Chisen Takeuchi
Tokyo, Japan
Last Updated: 09/26/2026
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Found 21 publications
Experiences and Information Needs of Families of Children With Organic Acid or Fatty Acid Metabolism Disorders in Japan.
Journal: Journal of genetic counseling
Published: February 04, 2026
Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C-Related Disease (Spastic Paraplegia 58): Two Long-Duration Cases.
Journal: Annals of clinical and translational neurology
Published: August 31, 2025
Pathological diagnosis and therapeutic management of hereditary leiomyomatosis and renal cell carcinoma syndrome-associated renal cell carcinoma.
Journal: International cancer conference journal
Published: July 19, 2025
Functional Analyses of SATB2 Variants Reveal Pathogenicity Mechanisms Linked With SATB2-Associated Syndrome.
Journal: American journal of medical genetics. Part A
Published: October 24, 2024
Amaurosis fugax in Marfan syndrome with myxomatous degeneration
Journal: Rinsho shinkeigaku = Clinical neurology
Published: September 23, 2024
Medical Needs of Adults with Down Syndrome Presenting at a Regional Medical and Rehabilitation Center in Japan.
Journal: Journal of Nippon Medical School = Nippon Ika Daigaku zasshi
Published: February 23, 2023
Worm-migration track of Paragonimus westermani infection.
Journal: QJM : monthly journal of the Association of Physicians
Published: January 12, 2023
Benefits and Challenges of Pediatric-to-Adult Health Care Transition in Childhood-Onset Neurologic Conditions.
Journal: Neurology. Clinical practice
Published: August 15, 2022
De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experiments.
Journal: Human molecular genetics
Published: April 24, 2022
Health care transition for cerebral palsy with intellectual disabilities: A systematic review.
Journal: Revue neurologique
Published: April 03, 2022
An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions.
Journal: BMC neurology
Published: August 20, 2021
Last Updated: 09/26/2026