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

Emil Ylikallio

Showing results (1-10 of 43) with videos related to

Pageof 5
Sort By:
Annals of Medicine|August 3, 2011
Mechanisms of mitochondrial diseasesEmil Ylikallio, Anu Suomalainen
Human Molecular Genetics|April 24, 2010
High mitochondrial DNA copy number has detrimental effects in miceEmil Ylikallio, Henna Tyynismaa, Hiroyuki Tsutsui, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesisEmil Ylikallio, Elisa Rahikkala, Riikka Keski-Filppula, et al.
Duodecim; Laaketieteellinen Aikakauskirja|April 15, 2014
[The many faces of neurosyphilis]Emil Ylikallio, Terttu Heikinheimo, Veli-Jukka Anttila, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegiaEmil Ylikallio, Doyoun Kim, Pirjo Isohanni, et al.
Neurology. Genetics|April 12, 2016
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth diseaseMari Auranen, Emil Ylikallio, Maria Shcherbii, et al.
Frontiers in Neurology|November 29, 2023
Lowered oxidative capacity in spinal muscular atrophy, Jokela type; comparison with mitochondrial muscle diseaseNadja Ratia, Edouard Palu, Hanna Lantto, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot-Marie-Tooth neuropathy and a mutation in HSPB1Emil Ylikallio, Mridul Johari, Svetlana Konovalova, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Annals of Medicine|August 3, 2011
Mechanisms of mitochondrial diseasesEmil Ylikallio, Anu Suomalainen
Human Molecular Genetics|April 24, 2010
High mitochondrial DNA copy number has detrimental effects in miceEmil Ylikallio, Henna Tyynismaa, Hiroyuki Tsutsui, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesisEmil Ylikallio, Elisa Rahikkala, Riikka Keski-Filppula, et al.
Duodecim; Laaketieteellinen Aikakauskirja|April 15, 2014
[The many faces of neurosyphilis]Emil Ylikallio, Terttu Heikinheimo, Veli-Jukka Anttila, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegiaEmil Ylikallio, Doyoun Kim, Pirjo Isohanni, et al.
Neurology. Genetics|April 12, 2016
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth diseaseMari Auranen, Emil Ylikallio, Maria Shcherbii, et al.
Frontiers in Neurology|November 29, 2023
Lowered oxidative capacity in spinal muscular atrophy, Jokela type; comparison with mitochondrial muscle diseaseNadja Ratia, Edouard Palu, Hanna Lantto, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot-Marie-Tooth neuropathy and a mutation in HSPB1Emil Ylikallio, Mridul Johari, Svetlana Konovalova, et al.
Pageof 5