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Talim

Showing results (91-100 of 159) with videos related to

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Neurology|March 26, 2003
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cystsH Topaloglu, M Brockington, Y Yuva, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 6, 2005
Focal segmental glomerulosclerosis associated with mitochondrial cytopathy: report of two cases with special emphasis on podocytesSafak Güçer, Beril Talim, Esin Aşan, et al.
American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.
Chemical Science|December 18, 2025
Sulfonyl-tuned amino DASAs for targeted photophysical and photoswitching controlAlexander Karr, Hye Joon Lee, A Talim G K, et al.
Pediatric Neurology|July 24, 2019
Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase DeficiencyYılmaz Yıldız, Beril Talim, Goknur Haliloglu, et al.
Seminars in Arthritis and Rheumatism|November 26, 2022
Early-onset juvenile dermatomyositis: A tertiary referral center experience and review of the literatureSeher Sener, Ozge Basaran, Ezgi Deniz Batu, et al.
Muscle & Nerve|September 2, 2022
Alterations in insulin-like growth factor system in spinal muscular atrophyAyse Yesbek Kaymaz, Sevgi Kostel Bal, Gamze Bora, et al.
Scientific Reports|September 14, 2021
Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular DystrophyEvrim Aksu-Menges, Cemil Can Eylem, Emirhan Nemutlu, et al.
Neuropediatrics|February 7, 2003
Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literatureG Haliloglu, A Chattopadhyay, L Skorodis, et al.
Muscle & Nerve|May 15, 2012
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-upLuciano Merlini, Monia Gennari, Elisabetta Malaspina, et al.
Pageof 16

Showing results (91-100 of 159) with videos related to

Sort By:
Pageof 16
Neurology|March 26, 2003
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cystsH Topaloglu, M Brockington, Y Yuva, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 6, 2005
Focal segmental glomerulosclerosis associated with mitochondrial cytopathy: report of two cases with special emphasis on podocytesSafak Güçer, Beril Talim, Esin Aşan, et al.
American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.
Chemical Science|December 18, 2025
Sulfonyl-tuned amino DASAs for targeted photophysical and photoswitching controlAlexander Karr, Hye Joon Lee, A Talim G K, et al.
Pediatric Neurology|July 24, 2019
Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase DeficiencyYılmaz Yıldız, Beril Talim, Goknur Haliloglu, et al.
Seminars in Arthritis and Rheumatism|November 26, 2022
Early-onset juvenile dermatomyositis: A tertiary referral center experience and review of the literatureSeher Sener, Ozge Basaran, Ezgi Deniz Batu, et al.
Muscle & Nerve|September 2, 2022
Alterations in insulin-like growth factor system in spinal muscular atrophyAyse Yesbek Kaymaz, Sevgi Kostel Bal, Gamze Bora, et al.
Scientific Reports|September 14, 2021
Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular DystrophyEvrim Aksu-Menges, Cemil Can Eylem, Emirhan Nemutlu, et al.
Neuropediatrics|February 7, 2003
Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literatureG Haliloglu, A Chattopadhyay, L Skorodis, et al.
Muscle & Nerve|May 15, 2012
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-upLuciano Merlini, Monia Gennari, Elisabetta Malaspina, et al.
Pageof 16