Garcia-Castro P, Giambo-Falian I, Carvacho I, Fuentes R
Front Cell Dev Biol. 2025; 13:1514461.
PMID: 39949602
PMC: 11821946.
DOI: 10.3389/fcell.2025.1514461.
Gomez-Lumbreras A, Leston Vazquez M, Vilaplana-Carnerero C, Prat-Vallverdu O, Vedia C, Morros R
Womens Health Rep (New Rochelle). 2024; 5(1):13-21.
PMID: 38249939
PMC: 10798141.
DOI: 10.1089/whr.2023.0123.
Turgut N, Boynukalin F, Gultomruk M, Yarkiner Z, Abali R, Bahceci M
Arch Gynecol Obstet. 2023; 308(5):1567-1575.
PMID: 37466688
DOI: 10.1007/s00404-023-07155-w.
Nikitina T, Lebedev I
Cells. 2022; 11(12).
PMID: 35741051
PMC: 9221414.
DOI: 10.3390/cells11121923.
Tang Y, Zhu C, Zhu C, Liang F, Lee A, Yao X
BMC Womens Health. 2020; 20(1):196.
PMID: 32912152
PMC: 7488519.
DOI: 10.1186/s12905-020-01064-9.
Count data regression modeling: an application to spontaneous abortion.
Verma P, Swain P, Singh K, Khetan M
Reprod Health. 2020; 17(1):106.
PMID: 32641058
PMC: 7346466.
DOI: 10.1186/s12978-020-00955-2.
Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss.
Nikitina T, Sazhenova E, Zhigalina D, Tolmacheva E, Sukhanova N, Lebedev I
J Assist Reprod Genet. 2020; 37(3):517-525.
PMID: 32009222
PMC: 7125272.
DOI: 10.1007/s10815-020-01703-y.
Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses.
Nikitina T, Sazhenova E, Tolmacheva E, Sukhanova N, Kashevarova A, Skryabin N
Biomed Hub. 2020; 1(1):1-11.
PMID: 31988885
PMC: 6945958.
DOI: 10.1159/000446099.
Impact of sitagliptin on endometrial mesenchymal stem-like progenitor cells: A randomised, double-blind placebo-controlled feasibility trial.
Tewary S, Lucas E, Fujihara R, Kimani P, Polanco A, Brighton P
EBioMedicine. 2020; 51:102597.
PMID: 31928963
PMC: 7000352.
DOI: 10.1016/j.ebiom.2019.102597.
Combination of QF-PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage.
Lovrecic L, Pereza N, Jaklic H, Ostojic S, Peterlin B
Mol Genet Genomic Med. 2019; 7(12):e980.
PMID: 31643138
PMC: 6900363.
DOI: 10.1002/mgg3.980.
Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia.
Turki R, Assidi M, Banni H, Zahed H, Karim S, Schulten H
BMC Med Genet. 2016; 17(Suppl 1):69.
PMID: 27766963
PMC: 5073987.
DOI: 10.1186/s12881-016-0331-1.
1(st) trimester miscarriage: four decades of study.
Hardy K, Hardy P
Transl Pediatr. 2016; 4(2):189-200.
PMID: 26835373
PMC: 4729087.
DOI: 10.3978/j.issn.2224-4336.2015.03.05.
Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.
Karatas A, Eroz R, Albayrak M, Ozlu T, Cakmak B, Keskin F
Afr Health Sci. 2015; 14(1):216-22.
PMID: 26060483
PMC: 4449075.
DOI: 10.4314/ahs.v14i1.34.
Chromosomal analysis of couples with repeated spontaneous abortions in northeastern iran.
Ghazaey S, Keify F, Mirzaei F, Maleki M, Tootian S, Ahadian M
Int J Fertil Steril. 2015; 9(1):47-54.
PMID: 25918592
PMC: 4410037.
DOI: 10.22074/ijfs.2015.4208.
Molecular analysis of products of conception obtained by hysteroembryoscopy from infertile couples.
Campos-Galindo I, Garcia-Herrero S, Martinez-Conejero J, Ferro J, Simon C, Rubio C
J Assist Reprod Genet. 2015; 32(5):839-48.
PMID: 25779005
PMC: 4429442.
DOI: 10.1007/s10815-015-0460-z.
Genetic considerations in recurrent pregnancy loss.
Hyde K, Schust D
Cold Spring Harb Perspect Med. 2015; 5(3):a023119.
PMID: 25659378
PMC: 4355257.
DOI: 10.1101/cshperspect.a023119.
Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases.
Choi T, Lee H, Park W, Jeong S, Moon H
Obstet Gynecol Sci. 2014; 57(6):518-25.
PMID: 25469342
PMC: 4245347.
DOI: 10.5468/ogs.2014.57.6.518.
Risk of chromosomal abnormalities in early spontaneous abortion after assisted reproductive technology: a meta-analysis.
Qin J, Pang L, Li M, Xu J, Zhou X
PLoS One. 2013; 8(10):e75953.
PMID: 24130752
PMC: 3795086.
DOI: 10.1371/journal.pone.0075953.
Rapid-prenatal diagnosis through fluorescence in situ hybridization for preventing aneuploidy related birth defects.
Fauzdar A, Chowdhry M, Makroo R, Mishra M, Srivastava P, Tyagi R
Indian J Hum Genet. 2013; 19(1):32-42.
PMID: 23901191
PMC: 3722628.
DOI: 10.4103/0971-6866.112881.
Chromosomal aneuploidy in the aging brain.
Faggioli F, Vijg J, Montagna C
Mech Ageing Dev. 2011; 132(8-9):429-36.
PMID: 21549743
PMC: 3168579.
DOI: 10.1016/j.mad.2011.04.008.