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Nath Pasutharnchat

Showing results (11-20 of 15) with videos related to

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Clinical Neurophysiology Practice|October 17, 2022
Sural-sparing pattern: A study against electrodiagnostic subtypes of Guillain-Barre syndromeNath Pasutharnchat, Varis Ratanasirisawad, Manasawan Santananukarn, et al.
American Journal of Physical Medicine & Rehabilitation|June 25, 2008
Safety profile of multilevel chemical denervation procedures using phenol or botulinum toxin or both in a pediatric populationKat Kolaski, Samuel J Ajizian, Leah Passmore, et al.
European Journal of Human Genetics : EJHG|September 25, 2020
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1Patra Yeetong, Chaipat Chunharas, Monnat Pongpanich, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28Patra Yeetong, Surasawadee Ausavarat, Roongroj Bhidayasiri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 8, 2025
Two distinct phenotypes and a novel mutation in limb-girdle muscular dystrophy R7 telethonin-related patients from Thai neuromuscular centerTanitnun Paprad, Jakkrit Amornvit, Thippamas Pobsuk, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Clinical Neurophysiology Practice|October 17, 2022
Sural-sparing pattern: A study against electrodiagnostic subtypes of Guillain-Barre syndromeNath Pasutharnchat, Varis Ratanasirisawad, Manasawan Santananukarn, et al.
American Journal of Physical Medicine & Rehabilitation|June 25, 2008
Safety profile of multilevel chemical denervation procedures using phenol or botulinum toxin or both in a pediatric populationKat Kolaski, Samuel J Ajizian, Leah Passmore, et al.
European Journal of Human Genetics : EJHG|September 25, 2020
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1Patra Yeetong, Chaipat Chunharas, Monnat Pongpanich, et al.
European Journal of Human Genetics : EJHG|June 21, 2012
A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28Patra Yeetong, Surasawadee Ausavarat, Roongroj Bhidayasiri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 8, 2025
Two distinct phenotypes and a novel mutation in limb-girdle muscular dystrophy R7 telethonin-related patients from Thai neuromuscular centerTanitnun Paprad, Jakkrit Amornvit, Thippamas Pobsuk, et al.
Pageof 2