Results 81 to 90 of about 1,997,971 (386)

Neonatal Morbidities of Fetal Growth Restriction: Pathophysiology and Impact

open access: yesFrontiers in Endocrinology, 2019
Being born small lays the foundation for short-term and long-term implications for life. Intrauterine or fetal growth restriction describes the pregnancy complication of pathological reduced fetal growth, leading to significant perinatal mortality and ...
A. Malhotra   +5 more
semanticscholar   +1 more source

Durability of Response to B‐Cell Maturation Antigen‐Directed mRNA Cell Therapy in Myasthenia Gravis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We report the 12‐month follow‐up outcomes from a Phase 2 clinical trial (NCT04146051) evaluating Descartes‐08, a BCMA‐directed RNA chimeric antigen receptor T‐cell (rCAR‐T) therapy for refractory generalized myasthenia gravis (MG).
Nizar Chahin   +10 more
wiley   +1 more source

SCAMP:standardised, concentrated, additional macronutrients, parenteral nutrition in very preterm infants: a phase IV randomised, controlled exploratory study of macronutrient intake, growth and other aspects of neonatal care [PDF]

open access: yes, 2011
Background Infants born
A Dinerstein   +66 more
core   +3 more sources

Dysbiosis of maternal and neonatal microbiota associated with gestational diabetes mellitus

open access: yesGut, 2018
Objective The initial colonisation of the human microbiota and the impact of maternal health on neonatal microbiota at birth remain largely unknown.
Jinfeng Wang   +12 more
semanticscholar   +1 more source

Characteristics of Cerebral Palsy in the Midwestern US

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cerebral palsy (CP) is the most common lifelong motor disability worldwide. Yet, data is limited on how CP manifests in the US. Our objective was to characterize and determine factors affecting functional outcomes in a large population of young people with CP in the Midwestern US.
Susie Kim   +6 more
wiley   +1 more source

A Rare Case of Fungaemia Due to Kodamaea ohmeri in a Neonate

open access: yesOnline Journal of Health & Allied Sciences, 2023
Background: K. ohmeri is seen predominantly in cutaneous, endocarditis, fungemia and catheter-related bloodstream infections. Neonates are predisposed to systemic fungal infections due to prematurity, immunocompromised state, invasive procedures ...
Asem Ali Ashraf   +5 more
doaj  

A retrospective audit of neonatal BCG vaccination in Grampian, Scotland

open access: yesHuman Vaccines & Immunotherapeutics, 2023
Bacillus Calmette–Guerin (BCG) vaccine confers protection against tuberculosis (TB) and works most effectively when given to infants. Scotland runs a risk-based program in which BCG vaccine is offered to infants whose parent or grandparent was born in a ...
Saba Savul, Susan Duthie
doaj   +1 more source

Expertise and the interpretation of computerized physiological data: implications for the design of computerized monitoring in neonatal intensive care [PDF]

open access: yes, 2001
This paper presents the outcomes from a cognitive engineering project addressing the design problems of computerized monitoring in neonatal intensive care.
ALBERDI   +65 more
core   +1 more source

The developing human connectome project: A minimal processing pipeline for neonatal cortical surface reconstruction

open access: yesNeuroImage, 2017
The Developing Human Connectome Project (dHCP) seeks to create the first 4-dimensional connectome of early life. Understanding this connectome in detail may provide insights into normal as well as abnormal patterns of brain development.
A. Makropoulos   +18 more
semanticscholar   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

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