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Gabor E Linthorst

Showing results (11-20 of 63) with videos related to

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Molecular Genetics and Metabolism|December 15, 2015
Discontinuation of enzyme replacement therapy in Fabry disease in the Dutch cohortMaarten Arends, Gabor E Linthorst, Carla E Hollak, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 26, 2012
[Using rare disease as a research model]Matthijs J V Scheltema, Maarten R Soeters, Gabor E Linthorst
Nederlands Tijdschrift Voor Geneeskunde|August 4, 2021
[Case reports of deceased patients]Corrette M C Ploem, Marieke A R Bak, Gabor E Linthorst
Medical Education|October 3, 2007
The majority of bold statements expressed during grand rounds lack scientific meritGabor E Linthorst, Johannes M A Daniels, David J van Westerloo
Journal of the American College of Cardiology|May 24, 2008
Enzyme activity for determination of presence of Fabry disease in women results in 40% false-negative resultsGabor E Linthorst, Ben J H M Poorthuis, Carla E M Hollak
Archives of Disease in Childhood|April 27, 2010
'Doctor Google' ending the diagnostic odyssey in lysosomal storage disorders: parents using internet search engines as an efficient diagnostic strategy in rare diseasesMachtelt G Bouwman, Quirine G A Teunissen, Frits A Wijburg, et al.
Current Pain and Headache Reports|September 3, 2013
Fabry disease: a rare cause of neuropathic painMarieke Biegstraaten, Gabor E Linthorst, Ivo N van Schaik, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 16, 2014
[Complaint to the disciplinary board about a resident]Gabor E Linthorst, Fanny N Lauw, Lilian A Hanekamp, et al.
Nature Reviews. Endocrinology|June 18, 2016
Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural historyStephan Kemp, Irene C Huffnagel, Gabor E Linthorst, et al.
Orphanet Journal of Rare Diseases|February 21, 2013
Cost-effectiveness of enzyme replacement therapy for Fabry diseaseSaskia M Rombach, Carla E M Hollak, Gabor E Linthorst, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Molecular Genetics and Metabolism|December 15, 2015
Discontinuation of enzyme replacement therapy in Fabry disease in the Dutch cohortMaarten Arends, Gabor E Linthorst, Carla E Hollak, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 26, 2012
[Using rare disease as a research model]Matthijs J V Scheltema, Maarten R Soeters, Gabor E Linthorst
Nederlands Tijdschrift Voor Geneeskunde|August 4, 2021
[Case reports of deceased patients]Corrette M C Ploem, Marieke A R Bak, Gabor E Linthorst
Medical Education|October 3, 2007
The majority of bold statements expressed during grand rounds lack scientific meritGabor E Linthorst, Johannes M A Daniels, David J van Westerloo
Journal of the American College of Cardiology|May 24, 2008
Enzyme activity for determination of presence of Fabry disease in women results in 40% false-negative resultsGabor E Linthorst, Ben J H M Poorthuis, Carla E M Hollak
Archives of Disease in Childhood|April 27, 2010
'Doctor Google' ending the diagnostic odyssey in lysosomal storage disorders: parents using internet search engines as an efficient diagnostic strategy in rare diseasesMachtelt G Bouwman, Quirine G A Teunissen, Frits A Wijburg, et al.
Current Pain and Headache Reports|September 3, 2013
Fabry disease: a rare cause of neuropathic painMarieke Biegstraaten, Gabor E Linthorst, Ivo N van Schaik, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 16, 2014
[Complaint to the disciplinary board about a resident]Gabor E Linthorst, Fanny N Lauw, Lilian A Hanekamp, et al.
Nature Reviews. Endocrinology|June 18, 2016
Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural historyStephan Kemp, Irene C Huffnagel, Gabor E Linthorst, et al.
Orphanet Journal of Rare Diseases|February 21, 2013
Cost-effectiveness of enzyme replacement therapy for Fabry diseaseSaskia M Rombach, Carla E M Hollak, Gabor E Linthorst, et al.
Pageof 7