Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis von Ihse, E, Ybo, A, Suhr, OB, Lindqvist, P, Backman, C, Westermark, P

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Transthyretin amyloid deposits in lumbar spinal stenosis and assessment of signs of systemic amyloidosis von Eldhagen, P., Berg, S., Lund, L.H., Sörensson, P., Suhr, O.B., Westermark, P.

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Survival After Transplantation in Patients With Mutations Other Than Val30Met: Extracts From the FAP World Transplant Registry von Suhr, Ole B, Larsson, Marie, Ericzon, Bo-Göran, Wilczek, Henryk E

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Transthyretin-derived amyloidosis: Probably a common cause of lumbar spinal stenosis von Westermark, Per, Westermark, Gunilla T., Suhr, Ole B., Berg, Svante

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Atrial Fibrillation and Central Nervous Complications in Liver Transplanted Hereditary Transthyretin Amyloidosis Patients von Wange, Niklas, Anan, Intissar, Ericzon, Bo-Göran, Pennlert, Johanna, Pilebro, Björn, Suhr, Ole B, Wixner, Jonas

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Liver Transplantation for Familial Amyloidotic Polyneuropathy (FAP): A Single‐Center Experience Over 16 Years von Yamamoto, S., Wilczek, H. E., Nowak, G., Larsson, M., Oksanen, A., Iwata, T., Gjertsen, H., Söderdahl, G., Wikström, L., Ando, Y., Suhr, O. B., Ericzon, B.‐G.

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Combining ECG and echocardiography to identify transthyretin cardiac amyloidosis in heart failure von Löfbacka, Viktor, Suhr, Ole B., Pilebro, Bjorn, Wixner, Jonas, Sundström, Torbjorn, Lindmark, Krister, Anan, Intissar, Lindqvist, Per

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Liver transplantation for familial amyloidotic polyneuropathy: Impact on Swedish patients' survival von Okamoto, Sadahisa, Wixner, Jonas, Obayashi, Konen, Ando, Yukio, Ericzon, Bo‐Göran, Friman, Styrbjörn, Uchino, Makoto, Suhr, Ole B.

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P.025 APOLLO, a phase 3 study of patisiran for the treatment of hereditary transthyretin amyloidosis (hATTR): 18-month safety and efficacy in subgroup with cardiac involvement von Vest, J, Solomon, S, Adams, D, Gonzalez-Duarte, A, O’Riordan, W, Yang, C, Coelho, T, Berk, J, Lin, K, Dyck, P, Gandhi, PJ, Sweetser, M, Suhr, OB, Kristen, A

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P.024 Long-term use of patisiran in patients with hereditary transthyretin amyloidosis (hATTR): 12 month efficacy & safety data from a global open label extension (OLE) study von Gonzalez-Duarte, A, Coelho, T, Adams, D, Yang, C, Polydefkis, M, Kristen, A, Tournev, I, Schmidt, H, Berk, J, Lin, K, Gandhi, PJ, Sweetser, M, White, M, Gollob, J, Suhr, OB

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Allele specific expression of the transthyretin gene in swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles von Norgren, Nina, Hellman, Urban, Ericzon, Bo Göran, Olsson, Malin, Suhr, Ole B

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Progression of cardiomyopathy after liver transplantation in patients with familial amyloidotic polyneuropathy, portuguese type von OLOFSSON, Bert-Ove, BACKMAN, Christer, KARP, Kjell, SUHR, Ole B

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Hereditary transthyretin amyloidosis from a Scandinavian perspective von Suhr, O. B., Svendsen, I. Hastrup, Andersson, R., Danielsson, Å., Holmgren, G., Ranløv, P. J.

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Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients von Olsson, M, Hellman, U, Planté-Bordeneuve, V, Jonasson, J, Lång, K, Suhr, OB

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PHASE 2 OPEN-LABEL EXTENSION (OLE) STUDY OF PATISIRAN, AN INVESTIGATIONAL RNA INTERFERENCE (RNAI) THERAPEUTIC FOR THE TREATMENT OF HEREDITARY ATTR AMYLOIDOSIS WITH POLYNEUROPATHY von Adams, D, Coelho, T, Conceicao, I, Waddington-Cruz, M, Schmidt, H, Buades, J, Campistol, JM, Pouget, J, BerkL, JL, Polydefkis, M, Ziyadeh, N, Partisano, AM, Chen, J, Gollob, J, Suhr, OB

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A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg ( p. His108Arg ) amyloidosis family von Hellman, Urban, Lundgren, Hans-Erik, Westermark, Per, Stafberg, Christina, Nahi, Hareth, Tachlinski, Sascha, Guggi, Michael, Flogegård, Max, Hamid, Mehmet, Escher, Stefan A, Suhr, Ole B

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Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs von Norgren, N, Olsson, M, Nystrom, H, Ericzon, BG, de Tayrac, M, Genin, E, Plante-Bordeneuve, V, Suhr, OB

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Liver transplantation does not prevent the development of life-threatening arrhythmia in familial amyloidotic polyneuropathy, Portuguese-type (ATTR Val30Met) patients von HÖRNSTEN, Rolf, WIKLUND, Urban, OLOFSSON, Bert-Ove, JENSEN, Steen M, SUHR, Ole B

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Amyloid heart disease mimicking hypertrophic cardiomyopathy von MÖRNER, S., HELLMAN, U., SUHR, O. B., KAZZAM, E., WALDENSTRÖM, A.

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Post Hoc Analysis of Nutritional Status in Patients with Transthyretin Familial Amyloid Polyneuropathy: Impact of Tafamidis von Suhr, Ole B., Conceição, Isabel M., Karayal, Onur N., Mandel, Francine S., Huertas, Pedro E., Ericzon, Bo‐Göran

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