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P Serdaroğlu

Showing results (11-20 of 19) with videos related to

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Muscle & Nerve|January 12, 1999
Electrical myotonia in heterozygous carriers of recessive myotonia congenitaF Deymeer, F Lehmann-Horn, P Serdaroğlu, et al.
Human Genetics|August 1, 1992
DNA analysis in Turkish Duchenne/Becker muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
The Turkish Journal of Pediatrics|April 1, 1992
Carrier detection by DNA analysis in Duchenne muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Annals of Human Genetics|June 5, 2001
Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and IndiansS Onengüt, G N Kavaslar, E Battaloğlu, et al.
Neuroradiology|May 1, 1996
A controlled study of reliability and validity of MRI findings in neuro-Behçet's diseaseO Coban, S Bahar, G Akman-Demir, et al.
Muscle & Nerve|August 14, 1998
The dominant chloride channel mutant G200R causing fluctuating myotonia: clinical findings, electrophysiology, and channel pathologyS Wagner, F Deymeer, L L Kürz, et al.
Journal of Neurology|February 24, 2001
Anti-alpha B-crystallin immunoreactivity in inflammatory nervous system diseasesB Celet, G Akman-Demir, P Serdaroğlu, et al.
Neurogenetics|August 29, 2001
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneityK Christodoulou, F Deymeer, P Serdaroğlu, et al.
Neurology|September 25, 1999
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit geneL Middleton, K Ohno, K Christodoulou, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Muscle & Nerve|January 12, 1999
Electrical myotonia in heterozygous carriers of recessive myotonia congenitaF Deymeer, F Lehmann-Horn, P Serdaroğlu, et al.
Human Genetics|August 1, 1992
DNA analysis in Turkish Duchenne/Becker muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
The Turkish Journal of Pediatrics|April 1, 1992
Carrier detection by DNA analysis in Duchenne muscular dystrophy familiesE Battaloğlu, M Telatar, F Deymeer, et al.
Annals of Human Genetics|June 5, 2001
Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and IndiansS Onengüt, G N Kavaslar, E Battaloğlu, et al.
Neuroradiology|May 1, 1996
A controlled study of reliability and validity of MRI findings in neuro-Behçet's diseaseO Coban, S Bahar, G Akman-Demir, et al.
Muscle & Nerve|August 14, 1998
The dominant chloride channel mutant G200R causing fluctuating myotonia: clinical findings, electrophysiology, and channel pathologyS Wagner, F Deymeer, L L Kürz, et al.
Journal of Neurology|February 24, 2001
Anti-alpha B-crystallin immunoreactivity in inflammatory nervous system diseasesB Celet, G Akman-Demir, P Serdaroğlu, et al.
Neurogenetics|August 29, 2001
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneityK Christodoulou, F Deymeer, P Serdaroğlu, et al.
Neurology|September 25, 1999
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit geneL Middleton, K Ohno, K Christodoulou, et al.
Pageof 2