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

Hanna Kolski

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Advances in Experimental Medicine and Biology|May 8, 2002
The Landau-Kleffner syndromeHanna Kolski, Hiroshi Otsubo
Expert Opinion on Biological Therapy|June 2, 2012
Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?Toshifumi Yokota, William Duddy, Yusuke Echigoya, et al.
Pediatric Neurology|October 13, 2009
A 10-month-old infant with reversible findings of brain deathAri R Joffe, Hanna Kolski, Jonathan Duff, et al.
Pediatric Neurology|July 22, 2008
Parental stress and quality of life in children with neuromuscular diseaseJean K Mah, Jennifer E Thannhauser, Hanna Kolski, et al.
Pediatrics|September 11, 2013
Clinical characteristics of pediatric myasthenia: a surveillance studyJuliana VanderPluym, Jiri Vajsar, Francois Dominique Jacob, et al.
Muscle & Nerve|January 8, 2014
Cooperative International Neuromuscular Research Group Duchenne Natural History Study demonstrates insufficient diagnosis and treatment of cardiomyopathy in Duchenne muscular dystrophyChristopher Spurney, Reiko Shimizu, Lauren P Morgenroth, et al.
Neuromuscular Disorders : NMD|December 28, 2010
Symptomatic dystrophinopathies in female childrenNatashia Seemann, Kathy Selby, Laura McAdam, et al.
Pediatric Pulmonology|October 4, 2022
Respiratory characteristics in children with spinal muscular atrophy type 1 receiving nusinersenLena Xiao, Jackie Chiang, Maria Castro-Codesal, et al.
Pediatrics|February 3, 2007
A 12-year prospective study of childhood herpes simplex encephalitis: is there a broader spectrum of disease?Jorina M Elbers, Ari Bitnun, Susan E Richardson, et al.
Human Mutation|July 13, 2019
The novel p.Ser263Phe mutation in the human high-affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndromeMayukh Banerjee, Denis Arutyunov, Daniel Brandwein, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|May 8, 2002
The Landau-Kleffner syndromeHanna Kolski, Hiroshi Otsubo
Expert Opinion on Biological Therapy|June 2, 2012
Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?Toshifumi Yokota, William Duddy, Yusuke Echigoya, et al.
Pediatric Neurology|October 13, 2009
A 10-month-old infant with reversible findings of brain deathAri R Joffe, Hanna Kolski, Jonathan Duff, et al.
Pediatric Neurology|July 22, 2008
Parental stress and quality of life in children with neuromuscular diseaseJean K Mah, Jennifer E Thannhauser, Hanna Kolski, et al.
Pediatrics|September 11, 2013
Clinical characteristics of pediatric myasthenia: a surveillance studyJuliana VanderPluym, Jiri Vajsar, Francois Dominique Jacob, et al.
Muscle & Nerve|January 8, 2014
Cooperative International Neuromuscular Research Group Duchenne Natural History Study demonstrates insufficient diagnosis and treatment of cardiomyopathy in Duchenne muscular dystrophyChristopher Spurney, Reiko Shimizu, Lauren P Morgenroth, et al.
Neuromuscular Disorders : NMD|December 28, 2010
Symptomatic dystrophinopathies in female childrenNatashia Seemann, Kathy Selby, Laura McAdam, et al.
Pediatric Pulmonology|October 4, 2022
Respiratory characteristics in children with spinal muscular atrophy type 1 receiving nusinersenLena Xiao, Jackie Chiang, Maria Castro-Codesal, et al.
Pediatrics|February 3, 2007
A 12-year prospective study of childhood herpes simplex encephalitis: is there a broader spectrum of disease?Jorina M Elbers, Ari Bitnun, Susan E Richardson, et al.
Human Mutation|July 13, 2019
The novel p.Ser263Phe mutation in the human high-affinity choline transporter 1 (CHT1/SLC5A7) causes a lethal form of fetal akinesia syndromeMayukh Banerjee, Denis Arutyunov, Daniel Brandwein, et al.
Pageof 2