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O B Suhr

Showing results (1-10 of 37) with videos related to

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Journal of Clinical Nursing|October 7, 2000
Waiting for a liver transplant: the experience of patients with familial amyloidotic polyneuropathyE Jonsén, E Athlin, O B Suhr
Journal of Internal Medicine|January 18, 2017
One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril compositionO B Suhr, E Lundgren, P Westermark
Journal of Advanced Nursing|February 15, 2000
Family members' experience of familial amyloidotic polyneuropathy disease--an infernal struggle and a fact of lifeE Jonsén, E Athlin, O B Suhr
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 11, 2001
Early liver transplantation is essential for familial amyloidotic polyneuropathy patients' quality of lifeE Jonsén, O B Suhr, K Tashima, et al.
Transplantation|September 26, 2000
Liver transplantation restores endocrine cells in patients with familial amyloidotic polyneuropathyI Anan, M El-Salhy, N Nyhlin, et al.
Journal of Internal Medicine|October 16, 2004
Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twinsG Holmgren, L Wikström, H-E Lundgren, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|May 29, 2000
Liver transplantation for hereditary transthyretin amyloidosisO B Suhr, G Herlenius, S Friman, et al.
European Journal of Haematology|November 20, 1998
Intestinal permeability in patients with acute myeloid leukemiaG M Sundström, A Wahlin, I Nordin-Andersson, et al.
Scandinavian Journal of Gastroenterology|November 4, 2000
Outcome of gastrointestinal complications after liver transplantation for familial amyloidotic polyneuropathyK Lång, L Wikström, A Danielsson, et al.
Journal of Internal Medicine|August 24, 2005
Amyloid heart disease mimicking hypertrophic cardiomyopathyS Mörner, U Hellman, O B Suhr, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Journal of Clinical Nursing|October 7, 2000
Waiting for a liver transplant: the experience of patients with familial amyloidotic polyneuropathyE Jonsén, E Athlin, O B Suhr
Journal of Internal Medicine|January 18, 2017
One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril compositionO B Suhr, E Lundgren, P Westermark
Journal of Advanced Nursing|February 15, 2000
Family members' experience of familial amyloidotic polyneuropathy disease--an infernal struggle and a fact of lifeE Jonsén, E Athlin, O B Suhr
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 11, 2001
Early liver transplantation is essential for familial amyloidotic polyneuropathy patients' quality of lifeE Jonsén, O B Suhr, K Tashima, et al.
Transplantation|September 26, 2000
Liver transplantation restores endocrine cells in patients with familial amyloidotic polyneuropathyI Anan, M El-Salhy, N Nyhlin, et al.
Journal of Internal Medicine|October 16, 2004
Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twinsG Holmgren, L Wikström, H-E Lundgren, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|May 29, 2000
Liver transplantation for hereditary transthyretin amyloidosisO B Suhr, G Herlenius, S Friman, et al.
European Journal of Haematology|November 20, 1998
Intestinal permeability in patients with acute myeloid leukemiaG M Sundström, A Wahlin, I Nordin-Andersson, et al.
Scandinavian Journal of Gastroenterology|November 4, 2000
Outcome of gastrointestinal complications after liver transplantation for familial amyloidotic polyneuropathyK Lång, L Wikström, A Danielsson, et al.
Journal of Internal Medicine|August 24, 2005
Amyloid heart disease mimicking hypertrophic cardiomyopathyS Mörner, U Hellman, O B Suhr, et al.
Pageof 4