Hans-Erik Lundgren

Publications

Author

Title

Year sorteringsordning

Fulltext

Suhr, Ole B
Wixner, Jonas
Pilebro, Björn; et al.

The Swedish landscape of hereditary ATTR amyloidosis
Amyloid, 24(1): 93-94

2017

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Wixner, Jonas
Pilebro, Bjorn
Lundgren, Hans-Erik; et al.

Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis
Amyloid, 24(1): 78-79

2017

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Hellman, Urban
Lundgren, Hans-Erik
Westermark, Per; et al.

A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family
European Journal of Medical Genetics, 58(4): 211-215

2015

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Suhr, Ole B
Andersen, Oluf
Aronsson, Thomas; et al.

Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.
Amyloid, 16(4): 208-214

2009

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Hellman, Urban
Alarcon, Flora
Lundgren, Hans-Erik; et al.

Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 15(3): 181-6

2008

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Holmgren, Gösta
Hellman, Urban
Anan, Intissar; et al.

Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
Amyloid, 12(3): 184-8

2005

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Holmgren, Gösta
Hellman, Urban
Lundgren, Hans-Erik; et al.

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.
Journal of Medical Genetics, 42(12): 953-6

2005

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