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M Pittman

Showing results (191-200 of 218) with videos related to

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Journal of Breast Imaging|March 1, 2024
Adaptations of Breast Imaging Centers to the COVID-19 Pandemic: A Survey of California and TexasJames S Chalfant, Ethan O Cohen, Jessica W T Leung, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
Blood|April 18, 2024
Standardized indolent systemic mastocytosis evaluations across a health care system: implications for screening accuracyJeremy C McMurray, Curtis S Pacheco, Brandon J Schornack, et al.
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2022
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalitiesElla F Whittle, Madison Chilian, Ehsan Ghayoor Karimiani, et al.
Neurobiology of Aging|February 6, 2018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseCornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, et al.
Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.
Pageof 22

Showing results (191-200 of 218) with videos related to

Sort By:
Pageof 22
Journal of Breast Imaging|March 1, 2024
Adaptations of Breast Imaging Centers to the COVID-19 Pandemic: A Survey of California and TexasJames S Chalfant, Ethan O Cohen, Jessica W T Leung, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
Blood|April 18, 2024
Standardized indolent systemic mastocytosis evaluations across a health care system: implications for screening accuracyJeremy C McMurray, Curtis S Pacheco, Brandon J Schornack, et al.
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2022
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalitiesElla F Whittle, Madison Chilian, Ehsan Ghayoor Karimiani, et al.
Neurobiology of Aging|February 6, 2018
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's diseaseCornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, et al.
Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.
Pageof 22