Detalhe da pesquisa
1.
Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome.
Birth Defects Res A Clin Mol Teratol
; 106(7): 549-62, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26970085
2.
The cervical mucus plug inhibits, but does not block, the passage of ascending bacteria from the vagina during pregnancy.
Acta Obstet Gynecol Scand
; 93(1): 102-8, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24266587
3.
A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability.
Am J Med Genet A
; 161A(12): 3191-5, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24254850
4.
Majocchi's Granuloma - The Great Mimicker: A Case Report.
Case Rep Dermatol
; 15(1): 190-193, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37899944
5.
The human fetal right ventricular myocardium appears without a sub-epicardial base-apex oriented layer of myocytes.
Pediatr Res
; 81(3): 396-397, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27861466
6.
Diagnosis and Treatment of Blau Syndrome/Early-onset Sarcoidosis, an Autoinflammatory Granulomatous Disease, in an Infant.
Acta Derm Venereol
; 97(1): 126-127, 2017 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27304707
7.
Idiopathic hypereosinophilic syndrome: A rare diagnosis in children.
Clin Case Rep
; 8(10): 2013-2016, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33088541
8.
Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease.
Cell Rep
; 33(4): 108304, 2020 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33113370
9.
Diagnostic and molecular genetic challenges in male incontinentia pigmenti: a case report.
Acta Derm Venereol
; 93(6): 741-2, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23572116
10.
Tinzaparin for the treatment of foetal growth retardation: An open-labelled randomized clinical trial.
Thromb Res
; 170: 38-44, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30114561
11.
Successful Topical Treatment of Pigmented Purpuric Lichenoid Dermatitis of Gougerot-Blum in a Young Patient: A Case Report and Summary of the Most Common Pigmented Purpuric Dermatoses.
Case Rep Dermatol
; 9(3): 169-176, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29033823
12.
First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray.
Clin Case Rep
; 5(5): 608-612, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28469860
13.
Constitutive transgene expression of Stem Cell Antigen-1 in the hair follicle alters the sensitivity to tumor formation and progression.
Stem Cell Res
; 23: 109-118, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28732240
14.
Positive effect of low-dose imatinib mesylate in a patient with nephrogenic systemic fibrosis.
Acta Derm Venereol
; 91(4): 478-9, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21537826
15.
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function.
Sci Rep
; 6: 24083, 2016 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27094867
16.
The development of hepatic stellate cells in normal and abnormal human fetuses - an immunohistochemical study.
Physiol Rep
; 3(8)2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26265759
17.
Treatment influencing down-staging in EORTC Melanoma Group sentinel node histological protocol compared with complete step-sectioning: a national multicentre study.
Eur J Cancer
; 48(3): 347-52, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22023888
18.
Elastosis Perforans Serpiginosa in a patient with Down syndrome treated with imiquimod 5% cream.
Dermatol Reports
; 2(2): 15, 2010 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-25386246
19.
Two cases of nephrogenic systemic fibrosis after exposure to the macrocyclic compound gadobutrol.
NDT Plus
; 3(3): 285-287, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28657062
20.
Concomitant Sweet's syndrome and relapsing polychondritis.
Acta Derm Venereol
; 87(5): 426-7, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17721651