Results 111 to 120 of about 47,410 (348)
Fractional order impedance models as rising tools for quantification of unconscious analgesia [PDF]
, 2013 This research focuses on modeling the diffusion process that occurs in the human body when an analgesic drug is taken up, by using fractional-order impedance models (FOIMs).
Chevalier, Amélie +3 more
core +1 more source
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison +3 more
wiley +1 more source
Beeinflussung der Mivacurium-induzierten Muskelrelaxation durch S(+)-Ketamin [PDF]
, 2019 Die Allgemeinanästhesie setzt sich aus einem Medikamentencocktail zusammen, das aus einem Hypnotikum, einem Muskelrelaxans sowie einem Analgetikum besteht. Die Analgetika sind der Opioidgruppe zugeordnet (z. B. Fentanyl oder Sufentanil).
Hescher-Jost, Ilona
core +1 more source
Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT Phelan‐McDermid syndrome (PMS) is a genetic condition caused by deletions of chromosome 22q13.3 or pathogenic variants in the SHANK3 gene. Neurologic features typically include intellectual disability, autism spectrum disorder, hypotonia, and absent speech, though there is considerable variability even among individuals with the same molecular
Rachel Gore Moses +21 more
wiley +1 more source
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT The National Institute of Health (NIH) Undiagnosed Diseases Program (UDP) is an NIH project with the goal of providing both a comprehensive diagnosis and a better understanding of the many mechanisms of disease for patients with rare and undiagnosed conditions.
Dee Adedipe +19 more
wiley +1 more source
Research advances in dysphagia animal models
Animal Models and Experimental Medicine, EarlyView.This review systematically summarizes the establishment, evaluation, and detection of dysphagia animal models in stroke, Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS) in three kinds of experimental animals (including rodents, nonhuman primates, and other mammals), providing a basis for the selection of appropriate animal models of ...
Junhui Bai +5 more
wiley +1 more source
AN ENDOTRACHBAL AND BRONCHOSCOPIC CABINET FOR NEUROMUSCULAR BLOCKADE [PDF]
, 1948 Robert M. Smith, Betty E. Lank
openalex +1 more source
Control of uncertain compartmental systems [PDF]
, 2007 \ A study of the performance of mass control for compartmental systems, under the presence of uncertainties, is presented. Bounds for the asymptotical mass offset are derived as a functional of the uncertainty bounds. The obtained results are illustrated
Mendonca, T, Rocha, P, Sousa, C
core +1 more source
HCN2‐Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models
Annals of Neurology, EarlyView.Objective We aimed to characterize the phenotypic spectrum and functional consequences associated with variants in HCN2, encoding for the hyperpolarization‐activated cyclic nucleotide (HCN) gated channel 2. Methods GeneMatcher facilitated the recruitment of 21 individuals with HCN2 variants from 15 unrelated families, carrying HCN2 variants.
Clara Houdayer +52 more
wiley +1 more source
The Changing Pattern of Neuromuscular Blockade Caused by Succinylcholine in Man [PDF]
, 1966 Jan F. Crul +3 more
openalex +1 more source