Results 251 to 260 of about 3,441,901 (408)

Single-platelet nanomechanics measured by high-throughput cytometry [PDF]

open access: yes, 2016
Ahn, B.   +20 more
core   +2 more sources

Clinical Impact of Graft Cryopreservation on Allogeneic Stem Cell Transplantation: An Italian, Registry‐Based Study on Behalf of the “Gruppo Italiano Per Il Trapianto di Midollo Osseo, Cellule Staminali Emopoietiche e Terapia Cellulare” (GITMO)

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT The coronavirus disease 2019 (COVID‐19) pandemic created major challenges for allogeneic hematopoietic stem cell transplantation (allo‐HSCT). Scientific societies and authorities recommended cryopreserving grafts before starting conditioning regimens, despite limited data on the clinical impact.
Irene Defrancesco   +52 more
wiley   +1 more source

Hemorrhagic Diathesis Associated with a Hereditary Platelet Disorder in Simmental Cattle

open access: bronze, 1993
Barbara A. Steficek   +3 more
openalex   +1 more source

Assessment of platelet activation in myeloproliferative disorders with complementary techniques [PDF]

open access: green, 2004
Emilsé Bermejo   +3 more
openalex   +1 more source

Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 7, July 2025.
ABSTRACT Hereditary multiple osteochondromas (HMO) is an autosomal dominant disorder caused by heterozygous deleterious variants in the EXT1 or EXT2 genes. While the clinical core phenotype is well established and mainly consists of bone deformities, limb length discrepancies, multiple benign bone neoplasms, and increased risk of chondrosarcoma, the ...
Francesco Comisi   +7 more
wiley   +1 more source

Use of recombinant factor VIIa in inherited platelet disorders [PDF]

open access: bronze, 2004
Mohamed Kaleelrahman   +2 more
openalex   +1 more source

Case Report: Unusual Neurological Features of Leigh Syndrome due to m.8993T>G Pathogenic Variant in the MT‐ATP6 Gene

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The MT‐ATP6 gene m.8993T>G pathogenic variant has been associated with Leigh syndrome, especially in patients exhibiting a high degree of heteroplasmy. Although patients may present with a wide phenotypic spectrum, characteristic findings include bilateral, symmetric hyperintensities in the basal ganglia and brainstem on brain MRI ...
Ramya Treitel   +2 more
wiley   +1 more source

Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy. [PDF]

open access: yesBlood Adv
Yu K   +15 more
europepmc   +1 more source

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