Pigg MH - Search Results

1

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.

Pigg MH, Bygum A, Gånemo A, Virtanen M, Brandrup F, Zimmer AD, Hotz A, Vahlquist A, Fischer J. Pigg MH, et al. Acta Derm Venereol. 2016 Nov 2;96(7):932-937. doi: 10.2340/00015555-2418. Acta Derm Venereol. 2016. PMID: 27025581 Free article.

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. 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. Acta Derm Venereol Suppl (Stockh). 2003 May;(213):34-47. Acta Derm Venereol Suppl (Stockh). 2003. PMID: 12822194

4

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.

Dahlqvist J, Klar J, Hausser I, Anton-Lamprecht I, Pigg MH, Gedde-Dahl T Jr, Gånemo A, Vahlquist A, Dahl N. Dahlqvist J, et al. Among authors: pigg mh. J Med Genet. 2007 Oct;44(10):615-20. doi: 10.1136/jmg.2007.050542. Epub 2007 Jun 8. J Med Genet. 2007. PMID: 17557927 Free PMC article.

5

Reply to Nellen et al's comment on the classification of clinical/genetic variants of Mal de Meleda.

Zhao L, Vahlquist A, Virtanen M, Wennerstrand L, Lind LK, Lundström A, Pigg MH. Zhao L, et al. Among authors: pigg mh. Acta Derm Venereol. 2015 Nov;95(8):1034-5. Acta Derm Venereol. 2015. PMID: 26844309 No abstract available.

6

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Pigg M, Annton-Lamprecht I, Braun-Quentin C, Gustavson KH, Wadelius C. Pigg M, et al. Acta Derm Venereol. 1999 Jan;79(1):41-3. doi: 10.1080/000155599750011688. Acta Derm Venereol. 1999. PMID: 10086857 Free article.

7

Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway.

Pigg M, Gedde-Dahl T Jr, Cox D, Hausser I, Anton-Lamprecht I, Dahl N. Pigg M, et al. Eur J Hum Genet. 1998 Nov-Dec;6(6):589-96. doi: 10.1038/sj.ejhg.5200224. Eur J Hum Genet. 1998. PMID: 9887377

8

Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13.

Klar J, Gedde-Dahl T Jr, Larsson M, Pigg M, Carlsson B, Tentler D, Vahlquist A, Dahl N. Klar J, et al. J Med Genet. 2004 Mar;41(3):208-12. doi: 10.1136/jmg.2003.012567. J Med Genet. 2004. PMID: 14985385 Free PMC article. No abstract available.

9

Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis.

Pigg M, Gedde-Dahl T Jr, Cox DW, Haugen G, Dahl N. Pigg M, et al. Prenat Diagn. 2000 Feb;20(2):132-7. doi: 10.1002/(sici)1097-0223(200002)20:2<132::aid-pd765>3.0.co;2-0. Prenat Diagn. 2000. PMID: 10694685

10

Self-reported quality of life, anxiety and depression in individuals with Ehlers-Danlos syndrome (EDS): a questionnaire study.

Berglund B, Pettersson C, Pigg M, Kristiansson P. Berglund B, et al. BMC Musculoskelet Disord. 2015 Apr 15;16:89. doi: 10.1186/s12891-015-0549-7. BMC Musculoskelet Disord. 2015. PMID: 25880527 Free PMC article.

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