Literature DB >> 35768702

Bartter syndrome with multiple renal and liver cysts: a case report.

Yemei He1,2, Yue Zhou3,4,5, Weihua Wu1,2, Yue Chen6,7,8, Santao Ou9,10.   

Abstract

Entities:  

Year:  2022        PMID： 35768702     DOI： 10.1007/s11255-022-03274-6

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN： 0301-1623            Impact factor:   2.370


× No keyword cloud information.
  10 in total

1.  Renal cysts and nephrocalcinosis in a patient with Bartter syndrome type III.

Authors:  Toru Watanabe; Toshihiro Tajima
Journal:  Pediatr Nephrol       Date:  2005-02-17       Impact factor: 3.714

2.  Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Authors:  Martin Konrad; Martin Vollmer; Henny H Lemmink; Lambertus P W J VAN DEN Heuvel; Nikola Jeck; Rosa Vargas-Poussou; Alicia Lakings; Rainer Ruf; Georges Deschênes; Corinne Antignac; Lisa Guay-Woodford; Nine V A M Knoers; Hannsjörg W Seyberth; Delphine Feldmann; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2000-08       Impact factor: 10.121

3.  Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.

Authors:  Hao Lu; Maria C Rondón Galeano; Elisabeth Ott; Geraldine Kaeslin; P Jaya Kausalya; Carina Kramer; Nadina Ortiz-Brüchle; Nadescha Hilger; Vicki Metzis; Milan Hiersche; Shang Yew Tay; Robert Tunningley; Shubha Vij; Andrew D Courtney; Belinda Whittle; Elke Wühl; Udo Vester; Björn Hartleben; Steffen Neuber; Valeska Frank; Melissa H Little; Daniel Epting; Peter Papathanasiou; Andrew C Perkins; Graham D Wright; Walter Hunziker; Heon Yung Gee; Edgar A Otto; Klaus Zerres; Friedhelm Hildebrandt; Sudipto Roy; Carol Wicking; Carsten Bergmann
Journal:  Nat Genet       Date:  2017-05-22       Impact factor: 38.330

Review 4.  Salt-Losing Tubulopathies in Children: What's New, What's Controversial?

Authors:  Robert Kleta; Detlef Bockenhauer
Journal:  J Am Soc Nephrol       Date:  2017-12-13       Impact factor: 10.121

5.  Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome.

Authors:  Alberto Bettinelli; Nicolò Borsa; Rosa Bellantuono; Marie-Louise Syrèn; Raffaele Calabrese; Alberto Edefonti; John Komninos; Marisa Santostefano; Luciano Beccaria; Ivana Pela; Mario G Bianchetti; Silvana Tedeschi
Journal:  Am J Kidney Dis       Date:  2007-01       Impact factor: 8.860

6.  Value of [68Ga]Ga-FAPI-04 imaging in the diagnosis of renal fibrosis.

Authors:  Yue Zhou; Xin Yang; Huipan Liu; Wenbin Luo; Hanxiang Liu; Taiyong Lv; Junzheng Wang; Jianhua Qin; Santao Ou; Yue Chen
Journal:  Eur J Nucl Med Mol Imaging       Date:  2021-04-07       Impact factor: 9.236

7.  Renal cysts and hypokalemia in primary aldosteronism: results of long-term follow-up after treatment.

Authors:  Marileda Novello; Cristiana Catena; Elisa Nadalini; Gian Luca Colussi; Sara Baroselli; Alessandra Chiuch; Roberta Lapenna; Massimo Bazzocchi; Leonardo A Sechi
Journal:  J Hypertens       Date:  2007-07       Impact factor: 4.844

8.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

9.  An Adult Case of Bartter Syndrome Type III Presenting with Proteinuria.

Authors:  Eun Jung Cha; Won Min Hwang; Sung-Ro Yun; Moon Hyang Park
Journal:  J Pathol Transl Med       Date:  2016-01-11

Review 10.  Bartter syndrome: causes, diagnosis, and treatment.

Authors:  Tamara da Silva Cunha; Ita Pfeferman Heilberg
Journal:  Int J Nephrol Renovasc Dis       Date:  2018-11-09
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.