Bodo B Beck

Bodo B Beck

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Bodo B Beck

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Proteome Analysis of Isolated Podocytes Reveals Stress Responses in Glomerular Sclerosis.

J Am Soc Nephrol 2020 Mar 11;31(3):544-559. Epub 2020 Feb 11.

Department II of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany;

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http://dx.doi.org/10.1681/ASN.2019030312DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062218PMC
March 2020

Case Report: Exome Sequencing Reveals LRBA Deficiency in a Patient With End-Stage Renal Disease.

Front Pediatr 2020 11;8:42. Epub 2020 Mar 11.

Faculty of Medicine and University Hospital Cologne, Institute of Human Genetics, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.3389/fped.2020.00042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078106PMC
March 2020

Subclinical myocardial disease in patients with primary hyperoxaluria and preserved left ventricular ejection fraction: a two-dimensional speckle-tracking imaging study.

Pediatr Nephrol 2019 12 22;34(12):2591-2600. Epub 2019 Aug 22.

Department of Pediatric Cardiology, Children's Hospital, University of Bonn, Adenauerallee 119, 53113, Bonn, Germany.

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http://dx.doi.org/10.1007/s00467-019-04330-7DOI Listing
December 2019

Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.

Stem Cell Res 2019 12 18;41:101626. Epub 2019 Oct 18.

Regenerative Medicine Program, CIMA Universidad de Navarra, Pamplona, Spain. Instituto de Investigación Sanitaria de Navarra, IdiSNA, Pamplona, Navarra, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2019.101626DOI Listing
December 2019

A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.

J Obstet Gynaecol 2019 Apr 12;39(3):395-397. Epub 2018 Jun 12.

b Service de Génétique Médicale, CHU Nantes , Nantes Cedex , France.

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http://dx.doi.org/10.1080/01443615.2018.1454415DOI Listing
April 2019

Correction to: Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow up of primary hyperoxaluria type III.

Pediatr Nephrol 2018 07;33(7):1275-1276

Division of Pediatric Nephrology, Department of Pediatrics, University of Bonn, Adenauerallee 119, 53113, Bonn, Germany.

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http://dx.doi.org/10.1007/s00467-018-3944-0DOI Listing
July 2018

Translation inhibition corrects aberrant localization of mutant alanine-glyoxylate aminotransferase: possible therapeutic approach for hyperoxaluria.

J Mol Med (Berl) 2018 07 18;96(7):621-630. Epub 2018 May 18.

Division of Pediatric Nephrology, Shaare Zedek Medical Center, Shmuel Bait Street, 91031, Jerusalem, Israel.

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http://dx.doi.org/10.1007/s00109-018-1651-8DOI Listing
July 2018

Single-nephron proteomes connect morphology and function in proteinuric kidney disease.

Kidney Int 2018 06 9;93(6):1308-1319. Epub 2018 Mar 9.

Department II of Internal Medicine, University of Cologne, Cologne, Germany; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany; Systems Biology of Ageing Cologne (Sybacol), University of Cologne, Cologne, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.kint.2017.12.012DOI Listing
June 2018

Autosomal Tubulointerstitial Kidney Disease-MUC1 Type: Differential Proteomics Suggests that Mutated MUC1 (insC) Affects Vesicular Transport in Renal Epithelial Cells.

Proteomics 2018 04 13;18(7):e1700456. Epub 2018 Mar 13.

Institute of Biochemistry II, Medical Faculty, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1002/pmic.201700456DOI Listing
April 2018

Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III.

Pediatr Nephrol 2017 Dec 15;32(12):2263-2271. Epub 2017 Jul 15.

Division of Pediatric Nephrology, Department of Pediatrics, University of Bonn, Adenauerallee 119, 53113, Bonn, Germany.

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http://dx.doi.org/10.1007/s00467-017-3731-3DOI Listing
December 2017

A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndrome.

Am J Med Genet A 2017 Aug 2;173(8):2132-2138. Epub 2017 Jun 2.

Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany.

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http://doi.wiley.com/10.1002/ajmg.a.38285
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http://dx.doi.org/10.1002/ajmg.a.38285DOI Listing
August 2017

Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.

Pediatr Nephrol 2017 Jul 31;32(7):1269-1273. Epub 2017 Mar 31.

Department of Pediatrics, University Hospital of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

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http://dx.doi.org/10.1007/s00467-017-3648-xDOI Listing
July 2017

Successful discontinuation of eculizumab under immunosuppressive therapy in DEAP-HUS.

Pediatr Nephrol 2017 06 20;32(6):1081-1087. Epub 2017 Feb 20.

Pediatric Nephrology, Children's and Adolescents' Hospital, University Hospital of Cologne, Kerpener Street 62, 50937, Cologne, Germany.

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http://link.springer.com/10.1007/s00467-017-3612-9
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http://dx.doi.org/10.1007/s00467-017-3612-9DOI Listing
June 2017

Renal thrombotic microangiopathy in patients with cblC defect: review of an under-recognized entity.

Pediatr Nephrol 2017 05 11;32(5):733-741. Epub 2016 Jun 11.

Division of Paediatric Nephrology, Beatrix Children's Hospital, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s00467-016-3399-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368212PMC
May 2017

Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.

Pediatr Nephrol 2017 05 12;32(5):791-800. Epub 2017 Jan 12.

Pediatric Nephrology, Children's and Adolescents' Hospital, University Hospital of Cologne, Kerpener Street 62, 50937, Cologne, Germany.

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http://dx.doi.org/10.1007/s00467-016-3556-5DOI Listing
May 2017

Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer.

BMC Med Genet 2017 05 12;18(1):53. Epub 2017 May 12.

Department II of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.

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http://dx.doi.org/10.1186/s12881-017-0416-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429543PMC
May 2017

Quiz Page December 2016: Anuria on the Second Day Following Kidney Transplantation.

Am J Kidney Dis 2016 Dec;68(6):A18-A21

Department of Pediatrics, University Hospital of Cologne, Cologne, Germany; Nephrology Research Laboratory, Renal Division and Department of Medicine, University Hospital of Cologne, Cologne, Germany; Center for Molecular Medicine, University of Cologne, Cologne, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S02726386163043
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http://dx.doi.org/10.1053/j.ajkd.2016.07.035DOI Listing
December 2016

Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With Nephrocalcinosis.

Kidney Blood Press Res 2015 22;40(5):443-51. Epub 2015 Aug 22.

Department of Nephrology and Hypertension, Friedrich-Alexander Universitx00E4;t Erlangen-Nx00FC;rnberg, Erlangen-Nx00FC;rnberg, Germany.

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http://dx.doi.org/10.1159/000368520DOI Listing
August 2016

Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.

N Engl J Med 2016 May 27;374(19):1853-63. Epub 2016 Apr 27.

From INSERM, Centre de Recherche des Cordeliers, Unité 1138, Centre National de la Recherche Scientifique, ERL8228 Université Pierre et Marie Curie and Université Paris-Descartes, Paris (K.L., E.S., S.D.); Institute of Human Genetics (B.B.B., A.W., B.R., J.A., G.Y.), Department of Pathology (H.G.), Cologne Center for Genomics and Center for Molecular Medicine (H.T., J.A., P.N.), Department II of Internal Medicine and Center for Molecular Medicine Cologne (M.P.B., T.B., M.M.R.), and Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases and Systems Biology of Aging Cologne (T.B., M.M.R.) - all at the University of Cologne, Cologne, the Department of Cellular and Integrative Physiology, University Medical Center Hamburg, Hamburg (H.V.), University Children's Hospital, Philipps University Marburg (H.W.S.), and Kuratorium für Heimdialyse, Pediatric Kidney Center (G.K.), Marburg, the Institute of Human Genetics, University Health Services Göttingen, Göttingen (G.Y.), and the Department of General Pediatrics, University Hospital Münster, Münster (K.P.S., M. Konrad) - all in Germany; the Division of Nephrology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center (S.-S.Y., S.-H.L.), and Institute of BioMedical Sciences, Academia Sinica (S.-S.Y.) - both in Taipei, Taiwan; the Department of Biomedical Molecular Biology, Inflammation Research Center, VIB/Ghent University, Ghent (D.P., M.J.M.B.), Unité de Recherche en Physiologie Moléculaire, University of Namur, Namur (C.D., O.B.), and the Division of Nephrology, University Children's Hospital Leuven (E.L.) - all in Belgium; the Divisions of Neonatology (K.B.) and Nephrology (M. Kömhoff), Beatrix Children's Hospital, and the Departments of Obstetrics and Gynecology (L.K.D., S.A.S.), Pathology and Medical Biology (A.T.), and Genetics (T.J.K.) - all at University Medical Center Groningen, Groningen, the Netherlands; and University Children's Hospital Graz

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http://dx.doi.org/10.1056/NEJMoa1507629DOI Listing
May 2016

Inhomogeneous Longitudinal Cardiac Rotation and Impaired Left Ventricular Longitudinal Strain in Children and Young Adults with End-Stage Renal Failure Undergoing Hemodialysis.

Echocardiography 2015 Aug 1;32(8):1250-60. Epub 2014 Dec 1.

Department of Pediatric Cardiology, Heart Center Cologne, University Hospital of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1111/echo.12842DOI Listing
August 2015

Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiency.

Pediatr Nephrol 2015 Jul 18;30(7):1203-6. Epub 2015 Apr 18.

University Children's Hospital Muenster, Muenster, NRW, Germany,

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http://dx.doi.org/10.1007/s00467-015-3110-xDOI Listing
July 2015

Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin.

Kidney Int 2014 Sep 26;86(3):589-99. Epub 2014 Mar 26.

1] Department of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany [2] Nikolaus-Fiebiger-Center of Molecular Medicine, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

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https://linkinghub.elsevier.com/retrieve/pii/S00852538153032
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http://dx.doi.org/10.1038/ki.2014.72DOI Listing
September 2014

A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype.

PLoS One 2013 4;8(10):e76414. Epub 2013 Oct 4.

Institute of Human Genetics, University of Cologne, Cologne, Germany ; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany ; Center of Familial Breast and Ovarian Cancer, University Hospital of Cologne, Cologne, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0076414PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790679PMC
May 2014

Kidney stones in primary hyperoxaluria: new lessons learnt.

PLoS One 2013 5;8(8):e70617. Epub 2013 Aug 5.

Department of Geosciences, Johannes Gutenberg University Mainz, Mainz, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0070617PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734250PMC
March 2014

Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice.

Clin J Am Soc Nephrol 2014 Mar 2;9(3):468-77. Epub 2014 Jan 2.

Division of Pediatric Nephrolgy and, †Pediatric Clinical Trial Unit, Department of Pediatrics and Adolescents Medicine, University Hospital Cologne, Cologne, Germany;, ‡Institute of Medical Statistics, Informatics and Epidemiology, and, §Institute of Human Genetics, University of Cologne, Cologne, Germany, ‖Department of Pediatrics, Division of Pediatric Nephrology, University Hospital Bonn, Bonn, Germany.

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http://dx.doi.org/10.2215/CJN.06820613DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944765PMC
March 2014

Apical sparing of longitudinal strain, left ventricular rotational abnormalities, and short-axis dysfunction in primary hyperoxaluria type 1.

Circ Heart Fail 2013 Jul;6(4):e45-7

Department of Pediatric Cardiology, Heart Center Cologne, University Hospital of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1161/CIRCHEARTFAILURE.113.000432DOI Listing
July 2013

Hyperoxaluria and systemic oxalosis: an update on current therapy and future directions.

Expert Opin Investig Drugs 2013 Jan 21;22(1):117-29. Epub 2012 Nov 21.

University of Cologne, Institute of Human Genetics, Cologne, Germany.

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http://dx.doi.org/10.1517/13543784.2013.741587DOI Listing
January 2013

Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?

Nephrol Dial Transplant 2012 Jul 28;27(7):2984-9. Epub 2012 Jan 28.

Institute of Human Genetics, Department of General, Visceral and Cancer Surgery, University of Cologne, and Division of Pediatric Nephrology, Department of Pediatric and Adolescent Medicine, University Hospital Cologne, Cologne, Germany.

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http://dx.doi.org/10.1093/ndt/gfr776DOI Listing
July 2012

Enteric hyperoxaluria, recurrent urolithiasis, and systemic oxalosis in patients with Crohn's disease.

Pediatr Nephrol 2012 Jul 25;27(7):1103-9. Epub 2012 Feb 25.

Division of Pediatric Nephrology, Department of Pediatric and Adolescent Medicine, University Hospital Cologne, Kerpenerstrasse 62, 50924, Cologne, Germany.

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http://dx.doi.org/10.1007/s00467-012-2126-8DOI Listing
July 2012

Respiratory and general outcome in neonates with renal oligohydramnios--a single-centre experience.

Nephrol Dial Transplant 2011 Nov 9;26(11):3514-22. Epub 2011 Mar 9.

Division of Neonatology and Paediatric Intensive Care Medicine, Children’s Hospital, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1093/ndt/gfr046DOI Listing
November 2011

Reduction of plasma oxalate levels by oral application of Oxalobacter formigenes in 2 patients with infantile oxalosis.

Am J Kidney Dis 2011 Sep 25;58(3):453-5. Epub 2011 Jun 25.

Department of Pediatric and Adolescent Medicine, Division of Pediatric Nephrology, University Hospital, Cologne, Germany.

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http://dx.doi.org/10.1053/j.ajkd.2011.05.012DOI Listing
September 2011

Late diagnosis of primary hyperoxaluria after failed kidney transplantation.

Int Urol Nephrol 2010 Sep 18;42(3):825-9. Epub 2009 Dec 18.

University Department of Nephrology, Medical Faculty, University of Skopje, Vodnjanska 17, 1000 Skopje, Macedonia.

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http://www.biopku.org/pdf/spasovski_2009_iun.pdf
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http://link.springer.com/10.1007/s11255-009-9690-2
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http://dx.doi.org/10.1007/s11255-009-9690-2DOI Listing
September 2010

Renal allograft calcification -- prevalence and etiology in pediatric patients.

Am J Nephrol 2009 30;30(3):194-200. Epub 2009 Apr 30.

Department of Pediatrics, Division of Pediatric Nephrology, University Hospital, Cologne, Germany.

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http://dx.doi.org/10.1159/000217585DOI Listing
February 2010

The primary hyperoxalurias.

Kidney Int 2009 Jun 18;75(12):1264-1271. Epub 2009 Feb 18.

Division of Nephrology, Department of Pediatrics, Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1038/ki.2009.32DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577278PMC
June 2009

Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT).

Pediatr Nephrol 2009 Jan 10;24(1):55-60. Epub 2008 Oct 10.

Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.

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http://dx.doi.org/10.1007/s00467-008-1016-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155267PMC
January 2009

The case: A boy with recurrent stones.

Kidney Int 2008 Jul;74(1):133-4

Division of Pediatric Nephrology, Department of Pediatrics, University Hospital Cologne, Cologne, Germany.

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http://dx.doi.org/10.1038/ki.2008.165DOI Listing
July 2008

Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasis.

Pediatr Nephrol 2003 Oct 13;18(10):996-9. Epub 2003 Aug 13.

Division of Pediatric Nephrology, University Children's Hospital, Josef-Stelzmann Strasse 9, 50924 Cologne, Germany.

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http://link.springer.com/content/pdf/10.1007/s00467-003-1229
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http://search.proquest.com/openview/73f7484c41be245989fb7c19
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http://link.springer.com/10.1007/s00467-003-1229-7
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http://dx.doi.org/10.1007/s00467-003-1229-7DOI Listing
October 2003