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Last Updated: 10/31/2025
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Found 47 publications
Clinical features of CAPOS syndrome caused by maternal ATP1A3 gene variation: a case report
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: November 13, 2023
Childhood fever and hearing loss associated with CAPOS syndrome.
Journal: Auris, nasus, larynx
Published: September 29, 2023
Is meal order timing and flexibility key to improving patient satisfaction with hospital foodservice?
Journal: Journal of human nutrition and dietetics : the official journal of the British Dietetic Association
Published: March 06, 2023
ATP1A3-related phenotypes in Chinese children: AHC, CAPOS, and RECA.
Journal: European journal of pediatrics
Published: April 08, 2022
Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.
Journal: Brain & development
Published: August 05, 2021
Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype-Phenotype Study and CI Management.
Journal: Frontiers in cell and developmental biology
Published: July 29, 2021
The diagnostic spectrum of ATP1A3-related disorders: 3 new patients.
Journal: Journal of the neurological sciences
Published: June 15, 2021
Long-Term Follow-Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene.
Journal: Movement disorders clinical practice
Published: April 19, 2021
ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum.
Journal: Frontiers in neurology
Published: December 04, 2020
An 88.8-kb Novel Deletion of 19q13.2 Encompassing the ATP1A3 Gene Detected by Array CGH in a Patient with Delayed Psychomotor Development, Generalized Hypotonia and Macrocephaly.
Journal: Molecular syndromology
Published: November 07, 2020
Cochlear Implantation Outcomes in Post Synaptic Auditory Neuropathies: A Systematic Review and Narrative Synthesis.
Journal: The journal of international advanced otology
Published: November 02, 2020
Last Updated: 10/31/2025