Results 121 to 130 of about 190,027 (315)
PSEUDO-BULBAR PALSY, CLINICALLY AND PATHOLOGICALLY CONSIDERED, WITH THE CLINICAL REPORT OF FIVE CASES [PDF]
, 1912 Frederick Tilney, Joseph Morrison
openalex +1 more source
Magnetic Skin for Voice Disorders with Real‐Time Lip Translation
Advanced Intelligent Systems, EarlyView.Soüti, a novel wearable technology combining flexible, biocompatible magnetic skin patches with a convolutional neural network to translate lip movements into speech with 92.54% accuracy. This innovative approach enhances therapeutic options for speech impairments and democratizes access to advanced healthcare technologies, particularly benefiting ...
Montserrat Ramirez‐De Angel +6 more
wiley +1 more source
BILATERAL OCULOMOTORIUS PALSY FROM SOFTENING IN EACH OCULOMOTORIUS NUCLEUS [PDF]
, 1913 WILLIAM G. SPILLER
openalex +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT SATB2‐associated syndrome (SAS) is characterized by intellectual disability, neurodevelopmental disorders, cleft palate, and dental abnormalities. SAS is caused by variants in the special AT‐rich sequence‐binding protein 2 (SATB2), which encodes a transcription factor containing two CUT domains and a homeobox (HOX) domain.
Nao Ukita +5 more
wiley +1 more source
Stem Cells Translational Medicine, 2016 Evidence for stem cells as a potential intervention for cerebral palsy is emerging. Our objective was to determine the efficacy and safety of stem cells for improving motor and cognitive function of people with cerebral palsy.
Iona Novak +5 more
doaj +1 more source
Rule Based Expert System for Diagnosis of Neuromuscular Disorders [PDF]
arXiv, 2012 In this paper, we discuss the implementation of a rule based expert system for diagnosing neuromuscular diseases. The proposed system is implemented as a rule based expert system in JESS for the diagnosis of Cerebral Palsy, Multiple Sclerosis, Muscular Dystrophy and Parkinson's disease. In the system, the user is presented with a list of questionnaires
arxiv
Phenotypic Expansion of Knobloch Syndrome Type 2 in an Individual With a De Novo PAK2 Variant
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT P21‐activated kinase 2 (PAK2) is a serine/threonine kinase essential for a variety of cellular processes including signal transduction, cellular survival, proliferation, and migration. A recent report proposed monoallelic PAK2 variants cause Knobloch syndrome type 2 (KNO2)—a developmental disorder primarily characterized by ocular anomalies ...
Elizabeth A. Werren +10 more
wiley +1 more source
Exploring a Multimodal Fusion-based Deep Learning Network for Detecting Facial Palsy [PDF]
arXivAlgorithmic detection of facial palsy offers the potential to improve current practices, which usually involve labor-intensive and subjective assessment by clinicians. In this paper, we present a multimodal fusion-based deep learning model that utilizes unstructured data (i.e. an image frame with facial line segments) and structured data (i.e. features
arxiv
Identification of Key Proteins Involved in Axon Guidance Related Disorders: A Systems Biology Approach [PDF]
arXiv, 2018 Axon guidance is a crucial process for growth of the central and peripheral nervous systems. In this study, 3 axon guidance related disorders, namely- Duane Retraction Syndrome (DRS) , Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS) and Congenital fibrosis of the extraocular muscles type 3 (CFEOM3) were studied using various Systems Biology ...
arxiv