Results 271 to 280 of about 683,747 (361)

Classical and Late‐Onset SOS/VOD After Allogeneic HSCT: A Japanese Transplant Registry Analysis

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Sinusoidal obstruction syndrome/veno‐occlusive disease (SOS/VOD) is a lethal complication of allogeneic hematopoietic stem cell transplantation (allo‐HSCT). According to the 2016 European Society for Blood and Marrow Transplantation criteria, SOS/VOD is classified into classical SOS/VOD and late‐onset SOS/VOD, but their similarities and ...
Kyoko Masuda   +20 more
wiley   +1 more source

The RAAS system SNPs polymorphism is associated with essential hypertension risk in rural areas in northern China. [PDF]

open access: yesInt J Med Sci
Cheng J   +12 more
europepmc   +1 more source

Applying the NIOSH Worker Well‐Being Framework to Migrant and Seasonal Farmworkers: Insights From the Literature

open access: yesAmerican Journal of Industrial Medicine, EarlyView.
ABSTRACT Background There is a growing appreciation of the importance of health and well‐being and of the complex set of factors, within and outside the workplace, that interact to affect the well‐being of workers. Migrant and seasonal farmworkers experience particular challenges, and measurement of factors that influence their health and well‐being is
Tessa Bonney   +3 more
wiley   +1 more source

Postnatal Progressive Craniosynostosis: An Unusual Case Presentation Leading to Cascade Diagnosis for Multiple Generations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT NM_000141.5: FGFR2 c.1032G>A is a pathogenic variant that causes Crouzon syndrome through activation of a new donor splice site. This clinical report highlights the intrafamilial variability that can exist with this specific variant. The proband is a 4‐year‐old boy who initially presented with concern for seizures.
Jessica T. Ogawa   +3 more
wiley   +1 more source

A New EP300‐Related Syndrome With Prominent Developmental and Immune Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rubinstein Taybi syndrome (RTS) is a disorder of chromatin remodeling and transcriptional regulation caused by heterozygous pathogenic variants in CREBBP and EP300. RTS is characterized by a distinct facial gestalt, intellectual disability, structural kidney and heart differences, feeding difficulties, and broad thumbs and great toes ...
Devi Priyanka Maripuri   +3 more
wiley   +1 more source

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