Výsledky vyhledávání - "Humphrey W H, Pullon"

Inhibition of C3 with pegcetacoplan results in normalization of hemolysis markers in paroxysmal nocturnal hemoglobinuria

Autor: Raymond S M, Wong, Humphrey W H, Pullon, Ismail, Amine, Andrija, Bogdanovic, Pascal, Deschatelets, Cedric G, Francois, Kalina, Ignatova, Surapol, Issaragrisil, Pimjai, Niparuck, Tontanai, Numbenjapon, Eloy, Roman, Jameela, Sathar, Raymond, Xu, Mohammed, Al-Adhami, Lisa, Tan, Eric, Tse, Federico V, Grossi

Publikováno v: Annals of Hematology. 101:1971-1986

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hematologic disorder characterized by complement-mediated hemolysis. C5 inhibitors (eculizumab/ravulizumab) control intravascular hemolysis but do not prevent residual extravascular hemoly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3bf846b1cc5dce676c8a819f23bd2e2
https://doi.org/10.1007/s00277-022-04903-x

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Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal

Autor: Rong Guo, Ana Raimundo, A. J. Bellingham, Humphrey W. H. Pullon, A. Gorchein, Chang Kee Lim

Publikováno v: Biomedical Chromatography. 12:350-356

Congenital erythropoietic porphyria is a rare genetic disorder in which deficiency of uroporphyrinogen III synthase results in excessive production of Type I porphyrins. The main clinical features are severe photodestruction of the skin and haemolyti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8e7d2997307ad6a8f32dcdd96ceafb8e
https://doi.org/10.1002/(sici)1099-0801(199811/12)12:6<350::aid-bmc761>3.0.co

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