D. Miranda

发表

Single Nucleotide Variants in A Family of Monozygotic Twins Discordant for the Phenotype Congenital Megaureter: A Genomic Analysis

R. G. C. C. L. Cardenas, A. C. S. D. S. Junior, L. B. Rodrigues, 2017 .

Possible involvement of ACSS2 gene in alcoholism

Valdir Ribeiro Campos, R. B. Lacerda, D. Miranda, 2017, Journal of Neural Transmission.

Immune markers in the RASopathy neurofibromatosis type 1

L. Rodrigues, M. Romano-Silva, D. Miranda, 2016, Journal of Neuroimmunology.

Urinary Levels of IL-1β and GDNF in Preterm Neonates as Potential Biomarkers of Motor Development: A Prospective Study

D. Miranda, É. Vieira, A. C. Simões e Silva, 2017, Mediators of inflammation.

Clinical Characteristics and Prognosis in Children and Adolescents With Autoimmune Hepatitis and Overlap Syndrome

Priscila Menezes Ferri Liu, D. Miranda, A. C. Simões e Silva, 2016, Journal of pediatric gastroenterology and nutrition.

Molecular Pathophysiology of Renal Tubular Acidosis

E. A. Oliveira, D. Miranda, P. Pereira, 2009, Current genomics.

Urinary chemokines and anti-inflammatory molecules in renal transplanted patients as potential biomarkers of graft function: a prospective study

M. Teixeira, N. Rezende, A. Teixeira, 2012, International Urology and Nephrology.

PAX2 Polymorphisms and Congenital Abnormalities of the Kidney and Urinary Tract in a Brazilian Pediatric Population: Evidence for a Role in Vesicoureteral Reflux

D. M. de Miranda, E. A. Oliveira, D. Miranda, 2014, Molecular Diagnosis & Therapy.

Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract.

L. Marco, E. A. Oliveira, D. Miranda, 2014, Jornal de pediatria.

Congenital anomalies of the kidney and urinary tract: An embryogenetic review

A. C. S. D. S. Junior, D. Miranda, A. Silva, 2014 .

Profile and scientific production of Brazilian National Council of Technological and Scientific Development researchers in Pediatrics

E. Colosimo, E. A. Oliveira, D. Miranda, 2013, Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo.

Interactions between Cytokines, Congenital Anomalies of Kidney and Urinary Tract and Chronic Kidney Disease

E. A. Oliveira, D. Miranda, A. C. Simões e Silva, 2013, Clinical & developmental immunology.

Usefulness of positron emission tomography in the differentiation between tumor and infectious lesions in pediatric oncology: a case report

D. Miranda, A. C. Simões e Silva, Karla Emília de Sá Rodrigues, 2015, BMC Pediatrics.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Craig S. Wong, H. Hakonarson, A. Latos-Bieleńska, 2018, Nature Genetics.

Comparison of the First and Second Waves of the Coronavirus Disease 2019 Pandemic in Children and Adolescents in a Middle-Income Country: Clinical Impact Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Gamma Lineage

E. Colosimo, R. Mak, E. A. Oliveira, 2022, The Journal of Pediatrics.

Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients

D. V. Rosa, E. A. Oliveira, D. Miranda, 2014, Nephrology.

Telomere Shortening and Psychiatric Disorders: A Systematic Review

D. Miranda, P. A. Pousa, T. S. Mendonça, 2021, Cells.

Cytokines in chronic kidney disease: potential link of MCP-1 and dyslipidemia in glomerular diseases

M. Teixeira, D. Miranda, A. C. Simões e Silva, 2013, Pediatric Nephrology.

Autoimmune Hepatitis and Autoimmune Hepatitis Overlap With Sclerosing Cholangitis: Immunophenotype Markers in Children and Adolescents

D. Miranda, A. C. Simões e Silva, K. Torres, 2017, Journal of pediatric gastroenterology and nutrition.

Whole-exome sequencing as a diagnostic tool for distal renal tubular acidosis.

E. A. Oliveira, D. Miranda, A. C. Simões e Silva, 2015, Jornal de pediatria.

Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter's Syndrome

R. Coletta, D. Miranda, H. Martelli-Júnior, 2012, Nephron Extra.

Case Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter’s Syndrome

R. Coletta, D. Miranda, H. Martelli-Júnior, 2012 .

Attention deficit and hyperactivity disorder and nocturnal enuresis co-occurrence in the pediatric population: a systematic review and meta-analysis

M. Albuquerque, D. Miranda, A. C. Simões e Silva, 2021, Pediatric Nephrology.

Association of SLITRK1 to Gilles de la Tourette Syndrome

Paul Sandor, P. Sandor, C. Barr, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Diagnostic criteria for autoimmune hepatitis in children: a challenge for pediatric hepatologists.

D. Miranda, A. C. Simões e Silva, P. Ferri, 2012, World journal of gastroenterology.

PAX2 Polymorphisms and Congenital Abnormalities of the Kidney and Urinary Tract in a Brazilian Pediatric Population: Evidence for a Role in Vesicoureteral Reflux

E. A. Oliveira, D. Miranda, A. C. Simões e Silva, 2014, Molecular Diagnosis & Therapy.