Results 251 to 260 of about 3,441,901 (408)
Single-platelet nanomechanics measured by high-throughput cytometry [PDF]
Ahn, B.+20 more
core +2 more sources
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
Barbara A. Steficek+3 more
openalex +1 more source
Assessment of platelet activation in myeloproliferative disorders with complementary techniques [PDF]
Emilsé Bermejo+3 more
openalex +1 more source
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]
Mohamed Kaleelrahman+2 more
openalex +1 more source
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]
Yu K+15 more
europepmc +1 more source