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S Cirak

Showing results (1-10 of 12) with videos related to

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Human & Experimental Toxicology|September 1, 1992
A case of porphyria due to carbaryl intoxicationH Sargin, S Cirak, S Gürçay
Der Nervenarzt|July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]G Wunderlich, A Abicht, A Brunn, et al.
Child: Care, Health and Development|June 9, 2012
Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophyM E Garralda, H McConachie, A Le Couteur, et al.
Revue Neurologique|July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathiesC Paketci, M Karakaya, P Edem, et al.
Neuropediatrics|June 15, 2006
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosumA Olmez, G Uyanik, R K Ozgül, et al.
Neurology|January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathiesM Lommel, S Cirak, T Willer, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United KingdomL Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD|July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvementT Cullup, P J Lamont, S Cirak, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
Neurology|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Human & Experimental Toxicology|September 1, 1992
A case of porphyria due to carbaryl intoxicationH Sargin, S Cirak, S Gürçay
Der Nervenarzt|July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]G Wunderlich, A Abicht, A Brunn, et al.
Child: Care, Health and Development|June 9, 2012
Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophyM E Garralda, H McConachie, A Le Couteur, et al.
Revue Neurologique|July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathiesC Paketci, M Karakaya, P Edem, et al.
Neuropediatrics|June 15, 2006
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosumA Olmez, G Uyanik, R K Ozgül, et al.
Neurology|January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathiesM Lommel, S Cirak, T Willer, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United KingdomL Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD|July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvementT Cullup, P J Lamont, S Cirak, et al.
Neurology|January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizuresR Straussberg, L Basel-Vanagaite, S Kivity, et al.
Neurology|June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patientsM Scoto, S Cirak, R Mein, et al.
Pageof 2