Suhr OB - Search Results

1

Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis.

Adams D, Gonzalez-Duarte A, O'Riordan WD, Yang CC, Ueda M, Kristen AV, Tournev I, Schmidt HH, Coelho T, Berk JL, Lin KP, Vita G, Attarian S, Planté-Bordeneuve V, Mezei MM, Campistol JM, Buades J, Brannagan TH 3rd, Kim BJ, Oh J, Parman Y, Sekijima Y, Hawkins PN, Solomon SD, Polydefkis M, Dyck PJ, Gandhi PJ, Goyal S, Chen J, Strahs AL, Nochur SV, Sweetser MT, Garg PP, Vaishnaw AK, Gollob JA, Suhr OB. Adams D, et al. Among authors: suhr ob. N Engl J Med. 2018 Jul 5;379(1):11-21. doi: 10.1056/NEJMoa1716153. N Engl J Med. 2018. PMID: 29972753 Free article. Clinical Trial.

2

Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis.

Holmgren G, Ericzon BG, Groth CG, Steen L, Suhr O, Andersen O, Wallin BG, Seymour A, Richardson S, Hawkins PN, et al. Holmgren G, et al. Lancet. 1993 May 1;341(8853):1113-6. doi: 10.1016/0140-6736(93)93127-m. Lancet. 1993. PMID: 8097803

3

Serum amyloid P component scintigraphy in familial amyloid polyneuropathy: regression of visceral amyloid following liver transplantation.

Rydh A, Suhr O, Hietala SO, Ahlström KR, Pepys MB, Hawkins PN. Rydh A, et al. Eur J Nucl Med. 1998 Jul;25(7):709-13. doi: 10.1007/s002590050273. Eur J Nucl Med. 1998. PMID: 9662592 Clinical Trial.

4

Gene therapy: lessons learned from liver transplantation for transthyretin-amyloidosis.

Suhr OB, Holmgren G, Lundgren E. Suhr OB, et al. Liver Transpl. 2004 Dec;10(12):1551-3. doi: 10.1002/lt.20302. Liver Transpl. 2004. PMID: 15558840 Free article. No abstract available.

5

Early liver transplantation improves familial amyloidotic polyneuropathy patients' survival.

Suhr OB, Friman S, Ericzon BG. Suhr OB, et al. Amyloid. 2005 Dec;12(4):233-8. doi: 10.1080/13506120500363609. Amyloid. 2005. PMID: 16399648

6

Do troponin and B-natriuretic peptide detect cardiomyopathy in transthyretin amyloidosis?

Suhr OB, Anan I, Backman C, Karlsson A, Lindqvist P, Mörner S, Waldenström A. Suhr OB, et al. J Intern Med. 2008 Mar;263(3):294-301. doi: 10.1111/j.1365-2796.2007.01888.x. Epub 2007 Dec 5. J Intern Med. 2008. PMID: 18069997 Free article.

7

On the origin of the transthyretin Val30Met familial amyloid polyneuropathy.

Zaros C, Genin E, Hellman U, Saporta MA, Languille L, Wadington-Cruz M, Suhr O, Misrahi M, Planté-Bordeneuve V. Zaros C, et al. Ann Hum Genet. 2008 Jul;72(Pt 4):478-84. doi: 10.1111/j.1469-1809.2008.00439.x. Epub 2008 May 5. Ann Hum Genet. 2008. PMID: 18460047

8

Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.

Obayashi K, Olsson M, Anan I, Ueda M, Nakamura M, Okamoto S, Yamashita T, Miida T, Ando Y, Suhr OB. Obayashi K, et al. Among authors: suhr ob. Clin Chim Acta. 2008 Dec;398(1-2):10-4. doi: 10.1016/j.cca.2008.07.033. Epub 2008 Aug 5. Clin Chim Acta. 2008. PMID: 18760272

9

Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population.

Hellman U, Alarcon F, Lundgren HE, Suhr OB, Bonaiti-Pellié C, Planté-Bordeneuve V. Hellman U, et al. Among authors: suhr ob. Amyloid. 2008 Sep;15(3):181-6. doi: 10.1080/13506120802193720. Amyloid. 2008. PMID: 18925456 Free PMC article.

10

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.

Olsson M, Hellman U, Planté-Bordeneuve V, Jonasson J, Lång K, Suhr OB. Olsson M, et al. Among authors: suhr ob. Clin Genet. 2009 Feb;75(2):163-8. doi: 10.1111/j.1399-0004.2008.01097.x. Epub 2008 Nov 1. Clin Genet. 2009. PMID: 19018796

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