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Robert Novo

Lille University Hospital
H指数:19
被引数:1,809

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Corrigendum to “Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children” [Kidney International Reports Volume 10, Issue 4, April 2025, Pages 1205-1212]

勘误:“儿童德尼-德拉斯综合征的基因型-表型相关性” [《国际肾脏报告》第10卷第4期,2025年4月,第1205-1212页]

2025-05-040
OA
Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

儿童Denys-Drash综合征中的基因型-表型相关性

2025-01-011
OAAI
Social Deprivation Is Associated With Lower Access to Pre-emptive Kidney Transplantation and More Urgent-Start Dialysis in the Pediatric Population
2022-04-0117
OAAI
An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
2021-11-0140
OAAI
Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
2019-09-0368
OAAI
Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome Retrospective Genetic and Clinical Study
2019-01-2334
OAAI
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice
2017-11-0176
OAAI
Observations of a large Dent disease cohort
2016-08-0173
OAAI
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1
2015-06-1178
OAAI
Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability
2014-06-0194
OAAI
Prospective, randomized trial comparing short and long intravenous antibiotic treatment of acute pyelonephritis in children: Dimercaptosuccinic acid scintigraphic evaluation at 9 months

比较儿童急性肾盂肾炎的短期和长期静脉抗生素治疗的前瞻性随机试验: 9个月时二巯基丁二酸闪烁显像评估

2008-03-0143
PREAI