Detalhe da pesquisa
1.
Fetal Mediastinal Fibrosarcoma. Report of Two Cases.
Fetal Pediatr Pathol
; 41(5): 843-851, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622726
2.
Inflammatory milieu of muscle biopsies in juvenile dermatomyositis.
Rheumatol Int
; 41(1): 77-85, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33106894
3.
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing.
Fetal Pediatr Pathol
; 39(2): 163-171, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31303091
4.
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.
Am J Hum Genet
; 98(6): 1130-1145, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27259049
5.
Are Congenital Urinary Tract Abnormalities Linked to Maternal Methylenetetrahydrofolate Reductase Polymorphisms in Fetuses of Intentionally Terminated Pregnancies with Oligo- or Anhydramnios ?
Fetal Pediatr Pathol
; 37(3): 177-183, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29737941
6.
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS.
J Am Soc Nephrol
; 27(1): 63-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25967120
7.
Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.
Fetal Pediatr Pathol
; 36(6): 445-451, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220612
8.
Acute kidney injury in a patient with COVID-19: Questions.
Pediatr Nephrol
; 36(12): 4109-4110, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491436
9.
Acute kidney injury in a patient with COVID-19: Answers.
Pediatr Nephrol
; 36(12): 4111-4113, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34491437
10.
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.
J Am Soc Nephrol
; 25(8): 1653-61, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24610927
11.
Giant cervical polyp with mesonephric duct remnants: unusual cause of vaginal bleeding in an adolescent girl.
Fetal Pediatr Pathol
; 33(3): 176-81, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24601846
12.
AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis.
Pathol Res Pract
; 258: 155334, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38718468
13.
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.
Am J Hum Genet
; 86(5): 789-96, 2010 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-20451171
14.
The histopathological effects of tamoxifen in the treatment of pubertal gynecomastia.
J Pediatr Endocrinol Metab
; 25(7-8): 753-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23155705
15.
Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
Pediatr Gastroenterol Hepatol Nutr
; 25(6): 441-452, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36451688
16.
Giant Right Atrial Myxoma with Fulminant Progression in an Infant.
J Pediatr Intensive Care
; 11(1): 77-82, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35178282
17.
Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages.
Turk J Pediatr
; 64(1): 59-68, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35286031
18.
Perianal giant condyloma acuminata in an infant: an alarming lesion for a pediatric surgeon.
Turk J Pediatr
; 53(3): 333-6, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21980819
19.
Clitoral epidermoid cyst secondary to blunt trauma in a 9-year-old child.
Turk J Pediatr
; 53(1): 108-10, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21534352
20.
A very rare cause of protein losing enteropathy: Gaucher disease.
Turk J Pediatr
; 63(4): 708-715, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34449155