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M Zuberi

Showing results (111-120 of 170) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2024
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 2Maike Josler, Ines El Naggar, Annikki Bertolini, et al.
Neuropediatrics|March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integumentY J Crow, J McMenamin, C A Haenggeli, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Anticancer Research|October 3, 2018
Differential Effects of <i>In Vitro</i> Treatment with Cinobufotalin on Three Types of Ovarian Cancer CellsSyeda H Afroze, Chander Peddaboina, Anthony B McDowell, et al.
Epilepsia|April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsyAilsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Journal of Medical Genetics|October 6, 2018
PEHO syndrome: the endpoint of different genetic epilepsiesManali Chitre, Michael S Nahorski, Kaitlin Stouffer, et al.
Brain : a Journal of Neurology|June 4, 1999
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsyS M Zuberi, L H Eunson, A Spauschus, et al.
Annals of Neurology|October 12, 2000
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variabilityL H Eunson, R Rea, S M Zuberi, et al.
Epilepsia|March 10, 2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and TerminologyRobert S Fisher, J Helen Cross, Jacqueline A French, et al.
Pediatrics|February 5, 2008
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardationAgatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, et al.
Pageof 17

Showing results (111-120 of 170) with videos related to

Sort By:
Pageof 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2024
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 2Maike Josler, Ines El Naggar, Annikki Bertolini, et al.
Neuropediatrics|March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integumentY J Crow, J McMenamin, C A Haenggeli, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Anticancer Research|October 3, 2018
Differential Effects of <i>In Vitro</i> Treatment with Cinobufotalin on Three Types of Ovarian Cancer CellsSyeda H Afroze, Chander Peddaboina, Anthony B McDowell, et al.
Epilepsia|April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsyAilsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Journal of Medical Genetics|October 6, 2018
PEHO syndrome: the endpoint of different genetic epilepsiesManali Chitre, Michael S Nahorski, Kaitlin Stouffer, et al.
Brain : a Journal of Neurology|June 4, 1999
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsyS M Zuberi, L H Eunson, A Spauschus, et al.
Annals of Neurology|October 12, 2000
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variabilityL H Eunson, R Rea, S M Zuberi, et al.
Epilepsia|March 10, 2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and TerminologyRobert S Fisher, J Helen Cross, Jacqueline A French, et al.
Pediatrics|February 5, 2008
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardationAgatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, et al.
Pageof 17