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S M Zuberi

Showing results (11-20 of 16) with videos related to

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Neurology|July 28, 2010
Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twinsT D Graves, S Rajakulendran, S M Zuberi, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, 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.
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.
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.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Neurology|July 28, 2010
Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twinsT D Graves, S Rajakulendran, S M Zuberi, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, 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.
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.
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.
Pageof 2