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

Talim

Showing results (111-120 of 159) with videos related to

Pageof 16
Sort By:
The American Journal of Pathology|July 11, 2020
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular DystrophiesEvrim Aksu-Menges, Yeliz Z Akkaya-Ulum, Didem Dayangac-Erden, et al.
Journal of Human Genetics|December 16, 2016
Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defectsGoknur Haliloglu, Kerstin Becker, Cagri Temucin, et al.
Pediatric Hematology and Oncology|July 7, 2007
Extranodal type T/NK-cell lymphoma with an atypical clinical presentationG Burça Aydin, Canan Akyuz, Beril Talim, et al.
Neuromuscular Disorders : NMD|May 28, 2024
Further expanding the phenotype of anti-Ku antibody associated disease in children and adolescentsEzgi Deniz Batu, Seher Şener, Göknur Haliloğlu, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.
European Journal of Pediatrics|January 18, 2006
Calpain-3 mutations in TurkeyBurcu Balci, Stefania Aurino, Göknur Haliloglu, et al.
Neuromuscular Disorders : NMD|February 15, 2025
Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotypeGöknur Haliloğlu, Sandra Donkervoort, Ülkühan Öztoprak, et al.
Archives of Neurology|November 15, 2006
Cardiac and pulmonary investigations in Bethlem myopathyAnneke J van der Kooi, Willem G de Voogt, Enrico Bertini, et al.
Neuromuscular Disorders : NMD|June 18, 2005
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genesA D'Amico, G Haliloglu, P Richard, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish originVilma-Lotta Lehtokari, Katarina Pelin, Kati Donner, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
The American Journal of Pathology|July 11, 2020
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular DystrophiesEvrim Aksu-Menges, Yeliz Z Akkaya-Ulum, Didem Dayangac-Erden, et al.
Journal of Human Genetics|December 16, 2016
Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defectsGoknur Haliloglu, Kerstin Becker, Cagri Temucin, et al.
Pediatric Hematology and Oncology|July 7, 2007
Extranodal type T/NK-cell lymphoma with an atypical clinical presentationG Burça Aydin, Canan Akyuz, Beril Talim, et al.
Neuromuscular Disorders : NMD|May 28, 2024
Further expanding the phenotype of anti-Ku antibody associated disease in children and adolescentsEzgi Deniz Batu, Seher Şener, Göknur Haliloğlu, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB lociB Talim, A Ferreiro, B Cormand, et al.
European Journal of Pediatrics|January 18, 2006
Calpain-3 mutations in TurkeyBurcu Balci, Stefania Aurino, Göknur Haliloglu, et al.
Neuromuscular Disorders : NMD|February 15, 2025
Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotypeGöknur Haliloğlu, Sandra Donkervoort, Ülkühan Öztoprak, et al.
Archives of Neurology|November 15, 2006
Cardiac and pulmonary investigations in Bethlem myopathyAnneke J van der Kooi, Willem G de Voogt, Enrico Bertini, et al.
Neuromuscular Disorders : NMD|June 18, 2005
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genesA D'Amico, G Haliloglu, P Richard, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish originVilma-Lotta Lehtokari, Katarina Pelin, Kati Donner, et al.
Pageof 16