Hendig D - Search Results

1

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect.

Brodehl A, Pour Hakimi SA, Stanasiuk C, Ratnavadivel S, Hendig D, Gaertner A, Gerull B, Gummert J, Paluszkiewicz L, Milting H. Brodehl A, et al. Among authors: hendig d. Genes (Basel). 2019 Nov 11;10(11):918. doi: 10.3390/genes10110918. Genes (Basel). 2019. PMID: 31718026 Free PMC article.

2

The Consideration of Pseudoxanthoma Elasticum as a Progeria Syndrome.

Tiemann J, Lindenkamp C, Wagner T, Brodehl A, Plümers R, Faust-Hinse I, Knabbe C, Hendig D. Tiemann J, et al. Among authors: hendig d. Front Biosci (Landmark Ed). 2023 Mar 20;28(3):55. doi: 10.31083/j.fbl2803055. Front Biosci (Landmark Ed). 2023. PMID: 37005749 Free article.

3

Heart Transplantation in Systemic Sclerosis: New Impulses for Conventional Scleroderma Transplantation Regimen and Scleroderma Diagnostic Monitoring: 2 Case Reports.

Faust I, Weile J, Fujita B, Kandolf R, Hendig D, Vollmer T, Stan AC, Kellner U, Kuhn J, Gummert JF, Knabbe C. Faust I, et al. Among authors: hendig d. Transplant Proc. 2019 Apr;51(3):865-870. doi: 10.1016/j.transproceed.2019.01.025. Epub 2019 Jan 9. Transplant Proc. 2019. PMID: 30979477

4

Homozygous XYLT2 variants as a cause of spondyloocular syndrome.

Umair M, Eckstein G, Rudolph G, Strom T, Graf E, Hendig D, Hoover J, Alanay J, Meitinger T, Schmidt H, Ahmad W. Umair M, et al. Among authors: hendig d. Clin Genet. 2018 Apr;93(4):913-918. doi: 10.1111/cge.13179. Epub 2018 Feb 20. Clin Genet. 2018. PMID: 29136277

5

Elevated xylosyltransferase I activities in pseudoxanthoma elasticum (PXE) patients as a marker of stimulated proteoglycan biosynthesis.

Götting C, Hendig D, Adam A, Schön S, Schulz V, Szliska C, Kuhn J, Kleesiek K. Götting C, et al. Among authors: hendig d. J Mol Med (Berl). 2005 Dec;83(12):984-92. doi: 10.1007/s00109-005-0693-x. Epub 2005 Aug 24. J Mol Med (Berl). 2005. PMID: 16133423

6

Polymorphisms in the xylosyltransferase genes cause higher serum XT-I activity in patients with pseudoxanthoma elasticum (PXE) and are involved in a severe disease course.

Schön S, Schulz V, Prante C, Hendig D, Szliska C, Kuhn J, Kleesiek K, Götting C. Schön S, et al. Among authors: hendig d. J Med Genet. 2006 Sep;43(9):745-9. doi: 10.1136/jmg.2006.040972. Epub 2006 Mar 29. J Med Genet. 2006. PMID: 16571645 Free PMC article.

7

Identification of a xylosyltransferase II gene haplotype marker for diabetic nephropathy in type 1 diabetes.

Hendig D, Tarnow L, Kuhn J, Kleesiek K, Götting C. Hendig D, et al. Clin Chim Acta. 2008 Dec;398(1-2):90-4. doi: 10.1016/j.cca.2008.08.019. Epub 2008 Aug 28. Clin Chim Acta. 2008. PMID: 18789912

8

Fast and sample cleanup-free measurement of nicotine and cotinine by stable isotope dilution ultra-performance liquid chromatography-tandem mass spectrometry.

Kuhn J, Vollmer T, Martin C, Hendig D, Knabbe C. Kuhn J, et al. Among authors: hendig d. J Pharm Biomed Anal. 2012 Aug-Sep;67-68:137-43. doi: 10.1016/j.jpba.2012.04.036. Epub 2012 May 3. J Pharm Biomed Anal. 2012. PMID: 22608097

9

Human xylosyltransferase-I - a new marker for myofibroblast differentiation in skin fibrosis.

Faust I, Roch C, Kuhn J, Prante C, Knabbe C, Hendig D. Faust I, et al. Among authors: hendig d. Biochem Biophys Res Commun. 2013 Jul 5;436(3):449-54. doi: 10.1016/j.bbrc.2013.05.125. Epub 2013 Jun 6. Biochem Biophys Res Commun. 2013. PMID: 23747722

10

New insights into the pathogenesis of pseudoxanthoma elasticum and related soft tissue calcification disorders by identifying genetic interactions and modifiers.

Hendig D, Knabbe C, Götting C. Hendig D, et al. Front Genet. 2013 Jun 19;4:114. doi: 10.3389/fgene.2013.00114. eCollection 2013. Front Genet. 2013. PMID: 23802012 Free PMC article.

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