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Items: 1 to 20 of 235

1.

A novel monoclonal antibody targeting carboxymethyllysine, an advanced glycation end product in atherosclerosis and pancreatic cancer.

Wendel U, Persson N, Risinger C, Bengtsson E, Nodin B, Danielsson L, Welinder C, Nordin Fredrikson G, Jansson B, Blixt O.

PLoS One. 2018 Feb 8;13(2):e0191872. doi: 10.1371/journal.pone.0191872. eCollection 2018.

2.

Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age.

Burgard P, Mönch E, Zschocke J, Wendel U, Langenbeck U; German Collaborative Study of Phenylketonuria (PKU)/Hyperphenylalaninaemia (HPA).

JIMD Rep. 2016;29:77-84. Epub 2015 Dec 19.

3.

Endogenous galactose formation in galactose-1-phosphate uridyltransferase deficiency.

Schadewaldt P, Kamalanathan L, Hammen HW, Kotzka J, Wendel U.

Arch Physiol Biochem. 2014 Dec;120(5):228-39. doi: 10.3109/13813455.2014.962547. Epub 2014 Sep 30.

PMID:
25268296
4.

Structural white matter changes in adolescents and young adults with maple syrup urine disease.

Klee D, Thimm E, Wittsack HJ, Schubert D, Primke R, Pentang G, Schaper J, Mödder U, Antoch A, Wendel U, Cohnen M.

J Inherit Metab Dis. 2013 Nov;36(6):945-53. doi: 10.1007/s10545-012-9582-y. Epub 2013 Jan 25.

PMID:
23355088
5.

Clinical and neurocognitive outcome in symptomatic isovaleric acidemia.

Grünert SC, Wendel U, Lindner M, Leichsenring M, Schwab KO, Vockley J, Lehnert W, Ensenauer R.

Orphanet J Rare Dis. 2012 Jan 25;7:9. doi: 10.1186/1750-1172-7-9.

6.

Differential glycomics of epithelial membrane glycoproteins from urinary exovesicles reveals shifts toward complex-type N-glycosylation in classical galactosemia.

Staubach S, Schadewaldt P, Wendel U, Nohroudi K, Hanisch FG.

J Proteome Res. 2012 Feb 3;11(2):906-16. doi: 10.1021/pr200711w. Epub 2011 Dec 2.

PMID:
22087537
7.

Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.

Lindner M, Gramer G, Haege G, Fang-Hoffmann J, Schwab KO, Tacke U, Trefz FK, Mengel E, Wendel U, Leichsenring M, Burgard P, Hoffmann GF.

Orphanet J Rare Dis. 2011 Jun 20;6:44. doi: 10.1186/1750-1172-6-44.

8.

Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemia.

Hoffmann B, Wendel U, Schweitzer-Krantz S.

J Inherit Metab Dis. 2011 Apr;34(2):421-7. doi: 10.1007/s10545-011-9297-5. Epub 2011 Feb 24.

PMID:
21347587
9.

Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.

Fukao T, Sass JO, Kursula P, Thimm E, Wendel U, Ficicioglu C, Monastiri K, Guffon N, Barić I, Zabot MT, Kondo N.

Biochim Biophys Acta. 2011 May;1812(5):619-24. doi: 10.1016/j.bbadis.2011.01.015. Epub 2011 Feb 2.

10.

Longitudinal assessment of intellectual achievement in patients with classical galactosemia.

Schadewaldt P, Hoffmann B, Hammen HW, Kamp G, Schweitzer-Krantz S, Wendel U.

Pediatrics. 2010 Feb;125(2):e374-81. doi: 10.1542/peds.2008-3325. Epub 2010 Jan 25.

PMID:
20100763
11.

A non-enzymatic function of 17beta-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival.

Rauschenberger K, Schöler K, Sass JO, Sauer S, Djuric Z, Rumig C, Wolf NI, Okun JG, Kölker S, Schwarz H, Fischer C, Grziwa B, Runz H, Nümann A, Shafqat N, Kavanagh KL, Hämmerling G, Wanders RJ, Shield JP, Wendel U, Stern D, Nawroth P, Hoffmann GF, Bartram CR, Arnold B, Bierhaus A, Oppermann U, Steinbeisser H, Zschocke J.

EMBO Mol Med. 2010 Feb;2(2):51-62. doi: 10.1002/emmm.200900055.

12.

Metabolic phenotypes of phenylketonuria. Kinetic and molecular evaluation of the Blaskovics protein loading test.

Langenbeck U, Burgard P, Wendel U, Lindner M, Zschocke J; German Collaborative Study on Phenylketonuria (PKU) / Hyperphenylalaninemia (HPA).

J Inherit Metab Dis. 2009 Aug;32(4):506-13. doi: 10.1007/s10545-009-1152-6. Epub 2009 Jul 16.

PMID:
19609714
13.

Molecular genetics of maple syrup urine disease in the Turkish population.

Gorzelany K, Dursun A, Coşkun T, Kalkanoğlu-Sivri SH, Gökçay GF, Demirkol M, Feyen O, Wendel U.

Turk J Pediatr. 2009 Mar-Apr;51(2):97-102. Erratum in: Turk J Pediatr. 2009 Sep-Oct;51(5):525.

PMID:
19480318
14.

Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop.

Spiekerkoetter U, Lindner M, Santer R, Grotzke M, Baumgartner MR, Boehles H, Das A, Haase C, Hennermann JB, Karall D, de Klerk H, Knerr I, Koch HG, Plecko B, Röschinger W, Schwab KO, Scheible D, Wijburg FA, Zschocke J, Mayatepek E, Wendel U.

J Inherit Metab Dis. 2009 Aug;32(4):498-505. doi: 10.1007/s10545-009-1126-8. Epub 2009 Apr 28.

PMID:
19452263
15.

Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshop.

Spiekerkoetter U, Lindner M, Santer R, Grotzke M, Baumgartner MR, Boehles H, Das A, Haase C, Hennermann JB, Karall D, de Klerk H, Knerr I, Koch HG, Plecko B, Röschinger W, Schwab KO, Scheible D, Wijburg FA, Zschocke J, Mayatepek E, Wendel U.

J Inherit Metab Dis. 2009 Aug;32(4):488-97. doi: 10.1007/s10545-009-1125-9. Epub 2009 Apr 29.

PMID:
19399638
16.

Biochemical and genetic analysis of 3-methylglutaconic aciduria type IV: a diagnostic strategy.

Wortmann SB, Rodenburg RJ, Jonckheere A, de Vries MC, Huizing M, Heldt K, van den Heuvel LP, Wendel U, Kluijtmans LA, Engelke UF, Wevers RA, Smeitink JA, Morava E.

Brain. 2009 Jan;132(Pt 1):136-46. doi: 10.1093/brain/awn296. Epub 2008 Nov 16.

PMID:
19015156
17.

Urinary excretion of pentose phosphate pathway-associated polyols in early postnatal life.

Koy A, Waldhaus A, Hammen HW, Wendel U, Mayatepek E, Schadewaldt P.

Neonatology. 2009;95(3):256-61. doi: 10.1159/000167789. Epub 2008 Nov 5.

PMID:
18987485
18.

Safety and efficacy of 22 weeks of treatment with sapropterin dihydrochloride in patients with phenylketonuria.

Lee P, Treacy EP, Crombez E, Wasserstein M, Waber L, Wolff J, Wendel U, Dorenbaum A, Bebchuk J, Christ-Schmidt H, Seashore M, Giovannini M, Burton BK, Morris AA; Sapropterin Research Group.

Am J Med Genet A. 2008 Nov 15;146A(22):2851-9. doi: 10.1002/ajmg.a.32562.

PMID:
18932221
19.

Maple syrup urine disease: newborn screening fails to discriminate between classic and variant forms.

Fingerhut R, Simon E, Maier EM, Hennermann JB, Wendel U.

Clin Chem. 2008 Oct;54(10):1739-41. doi: 10.1373/clinchem.2008.105270. No abstract available.

20.

Biochemical monitoring of pregnancy and breast feeding in five patients with classical galactosaemia--and review of the literature.

Schadewaldt P, Hammen HW, Kamalanathan L, Wendel U, Schwarz M, Bosch AM, Guion N, Janssen M, Boers GH.

Eur J Pediatr. 2009 Jun;168(6):721-9. doi: 10.1007/s00431-008-0832-9. Epub 2008 Sep 24.

PMID:
18813948

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