Qian Fu
Beijing, China
Last Updated: 09/26/2026
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Found 12 publications
Clinical Characteristics of 30 Cases of Childhood Haemolytic Uremic Syndrome in a Single Centre.
Journal: Nephrology (Carlton, Vic.)
Published: October 31, 2025
Xanthogranulomatous pyelonephritis in a 47-day-old male infant: a case report.
Journal: Frontiers in pediatrics
Published: May 09, 2025
Compound heterozygous mutations in BBS7 cause kidney abnormalities in Bardet-Biedl syndrome.
Journal: Genes & diseases
Published: March 03, 2025
Alport syndrome complicated with steroid-sensitive nephrotic syndrome: a case report.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 07, 2025
Characteristics of children with IgA nephropathy.
Journal: Pediatric research
Published: June 30, 2021
Generation of a human iPSC line from a Bardet-Biedl syndrome patient compound heterozygous for the BBS7 variants c.849 + 1G > C/c.754G > A.
Journal: Stem cell research
Published: May 18, 2021
Lung ultrasound methods for assessing fluid volume change and monitoring dry weight in pediatric hemodialysis patients.
Journal: Pediatric nephrology (Berlin, Germany)
Published: May 06, 2020
Simpson-Golabi-Behmel syndrome with 46,XY disorders of sex development: A case report.
Journal: American journal of medical genetics. Part A
Published: April 26, 2018
Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome.
Journal: Science China. Life sciences
Published: March 30, 2017
Corneal cystine crystals in cystinosis.
Journal: Archives of disease in childhood
Published: March 02, 2017
Clinical features of Bardet-Biedl syndrome with renal abnormalities as initial manifestations
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: September 17, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026