scispace - formally typeset
J

Johan Aschan

Researcher at Janssen-Cilag

Publications -  81
Citations -  5207

Johan Aschan is an academic researcher from Janssen-Cilag. The author has contributed to research in topics: Transplantation & Hematopoietic stem cell transplantation. The author has an hindex of 38, co-authored 80 publications receiving 5055 citations. Previous affiliations of Johan Aschan include Karolinska University Hospital & Sahlgrenska University Hospital.

Papers
More filters
Journal ArticleDOI

Mesenchymal stem cells for treatment of therapy-resistant graft-versus-host disease.

TL;DR: MSC is a very promising treatment for severe steroid-resistant acute GVHD and five patients are still alive between 2 months and 3 years after the transplantation and their survival rate was significantly better than that of 16 patients with steroid- resistant biopsy-proven gastrointestinal GV HD, not treated with MSC during the same period.
Journal ArticleDOI

Risk factors for chronic graft-versus-host disease after bone marrow transplantation: a retrospective single centre analysis.

TL;DR: Among 551 consecutive recipients of allogeneic bone marrow transplants, 451 survived more than 3 months and were evaluated for chronic graft-versus-host disease (GVHD), and high recipient age was the single most important risk factor (P < 0.001).
Journal Article

Similar incidence of graft-versus-host disease using HLA-A, -B and -DR identical unrelated bone marrow donors as with HLA-identical siblings.

TL;DR: Among 42 consecutive recipients of unrelated marrow were 39 HLA-A, -B, -DR identical, matched unrelated donors (MUD) and three with one HLA antigen mismatch, which included 24 patients with hematological malignancies, 6 with severe aplastic anemia and 9 inherited disorders.
Journal ArticleDOI

Results of different strategies for reducing cytomegalovirus-associated mortality in allogeneic stem cell transplant recipients.

TL;DR: Preemptive therapy based on polymerase chain reaction for CMV DNA was associated with reduced risks forCMV disease, CMV-associated death, and TRM, whereas other prophylactic modalities did not give additional benefit.
Journal ArticleDOI

Pharmacokinetics of high-dose busulphan in relation to age and chronopharmacology.

TL;DR: It is concluded that the busulphan dosage for children must be reconsidered and that further studies are urgently needed to develop an optimal therapy.