Detalhe da pesquisa
1.
COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.
Prenat Diagn
; 42(5): 601-610, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35150448
2.
Associations between fetal heart rate variability and umbilical cord occlusions-induced neural injury: An experimental study in a fetal sheep model.
Acta Obstet Gynecol Scand
; 101(7): 758-770, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35502642
3.
The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.
Clin Genet
; 100(4): 462-467, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34212369
4.
WNT10B variants in split hand/foot malformation: Report of three novel families and review of the literature.
Am J Med Genet A
; 179(7): 1351-1356, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31050392
5.
Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.
Genet Med
; 19(9): 1013-1021, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28301459
6.
Perinatal outcome of placental massive perivillous fibrin deposition: a case-control study.
Prenat Diagn
; 37(4): 323-328, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28152557
7.
Confirmation of risk of cancer in blepharocheilodontic syndrome.
Genet Med
; 22(10): 1727-1728, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32483297
8.
Pregnancy as a susceptible state for thrombotic microangiopathies.
Front Med (Lausanne)
; 11: 1343060, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38476448
9.
Total alkaline phosphatase levels by gestational age in a large sample of pregnant women.
Placenta
; 132: 32-37, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36623417
10.
The challenging follow-up of pregnancy in women with known thrombotic thrombocytopenic purpura: a single-center experience of a preemptive management protocol.
J Nephrol
; 36(9): 2519-2529, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37816989
11.
A new case of bent bone dysplasia--FGFR2 type and review of the literature.
Am J Med Genet A
; 170(3): 785-9, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26573129
12.
Risk factors for spontaneous hematoma of the umbilical cord: A case-control study.
Placenta
; 99: 152-156, 2020 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32798767
13.
Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome.
Eur J Med Genet
; 61(10): 585-595, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29605658
14.
SALL4 expression in gestational trophoblastic tumors: a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor.
Hum Pathol
; 54: 121-6, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27068524