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P I Tomlin

Showing results (1-10 of 6) with videos related to

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Developmental Medicine and Child Neurology|December 1, 1986
A study on carbamazepine levels, including estimation of 10-11 epoxy-carbamazepine and levels in free plasma and salivaP I Tomlin, I McKinlay, I Smith
Clinical Dysmorphology|June 3, 2005
Kohlschutter syndrome in siblingsD Donnai, P I Tomlin, R M Winter
Seizure|June 1, 1992
Fatal liver failure following generalized tonic-clonic seizuresS W Brown, M A Clarke, P I Tomlin
Journal of Medical Genetics|January 1, 1996
Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisationH M Kingston, D H Ledbetter, P I Tomlin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 28, 2012
Distinctive neurological phenotype associated with partial trisomy of chromosome 16B G McCullagh, B Kerr, S Trueman, et al.
Clinical and Experimental Immunology|November 28, 2002
Hyper IgD syndrome (HIDS) associated with in vitro evidence of defective monocyte TNFRSF1A shedding and partial response to TNF receptor blockade with etanerceptP D Arkwright, M F McDermott, S M Houten, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Developmental Medicine and Child Neurology|December 1, 1986
A study on carbamazepine levels, including estimation of 10-11 epoxy-carbamazepine and levels in free plasma and salivaP I Tomlin, I McKinlay, I Smith
Clinical Dysmorphology|June 3, 2005
Kohlschutter syndrome in siblingsD Donnai, P I Tomlin, R M Winter
Seizure|June 1, 1992
Fatal liver failure following generalized tonic-clonic seizuresS W Brown, M A Clarke, P I Tomlin
Journal of Medical Genetics|January 1, 1996
Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisationH M Kingston, D H Ledbetter, P I Tomlin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 28, 2012
Distinctive neurological phenotype associated with partial trisomy of chromosome 16B G McCullagh, B Kerr, S Trueman, et al.
Clinical and Experimental Immunology|November 28, 2002
Hyper IgD syndrome (HIDS) associated with in vitro evidence of defective monocyte TNFRSF1A shedding and partial response to TNF receptor blockade with etanerceptP D Arkwright, M F McDermott, S M Houten, et al.
Pageof 1