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Yesim Parman

Showing results (31-40 of 61) with videos related to

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Clinical and Experimental Immunology|August 28, 2023
Disease activity in chronic inflammatory demyelinating polyneuropathy: association between circulating B-cell subsets, cytokine levels, and clinical outcomesAyse Nur Ozdag Acarli, Erdem Tuzun, Elif Sanli, et al.
Journal of the Peripheral Nervous System : JPNS|June 2, 2026
Significance of Phrenic Nerve Conduction Study in the Electrodiagnosis of Guillain Barré SyndromeVolkan Tasdemir, Nermin Gorkem Sirin, Sezin Alpaydın Baslo, et al.
Clinical Rheumatology|January 12, 2012
Association of amyotrophic lateral sclerosis and Behcet's disease: is there a relationship? A multi-national case seriesHela Mrabet, Afshin Borhani-Haghighi, Emel Koseoglu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2015
Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencingDaliya Kancheva, Derek Atkinson, Peter De Rijk, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2021
Dysregulation of myelin synthesis and actomyosin function underlies aberrant myelin in CMT4B1 neuropathyMarta Guerrero-Valero, Federica Grandi, Silvia Cipriani, et al.
Brain : a Journal of Neurology|October 8, 2004
Clinicopathological and genetic study of early-onset demyelinating neuropathyYesim Parman, Esra Battaloglu, Ibrahim Baris, et al.
European Journal of Medical Genetics|September 16, 2014
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathyAhmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2013
Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4DYuji Okamoto, Meryem Tuba Goksungur, Davut Pehlivan, et al.
American Journal of Human Genetics|June 15, 2007
Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4Claudia Stendel, Andreas Roos, Tine Deconinck, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Clinical and Experimental Immunology|August 28, 2023
Disease activity in chronic inflammatory demyelinating polyneuropathy: association between circulating B-cell subsets, cytokine levels, and clinical outcomesAyse Nur Ozdag Acarli, Erdem Tuzun, Elif Sanli, et al.
Journal of the Peripheral Nervous System : JPNS|June 2, 2026
Significance of Phrenic Nerve Conduction Study in the Electrodiagnosis of Guillain Barré SyndromeVolkan Tasdemir, Nermin Gorkem Sirin, Sezin Alpaydın Baslo, et al.
Clinical Rheumatology|January 12, 2012
Association of amyotrophic lateral sclerosis and Behcet's disease: is there a relationship? A multi-national case seriesHela Mrabet, Afshin Borhani-Haghighi, Emel Koseoglu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2015
Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencingDaliya Kancheva, Derek Atkinson, Peter De Rijk, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2021
Dysregulation of myelin synthesis and actomyosin function underlies aberrant myelin in CMT4B1 neuropathyMarta Guerrero-Valero, Federica Grandi, Silvia Cipriani, et al.
Brain : a Journal of Neurology|October 8, 2004
Clinicopathological and genetic study of early-onset demyelinating neuropathyYesim Parman, Esra Battaloglu, Ibrahim Baris, et al.
European Journal of Medical Genetics|September 16, 2014
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathyAhmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2013
Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4DYuji Okamoto, Meryem Tuba Goksungur, Davut Pehlivan, et al.
American Journal of Human Genetics|June 15, 2007
Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4Claudia Stendel, Andreas Roos, Tine Deconinck, et al.
Pageof 7