Schönherr N[au] - Search Results

Year	Number of Results
2005	1
2006	4
2007	5
2008	7
2009	5
2010	2
2021	1
2022	1
2023	0

1

Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.

Eggermann T, Eggermann K, Schönherr N. Eggermann T, et al. Among authors: schonherr n. Trends Genet. 2008 Apr;24(4):195-204. doi: 10.1016/j.tig.2008.01.003. Epub 2008 Mar 7. Trends Genet. 2008. PMID: 18329128 Review.

2

Reagent-Free Immobilization of Industrial Lipases to Develop Lipolytic Membranes with Self-Cleaning Surfaces.

Schmidt M, Prager A, Schönherr N, Gläser R, Schulze A. Schmidt M, et al. Among authors: schonherr n. Membranes (Basel). 2022 Jun 9;12(6):599. doi: 10.3390/membranes12060599. Membranes (Basel). 2022. PMID: 35736306 Free PMC article.

3

Segmental maternal UPD(7q) in Silver-Russell syndrome.

Eggermann T, Schönherr N, Jäger S, Spaich C, Ranke MB, Wollmann HA, Binder G. Eggermann T, et al. Among authors: schonherr n. Clin Genet. 2008 Nov;74(5):486-9. doi: 10.1111/j.1399-0004.2008.01057.x. Epub 2008 Aug 12. Clin Genet. 2008. PMID: 18700897 No abstract available.

4

Impact of high-energy electron irradiation on mechanical, structural and chemical properties of agarose hydrogels.

Krömmelbein C, Mütze M, Konieczny R, Schönherr N, Griebel J, Gerdes W, Mayr SG, Riedel S. Krömmelbein C, et al. Among authors: schonherr n. Carbohydr Polym. 2021 Jul 1;263:117970. doi: 10.1016/j.carbpol.2021.117970. Epub 2021 Mar 21. Carbohydr Polym. 2021. PMID: 33858571

5

Are H19 variants associated with Silver-Russell syndrome?

Schönherr N, Binder G, Korsch E, Kämmerer E, Wollmann HA, Eggermann T. Schönherr N, et al. J Pediatr Endocrinol Metab. 2008 Oct;21(10):985-93. doi: 10.1515/jpem.2008.21.10.985. J Pediatr Endocrinol Metab. 2008. PMID: 19209620

6

Mutation analysis of GNAS1 and overlapping transcripts in Silver-Russell syndrome patients.

Eggermann T, Meyer E, Schönherr N, Flick F, Chauvistré H, Mavany M, Wollmann HA. Eggermann T, et al. Among authors: schonherr n. Mol Genet Metab. 2007 Feb;90(2):224-6. doi: 10.1016/j.ymgme.2006.09.004. Epub 2006 Oct 23. Mol Genet Metab. 2007. PMID: 17056291 No abstract available.

7

Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations.

Spengler S, Gogiel M, Schönherr N, Binder G, Eggermann T. Spengler S, et al. Among authors: schonherr n. Eur J Med Genet. 2009 Nov-Dec;52(6):415-6. doi: 10.1016/j.ejmg.2009.07.005. Epub 2009 Jul 24. Eur J Med Genet. 2009. PMID: 19632365

8

LOT1 (ZAC1/PLAGL1) as member of an imprinted gene network does not harbor Silver-Russell specific variants.

Jäger S, Schönherr N, Spengler S, Ranke MB, Wollmann HA, Binder G, Eggermann T. Jäger S, et al. Among authors: schonherr n. J Pediatr Endocrinol Metab. 2009 Jun;22(6):555-9. doi: 10.1515/jpem.2009.22.6.555. J Pediatr Endocrinol Metab. 2009. PMID: 19694203

9

ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features.

Eggermann T, Meyer E, Caglayan AO, Dundar M, Schönherr N. Eggermann T, et al. Among authors: schonherr n. J Pediatr Endocrinol Metab. 2008 Jan;21(1):59-62. doi: 10.1515/jpem.2008.21.1.59. J Pediatr Endocrinol Metab. 2008. PMID: 18404973

10

Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation.

Eggermann T, Gonzalez D, Spengler S, Arslan-Kirchner M, Binder G, Schönherr N. Eggermann T, et al. Among authors: schonherr n. Pediatrics. 2009 May;123(5):e929-31. doi: 10.1542/peds.2008-3228. Epub 2009 Apr 13. Pediatrics. 2009. PMID: 19364767

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