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

H M Lai

Showing results (31-40 of 44) with videos related to

Pageof 5
Sort By:
Gene|January 15, 2020
Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disordersChui-Sun Yap, Saumya Shekhar Jamuar, Angeline H M Lai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 16, 2021
Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromesPravin Rr, Catherine Douch, Mark Jean Aan Koh, et al.
Brain : a Journal of Neurology|December 1, 1996
Progressive cerebral atrophy in multiple sclerosis. A serial MRI studyN A Losseff, L Wang, H M Lai, et al.
Journal of Pediatric Genetics|April 24, 2023
Novel Variants and Clinical Characteristics of 16 Patients from Southeast Asia with Genetic Variants in Neurofibromin-1Grace Lin, Heming Wei, Angeline H M Lai, et al.
Journal of Neurology|May 1, 1997
Serial magnetisation transfer ratios in gadolinium-enhancing lesions in multiple sclerosisH M Lai, C A Davie, A Gass, et al.
Annals of Neurology|March 20, 1998
Correlations between monthly enhanced MRI lesion rate and changes in T2 lesion volume in multiple sclerosisP D Molyneux, M Filippi, F Barkhof, et al.
Human Genomics|December 16, 2015
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patientsEileen C P Lim, Maggie Brett, Angeline H M Lai, et al.
Lupus|July 2, 2011
Age- and gender-related long-term renal outcome in patients with lupus nephritisC-Y Hsu, W-C Chiu, T-S Yang, et al.
Clinical Rheumatology|April 14, 2007
Association of tri-nucleotide (CAG and GGC) repeat polymorphism of androgen receptor gene in Taiwanese women with refractory or remission rheumatoid arthritisS F Yu, T T Cheng, Y H Hsu, et al.
Neuropathology and Applied Neurobiology|November 4, 2015
Bringing CLARITY to the human brain: visualization of Lewy pathology in three dimensionsA K L Liu, M E D Hurry, O T W Ng, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Gene|January 15, 2020
Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disordersChui-Sun Yap, Saumya Shekhar Jamuar, Angeline H M Lai, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 16, 2021
Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromesPravin Rr, Catherine Douch, Mark Jean Aan Koh, et al.
Brain : a Journal of Neurology|December 1, 1996
Progressive cerebral atrophy in multiple sclerosis. A serial MRI studyN A Losseff, L Wang, H M Lai, et al.
Journal of Pediatric Genetics|April 24, 2023
Novel Variants and Clinical Characteristics of 16 Patients from Southeast Asia with Genetic Variants in Neurofibromin-1Grace Lin, Heming Wei, Angeline H M Lai, et al.
Journal of Neurology|May 1, 1997
Serial magnetisation transfer ratios in gadolinium-enhancing lesions in multiple sclerosisH M Lai, C A Davie, A Gass, et al.
Annals of Neurology|March 20, 1998
Correlations between monthly enhanced MRI lesion rate and changes in T2 lesion volume in multiple sclerosisP D Molyneux, M Filippi, F Barkhof, et al.
Human Genomics|December 16, 2015
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patientsEileen C P Lim, Maggie Brett, Angeline H M Lai, et al.
Lupus|July 2, 2011
Age- and gender-related long-term renal outcome in patients with lupus nephritisC-Y Hsu, W-C Chiu, T-S Yang, et al.
Clinical Rheumatology|April 14, 2007
Association of tri-nucleotide (CAG and GGC) repeat polymorphism of androgen receptor gene in Taiwanese women with refractory or remission rheumatoid arthritisS F Yu, T T Cheng, Y H Hsu, et al.
Neuropathology and Applied Neurobiology|November 4, 2015
Bringing CLARITY to the human brain: visualization of Lewy pathology in three dimensionsA K L Liu, M E D Hurry, O T W Ng, et al.
Pageof 5