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1.
Discordant Eosinophilic/T-Cell Chorionic Vasculitis in a Dichorionic Diamniotic Placenta.
Int J Mol Sci
; 24(11)2023 May 24.
Article
in English
| MEDLINE | ID: mdl-37298167
2.
Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous POMT2 Missense Mutations.
Fetal Pediatr Pathol
; 42(2): 334-341, 2023 Apr.
Article
in English
| MEDLINE | ID: mdl-36048137
3.
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation.
Acta Neuropathol
; 142(4): 761-776, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34347142
4.
Role of fetal MRI in the evaluation of isolated and non-isolated corpus callosum dysgenesis: results of a cross-sectional study.
Prenat Diagn
; 37(3): 244-252, 2017 Mar.
Article
in English
| MEDLINE | ID: mdl-27992967
5.
Axial skeletogenesis in human autosomal aneuploidies: A radiographic study of 145 second trimester fetuses.
Am J Med Genet A
; 170(3): 676-87, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26687031
6.
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome.
Birth Defects Res A Clin Mol Teratol
; 103(6): 554-66, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25360518
7.
Dandy-Walker Malformation: is the 'tail sign' the key sign?
Prenat Diagn
; 35(13): 1358-64, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26448595
8.
Role of foetal MRI in the evaluation of ischaemic-haemorrhagic lesions of the foetal brain.
J Perinat Med
; 40(4): 419-26, 2012 Apr 13.
Article
in English
| MEDLINE | ID: mdl-22752774
9.
Sirenomelia and VACTERL association in the offspring of a woman with diabetes.
Am J Med Genet A
; 152A(7): 1803-7, 2010 Jul.
Article
in English
| MEDLINE | ID: mdl-20583159
10.
The splice c.1815G>A variant in KIAA0586 results in a phenotype bridging short-rib-polydactyly and oral-facial-digital syndrome: A case report and literature review.
Medicine (Baltimore)
; 99(8): e19169, 2020 Feb.
Article
in English
| MEDLINE | ID: mdl-32080096
11.
Fontaine-Farriaux syndrome: a recognizable craniosynostosis syndrome with nail, skeletal, abdominal, and central nervous system anomalies.
Am J Med Genet A
; 149A(10): 2193-9, 2009 Oct.
Article
in English
| MEDLINE | ID: mdl-19731360
12.
Incidental endometrial adenocarcinoma in early pregnancy: a case report and review of the literature.
Int J Gynecol Cancer
; 19(9): 1580-4, 2009 Dec.
Article
in English
| MEDLINE | ID: mdl-19955941
13.
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum.
Science
; 366(6464): 454-460, 2019 10 25.
Article
in English
| MEDLINE | ID: mdl-31624095
14.
A 22-Week-Old Fetus with Nager Syndrome and Congenital Diaphragmatic Hernia due to a Novel SF3B4 Mutation.
Mol Syndromol
; 5(5): 241-4, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-25337072
15.
Bilateral subependymal heterotopia, ventriculomegaly and cerebellar asymmetry: fetal MRI findings of a rare association of brain anomalies.
J Radiol Case Rep
; 7(11): 38-45, 2013 Nov.
Article
in English
| MEDLINE | ID: mdl-24421929
16.
Prenatal diagnosis and post-mortem examination in a fetus with thrombocytopenia-absent radius (TAR) syndrome due to compound heterozygosity for a 1q21.1 microdeletion and a RBM8A hypomorphic allele: a case report.
BMC Res Notes
; 6: 376, 2013 Sep 22.
Article
in English
| MEDLINE | ID: mdl-24053387
17.
Histomorphometric characteristics of first trimester chorionic villi in pregnancies with low serum pregnancy-associated plasma protein-A levels: relationship with placental three-dimensional power doppler ultrasonographic vascularization.
J Matern Fetal Neonatal Med
; 24(2): 253-7, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-20459339
18.
Embolism of brain tissue in intrapartum and early neonatal deaths: report of 9 cases.
Pediatr Dev Pathol
; 12(6): 464-8, 2009.
Article
in English
| MEDLINE | ID: mdl-19594200
19.
Short-term surviving sirenomelia neonate followed by a complex mesodermal malformation in a sibling.
BMJ Case Rep
; 20132013 Jan 29.
Article
in English
| MEDLINE | ID: mdl-23365163
20.
Reassessment of holoprosencephaly-diencephalic hamartoblastoma (HDH) association.
Am J Med Genet A
; 143A(3): 277-84, 2007 Feb 01.
Article
in English
| MEDLINE | ID: mdl-17230485