Bygum A - Search Results

1

[New classification and genetic background of inherited ichthyoses].

Andersen RE, Hertz JM, Bygum A. Andersen RE, et al. Among authors: bygum a. Ugeskr Laeger. 2014 Jul 14;176(29):V11130688. Ugeskr Laeger. 2014. PMID: 25292205 Free article. Review. Danish.

2

[Prurigo pigmentosa].

Andersen R, Vasilescu IC, Bygum A. Andersen R, et al. Among authors: bygum a. Ugeskr Laeger. 2020 Mar 9;182(11):V70775. Ugeskr Laeger. 2020. PMID: 32285778 Free article. Danish. No abstract available.

3

[A patient diagnosed herself with erythropoietic protoporphyria after googling photosensitivity].

Christiansen AL, Brusgaard K, Hertz JM, Bygum A. Christiansen AL, et al. Among authors: bygum a. Ugeskr Laeger. 2015 Jul 20;177(30):V01150015. Ugeskr Laeger. 2015. PMID: 26240047 Free article. Danish.

4

Ichthyosis with Confetti Inherited from a Mosaic Father.

Pallesen KAU, Clemmensen O, Fischer J, Hertz JM, Bygum A. Pallesen KAU, et al. Among authors: bygum a. Acta Derm Venereol. 2018 Jan 12;98(1):130-131. doi: 10.2340/00015555-2776. Acta Derm Venereol. 2018. PMID: 29135017 Free article. No abstract available.

5

Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation.

Krøigård AB, Clemmensen O, Gjørup H, Hertz JM, Bygum A. Krøigård AB, et al. Among authors: bygum a. BMC Dermatol. 2016 Mar 10;16:3. doi: 10.1186/s12895-016-0040-7. BMC Dermatol. 2016. PMID: 26964878 Free PMC article.

6

Newborn with severe epidermolysis bullosa: to treat or not to treat?

Boesen ML, Bygum A, Hertz JM, Zachariassen G. Boesen ML, et al. Among authors: bygum a. BMJ Case Rep. 2016 Apr 26;2016:bcr2016214727. doi: 10.1136/bcr-2016-214727. BMJ Case Rep. 2016. PMID: 27118747 Free PMC article.

7

[Congenital hair shaft anomalies].

Drivenes JL, Bygum A, Hertz JM, Grimalt R, Puente-Pablo N. Drivenes JL, et al. Among authors: bygum a. Ugeskr Laeger. 2021 May 31;183(22):V02210125. Ugeskr Laeger. 2021. PMID: 34060455 Free article. Review. Danish.

8

A retrospective study of clinical and mutational findings in 45 Danish families with ectodermal dysplasia.

Svendsen T, Henningsen E, Hertz JM, Vestergaard Grejsen D, Bygum A. Svendsen T, et al. Among authors: bygum a. Acta Derm Venereol. 2014 Sep;94(5):531-3. doi: 10.2340/00015555-1799. Acta Derm Venereol. 2014. PMID: 24514865 Free article.

9

Manifestations of Gorlin-Goltz syndrome.

Larsen AK, Mikkelsen DB, Hertz JM, Bygum A. Larsen AK, et al. Among authors: bygum a. Dan Med J. 2014 May;61(5):A4829. Dan Med J. 2014. PMID: 24814739 Free article.

10

The first Danish family reported with an AQP5 mutation presenting diffuse non-epidermolytic palmoplantar keratoderma of Bothnian type, hyperhidrosis and frequent Corynebacterium infections: a case report.

Krøigård AB, Hetland LE, Clemmensen O, Blaydon DC, Hertz JM, Bygum A. Krøigård AB, et al. Among authors: bygum a. BMC Dermatol. 2016 Jun 3;16(1):7. doi: 10.1186/s12895-016-0044-3. BMC Dermatol. 2016. PMID: 27255181 Free PMC article.

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