Results 211 to 220 of about 298,071 (357)
Multi‐Diseases Detection with Memristive System on Chip
Advanced Intelligent Systems, EarlyView.A robust disease detection system, which is capable of the early prevention of acute myocardial infarction and the detection of liver cancer, is implemented on a memristive system‐on‐chip (SoC). A fully integrated SoC is utilized to ensure the system's portability, low latency, high accuracy, and energy efficiency for medical analysis.
Zihan Wang +7 more
wiley +1 more source
Taiwanese Journal of Obstetrics & Gynecology, 2019 Breast-feeding initiation within the first half hour after birth is one of the World Health Organization recommendations. However, in most hospitals, mother-infant contact and breast-feeding initiation are delayed due to routine mother and infant care ...
Fatemeh Zahra Karimi +3 more
doaj
Establishing breast feeding in infants with Down syndrome: the FADES cohort experience. [PDF]
BMJ Paediatr Open, 2022 Williams GM +7 more
europepmc +1 more source
TP53‐Mutated Myeloid Neoplasms: 2024 Update on Diagnosis, Risk‐Stratification, and Management
American Journal of Hematology, EarlyView.ABSTRACT Alterations in the tumor suppressor gene TP53 are common in human cancers and are associated with an aggressive nature. Approximately 8%–12% of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) harbor TP53 mutations (TP53mut) and present immense challenges due to inherent chemoresistance and poor outcomes.
Mithun Vinod Shah +2 more
wiley +1 more source
Breast Feeding Among Urban Women And Promotion
Indian Journal of Community Medicine, 1987 Breast feeding practices among 925 urban women are described. Advantage of breast-feeding in infant morbidity is highlighted. An outline is given for promotion of infant health through breast-feeding.
Kumari Sudarshan +3 more
doaj
Investigating short-stay admission to a neonatal intensive care unit as a risk factor for reduced breast feeding at discharge in infants ≥36 weeks' gestation: a retrospective cohort study. [PDF]
BMJ Open, 2023 Jones RA +7 more
europepmc +1 more source
A New EP300‐Related Syndrome With Prominent Developmental and Immune Phenotypes
American 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
Safety of breast feeding during rituximab treatment in multiple sclerosis. [PDF]
J Neurol Neurosurg Psychiatry, 2022 Rød BE +4 more
europepmc +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Prader‐Willi syndrome (PWS) is a neurodevelopmental disorder typically caused by large deletions or imprinting defects on chromosome 15q11.2, encompassing multiple genes. While the contribution of individual genes to the PWS phenotype remains unclear, previous studies suggested that isolated deletions of MAGEL2, NDN, and MKRN3, excluding the ...
Jannis Buecking +6 more
wiley +1 more source