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

Jakkrit Amornvit

Showing results (1-10 of 22) with videos related to

Pageof 3
Sort By:
Journal of Child Neurology|May 12, 2026
Diagnostic Accuracy of the Combined Bedside Tests (Icepack and Fatigability) in Diagnosing Juvenile Myasthenia GravisPechpailin Kortnoi, Jakkrit Amornvit, Tanitnun Paprad
Heliyon|June 26, 2023
Syncope with autonomic dysfunction assessed with the Thai-COMPASS 31 questionnaireNithit Singtokum, Jakkrit Amornvit, Stephen Kerr, et al.
Clinical Neurophysiology Practice|April 14, 2020
Mid-palm recording technique, a new electrodiagnostic approach in Martin-Gruber anastomosisNath Pasutharnchat, Jakkrit Amornvit, Chamaiporn Taychargumpoo, et al.
BMC Neurology|May 23, 2021
Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohortNath Pasutharnchat, Chamaiporn Taychargumpoo, Yongkasem Vorasettakarnkij, et al.
American Journal of Physical Medicine & Rehabilitation|May 29, 2019
Needle EMG, a Jigsaw to Disclose Lipid Storage Myopathy Due to Multiple Acyl-CoA Dehydrogenase DeficiencyManasawan Santananukarn, Jakkrit Amornvit, Nath Pasutharnchat, et al.
Journal of Medical Case Reports|October 29, 2025
Possible shared pathogenesis between idiopathic sensory ganglionopathy and achalasia: a case reportPunchai Pureesatien, Nath Pasuthanchat, Tanisa Patcharatrakul, et al.
Brain and Behavior|August 23, 2017
A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a familyJakkrit Amornvit, Mehmet E Yalvac, Lei Chen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 12, 2024
Clinical and neurophysiological characterization of p.Gly59Ser mutation in DCTN1: a study in a Thai family and a brief reviewNath Pasutharnchat, Chamaiporn Taychargumpoo, Jakkrit Amornvit, et al.
The Neurohospitalist|September 29, 2025
Subacute Combined Degeneration From Isolated Folate Deficiency Secondary to Nutrition and Co-Trimoxazole Use in a Patient With IgG4-Related DiseaseManta Yonpiam, Thanakit Pongpitakmetha, Wattakorn Laohapiboolrattana, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|June 27, 2014
Fulminant respiratory muscle paralysis, an expanding clinical spectrum of mitochondrial A3243G tRNALeu mutationJakkrit Amornvit, Nath Pasutharnchat, Monvasi Pachinburavan, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Child Neurology|May 12, 2026
Diagnostic Accuracy of the Combined Bedside Tests (Icepack and Fatigability) in Diagnosing Juvenile Myasthenia GravisPechpailin Kortnoi, Jakkrit Amornvit, Tanitnun Paprad
Heliyon|June 26, 2023
Syncope with autonomic dysfunction assessed with the Thai-COMPASS 31 questionnaireNithit Singtokum, Jakkrit Amornvit, Stephen Kerr, et al.
Clinical Neurophysiology Practice|April 14, 2020
Mid-palm recording technique, a new electrodiagnostic approach in Martin-Gruber anastomosisNath Pasutharnchat, Jakkrit Amornvit, Chamaiporn Taychargumpoo, et al.
BMC Neurology|May 23, 2021
Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohortNath Pasutharnchat, Chamaiporn Taychargumpoo, Yongkasem Vorasettakarnkij, et al.
American Journal of Physical Medicine & Rehabilitation|May 29, 2019
Needle EMG, a Jigsaw to Disclose Lipid Storage Myopathy Due to Multiple Acyl-CoA Dehydrogenase DeficiencyManasawan Santananukarn, Jakkrit Amornvit, Nath Pasutharnchat, et al.
Journal of Medical Case Reports|October 29, 2025
Possible shared pathogenesis between idiopathic sensory ganglionopathy and achalasia: a case reportPunchai Pureesatien, Nath Pasuthanchat, Tanisa Patcharatrakul, et al.
Brain and Behavior|August 23, 2017
A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a familyJakkrit Amornvit, Mehmet E Yalvac, Lei Chen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 12, 2024
Clinical and neurophysiological characterization of p.Gly59Ser mutation in DCTN1: a study in a Thai family and a brief reviewNath Pasutharnchat, Chamaiporn Taychargumpoo, Jakkrit Amornvit, et al.
The Neurohospitalist|September 29, 2025
Subacute Combined Degeneration From Isolated Folate Deficiency Secondary to Nutrition and Co-Trimoxazole Use in a Patient With IgG4-Related DiseaseManta Yonpiam, Thanakit Pongpitakmetha, Wattakorn Laohapiboolrattana, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|June 27, 2014
Fulminant respiratory muscle paralysis, an expanding clinical spectrum of mitochondrial A3243G tRNALeu mutationJakkrit Amornvit, Nath Pasutharnchat, Monvasi Pachinburavan, et al.
Pageof 3