Treatment of gastrointestinal complication in transthyretin amyloidosis. A single centre’s experience

por Suhr, Ole B
Publicado 2015

Diagnosis and treatment of gastrointestinal dysfunction in hereditary TTR amyloidosis

por Obici, Laura, Suhr, Ole B.
Publicado 2019

Variation in amount of wild-type transthyretin in different fibril and tissue types in ATTR amyloidosis

por Ihse, Elisabet, Suhr, Ole B., Hellman, Ulf, Westermark, Per
Publicado 2010

Transthyretin-derived amyloidosis: Probably a common cause of lumbar spinal stenosis

por Westermark, Per, Westermark, Gunilla T., Suhr, Ole B., Berg, Svante
Publicado 2014

Irritable bowel syndrome-like symptoms in treated microscopic colitis patients compared with controls: a cross-sectional study

por Pagoldh, Jenny, Lundgren, David, Suhr, Ole B, Karling, Pontus
Publicado 2019

Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis

por Wixner, Jonas, Sundström, Torbjörn, Karling, Pontus, Anan, Intissar, Suhr, Ole B
Publicado 2015

Amyloid Cardiomyopathy in Hereditary Transthyretin V30M Amyloidosis - Impact of Sex and Amyloid Fibril Composition

por Arvidsson, Sandra, Pilebro, Björn, Westermark, Per, Lindqvist, Per, Suhr, Ole B.
Publicado 2015

Survival After Transplantation in Patients With Mutations Other Than Val30Met: Extracts From the FAP World Transplant Registry

por Suhr, Ole B., Larsson, Marie, Ericzon, Bo-Göran, Wilczek, Henryk E.
Publicado 2016

Allele Specific Expression of the Transthyretin Gene in Swedish Patients with Hereditary Transthyretin Amyloidosis (ATTR V30M) Is Similar between the Two Alleles

por Norgren, Nina, Hellman, Urban, Ericzon, Bo Göran, Olsson, Malin, Suhr, Ole B.
Publicado 2012

(99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosis

por Pilebro, Björn, Suhr, Ole B., Näslund, Ulf, Westermark, Per, Lindqvist, Per, Sundström, Torbjörn
Publicado 2016

Cardiac transthyretin amyloidosis (99m)Tc-DPD SPECT correlates with strain echocardiography and biomarkers

por Löfbacka, Viktor, Axelsson, Jan, Pilebro, Björn, Suhr, Ole B., Lindqvist, Per, Sundström, Torbjörn
Publicado 2020

THAOS: Gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease

por Wixner, Jonas, Mundayat, Rajiv, Karayal, Onur N, Anan, Intissar, Karling, Pontus, Suhr, Ole B
Publicado 2014

Impact of genotype and phenotype on cardiac biomarkers in patients with transthyretin amyloidosis – Report from the Transthyretin Amyloidosis Outcome Survey (THAOS)

por Kristen, Arnt V., Maurer, Mathew S., Rapezzi, Claudio, Mundayat, Rajiv, Suhr, Ole B., Damy, Thibaud
Publicado 2017

Evolving landscape in the management of transthyretin amyloidosis

por Hawkins, Philip N., Ando, Yukio, Dispenzeri, Angela, Gonzalez-Duarte, Alejandra, Adams, David, Suhr, Ole B.
Publicado 2015

Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns...

por Parman, Yesim, Adams, David, Obici, Laura, Galán, Lucía, Guergueltcheva, Velina, Suhr, Ole B., Coelho, Teresa
Publicado 2016

The clinical course after glucocorticoid treatment in patients with inflammatory bowel disease is linked to suppression of the hypothalamic–pituitary–adrenal axis: a retrospective...

por Ibrahim, Aghil, Dahlqvist, Per, Olsson, Tommy, Lundgren, David, Werner, Mårten, Suhr, Ole B., Karling, Pontus
Publicado 2017

A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers

por Olsson, Malin, Norgren, Nina, Obayashi, Konen, Plante-Bordeneuve, Violaine, Suhr, Ole B, Cederquist, Kristina, Jonasson, Jenni
Publicado 2010

Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis

por Obici, Laura, Kuks, Jan B., Buades, Juan, Adams, David, Suhr, Ole B., Coelho, Teresa, Kyriakides, Theodore
Publicado 2016

Atrial Fibrillation and Central Nervous Complications in Liver Transplanted Hereditary Transthyretin Amyloidosis Patients

por Wange, Niklas, Anan, Intissar, Ericzon, Bo-Göran, Pennlert, Johanna, Pilebro, Björn, Suhr, Ole B., Wixner, Jonas
Publicado 2018

Amyloid fibril composition type is consistent over time in patients with Val30Met (p.Val50Met) transthyretin amyloidosis

por Anan, Intissar, Suhr, Ole B., Liszewska, Katarzyna, Mejia Baranda, Jorge, Pilebro, Björn, Wixner, Jonas, Ihse, Elisabet
Publicado 2022