Schulz S - Search Results

1

A case of Brooke-Spiegler syndrome with a novel mutation in the CYLD gene in a patient with aggressive non-Hodgkin's lymphoma.

Hunstig F, Schulz S, Nieten I, Froster U, Boltze C, Schliemann S, Hochhaus A, La Rosée P. Hunstig F, et al. Among authors: schulz s. J Cancer Res Clin Oncol. 2016 Apr;142(4):845-8. doi: 10.1007/s00432-015-2079-y. Epub 2015 Dec 11. J Cancer Res Clin Oncol. 2016. PMID: 26660106

2

Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia.

Darr-Foit S, Schliemann S, Schulz S, Elsner P. Darr-Foit S, et al. Among authors: schulz s. J Dtsch Dermatol Ges. 2018 Mar;16(3):348-349. doi: 10.1111/ddg.13446. Epub 2018 Feb 21. J Dtsch Dermatol Ges. 2018. PMID: 29465813 No abstract available.

3

Buschke-Ollendorff-Syndrom mit einer neuartigen LEMD3-Mutation - Der Fall einer ungewöhnlichen Alopezie.

Darr-Foit S, Schliemann S, Schulz S, Elsner P. Darr-Foit S, et al. Among authors: schulz s. J Dtsch Dermatol Ges. 2018 Mar;16(3):348-350. doi: 10.1111/ddg.13446_g. J Dtsch Dermatol Ges. 2018. PMID: 29537144 No abstract available.

4

[Gastroparesis in Noonan syndrome].

Heimrich KG, Gühne F, Schulz S, Mutschke S, Stallmach A, Rüddel J. Heimrich KG, et al. Among authors: schulz s. Z Gastroenterol. 2017 Feb;55(2):145-148. doi: 10.1055/s-0042-121551. Epub 2017 Feb 13. Z Gastroenterol. 2017. PMID: 28192847 German.

5

Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.

Goetze S, Raessler F, Hipler UC, Schulz S, Kohlhase J, Elsner P. Goetze S, et al. Among authors: schulz s. J Eur Acad Dermatol Venereol. 2016 Mar;30(3):493-4. doi: 10.1111/jdv.12880. Epub 2015 Jan 20. J Eur Acad Dermatol Venereol. 2016. PMID: 25600101 No abstract available.

6

Novel Association of a Familial TGFBR1 Mutation in Loeys-Dietz Syndrome with Concomitant Hematologic Malignancy.

Disha K, Schulz S, Breuer M, Owais T, Girdauskas E, Kuntze T. Disha K, et al. Among authors: schulz s. Korean J Thorac Cardiovasc Surg. 2019 Oct;52(5):376-379. doi: 10.5090/kjtcs.2019.52.5.376. Epub 2019 Oct 5. Korean J Thorac Cardiovasc Surg. 2019. PMID: 31624717 Free PMC article.

7

Transforming Growth Factor Beta-2 Mutations in Barlow's Disease and Aortic Dilatation.

Disha K, Schulz S, Kuntze T, Girdauskas E. Disha K, et al. Among authors: schulz s. Ann Thorac Surg. 2017 Jul;104(1):e19-e21. doi: 10.1016/j.athoracsur.2017.01.103. Ann Thorac Surg. 2017. PMID: 28633253

8

Transforming growth factor-beta receptor type II mutation in a patient with bicuspid aortic valve disease and intraoperative aortic dissection.

Girdauskas E, Schulz S, Borger MA, Mierzwa M, Kuntze T. Girdauskas E, et al. Among authors: schulz s. Ann Thorac Surg. 2011 May;91(5):e70-1. doi: 10.1016/j.athoracsur.2010.12.060. Ann Thorac Surg. 2011. PMID: 21524434

9

Novel MECP2 Mutation c.1162_1172del; p.Pro388* in Two Patients with Symptoms of Atypical Rett Syndrome.

Bernstein U, Demuth S, Puk O, Eichhorn B, Schulz S. Bernstein U, et al. Among authors: schulz s. Mol Syndromol. 2019 Jul;10(4):223-228. doi: 10.1159/000501183. Epub 2019 Jul 2. Mol Syndromol. 2019. PMID: 31602196 Free PMC article.

10

Double-Hit Mutations in Bicuspid Aortic Valve and Blunt Traumatic Acute Aortic Dissection.

Disha K, Schulz S, Mierzwa M, Owais T, Girdauskas E, Kuntze T. Disha K, et al. Among authors: schulz s. Ann Thorac Surg. 2021 Jan;111(1):e5-e6. doi: 10.1016/j.athoracsur.2020.04.121. Epub 2020 Jun 13. Ann Thorac Surg. 2021. PMID: 32544455

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

2,229 results

Search Page

Filters