Results 41 to 50 of about 92,950 (263)
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane +43 more
wiley +1 more source
Homologous human milk supplement for very low birth weight preterm infant feeding
Revista Paulista de Pediatria, 2015 OBJECTIVE: To develop a homologous human milk supplement for very low-birth weight infant feeding, using an original and simplified methodology, to know the nutritional composition of human milk fortified with this supplement and to evaluate its ...
Thayana Regina de Souza Grance +3 more
doaj +1 more source
Effect of Delayed Elevation of Thyrotropin on Feeding Intolerance in Very Low Birth Weight Infants [PDF]
Neonatal Medicine, 2019 Purpose We investigated the effect of delayed elevation of thyrotropin (TSH) (deTSH) on gastrointestinal motility in very low birth weight infants (VLBWI).
Ju Kyung Hyun +3 more
doaj +1 more source
Van Tıp Dergisi, 2021 INTRODUCTION: This study aimed to evaluate the relationship between necrotizing enterocolitis (NEC), risk factors, and feeding intolerance in very low birth weight premature newborns. METHODS: The cases who were born under 30 weeks of gestational age and
Meliha Aksoy Okan +4 more
doaj +1 more source
Incidence of bronchopulmonary dysplasia and mortality of very low birth weight infants in Vojvodina [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2020 Introduction/Objective. The incidence of bronchopulmonary dysplasia (BPD) varies depending on the prematurity rate, definition, and therapy that are applied at a certain center.
Vilotijević-Dautović Gordana +3 more
doaj +1 more source
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
The Effect of Maternal Pre-pregnancy Body Mass Index on Very Low Birth Weight Infants [PDF]
Neonatal Medicine, 2018 Purpose The pre-pregnancy body mass index (BMI) is associated with adverse neonatal outcomes. However, studies on very low birth weight (VLBW) infants are rare.
Kyung Suk Baek +3 more
doaj +1 more source
Cost of Morbidities in Very Low Birth Weight Infants [PDF]
The Journal of Pediatrics, 2013 To determine the association between direct costs for the initial neonatal intensive care unit hospitalization and 4 potentially preventable morbidities in a retrospective cohort of very low birth weight (VLBW) infants (birth weight
Tricia J, Johnson +4 more
openaire +2 more sources
Onasemnogene Abeparvovec in Patients With SMA: Interim Results of the RESTORE Registry in Japan
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective There are limited real‐world data regarding the safety and effectiveness of onasemnogene abeparvovec (OA; Zolgensma) infusion, a one‐time gene replacement therapy, for Japanese patients with spinal muscular atrophy (SMA). We aimed to improve understanding of the real‐world outcomes for OA in Japan.
Kayoko Saito +8 more
wiley +1 more source
Jornal de Pediatria, 2021 Objective: This study aimed to evaluate annual trends of early neonatal sepsis and antimicrobial use in very low birth weight infants for 12 years, as well as to identify microbiological agents, antimicrobial sensitivity profiles, and association with ...
Jamil Pedro de Siqueira Caldas +3 more
doaj +1 more source