Detalhe da pesquisa
1.
The types and frequencies of X chromosome abnormalities in women with reproductive problems.
Cytogenet Genome Res
; 2023 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37788650
2.
The impact of preimplantation genetic testing for aneuploidies (PGT-A) on clinical outcomes in high risk patients.
J Assist Reprod Genet
; 39(6): 1341-1349, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35338417
3.
Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF.
Cytogenet Genome Res
; 161(12): 551-555, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35051945
4.
Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype.
Gynecol Endocrinol
; 37(4): 377-381, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33356667
5.
Bone Marrow Failure in Fanconi Anemia: Clinical and Genetic Spectrum in a Cohort of 20 Pediatric Patients.
J Pediatr Hematol Oncol
; 41(8): 612-617, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31259830
6.
Plasma biomarkers for the identification of women at risk for early-onset preeclampsia.
Expert Rev Proteomics
; 14(3): 269-276, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28222616
7.
RASSF1A in maternal plasma as a molecular marker of preeclampsia.
Prenat Diagn
; 33(7): 682-7, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23526657
8.
A 46,XX Karyotype in Men with Infertility: Two New Cases and Review of the Literature.
J Hum Reprod Sci
; 15(3): 307-317, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341017
9.
Proteomic analysis of amniotic fluid for the diagnosis of fetal aneuploidies.
Expert Rev Proteomics
; 8(2): 175-85, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21501011
10.
Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature.
Eur J Obstet Gynecol Reprod Biol
; 264: 212-218, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34332218
11.
Potential biomarkers for Turner in maternal plasma: possibility for noninvasive prenatal diagnosis.
J Proteome Res
; 9(10): 5164-70, 2010 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20738094
12.
Coffin-Siris Syndrome 4-Related Spectrum in a Young Woman Caused by a Heterozygous SMARCA4 Deletion Detected by High-Resolution aCGH.
Mol Syndromol
; 11(3): 141-145, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32903985
13.
Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF.
In Vivo
; 34(3): 1433-1437, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32354942
14.
Mass spectrometry-based proteomics in reproductive medicine.
Mass Spectrom Rev
; 27(6): 624-34, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18618655
15.
Three novel mutations in greek sotos patients with rare clinical manifestations.
Horm Res
; 71(1): 45-51, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19039236
16.
Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.
Eur J Med Genet
; 51(1): 61-7, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-17998173
17.
The ATM gene and ataxia telangiectasia.
Anticancer Res
; 28(1B): 401-5, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18383876
18.
Development of cancer in patients with primary immunodeficiencies.
Anticancer Res
; 28(2B): 1263-9, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18505064
19.
Androgen insensitivity syndrome: clinical features and molecular defects.
Hormones (Athens)
; 7(3): 217-29, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18694860
20.
Dysregulated placental microRNAs in Early and Late onset Preeclampsia.
Placenta
; 61: 24-32, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29277268