Publications by authors named "Matthias T F Wolf"

34Publications

A rare case of hyporeninemic hypertension: Answers.

Pediatr Nephrol 2020 Jun 30. Epub 2020 Jun 30.

Pediatric Nephrology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

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http://dx.doi.org/10.1007/s00467-020-04667-4DOI Listing
June 2020

A rare case of hyporeninemic hypertension: Questions.

Pediatr Nephrol 2020 Jun 30. Epub 2020 Jun 30.

Pediatric Nephrology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

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http://dx.doi.org/10.1007/s00467-020-04658-5DOI Listing
June 2020

Homozygous NEK8 Mutations in Siblings With Neonatal Cholestasis Progressing to End-stage Liver, Renal, and Cardiac Disease.

J Pediatr Gastroenterol Nutr 2020 01;70(1):e19-e22

Division of Pediatric Gastroenterology, Hepatology, and Nutrition.

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http://dx.doi.org/10.1097/MPG.0000000000002517DOI Listing
January 2020

Uromodulin in mineral metabolism.

Curr Opin Nephrol Hypertens 2019 09;28(5):481-489

Pediatric Nephrology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

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http://dx.doi.org/10.1097/MNH.0000000000000522DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764599PMC
September 2019

Mercury Intoxication as a Rare Cause of Membranous Nephropathy in a Child.

Am J Kidney Dis 2018 10 21;72(4):601-605. Epub 2018 Jul 21.

Division of Pediatric Nephrology, Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX. Electronic address:

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http://dx.doi.org/10.1053/j.ajkd.2018.05.013DOI Listing
October 2018

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

Authors:
Daniela A Braun Jia Rao Geraldine Mollet David Schapiro Marie-Claire Daugeron Weizhen Tan Olivier Gribouval Olivia Boyer Patrick Revy Tilman Jobst-Schwan Johanna Magdalena Schmidt Jennifer A Lawson Denny Schanze Shazia Ashraf Jeremy F P Ullmann Charlotte A Hoogstraten Nathalie Boddaert Bruno Collinet Gaëlle Martin Dominique Liger Svjetlana Lovric Monica Furlano I Chiara Guerrera Oraly Sanchez-Ferras Jennifer F Hu Anne-Claire Boschat Sylvia Sanquer Björn Menten Sarah Vergult Nina De Rocker Merlin Airik Tobias Hermle Shirlee Shril Eugen Widmeier Heon Yung Gee Won-Il Choi Carolin E Sadowski Werner L Pabst Jillian K Warejko Ankana Daga Tamara Basta Verena Matejas Karin Scharmann Sandra D Kienast Babak Behnam Brendan Beeson Amber Begtrup Malcolm Bruce Gaik-Siew Ch'ng Shuan-Pei Lin Jui-Hsing Chang Chao-Huei Chen Megan T Cho Patrick M Gaffney Patrick E Gipson Chyong-Hsin Hsu Jameela A Kari Yu-Yuan Ke Cathy Kiraly-Borri Wai-Ming Lai Emmanuelle Lemyre Rebecca Okashah Littlejohn Amira Masri Mastaneh Moghtaderi Kazuyuki Nakamura Fatih Ozaltin Marleen Praet Chitra Prasad Agnieszka Prytula Elizabeth R Roeder Patrick Rump Rhonda E Schnur Takashi Shiihara Manish D Sinha Neveen A Soliman Kenza Soulami David A Sweetser Wen-Hui Tsai Jeng-Daw Tsai Rezan Topaloglu Udo Vester David H Viskochil Nithiwat Vatanavicharn Jessica L Waxler Klaas J Wierenga Matthias T F Wolf Sik-Nin Wong Sebastian A Leidel Gessica Truglio Peter C Dedon Annapurna Poduri Shrikant Mane Richard P Lifton Maxime Bouchard Peter Kannu David Chitayat Daniella Magen Bert Callewaert Herman van Tilbeurgh Martin Zenker Corinne Antignac Friedhelm Hildebrandt

Nat Genet 2017 Oct 14;49(10):1529-1538. Epub 2017 Aug 14.

Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

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http://www.nature.com/doifinder/10.1038/ng.3933
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http://dx.doi.org/10.1038/ng.3933DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819591PMC
October 2017

Omental Arteriopathy in Primary Atypical Hemolytic Uremic Syndrome.

Int J Surg Pathol 2017 Sep 22;25(6):515-517. Epub 2017 Mar 22.

1 University of Texas Southwestern Medical Center, Dallas, TX, USA.

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http://dx.doi.org/10.1177/1066896917699703DOI Listing
September 2017

Nephronophthisis and related syndromes.

Curr Opin Pediatr 2015 Apr;27(2):201-11

Division of Pediatric Nephrology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

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http://dx.doi.org/10.1097/MOP.0000000000000194DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422489PMC
April 2015

Klotho up-regulates renal calcium channel transient receptor potential vanilloid 5 (TRPV5) by intra- and extracellular N-glycosylation-dependent mechanisms.

J Biol Chem 2014 Dec 5;289(52):35849-57. Epub 2014 Nov 5.

Internal Medicine, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390

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http://dx.doi.org/10.1074/jbc.M114.616649DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276853PMC
December 2014

Uromodulin upregulates TRPV5 by impairing caveolin-mediated endocytosis.

Kidney Int 2013 Jul 6;84(1):130-7. Epub 2013 Mar 6.

Division of Pediatric Nephrology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9063, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S00852538155592
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http://dx.doi.org/10.1038/ki.2013.63DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700562PMC
July 2013

Nephronophthisis.

Pediatr Nephrol 2011 Feb 22;26(2):181-94. Epub 2010 Jul 22.

Divison of Pediatric Nephrology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USA.

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http://link.springer.com/10.1007/s00467-010-1585-z
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http://dx.doi.org/10.1007/s00467-010-1585-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160028PMC
February 2011

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

Evidence of oligogenic inheritance in nephronophthisis.

J Am Soc Nephrol 2007 Oct 12;18(10):2789-95. Epub 2007 Sep 12.

Departments of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.

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http://dx.doi.org/10.1681/ASN.2007020243DOI Listing
October 2007

Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing.

Hum Genet 2006 Jul 26;119(6):649-58. Epub 2006 Apr 26.

Department of Pediatrics, University of Michigan, Ann Arbor, MI 48109-0646, USA, and University Children's Hospital, Freiburg University, Germany.

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http://dx.doi.org/10.1007/s00439-006-0176-3DOI Listing
July 2006

Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.

Nephrol Dial Transplant 2005 May 1;20(5):909-14. Epub 2005 Mar 1.

Department of Pediatrics and Communicable Diseases, University of Michigan, 8220C MSRB III, 1150 West Medical Center Drive, Ann Arbor, MI 48109-0646, USA.

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http://dx.doi.org/10.1093/ndt/gfh754DOI Listing
May 2005

Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegans.

J Am Soc Nephrol 2005 Mar 19;16(3):676-87. Epub 2005 Jan 19.

Department of Pediatrics and Communicable Diseases, University of Michigan, 8220C MSRB III, 1150 West Medical Center Drive, Ann Arbor, MI 48109-0646, USA.

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http://dx.doi.org/10.1681/ASN.2003121025DOI Listing
March 2005

Medullary cystic kidney disease type 1 in a large Native-American kindred.

Am J Kidney Dis 2004 Oct;44(4):611-7

Division of Nephrology and Hypertension, University of North Carolina, Chapel Hill, NC, USA.

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October 2004

Refinement of the critical region for MCKD1 by detection of transcontinental haplotype sharing.

Kidney Int 2003 Sep;64(3):788-92

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan 48109-0640, USA.

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http://dx.doi.org/10.1046/j.1523-1755.2003.00161.xDOI Listing
September 2003

Pulmonary re-occurrence of post-transplant lymphoproliferative disease with hypogammaglobulinaemia.

Eur J Pediatr 2003 Mar 28;162(3):180-183. Epub 2003 Jan 28.

Department of Paediatrics, Universitätsklinikum Benjamin Franklin, Freie Universität Berlin, Hindenburgdamm 30, 12200 , Berlin, Germany.

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http://dx.doi.org/10.1007/s00431-002-1120-8DOI Listing
March 2003

Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.

Pediatr Nephrol 2002 Aug 11;17(8):602-8. Epub 2002 Jun 11.

Klinik für Kinder und Jugendliche, University of Erlangen - Nürnberg, 91054 Erlangen, Germany.

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http://dx.doi.org/10.1007/s00467-002-0884-4DOI Listing
August 2002