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H G Marks

Showing results (21-30 of 29) with videos related to

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Journal of Pediatric Orthopedics|May 1, 1991
Intraspinal epidermoid tumors in children: problems in recognition and imaging techniques for diagnosisP A Caro, H G Marks, D Keret, et al.
Nature Genetics|November 1, 1993
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneB B Roa, P J Dyck, H G Marks, et al.
Electroencephalography and Clinical Neurophysiology|January 1, 1986
Effects of halothane on intraoperative scalp-recorded somatosensory evoked potentials to posterior tibial nerve stimulation in manS K Salzman, A L Beckman, H G Marks, et al.
The Journal of Pediatrics|August 1, 1978
Catch-up brain growth-demonstration by CAT scanH G Marks, P Borns, N L Steg, et al.
Molecular Genetics and Metabolism|October 11, 2001
Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophyR Frisch, K R Singleton, P A Moses, et al.
Annals of Neurology|July 1, 1991
Use of computed tomography, magnetic resonance imaging, and localized 1H magnetic resonance spectroscopy in Canavan's disease: a case reportH G Marks, P A Caro, Z Y Wang, et al.
Neurology|October 1, 1996
Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effectP P Koty, E Pegoraro, G Hobson, et al.
Neuropediatrics|May 28, 2008
Epilepsy and respiratory chain defects in children with mitochondrial encephalopathiesD S Khurana, L Salganicoff, J J Melvin, et al.
Neurology|November 9, 2000
Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseG M Hobson, A P Davis, N C Stowell, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Pediatric Orthopedics|May 1, 1991
Intraspinal epidermoid tumors in children: problems in recognition and imaging techniques for diagnosisP A Caro, H G Marks, D Keret, et al.
Nature Genetics|November 1, 1993
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) geneB B Roa, P J Dyck, H G Marks, et al.
Electroencephalography and Clinical Neurophysiology|January 1, 1986
Effects of halothane on intraoperative scalp-recorded somatosensory evoked potentials to posterior tibial nerve stimulation in manS K Salzman, A L Beckman, H G Marks, et al.
The Journal of Pediatrics|August 1, 1978
Catch-up brain growth-demonstration by CAT scanH G Marks, P Borns, N L Steg, et al.
Molecular Genetics and Metabolism|October 11, 2001
Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophyR Frisch, K R Singleton, P A Moses, et al.
Annals of Neurology|July 1, 1991
Use of computed tomography, magnetic resonance imaging, and localized 1H magnetic resonance spectroscopy in Canavan's disease: a case reportH G Marks, P A Caro, Z Y Wang, et al.
Neurology|October 1, 1996
Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effectP P Koty, E Pegoraro, G Hobson, et al.
Neuropediatrics|May 28, 2008
Epilepsy and respiratory chain defects in children with mitochondrial encephalopathiesD S Khurana, L Salganicoff, J J Melvin, et al.
Neurology|November 9, 2000
Mutations in noncoding regions of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseG M Hobson, A P Davis, N C Stowell, et al.
Pageof 3