Beicht S - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.

Weber S, Strasser K, Rath S, Kittke A, Beicht S, Alberer M, Lange-Sperandio B, Hoyer PF, Benz MR, Ponsel S, Weber LT, Klein HG, Hoefele J. Weber S, et al. Among authors: beicht s. Pediatr Nephrol. 2016 Jun;31(6):941-55. doi: 10.1007/s00467-015-3302-4. Epub 2016 Jan 25. Pediatr Nephrol. 2016. PMID: 26809805

Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome.

Beicht S, Strobl-Wildemann G, Rath S, Wachter O, Alberer M, Kaminsky E, Weber LT, Hinrichsen T, Klein HG, Hoefele J. Beicht S, et al. Gene. 2013 Sep 10;526(2):474-7. doi: 10.1016/j.gene.2013.05.045. Epub 2013 May 31. Gene. 2013. PMID: 23732293

IMPROVE 1.0: Individual Monitoring of Psoriasis Activity by Regular Online App Questionnaires and Outpatient Visits.

Garzorz-Stark N, Beicht S, Baghin V, Stark SP, Biedermann T, Lauffer F. Garzorz-Stark N, et al. Among authors: beicht s. Front Med (Lausanne). 2021 Jun 22;8:648233. doi: 10.3389/fmed.2021.648233. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34239885 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3 results

Search Page

Filters