Giehl KA - Search Results

1

[Recurrent pyoderma in Kindler syndrome].

Niculescu L, Ruzicka T, Braunmühl TV, Giehl KA. Niculescu L, et al. Among authors: giehl ka. Hautarzt. 2018 Oct;69(Suppl 1):16-18. doi: 10.1007/s00105-018-4198-2. Hautarzt. 2018. PMID: 30264319 German. No abstract available.

2

A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/Palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders.

Niculescu L, Wagner M, Westphal DS, Fischer M, Mihatsch W, Prothmann A, Ruzicka T, Wollenberg A, Wolff H, Schmidt H, Giehl KA. Niculescu L, et al. Among authors: giehl ka. Acta Derm Venereol. 2019 Jan 1;99(1):111-112. doi: 10.2340/00015555-2997. Acta Derm Venereol. 2019. PMID: 29956718 Free article. No abstract available.

3

Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome.

Niculescu L, Ruini C, Srour J, Salzer S, Schönbuchner I, von Braunmühl T, Ruzicka T, Hohenleutner U, Giehl KA, Fischer J, Wollenberg A. Niculescu L, et al. Among authors: giehl ka. Acta Derm Venereol. 2019 Mar 1;99(3):345-346. doi: 10.2340/00015555-3087. Acta Derm Venereol. 2019. PMID: 30460372 Free article. No abstract available.

4

A controlled trial of photodynamic therapy of actinic keratosis comparing different red light sources.

Giehl KA, Kriz M, Grahovac M, Ruzicka T, Berking C. Giehl KA, et al. Eur J Dermatol. 2014 May-Jun;24(3):335-41. doi: 10.1684/ejd.2014.2364. Eur J Dermatol. 2014. PMID: 24876164 Clinical Trial.

5

Nonsense mutations in AAGAB cause punctate palmoplantar keratoderma type Buschke-Fischer-Brauer.

Giehl KA, Eckstein GN, Pasternack SM, Praetzel-Wunder S, Ruzicka T, Lichtner P, Seidl K, Rogers M, Graf E, Langbein L, Braun-Falco M, Betz RC, Strom TM. Giehl KA, et al. Am J Hum Genet. 2012 Oct 5;91(4):754-9. doi: 10.1016/j.ajhg.2012.08.024. Epub 2012 Sep 20. Am J Hum Genet. 2012. PMID: 23000146 Free PMC article.

6

Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability.

Giehl KA, Herzinger T, Wolff H, Sárdy M, von Braunmühl T, Dekeuleneer V, Sznajer Y, Tennstedt D, Boes P, Rapprich S, Wagner N, Betz RC, Braun-Falco M, Strom T, Ruzicka T, Eckstein GN. Giehl KA, et al. Acta Derm Venereol. 2016 May;96(4):468-72. doi: 10.2340/00015555-2304. Acta Derm Venereol. 2016. PMID: 26608363 Free article.

7

Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysis.

Giehl KA, Rogers MA, Radivojkov M, Tosti A, de Berker DA, Weinlich G, Schmuth M, Ruzicka T, Eckstein GN. Giehl KA, et al. Br J Dermatol. 2009 Mar;160(3):527-33. doi: 10.1111/j.1365-2133.2008.08948.x. Epub 2008 Nov 25. Br J Dermatol. 2009. PMID: 19067701

8

[Focal dermal hypoplasia (Goltz-Gorlin syndrome) : The cause is now known].

Giehl KA. Giehl KA. Hautarzt. 2016 Jul;67(7):583-5. doi: 10.1007/s00105-016-3823-1. Hautarzt. 2016. PMID: 27341828 German. No abstract available.

9

[Hereditary pigmentary disorders].

Giehl K, Braun-Falco M. Giehl K, et al. Hautarzt. 2010 Jul;61(7):567-77. doi: 10.1007/s00105-009-1917-8. Hautarzt. 2010. PMID: 20556350 German.

10

[6-month-old female with increasing hyperpigmentation following suspected neonatal HSV infection : Preparation for the specialist examination: part 30].

Salzer S, Giehl K. Salzer S, et al. Hautarzt. 2019 Apr;70(Suppl 1):16-19. doi: 10.1007/s00105-018-4311-6. Hautarzt. 2019. PMID: 30976862 German. No abstract available.

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