Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.
Journal: Human molecular genetics
Published: May 22, 2026
Protocol for quantitative analysis of adult zebrafish swimming behavior using DeepLabCut.
Journal: STAR protocols
Published: November 21, 2025
Letter: Advance Care Planning Documentation Changes Among Neurologists in an Amyotrophic Lateral Sclerosis Clinic with Addition of Specialist Palliative Care.
Journal: Journal of palliative medicine
Published: August 05, 2025
Oligodendrocyte dysfunction contributes to motor deficits and Purkinje cell axonopathy in spinocerebellar ataxia type 1.
Journal: The Journal of clinical investigation
Published: May 15, 2025
Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network Study.
Journal: American journal of medical genetics. Part A
Published: September 08, 2024
Respiratory Function Changes as Early Signs of Amyotrophic Lateral Sclerosis.
Journal: Respiration; international review of thoracic diseases
Published: April 17, 2023
Reduction of mutant ATXN1 rescues premature death in a conditional SCA1 mouse model.
Journal: JCI insight
Published: March 15, 2022
Charcot Marie Tooth disease type 4J with complex central nervous system features.
Journal: Annals of clinical and translational neurology
Published: November 15, 2017
Motor neuron degeneration correlates with respiratory dysfunction in SCA1.
Journal: Disease models & mechanisms
Published: October 23, 2017
Simultaneous serum aquaporin-4 antibody and CSF NMDA receptor antibody-positive encephalitis.
Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: April 21, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026