Detalhe da pesquisa
1.
Recessive CHRM5 variant as a potential cause of neurogenic bladder.
Am J Med Genet A;
191(8): 2083-2091, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37213061
2.
Relapsing and refractory peritoneal dialysis peritonitis caused by Corynebacterium amycolatum.
Pediatr Nephrol;
38(5): 1687-1692, 2023 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36352270
3.
Pediatric peritoneal dialysis training program and its relationship to peritonitis: a study of the International Pediatric Peritoneal Dialysis Network.
Pediatr Nephrol;
38(12): 4111-4118, 2023 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37405492
4.
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Genet Med;
24(2): 307-318, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34906515
5.
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Am J Med Genet A;
188(1): 310-313, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34525250
6.
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.
Am J Med Genet A;
188(5): 1355-1367, 2022 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35040250
7.
Treatment and long-term outcome in primary nephrogenic diabetes insipidus.
Nephrol Dial Transplant;
2020 Dec 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33367818
8.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
J Am Soc Nephrol;
29(9): 2348-2361, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30143558
9.
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease.
J Pediatr;
199: 22-28.e6, 2018 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29753540
10.
Clinical Factors and Adverse Kidney Outcomes in Children With Antineutrophil Cytoplasmic Antibody-Associated Glomerulonephritis.
Am J Kidney Dis;
81(1): 119-122, 2023 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35810826
11.
Late acute rejection: incidence, risk factors, and effect on graft survival and function.
Pediatr Transplant;
18(2): 155-62, 2014 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24372967
12.
A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome.
Children (Basel);
9(11)2022 Nov 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36421183
13.
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease.
Kidney Int Rep;
7(7): 1643-1652, 2022 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35812281
14.
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Eur Urol Open Sci;
44: 106-112, 2022 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36185583
15.
An unusual cause of pink diapers in an infant: Questions and Answers.
Pediatr Nephrol;
31(4): 575, 577-80, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25823987
16.
An unusual cause of "pink diaper" in an infant: Answers.
Pediatr Nephrol;
31(4): 577-80, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25823988
17.
Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKD.
Sci Rep;
11(1): 21677, 2021 11 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34737334
18.
Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome.
Kidney Int Rep;
6(2): 472-483, 2021 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33615072
19.
Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network.
Sci Rep;
9(1): 4886, 2019 03 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30894599