi, Niklas Darín, M. Tulinius, +3

Neuropediatrics

GeneticsPathologyMolecular GeneticsDisease Gene IdentificationLeigh Syndrome +16

Humoral and cellular immune responses up to 7·5 years after administration of streptokinase for acute myocardial infarction

Iain Squire, Wendy J. Lawley, Sue Fletcher, +4

European Heart Journal

Complement activation in Henoch-Schönlein purpura

Graham Smith, Joyce Davidson, David A. Hughes, +2

Pediatric Nephrology

BiologyComplement SystemAutoimmune DiseaseDisease MechanismNatural Sciences +5

IgA class anticardiolipin antibodies in cutaneous leukocytoclastic vasculitis

A. David Burden, David M. Tillman, P. Foley, +1

Journal of the American Academy of Dermatology

Autoimmune DiseaseVasculitisHematologyImmunologyPathology +5

C3b receptor (CR1) expression on the polymorphonuclear leukocytes from patients with systemic lupus erythematosus.

Alistair I. Fyfe, E Holme, Asad Zoma, +1

PubMed

ImmunologyPolymorphonuclear LeukocytesCellular PhysiologyImmune DysregulationInflammation +17

Properties of intact and univalent (Fab) antibodies raised against isolated, solubilized, mouse zonae pellucidae

R. John Aitken, E Holme, D. C. Richardson, +1

Reproduction

Measurement of complement activation products in patients with chronic rheumatic diseases

Ghazi Auda, E Holme, Julie Davidson, +3

Rheumatology International

InflammationRheumatologyComplement SystemChronic Rheumatic DiseasesRheumatoid Disorder +13

Prevention of immune precipitation by purified components of the alternative pathway.

J K Naama, E Holme, E B Hamilton, +1

PubMed

Alternative Pathway ComponentsImmune RegulationImmunologyImmunologic MechanismImmunotherapy +16

Mutation analysis of the FAH gene in Israeli patients with tyrosinemia type I

Orly Elpeleg, Avraham Shaag, E Holme, +4

Human Mutation

Tyrosinemia TypePro261leu MutationGeneticsGenetic EpidemiologyImmunology +17