Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yutaka Furuta

Showing results (11-20 of 31) with videos related to

Pageof 4
Sort By:
Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|June 19, 2024
Ascites Caused by Intestinal Anisakiasis: A Case Report and Literature ReviewYutaka Furuta, Naoto Matsuda, Hiroaki Wakakuri, et al.
Cureus|January 30, 2024
The International Transfer of Patients With Positive SARS-CoV-2 Test Using a FrameworkYutaka Furuta, Yoji Hoshina, Yusuke Matsuura, et al.
American Journal of Medical Genetics. Part A|June 26, 2026
Positron Emission Tomography (PET) in Phenylketonuria: A Systematic Review of Brain Metabolism Beyond PhenylalanineYutaka Furuta, Shoji Yano, John A Phillips, et al.
American Journal of Medical Genetics. Part A|January 16, 2024
Data from electronic healthcare records expand our understanding of X-linked genetic diseasesRory J Tinker, Lisa Bastarache, Kimberly Ezell, et al.
The Neurohospitalist|June 9, 2025
Unexplained Progressive Respiratory Insufficiency and Weakness Diagnosed as Late-Onset Pompe Disease Through Biochemical and Molecular Genetic TestingYutaka Furuta, Neena S Agrawal, Angela R Grochowsky, et al.
Orphanet Journal of Rare Diseases|November 15, 2024
A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseasesYutaka Furuta, Rory J Tinker, Rizwan Hamid, et al.
International Journal of Dermatology|January 7, 2026
Decoding Genetic Disease Through the Skin: Lessons From the UDN AuthorsAthira Sivadas, Katelyn Moore, Kimberly Ezell, et al.
American Journal of Medical Genetics. Part A|August 25, 2023
A medical odyssey of a 72-year-old man with Charcot-Marie-Tooth disease type 2 newly diagnosed with biallelic variants in SORD gene causing sorbitol dehydrogenase deficiencyYutaka Furuta, Erica T Nelson, Serena M Neumann, et al.
Biomolecules|March 28, 2026
Expanded Clinical Spectrum of Autosomal-Dominant STT3A-CDGHamdan Al-Shahrani, Evelin Szabó, Caroline Staccone, et al.
American Journal of Ophthalmology|August 8, 2025
The Undiagnosed Diseases Network (UDN) Solves Ocular Syndromic Diagnostic DilemmasRory J Tinker, Logan M Smith, Lisa A Bastarache, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi|June 19, 2024
Ascites Caused by Intestinal Anisakiasis: A Case Report and Literature ReviewYutaka Furuta, Naoto Matsuda, Hiroaki Wakakuri, et al.
Cureus|January 30, 2024
The International Transfer of Patients With Positive SARS-CoV-2 Test Using a FrameworkYutaka Furuta, Yoji Hoshina, Yusuke Matsuura, et al.
American Journal of Medical Genetics. Part A|June 26, 2026
Positron Emission Tomography (PET) in Phenylketonuria: A Systematic Review of Brain Metabolism Beyond PhenylalanineYutaka Furuta, Shoji Yano, John A Phillips, et al.
American Journal of Medical Genetics. Part A|January 16, 2024
Data from electronic healthcare records expand our understanding of X-linked genetic diseasesRory J Tinker, Lisa Bastarache, Kimberly Ezell, et al.
The Neurohospitalist|June 9, 2025
Unexplained Progressive Respiratory Insufficiency and Weakness Diagnosed as Late-Onset Pompe Disease Through Biochemical and Molecular Genetic TestingYutaka Furuta, Neena S Agrawal, Angela R Grochowsky, et al.
Orphanet Journal of Rare Diseases|November 15, 2024
A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseasesYutaka Furuta, Rory J Tinker, Rizwan Hamid, et al.
International Journal of Dermatology|January 7, 2026
Decoding Genetic Disease Through the Skin: Lessons From the UDN AuthorsAthira Sivadas, Katelyn Moore, Kimberly Ezell, et al.
American Journal of Medical Genetics. Part A|August 25, 2023
A medical odyssey of a 72-year-old man with Charcot-Marie-Tooth disease type 2 newly diagnosed with biallelic variants in SORD gene causing sorbitol dehydrogenase deficiencyYutaka Furuta, Erica T Nelson, Serena M Neumann, et al.
Biomolecules|March 28, 2026
Expanded Clinical Spectrum of Autosomal-Dominant STT3A-CDGHamdan Al-Shahrani, Evelin Szabó, Caroline Staccone, et al.
American Journal of Ophthalmology|August 8, 2025
The Undiagnosed Diseases Network (UDN) Solves Ocular Syndromic Diagnostic DilemmasRory J Tinker, Logan M Smith, Lisa A Bastarache, et al.
Pageof 4