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

P Lertrit

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Human Genetics|December 1, 1991
Normal variants of human mitochondrial DNA and translation products: the building of a reference data baseS Marzuki, A S Noer, P Lertrit, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Molecular examination of GH gene deletion in familial growth hormone deficiencyS Lekhakula, P Lertrit, C Tuchinda, et al.
Human Genetics|September 10, 1999
A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndromeP Lertrit, A Imsumran, P Karnkirawattana, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|May 5, 2001
Experience of ApoE study in Thai elderlyV Senanarong, K Harnphadungkit, P Lertrit, et al.
Australian and New Zealand Journal of Medicine|April 1, 1994
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathiesM J Jean-Francois, P Lertrit, S F Berkovic, et al.
European Journal of Neurology|April 5, 2005
An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophyW L Chuenkongkaew, P Lertrit, C Limwongse, et al.
American Journal of Human Genetics|October 1, 1991
A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndromeA S Noer, H Sudoyo, P Lertrit, et al.
Human Molecular Genetics|November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunctionP Lertrit, R M Kapsa, M J Jean-Francois, et al.
American Journal of Human Genetics|September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex IP Lertrit, A S Noer, M J Jean-Francois, et al.
Journal of the Neurological Sciences|December 1, 1996
Mitochondrial DNA polymorphism in substantia nigraR M Kapsa, M J Jean-Francois, P Lertrit, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Human Genetics|December 1, 1991
Normal variants of human mitochondrial DNA and translation products: the building of a reference data baseS Marzuki, A S Noer, P Lertrit, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Molecular examination of GH gene deletion in familial growth hormone deficiencyS Lekhakula, P Lertrit, C Tuchinda, et al.
Human Genetics|September 10, 1999
A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndromeP Lertrit, A Imsumran, P Karnkirawattana, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|May 5, 2001
Experience of ApoE study in Thai elderlyV Senanarong, K Harnphadungkit, P Lertrit, et al.
Australian and New Zealand Journal of Medicine|April 1, 1994
Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathiesM J Jean-Francois, P Lertrit, S F Berkovic, et al.
European Journal of Neurology|April 5, 2005
An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophyW L Chuenkongkaew, P Lertrit, C Limwongse, et al.
American Journal of Human Genetics|October 1, 1991
A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndromeA S Noer, H Sudoyo, P Lertrit, et al.
Human Molecular Genetics|November 1, 1994
Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunctionP Lertrit, R M Kapsa, M J Jean-Francois, et al.
American Journal of Human Genetics|September 1, 1992
A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex IP Lertrit, A S Noer, M J Jean-Francois, et al.
Journal of the Neurological Sciences|December 1, 1996
Mitochondrial DNA polymorphism in substantia nigraR M Kapsa, M J Jean-Francois, P Lertrit, et al.
Pageof 3