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Indications for haematopoietic stem cell transplantation for haematological diseases, solid tumours and immune disorders: current practice in Europe, 2019
This is the seventh special EBMT report on the indications for haematopoietic stem cell
transplantation for haematological diseases, solid tumours and immune disorders. Our aim …
transplantation for haematological diseases, solid tumours and immune disorders. Our aim …
Indications for allo-and auto-SCT for haematological diseases, solid tumours and immune disorders: current practice in Europe, 2015
This is the sixth special report that the European Society for Blood and Marrow
Transplantation regularly publishes on the current practice and indications for …
Transplantation regularly publishes on the current practice and indications for …
Indications for haematopoietic cell transplantation for haematological diseases, solid tumours and immune disorders: current practice in Europe, 2022
JA Snowden, I Sánchez-Ortega… - Bone marrow …, 2022 - nature.com
For over two decades, the EBMT has updated recommendations on indications for
haematopoietic cell transplantation (HCT) practice based on clinical and scientific …
haematopoietic cell transplantation (HCT) practice based on clinical and scientific …
Bone marrow failure and the telomeropathies
DM Townsley, B Dumitriu… - Blood, The Journal of the …, 2014 - ashpublications.org
Our understanding of the pathophysiology of aplastic anemia is undergoing significant
revision, with implications for diagnosis and treatment. Constitutional and acquired disease …
revision, with implications for diagnosis and treatment. Constitutional and acquired disease …
Dyskeratosis congenita: a literature review
MM AlSabbagh - JDDG: Journal der Deutschen …, 2020 - Wiley Online Library
Dyskeratosis congenita is a rare hereditary disease that occurs predominantly in males and
manifests clinically as the classic triad of reticulate hyperpigmentation, nail dystrophy and …
manifests clinically as the classic triad of reticulate hyperpigmentation, nail dystrophy and …
The diagnosis and treatment of dyskeratosis congenita: a review
MS Fernández García… - Journal of blood …, 2014 - Taylor & Francis
Dyskeratosis congenita (DC) is an inherited bone marrow failure (BMF) syndrome
characterized by the classic triad of abnormal skin pigmentation, nail dystrophy, and oral …
characterized by the classic triad of abnormal skin pigmentation, nail dystrophy, and oral …
[HTML][HTML] Extracorporeal photopheresis in steroid-refractory acute or chronic graft-versus-host disease: results of a systematic review of prospective studies
Acute and chronic graft-versus-host disease (GVHD) remain major obstacles for successful
allogeneic hematopoietic cell transplantation. Extracorporeal photopheresis (ECP) …
allogeneic hematopoietic cell transplantation. Extracorporeal photopheresis (ECP) …
[HTML][HTML] Outcomes of allogeneic hematopoietic cell transplantation in patients with dyskeratosis congenita
SM Gadalla, C Sales-Bonfim, J Carreras… - Biology of Blood and …, 2013 - Elsevier
We describe outcomes after allogeneic transplantation in 34 patients with dyskeratosis
congenita who underwent transplantation between 1981 and 2009. The median age at …
congenita who underwent transplantation between 1981 and 2009. The median age at …
Outcome of haematopoietic stem cell transplantation in dyskeratosis congenita
F Fioredda, S Iacobelli, ET Korthof… - British journal of …, 2018 - Wiley Online Library
Dyskeratosis congenita (DC) is a genetic multisystem disorder with frequent involvement of
the bone marrow. Haematopoietic stem cell transplantation (HSCT) is the only definitive cure …
the bone marrow. Haematopoietic stem cell transplantation (HSCT) is the only definitive cure …
Evaluation and management of hematopoietic failure in dyskeratosis congenita
S Agarwal - Hematology/Oncology Clinics, 2018 - hemonc.theclinics.com
Dyskeratosis congenita (DC) is a rare, inherited bone marrow failure (BMF) syndrome
characterized by variable manifestations and ages of onset, and predisposition to cancer …
characterized by variable manifestations and ages of onset, and predisposition to cancer …