Results 61 to 70 of about 4,292 (213)

Innovative Approaches in Dyskinetic Cerebral Palsy Management with Taila Dahana Agnikarma Integrated with Panchakarma Therapies: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Cerebral Palsy (CP) is a group of neurological disorders affecting movement, muscle tone, and posture due to brain injury occurring during early development.
Jeeru Ojaswini Reddy, Uma Shetti, Azizahmed Arbar, Kh Veena, Sonu Prakash   +4 more
doaj   +1 more source

Real world testing and cost‐effectiveness analysis of subcutaneous EEG (REAL‐ASE): Protocol for a prospective multicentre interventional trial

Epilepsia Open, EarlyView.
Abstract Objective Epilepsy is a common condition associated with significant morbidity, mortality, and costs. Poor documentation of seizures is a major challenge in epilepsy care. Objective seizure counting with mobile devices may mitigate this challenge and improve patient management.
Matthew McWilliam, Pedro F. Viana, Eren Dursun, Joe Davies, Joel S. Winston, Jessica Agren, Harutomo Hasegawa, Jonas Duun‐Henriksen, Mark P. Richardson   +8 more
wiley   +1 more source

Patient outcomes in KCNQ2 developmental and epileptic encephalopathy

Developmental Medicine &Child Neurology, EarlyView.
Abstract The aim of this study was to review and summarize the literature describing clinically observed or caregiver‐reported and patient‐reported KCNQ2 developmental and epileptic encephalopathy (DEE) outcomes. Three online databases and selected congress proceedings were searched (August 2023).
Grant Maclaine, Michele H. Potashman, Deepshikha Pawar, Sugandh Sharma, Katja Rudell, Jason Lerner, Vlad Coric, Anne T. Berg, John Millichap, Gil L'Italien   +9 more
wiley   +1 more source

MUTATIONS IN THE ARX GENE: CLINICAL, ELECTROENCEPHALOGRAPHIC AND NEUROIMAGING FEATURES IN 3 PATIENTS

Русский журнал детской неврологии, 2017
The Aristaless-related homeobox (ARX) gene is a member of the paired-type homeodomain transcription factor family with critical roles in embryonic development, particularly in the developing brain.
I. V. Ivanova, K. Yu. Mukhin, O. A. Pylaeva, M. Yu. Bobylova, N. E. Kvaskova, A. S. Petrukhin   +5 more
doaj   +1 more source

Diagnosis of multiple sclerosis and Fahr's Disease in a young woman: A case report (PP-15) [PDF]

Neurology Letters, 2023
Fahr’s disease is a progressive and idiopathic basal ganglia calcification with normal metabolism of calcium and phosphore with motor and psychiatric sings and symptoms.
Mohammadreza Malek Zadeh, Pourandokht Mousavian, Mohammad Ali Nahayati   +2 more
doaj  

Characteristics of Cerebral Palsy in the Midwestern US

Annals of Clinical and Translational Neurology, Volume 13, Issue 1, Page 21-35, January 2026.
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, Kelsey Steffen, Lauren Gottschalk‐Henneberry, Jennifer Miros, Amy Robichaux‐Viehoever, Karen Taca, Bhooma R. Aravamuthan   +6 more
wiley   +1 more source

Nutrition Support Interventions for Children and Young People Treated for Osteosarcoma: A Scoping Review

Journal of Human Nutrition and Dietetics, Volume 38, Issue 6, December 2025.
Whilst a range of nutrition support interventions for those undergoing osteosarcoma treatment has been studied and interest is growing, the evidence is fragmented, methodologically weak and indicates wide variation in clinical practice. We identify priority research needed to establish evidence‐based clinical practice guidance.
Laura Sealy, Maddie Smith, Sarah Barrett, Divyalakshmi Bhaskaran, Helen Rees, Raquel Revuelta Iniesta   +5 more
wiley   +1 more source

A case report of PRRT2 mutation-associated familial convulsions with paroxysmal choreoathetosis syndrome

Zaporožskij Medicinskij Žurnal, 2019
Diagnostics and differential diagnostics of inherited metabolic diseases in children have still been complicated. The diagnostic difficulties are due to the fact that the diseases are orphan and their recognition is not always timely. Objective.
M. A. Trishchynska, V. O. Svystilnyk
doaj   +1 more source

Infantile Cerebellar‐Retinal Degeneration Associated With Novel ACO2 Variants: Clinical Features and Insights From a Drosophila Model

Clinical Genetics, Volume 108, Issue 3, Page 266-278, September 2025.
Our Translational Loop integrates patient genetic data with Drosophila models to study disease mechanisms. We identified ACO2 variants in a patient linked to ICRD and show that our animal model mirrors key aspects of the disease. These insights help pinpoint therapeutic targets, advancing research toward treatments for rare genetic disorders.
Edgar Buhl, Suchika Garg, Marie Monaghan, Amy Preston, Marcus Likeman, Julianne Dare, Julie Evans, Lucie S. Taylor, Ian Berry, Kathryn Urankar, Paul G. D. Spry, Cathy Williams, Robert W. Taylor, Charlotte L. Alston, James J. L. Hodge, Anirban Majumdar   +15 more
wiley   +1 more source

Paroxysmal Nonkinesigenic Dyskinesia with Tremor

Case Reports in Neurological Medicine, 2013
Introduction. Paroxysmal nonkinesigenic dyskinesia (PNKD) consists of episodes of chorea, athetosis, or dystonia which are not triggered by movement, with complete remission between episodes.
Robert Fekete
doaj   +1 more source