Results 141 to 150 of about 399,686 (316)

Xenogeneic Mitochondrial Transplantation Improves Selected Age‐Associated Phenotypes in Mice

open access: yesAdvanced Science, EarlyView.
Yak‐derived xenogeneic mitochondrial transplantation improves selected age‐associated phenotypes in mice, enhances mitochondrial functional readouts, and engages host mitochondrial quality‐control pathways. Broad tissue biodistribution, increased ATP production and mtDNA copy number, reduced ROS levels and dysfunctional mitochondria, improved motility ...
Wenpeng Li   +5 more
wiley   +1 more source

BODY MASS INDEX AS A PREDICTOR OF EXERCISE CAPACITY AMONG POSTPARTUM WOMEN: A CROSS-SECTIONAL STUDY

open access: yesThe Indonesian Journal of Public Health
Introduction: Maternal obesity is a major global health issue, affecting 14.6% of women in Malaysia. An abnormally higher body mass index (BMI) is associated with various health problems, including reduced exercise capacity, affecting daily activities ...
Rabiatul Adawiah Abdul Rahman   +1 more
doaj   +1 more source

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden   +2 more
wiley   +1 more source

Gastrointestinal Manifestations in Rubinstein‐Taybi Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rubinstein–Taybi syndrome is a rare genetic condition associated with a wide range of physical, cognitive, and developmental impairments, yet its gastrointestinal manifestations remain poorly characterized. Case reports and small series suggest a high prevalence of gastroesophageal reflux, constipation, dysphagia, and nutritional compromise ...
Mohamad Abi Nassif   +3 more
wiley   +1 more source

Maternal postpartum blood pressure screening at newborn visits and its impact on postpartum care utilization

open access: yesPregnancy
Background To assess the impact of a maternal cardiovascular (CV) and blood pressure (BP) screening and standardized referral protocol at newborn visits on care utilization in the first 12 weeks postpartum.
Paige M. Anderson   +9 more
doaj   +1 more source

Men’s Perinatal Mental Health in the Transition to Fatherhood [PDF]

open access: yes, 2015
While fathers have come to be more involved with their partners and infants throughout the perinatal period, recent research has shown that roughly 10% of new dads experience mental health difficulties including depression and anxiety. Unfortunately, few
Edwards, Lisa, Singley, Daniel B.
core   +1 more source

Postpartum Headaches [PDF]

open access: yesAnnals of Emergency Medicine, 2017
Michael B, Weinstock   +3 more
openaire   +2 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Postpartum emergency department visits and readmissions in the 90 days after a singleton delivery

open access: yesPregnancy
Introduction Maternal morbidity and mortality are often concentrated in the first 90 days postpartum. Postpartum emergency department (ED) and hospital use provide valuable insight into peripartum health outcomes.
Jecca R. Steinberg   +4 more
doaj   +1 more source

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi   +11 more
wiley   +1 more source

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