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Showing results (11-20 of 89) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|August 31, 2000
[New insights in frontotemporal dementia]S M Rosso, P Heutink, A Tibben, et al.
Journal of Medical Virology|November 1, 1988
Natural antibodies to HIV-tat epitopes and expression of HIV-1 genes in vivoW J Krone, C Debouck, L G Epstein, et al.
American Journal of Ophthalmology|June 1, 1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS geneC B Hoyng, P Heutink, L Testers, et al.
Journal of Medical Genetics|June 1, 1994
Phenotypic analysis of triphalangeal thumb and associated hand malformationsJ Zguricas, P J Snijders, S E Hovius, et al.
Plant Physiology|May 1, 1989
Rhizosphere Acidification by Iron Deficient Bean Plants: The Role of Trace Amounts of Divalent Metal Ions: A Study on Roots of Intact Plants with the Use of C- and P-NMRH F Bienfait, H J Lubberding, P Heutink, et al.
The American Journal of Pathology|February 13, 2001
Molecular analysis of mutant and wild-type tau deposited in the brain affected by the FTDP-17 R406W mutationT Miyasaka, M Morishima-Kawashima, R Ravid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 16, 1999
N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam studyB S Harhangi, B A Oostra, P Heutink, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2001
CYP2D6 polymorphism in Parkinson's disease: the Rotterdam StudyB S Harhangi, B A Oostra, P Heutink, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
Human Molecular Genetics|December 15, 2000
Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patientsP Rizzu, M Joosse, R Ravid, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Nederlands Tijdschrift Voor Geneeskunde|August 31, 2000
[New insights in frontotemporal dementia]S M Rosso, P Heutink, A Tibben, et al.
Journal of Medical Virology|November 1, 1988
Natural antibodies to HIV-tat epitopes and expression of HIV-1 genes in vivoW J Krone, C Debouck, L G Epstein, et al.
American Journal of Ophthalmology|June 1, 1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS geneC B Hoyng, P Heutink, L Testers, et al.
Journal of Medical Genetics|June 1, 1994
Phenotypic analysis of triphalangeal thumb and associated hand malformationsJ Zguricas, P J Snijders, S E Hovius, et al.
Plant Physiology|May 1, 1989
Rhizosphere Acidification by Iron Deficient Bean Plants: The Role of Trace Amounts of Divalent Metal Ions: A Study on Roots of Intact Plants with the Use of C- and P-NMRH F Bienfait, H J Lubberding, P Heutink, et al.
The American Journal of Pathology|February 13, 2001
Molecular analysis of mutant and wild-type tau deposited in the brain affected by the FTDP-17 R406W mutationT Miyasaka, M Morishima-Kawashima, R Ravid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 16, 1999
N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam studyB S Harhangi, B A Oostra, P Heutink, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2001
CYP2D6 polymorphism in Parkinson's disease: the Rotterdam StudyB S Harhangi, B A Oostra, P Heutink, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
Human Molecular Genetics|December 15, 2000
Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patientsP Rizzu, M Joosse, R Ravid, et al.
Pageof 9