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 (101-110 of 159) with videos related to

Pageof 16
Sort By:
Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.
Current Microbiology|January 16, 2026
First Report of Aspergillus aculeatus Colonizing Protaetia brevitarsis Larvae: Pathogenicity and Dose-Dependent VirulenceHaokun Cheng, Jialin Qiu, Muhammad Adeel Ghafar, et al.
Rheumatology International|October 27, 2020
Inflammatory milieu of muscle biopsies in juvenile dermatomyositisErdal Sag, Gulsev Kale, Goknur Haliloglu, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 5, 2016
Surgical Treatment of Childhood Inflammatory Myofibroblastic TumorsTutku Soyer, Beril Talim, İbrahim Karnak, et al.
Journal of Neuromuscular Diseases|January 9, 2023
A Child with Refractory and Relapsing Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Myopathy: Case-Based ReviewSeher Sener, Ezgi Deniz Batu, Seher Sari, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Journal of Medical Genetics|May 21, 2013
A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathiesNilgun Cetin, Burcu Balci-Hayta, Hulya Gundesli, et al.
Multiple Sclerosis and Related Disorders|May 8, 2023
Neuromyelitis optica spectrum disorders with a benign course. Analysis of 544 patientsMarco A Lana-Peixoto, Natália C Talim, Dagoberto Callegaro, et al.
Archives of Neurology|February 16, 2006
Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutationsEugenio Mercuri, Haluk Topaloglu, Martin Brockington, et al.
Pageof 16

Showing results (101-110 of 159) with videos related to

Sort By:
Pageof 16
Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.
Current Microbiology|January 16, 2026
First Report of Aspergillus aculeatus Colonizing Protaetia brevitarsis Larvae: Pathogenicity and Dose-Dependent VirulenceHaokun Cheng, Jialin Qiu, Muhammad Adeel Ghafar, et al.
Rheumatology International|October 27, 2020
Inflammatory milieu of muscle biopsies in juvenile dermatomyositisErdal Sag, Gulsev Kale, Goknur Haliloglu, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|October 5, 2016
Surgical Treatment of Childhood Inflammatory Myofibroblastic TumorsTutku Soyer, Beril Talim, İbrahim Karnak, et al.
Journal of Neuromuscular Diseases|January 9, 2023
A Child with Refractory and Relapsing Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Myopathy: Case-Based ReviewSeher Sener, Ezgi Deniz Batu, Seher Sari, et al.
Neuromuscular Disorders : NMD|June 19, 1998
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblingsH Topaloğlu, B Talim, N Vignier, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Journal of Medical Genetics|May 21, 2013
A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathiesNilgun Cetin, Burcu Balci-Hayta, Hulya Gundesli, et al.
Multiple Sclerosis and Related Disorders|May 8, 2023
Neuromyelitis optica spectrum disorders with a benign course. Analysis of 544 patientsMarco A Lana-Peixoto, Natália C Talim, Dagoberto Callegaro, et al.
Archives of Neurology|February 16, 2006
Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutationsEugenio Mercuri, Haluk Topaloglu, Martin Brockington, et al.
Pageof 16