Results 221 to 230 of about 3,140,235 (395)
Hardware in Mechanical Ventilator : Mechanics of Ventilator
openaire +2 more sources
Expanding the SIAH1‐Associated Phenotypic Spectrum: Insights From Loss‐of‐Function Variants
ABSTRACT SIAH1 encodes for a RING‐type E3 ubiquitin ligase involved in protein ubiquitination. More specifically, it positively regulates Wnt signaling through promoting the accumulation of β‐catenin and mediates ubiquitination and degradation of Akt3 in neural development.
Liza Douiev+14 more
wiley +1 more source
Lung Ultrasound in Mechanical Ventilation: A Purposive Review. [PDF]
Bianchini A+9 more
europepmc +1 more source
Mechanical aids to ventilation for use in the field. [PDF]
M G Harries
openalex +1 more source
Children With 22.Q.11.2 Deletion Syndrome: Sleep‐Disordered Breathing and Management
ABSTRACT Patients with 22q11.2 deletion syndrome (22q11DS) are predisposed to obstructive sleep apnea (OSA) due to an abnormal craniofacial anatomy with pharyngeal hypotonia, retrognathia, micrognathia, and glossoptosis. The aim of the study was to describe the prevalence and management of OSA in a cohort of children with 22q11DS.
Domenico Paolo La Regina+6 more
wiley +1 more source
Outcome of Cerebral Venous Thrombosis Requiring Mechanical Ventilation. [PDF]
Kalita J+5 more
europepmc +1 more source
A New Treatment Modality for Pneumoperitoneum Associated with Mechanical Ventilation [PDF]
Victor Gordon
openalex +1 more source
Prenatal Brain Abnormalities in Sodium‐Dependent Multivitamin Transporter Deficiency
ABSTRACT In treatable neurometabolic disorders, early diagnosis and prompt initiation of treatment are key to improved survival and outcomes. Biallelic variants in SLC5A6 cause sodium‐dependent multivitamin transporter deficiency (OMIM # 618973), which is treatable with high‐dose pantothenic acid, biotin, and alpha lipoic acid.
Eri Ogawa+2 more
wiley +1 more source
Anaesthesia, mechanical ventilation and the training of surgeons [PDF]
J.F. Searle
openalex +1 more source
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun+2 more
wiley +1 more source