Westermark P - Search Results

1

Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.

Rasool M, Nawaz S, Azhar A, Wajid M, Westermark P, Baig SM, Klar J, Dahl N. Rasool M, et al. Among authors: westermark p. Eur J Dermatol. 2010 Jul-Aug;20(4):443-6. doi: 10.1684/ejd.2010.0962. Epub 2010 Apr 21. Eur J Dermatol. 2010. PMID: 20409997

2

Autosomal recessive congenital ichthyosis in Sweden and Estonia: clinical, genetic and ultrastructural findings in eighty-three patients.

Gånemo A, Pigg M, Virtanen M, Kukk T, Raudsepp H, Rossman-Ringdahl I, Westermark P, Niemi KM, Dahl N, Vahlquist A. Gånemo A, et al. Among authors: westermark p. Acta Derm Venereol. 2003;83(1):24-30. doi: 10.1080/00015550310002666. Acta Derm Venereol. 2003. PMID: 12636018 Free article.

3

The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases.

Vahlquist A, Gånemo A, Pigg M, Virtanen M, Westermark P. Vahlquist A, et al. Among authors: westermark p. Acta Derm Venereol Suppl (Stockh). 2003 May;(213):34-47. Acta Derm Venereol Suppl (Stockh). 2003. PMID: 12822194

4

[Burdensome rules for clinical trials are not in proportion to benefits for the patient].

Vahlquist A, Westermark P, Ståhle E, Venge P, Påhlman L, Hällgren R, Rönnblom L, Kämpe O, Wiklund L, Aquilonius SM, Alm A. Vahlquist A, et al. Among authors: westermark p. Lakartidningen. 2005 Jun 6-12;102(23):1832, 1834; discussion 1834. Lakartidningen. 2005. PMID: 15997556 Swedish. No abstract available.

5

Lars Grimelius and his silver impregnation method--Commentaries on the paper in Upsala Journal of Medical Sciences with the highest number of citations.

Westermark P. Westermark P. Ups J Med Sci. 2015 May;120(2):113-6. doi: 10.3109/03009734.2015.1023910. Epub 2015 Mar 17. Ups J Med Sci. 2015. PMID: 25783841 Free PMC article. No abstract available.

6

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: westermark p. 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

7

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: westermark p. Amyloid. 2005 Sep;12(3):189-92. doi: 10.1080/13506120500221989. Amyloid. 2005. PMID: 16194875

8

Transthyretin-derived amyloidosis: probably a common cause of lumbar spinal stenosis.

Westermark P, Westermark GT, Suhr OB, Berg S. Westermark P, et al. Among authors: westermark gt. Ups J Med Sci. 2014 Aug;119(3):223-8. doi: 10.3109/03009734.2014.895786. Epub 2014 Mar 12. Ups J Med Sci. 2014. PMID: 24620715 Free PMC article.

9

Amyloid Cardiomyopathy in Hereditary Transthyretin V30M Amyloidosis - Impact of Sex and Amyloid Fibril Composition.

Arvidsson S, Pilebro B, Westermark P, Lindqvist P, Suhr OB. Arvidsson S, et al. Among authors: westermark p. PLoS One. 2015 Nov 23;10(11):e0143456. doi: 10.1371/journal.pone.0143456. eCollection 2015. PLoS One. 2015. PMID: 26600306 Free PMC article.

10

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: westermark p. PLoS One. 2019 Feb 27;14(2):e0211983. doi: 10.1371/journal.pone.0211983. eCollection 2019. PLoS One. 2019. PMID: 30811423 Free PMC article.

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