Volz A - Search Results

1

Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.

Omran H, Sasmaz G, Häffner K, Volz A, Olbrich H, Melkaoui R, Otto E, Wienker TF, Korinthenberg R, Brandis M, Antignac C, Hildebrandt F. Omran H, et al. Among authors: volz a. J Am Soc Nephrol. 2002 Jan;13(1):75-79. doi: 10.1681/ASN.V13175. J Am Soc Nephrol. 2002. PMID: 11752023

2

Candidate gene analysis of KIAA0678 encoding a DnaJ-like protein for adolescent nephronophthisis and Senior-Løken syndrome type 3.

Volz A, Melkaoui R, Hildebrandt F, Omran H. Volz A, et al. Cytogenet Genome Res. 2002;97(3-4):163-6. doi: 10.1159/000066617. Cytogenet Genome Res. 2002. PMID: 12438707

3

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.

Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E, Volz A, Wolf MT, Sasmaz G, Trauer U, Reinhardt R, Sudbrak R, Antignac C, Gretz N, Walz G, Schermer B, Benzing T, Hildebrandt F, Omran H. Olbrich H, et al. Among authors: volz a. Nat Genet. 2003 Aug;34(4):455-9. doi: 10.1038/ng1216. Nat Genet. 2003. PMID: 12872122

4

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

Olbrich H, Häffner K, Kispert A, Völkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H. Olbrich H, et al. Among authors: volz a. Nat Genet. 2002 Feb;30(2):143-4. doi: 10.1038/ng817. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788826

5

Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations.

Kispert A, Petry M, Olbrich H, Volz A, Ketelsen UP, Horvath J, Melkaoui R, Omran H, Zariwala M, Noone PG, Knowles M. Kispert A, et al. Among authors: volz a. Thorax. 2003 Jun;58(6):552-4. doi: 10.1136/thorax.58.6.552-b. Thorax. 2003. PMID: 12775878 Free PMC article. No abstract available.

6

Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene.

Schumann H, Roth W, Has C, Volz A, Erfurt-Berge C, Magin TM, Bruckner-Tuderman L. Schumann H, et al. Among authors: volz a. Br J Dermatol. 2012 Oct;167(4):929-36. doi: 10.1111/j.1365-2133.2012.11075.x. Epub 2012 Sep 7. Br J Dermatol. 2012. PMID: 22639907

7

Network epidermolysis bullosa: molecular pathomechanisms and novel therapeutic approaches.

Volz A, Has C, Schumann H, Bruckner-Tuderman L. Volz A, et al. J Dtsch Dermatol Ges. 2007 Apr;5(4):274-9. doi: 10.1111/j.1610-0387.2006.06181.x. J Dtsch Dermatol Ges. 2007. PMID: 17376090 Review. English, German.

8

Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer.

Has C, Burger B, Volz A, Kohlhase J, Bruckner-Tuderman L, Itin P. Has C, et al. Among authors: volz a. Dermatology. 2010;221(4):309-12. doi: 10.1159/000320235. Epub 2010 Oct 11. Dermatology. 2010. PMID: 20938162

9

Perifollicular protrusions--mid-dermal elastolysis.

Volz A, Pfister-Wartha A, Bruckner-Tuderman L, Braun-Falco M. Volz A, et al. J Dtsch Dermatol Ges. 2009 Jan;7(1):68-9. doi: 10.1111/j.1610-0387.2008.06959.x. Epub 2008 Nov 18. J Dtsch Dermatol Ges. 2009. PMID: 19054426

10

Non-infectious granulomatous dermatoses.

Schmitt A, Volz A. Schmitt A, et al. Among authors: volz a. J Dtsch Dermatol Ges. 2019 May;17(5):518-533. doi: 10.1111/ddg.13848. J Dtsch Dermatol Ges. 2019. PMID: 31115996

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