Lundgren HE - Search Results

1

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: lundgren he. Amyloid. 2008 Sep;15(3):181-6. doi: 10.1080/13506120802193720. Amyloid. 2008. PMID: 18925456 Free PMC article.

2

The Swedish landscape of hereditary ATTR amyloidosis.

Suhr OB, Wixner J, Pilebro B, Lundgren HE, Anan I. Suhr OB, et al. Among authors: lundgren he. Amyloid. 2017 Mar;24(sup1):93-94. doi: 10.1080/13506129.2017.1286580. Amyloid. 2017. PMID: 28434364 No abstract available.

3

A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family.

Hellman U, Lundgren HE, Westermark P, Stafberg C, Nahi H, Tachlinski S, Guggi M, Flogegård M, Hamid M, Escher SA, Suhr OB. Hellman U, et al. Among authors: lundgren he. Eur J Med Genet. 2015 Apr;58(4):211-5. doi: 10.1016/j.ejmg.2015.02.005. Epub 2015 Feb 24. Eur J Med Genet. 2015. PMID: 25721874

4

Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families.

Suhr OB, Wixner J, Anan I, Lundgren HE, Wijayatunga P, Westermark P, Ihse E. Suhr OB, et al. Among authors: lundgren he. PLoS One. 2019 Feb 27;14(2):e0211983. doi: 10.1371/journal.pone.0211983. eCollection 2019. PLoS One. 2019. PMID: 30811423 Free PMC article.

5

Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type.

Hellman U, Lång K, Ihse E, Jonasson J, Olsson M, Lundgren HE, Pilebro B, Westermark P, Wixner J, Anan I. Hellman U, et al. Among authors: lundgren he. Scand J Clin Lab Invest. 2019 Oct;79(6):372-376. doi: 10.1080/00365513.2019.1624977. Epub 2019 Jun 6. Scand J Clin Lab Invest. 2019. PMID: 31169435

6

Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial.

Berk JL, Suhr OB, Obici L, Sekijima Y, Zeldenrust SR, Yamashita T, Heneghan MA, Gorevic PD, Litchy WJ, Wiesman JF, Nordh E, Corato M, Lozza A, Cortese A, Robinson-Papp J, Colton T, Rybin DV, Bisbee AB, Ando Y, Ikeda S, Seldin DC, Merlini G, Skinner M, Kelly JW, Dyck PJ; Diflunisal Trial Consortium. Berk JL, et al. JAMA. 2013 Dec 25;310(24):2658-67. doi: 10.1001/jama.2013.283815. JAMA. 2013. PMID: 24368466 Free PMC article. Clinical Trial.

7

The Swedish open-label diflunisal trial (DFNS01) on hereditary transthyretin amyloidosis and the impact of amyloid fibril composition.

Wixner J, Westermark P, Ihse E, Pilebro B, Lundgren HE, Anan I. Wixner J, et al. Among authors: lundgren he. Amyloid. 2019;26(sup1):39-40. doi: 10.1080/13506129.2019.1593133. Amyloid. 2019. PMID: 31343354 Clinical Trial. No abstract available.

8

Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis.

Wixner J, Pilebro B, Lundgren HE, Olsson M, Anan I. Wixner J, et al. Among authors: lundgren he. Amyloid. 2017 Mar;24(sup1):78-79. doi: 10.1080/13506129.2016.1269739. Epub 2016 Dec 31. Amyloid. 2017. PMID: 28042702 Clinical Trial. No abstract available.

9

A case report of osteoarthritis associated with hereditary transthyretin amyloidosis ATTRV30M.

Anan I, Bång J, Lundgren HE, Wixner J, Westermark P. Anan I, et al. Among authors: lundgren he. Amyloid. 2019;26(sup1):29-30. doi: 10.1080/13506129.2019.1593132. Amyloid. 2019. PMID: 31343355 No abstract available.

10

Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.

Suhr OB, Andersen O, Aronsson T, Jonasson J, Kalimo H, Lundahl C, Lundgren HE, Melberg A, Nyberg J, Olsson M, Sandberg A, Westermark P. Suhr OB, et al. Among authors: lundgren he. Amyloid. 2009 Dec;16(4):208-14. doi: 10.3109/13506120903421587. Amyloid. 2009. PMID: 19922332

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