Alexey Tsygin

Alexey Tsygin

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Alexey Tsygin

Alexey Tsygin

Publications by authors named "Alexey Tsygin"

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7Publications

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Management of bone disease in cystinosis: Statement from an international conference.

Authors:
Katharina Hohenfellner Frank Rauch Gema Ariceta Atif Awan Justine Bacchetta Carsten Bergmann Susanne Bechtold Noelle Cassidy Geroges Deschenes Ewa Elenberg William A Gahl Oliver Greil Erik Harms Nadine Herzig Bernd Hoppe Christian Koeppl Malcolm A Lewis Elena Levtchenko Galina Nesterova Fernando Santos Karl P Schlingmann Aude Servais Neveen A Soliman Guenther Steidle Clodagh Sweeney Ulrike Treikauskas Rezan Topaloglu Alexey Tsygin Koenraad Veys Rodo V Vigier Jozef Zustin Dieter Haffner

J Inherit Metab Dis 2019 Sep 5;42(5):1019-1029. Epub 2019 Aug 5.

Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1002/jimd.12134DOI Listing
September 2019

Treatment and long-term outcome in primary distal renal tubular acidosis.

Authors:
Sergio Camilo Lopez-Garcia Francesco Emma Stephen B Walsh Marc Fila Nakysa Hooman Marcin Zaniew Aurélia Bertholet-Thomas Giacomo Colussi Kathrin Burgmaier Elena Levtchenko Jyoti Sharma Jyoti Singhal Neveen A Soliman Gema Ariceta Biswanath Basu Luisa Murer Velibor Tasic Alexey Tsygin Stéphane Decramer Helena Gil-Peña Linda Koster-Kamphuis Claudio La Scola Jutta Gellermann Martin Konrad Marc Lilien Telma Francisco Despoina Tramma Peter Trnka Selçuk Yüksel Maria Rosa Caruso Milan Chromek Zelal Ekinci Giovanni Gambaro Jameela A Kari Jens König Francesca Taroni Julia Thumfart Francesco Trepiccione Louise Winding Elke Wühl Ayşe Ağbaş Anna Belkevich Rosa Vargas-Poussou Anne Blanchard Giovanni Conti Olivia Boyer Ismail Dursun Ayşe Seda Pınarbaşı Engin Melek Marius Miglinas Robert Novo Andrew Mallett Danko Milosevic Maria Szczepanska Sarah Wente Hae Il Cheong Rajiv Sinha Zoran Gucev Stephanie Dufek Daniela Iancu Robert Kleta Franz Schaefer Detlef Bockenhauer

Nephrol Dial Transplant 2019 06;34(6):981-991

Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

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http://dx.doi.org/10.1093/ndt/gfy409DOI Listing
June 2019

Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.

Authors:
Verena Matejas Bernward Hinkes Faisal Alkandari Lihadh Al-Gazali Ellen Annexstad Mehmet B Aytac Margaret Barrow Kveta Bláhová Detlef Bockenhauer Hae Il Cheong Iwona Maruniak-Chudek Pierre Cochat Jörg Dötsch Priya Gajjar Raoul C Hennekam Françoise Janssen Mikhail Kagan Ariana Kariminejad Markus J Kemper Jens Koenig Jillene Kogan Hester Y Kroes Eberhard Kuwertz-Bröking Amy F Lewanda Ana Medeira Jutta Muscheites Patrick Niaudet Michel Pierson Anand Saggar Laurie Seaver Mohnish Suri Alexey Tsygin Elke Wühl Aleksandra Zurowska Steffen Uebe Friedhelm Hildebrandt Corinne Antignac Martin Zenker

Hum Mutat 2010 Sep;31(9):992-1002

Institute of Human Genetics, University Hospital Erlangen, University of Erlangen-Nuremberg, Germany.

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http://dx.doi.org/10.1002/humu.21304DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978072PMC
September 2010

Novel human pathological mutations. Gene symbol: NPHS1. Disease: congenital nephrotic syndrome, Finnish type.

Authors:
Eugeny Tikhomirov Tatjiana Voznesenskaya Alexey Tsygin

Hum Genet 2009 Apr;125(3):334

Scientific Centre of Children Health, Moscow, Russian Federation.

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April 2009

Gene symbol: NPHS1. Disease: Congenital nephrotic syndrome, Finnish type.

Authors:
Eugeny Tikhomirov Natalia Averyanova Tatiana Voznesenskaya Alexey Tsygin

Hum Genet 2008 Oct;124(3):304

Scientific Centre of Children Health, Genetic Group, Lomonosovsky Prospect, 2/62, 119991 Moscow, Russian Federation.

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October 2008

Novel human pathological mutations. Gene symbol: NPHS2. Disease: steroid-resistant nephrotic syndrome.

Authors:
Eugeny Tikhomirov Natalia Averyanova Gulnara Bayazutdinova Tatiana Voznesenskaya Alexey Tsygin

Hum Genet 2007 Dec;122(5):549

Scientific Centre of Children Health, Genetic Group, Lomonosovsky Prospect, 2/62, 119991, Moscow, RussianFederation.

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December 2007

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.

Authors:
Bernward Hinkes Roger C Wiggins Rasheed Gbadegesin Christopher N Vlangos Dominik Seelow Gudrun Nürnberg Puneet Garg Rakesh Verma Hassan Chaib Bethan E Hoskins Shazia Ashraf Christian Becker Hans Christian Hennies Meera Goyal Bryan L Wharram Asher D Schachter Sudha Mudumana Iain Drummond Dontscho Kerjaschki Rüdiger Waldherr Alexander Dietrich Fatih Ozaltin Aysin Bakkaloglu Roxana Cleper Lina Basel-Vanagaite Martin Pohl Martin Griebel Alexey N Tsygin Alper Soylu Dominik Müller Caroline S Sorli Tom D Bunney Matilda Katan Jinhong Liu Massimo Attanasio John F O'toole Katrin Hasselbacher Bettina Mucha Edgar A Otto Rannar Airik Andreas Kispert Grant G Kelley Alan V Smrcka Thomas Gudermann Lawrence B Holzman Peter Nürnberg Friedhelm Hildebrandt

Nat Genet 2006 Dec 5;38(12):1397-405. Epub 2006 Nov 5.

Department of Pediatrics, University of Michigan, Ann Arbor, Michigan 48109, USA.

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http://dx.doi.org/10.1038/ng1918DOI Listing
December 2006