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K Foster

Showing results (401-410 of 446) with videos related to

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Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Human Molecular Genetics|July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresisF M Richards, M E Phipps, F Latif, et al.
Mycoses|December 14, 2007
Naildex: pilot evaluation of an onychodystrophy severity instrumentErin M Warshaw, Carmen A Traywick, Allison A Hoffman, et al.
Diabetologia|October 14, 2006
Vascular depression in older people with diabetesD G Bruce, G Casey, W A Davis, et al.
Journal of Alzheimer'S Disease : JAD|June 5, 2009
The relationship between memory complaints, perceived quality of life and mental health in apolipoprotein Eepsilon4 carriers and non-carriersHamid R Sohrabi, Kristyn A Bates, Mark Rodrigues, et al.
Clinical Biochemistry|August 11, 2000
Use of a dual monoclonal solid phase and a polyclonal detector to create an immunoassay for the detection of human cardiac troponin IS K Oh, K Foster, P Datta, et al.
Journal of Alzheimer'S Disease : JAD|July 16, 2014
Grey matter changes associated with deficit awareness in mild cognitive impairment: a voxel-based morphometry studyAndrew H Ford, Osvaldo P Almeida, Leon Flicker, et al.
Neuropsychologia|June 24, 2015
Longitudinal cognitive decline in the AIBL cohort: The role of APOE ε4 statusMatthew A Albrecht, Cassandra Szoeke, Paul Maruff, et al.
Brain : a Journal of Neurology|June 6, 2013
Lack of reliable evidence for a distinctive ε4-related cognitive phenotype that is independent from clinical diagnostic status: findings from the Australian Imaging, Biomarkers and Lifestyle StudyJonathan K Foster, Matthew A Albrecht, Greg Savage, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Pageof 45

Showing results (401-410 of 446) with videos related to

Sort By:
Pageof 45
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Human Molecular Genetics|July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresisF M Richards, M E Phipps, F Latif, et al.
Mycoses|December 14, 2007
Naildex: pilot evaluation of an onychodystrophy severity instrumentErin M Warshaw, Carmen A Traywick, Allison A Hoffman, et al.
Diabetologia|October 14, 2006
Vascular depression in older people with diabetesD G Bruce, G Casey, W A Davis, et al.
Journal of Alzheimer'S Disease : JAD|June 5, 2009
The relationship between memory complaints, perceived quality of life and mental health in apolipoprotein Eepsilon4 carriers and non-carriersHamid R Sohrabi, Kristyn A Bates, Mark Rodrigues, et al.
Clinical Biochemistry|August 11, 2000
Use of a dual monoclonal solid phase and a polyclonal detector to create an immunoassay for the detection of human cardiac troponin IS K Oh, K Foster, P Datta, et al.
Journal of Alzheimer'S Disease : JAD|July 16, 2014
Grey matter changes associated with deficit awareness in mild cognitive impairment: a voxel-based morphometry studyAndrew H Ford, Osvaldo P Almeida, Leon Flicker, et al.
Neuropsychologia|June 24, 2015
Longitudinal cognitive decline in the AIBL cohort: The role of APOE ε4 statusMatthew A Albrecht, Cassandra Szoeke, Paul Maruff, et al.
Brain : a Journal of Neurology|June 6, 2013
Lack of reliable evidence for a distinctive ε4-related cognitive phenotype that is independent from clinical diagnostic status: findings from the Australian Imaging, Biomarkers and Lifestyle StudyJonathan K Foster, Matthew A Albrecht, Greg Savage, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Pageof 45