Hellman U - Search Results

1

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. 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

2

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.

Holmgren G, Hellman U, Lundgren HE, Sandgren O, Suhr OB. Holmgren G, et al. Among authors: hellman u. J Med Genet. 2005 Dec;42(12):953-6. doi: 10.1136/jmg.2005.033720. Epub 2005 Jun 1. J Med Genet. 2005. PMID: 15930086 Free PMC article.

3

Amyloid heart disease mimicking hypertrophic cardiomyopathy.

Mörner S, Hellman U, Suhr OB, Kazzam E, Waldenström A. Mörner S, et al. Among authors: hellman u. J Intern Med. 2005 Sep;258(3):225-30. doi: 10.1111/j.1365-2796.2005.01522.x. J Intern Med. 2005. PMID: 16115295 Free article.

4

Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.

Holmgren G, Hellman U, Anan I, Lundgren HE, Jonasson J, Stafberg C, Fahoum S, Suhr OB. Holmgren G, et al. Among authors: hellman u. Amyloid. 2005 Sep;12(3):184-8. doi: 10.1080/13506120500223126. Amyloid. 2005. PMID: 16194874

5

A Swedish family with the rare Phe33Leu transthyretin mutation.

Holmgren G, Hellman U, Jonasson J, Lundgren HE, Westermark P, Suhr OB. Holmgren G, et al. Among authors: hellman u. Amyloid. 2005 Sep;12(3):189-92. doi: 10.1080/13506120500221989. Amyloid. 2005. PMID: 16194875

6

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. Among authors: hellman u. 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

7

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

8

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: hellman u. 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

9

TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?

Bonaïti B, Olsson M, Hellman U, Suhr O, Bonaïti-Pellié C, Planté-Bordeneuve V. Bonaïti B, et al. Among authors: hellman u. Eur J Hum Genet. 2010 Aug;18(8):948-52. doi: 10.1038/ejhg.2010.36. Epub 2010 Mar 17. Eur J Hum Genet. 2010. PMID: 20234390 Free PMC article.

10

Regional differences and similarities of FAP in Sweden.

Hellman U, Suhr O. Hellman U, et al. Amyloid. 2012 Jun;19 Suppl 1:53-4. doi: 10.3109/13506129.2012.670813. Epub 2012 Apr 2. Amyloid. 2012. PMID: 22468675

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