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E Scheffer

Showing results (231-240 of 740) with videos related to

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Ebiomedicine|October 30, 2024
Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' familiesKaren L Oliver, Ingrid E Scheffer, Colin A Ellis, et al.
Journal of Paediatrics and Child Health|September 2, 2022
Response to sequential treatment with prednisolone and vigabatrin in infantile spasmsWinston Dzau, Sally Cheng, Penny Snell, et al.
The Journal of Pathology|July 1, 1997
Quality assessment by expert opinion in melanoma pathology: experience of the pathology panel of the Dutch Melanoma Working PartyK C Veenhuizen, P E De Wit, W J Mooi, et al.
Developmental Medicine and Child Neurology|February 12, 2009
Electroencephalographic abnormalities during sleep in children with developmental speech-language disorders: a case-control studyBronwyn Parry-Fielder, Kevin Collins, John Fisher, et al.
Expert Review of Neurotherapeutics|September 14, 2021
Cutting edge approaches to detecting brain mosaicism associated with common focal epilepsies: implications for diagnosis and potential therapiesZimeng Ye, Mark F Bennett, Melanie Bahlo, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|May 2, 2003
A twin study of genetic influences on epilepsy outcomeMichael R Johnson, Roger L Milne, Yvonne Torn-Broers, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
Cancer|April 1, 1984
Immunohistochemical and histochemical tools in the diagnosis of amelanotic melanomaS G van Duinen, D J Ruiter, P Hageman, et al.
Epilepsia|March 14, 2025
Sleep-related hypermotor epilepsy-No longer controversialFrancesca Bisulli, Samuel F Berkovic, Ingrid E Scheffer, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Pageof 74

Showing results (231-240 of 740) with videos related to

Sort By:
Pageof 74
Ebiomedicine|October 30, 2024
Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' familiesKaren L Oliver, Ingrid E Scheffer, Colin A Ellis, et al.
Journal of Paediatrics and Child Health|September 2, 2022
Response to sequential treatment with prednisolone and vigabatrin in infantile spasmsWinston Dzau, Sally Cheng, Penny Snell, et al.
The Journal of Pathology|July 1, 1997
Quality assessment by expert opinion in melanoma pathology: experience of the pathology panel of the Dutch Melanoma Working PartyK C Veenhuizen, P E De Wit, W J Mooi, et al.
Developmental Medicine and Child Neurology|February 12, 2009
Electroencephalographic abnormalities during sleep in children with developmental speech-language disorders: a case-control studyBronwyn Parry-Fielder, Kevin Collins, John Fisher, et al.
Expert Review of Neurotherapeutics|September 14, 2021
Cutting edge approaches to detecting brain mosaicism associated with common focal epilepsies: implications for diagnosis and potential therapiesZimeng Ye, Mark F Bennett, Melanie Bahlo, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|May 2, 2003
A twin study of genetic influences on epilepsy outcomeMichael R Johnson, Roger L Milne, Yvonne Torn-Broers, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
Cancer|April 1, 1984
Immunohistochemical and histochemical tools in the diagnosis of amelanotic melanomaS G van Duinen, D J Ruiter, P Hageman, et al.
Epilepsia|March 14, 2025
Sleep-related hypermotor epilepsy-No longer controversialFrancesca Bisulli, Samuel F Berkovic, Ingrid E Scheffer, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Pageof 74