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R G Feldman

Showing results (141-150 of 150) with videos related to

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Science (New York, N.Y.)|February 20, 1987
The genetic defect causing familial Alzheimer's disease maps on chromosome 21P H St George-Hyslop, R E Tanzi, R J Polinsky, et al.
Infection and Immunity|March 1, 1994
Epitope specificity of rabbit immunoglobulin G (IgG) elicited by pneumococcal type 23F synthetic oligosaccharide- and native polysaccharide-protein conjugate vaccines: comparison with human anti-polysaccharide 23F IgGE Alonso de Velasco, A F Verheul, A M van Steijn, et al.
Climacteric : the Journal of the International Menopause Society|June 2, 2015
Treatment with denosumab reduces secondary fracture risk in women with postmenopausal osteoporosisS Palacios, L Kalouche-Khalil, R Rizzoli, et al.
American Journal of Medical Genetics|April 27, 2002
Segregation analysis of Parkinson disease revealing evidence for a major causative geneN E Maher, L J Currie, A M Lazzarini, et al.
Neurology|March 17, 2000
Transplantation of embryonic porcine mesencephalic tissue in patients with PDJ M Schumacher, S A Ellias, E P Palmer, et al.
Neurobiology of Aging|March 1, 1997
Moderate and advanced Alzheimer's patients exhibit platelet activation differencesT A Davies, H J Long, H E Tibbles, et al.
Neurology|January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.
Neurology|September 26, 2001
Genome-wide scan for Parkinson's disease: the GenePD StudyA L DeStefano, L I Golbe, M H Mark, et al.
Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Science (New York, N.Y.)|February 20, 1987
The genetic defect causing familial Alzheimer's disease maps on chromosome 21P H St George-Hyslop, R E Tanzi, R J Polinsky, et al.
Infection and Immunity|March 1, 1994
Epitope specificity of rabbit immunoglobulin G (IgG) elicited by pneumococcal type 23F synthetic oligosaccharide- and native polysaccharide-protein conjugate vaccines: comparison with human anti-polysaccharide 23F IgGE Alonso de Velasco, A F Verheul, A M van Steijn, et al.
Climacteric : the Journal of the International Menopause Society|June 2, 2015
Treatment with denosumab reduces secondary fracture risk in women with postmenopausal osteoporosisS Palacios, L Kalouche-Khalil, R Rizzoli, et al.
American Journal of Medical Genetics|April 27, 2002
Segregation analysis of Parkinson disease revealing evidence for a major causative geneN E Maher, L J Currie, A M Lazzarini, et al.
Neurology|March 17, 2000
Transplantation of embryonic porcine mesencephalic tissue in patients with PDJ M Schumacher, S A Ellias, E P Palmer, et al.
Neurobiology of Aging|March 1, 1997
Moderate and advanced Alzheimer's patients exhibit platelet activation differencesT A Davies, H J Long, H E Tibbles, et al.
Neurology|January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.
Neurology|September 26, 2001
Genome-wide scan for Parkinson's disease: the GenePD StudyA L DeStefano, L I Golbe, M H Mark, et al.
Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.
Pageof 15