Results 11 to 20 of about 23,388 (267)

Inhibitory serum factor of lymphoproliferative response to allogeneic cells in pregnancy [PDF]

open access: yesSão Paulo Medical Journal, 1997
INTRODUCTION: An inhibitory serum factor of mixed lymphocyte culture (MLC) has been associated with successful pregnancy after lymphocyte transfusion in women with unexplained recurrent spontaneous abortions (RSA).
Silvia Daher   +4 more
doaj   +3 more sources

An “inexplicable” problem of habitual abortion

open access: yesClinical Management Issues, 2007
Thyroid autoimmunity (TAI) appears to be a determining factor in pregnancy loss. Many studies have confirmed this association, not only in hypo- and hyperthyroid women but also in euthyroid ones.
Gabriella Gallone
doaj   +1 more source

Significant correlation of angiotensin converting enzyme and glycoprotein IIIa genes polymorphisms with unexplained recurrent pregnancy loss in north of Iran [PDF]

open access: yes, 2016
Background: Spontaneous abortion is considered as the most complex problem during pregnancy. Thrombophilia is resumed as a cause of recurrent pregnancy loss (RPL). Glycoprotein IIIa (GPIIIa) gene is involved in thrombosis and abortion.
Farazmandfar, T.   +2 more
core   +1 more source

The structure of immunocompetent decidual cells in recurrent missed abortions [PDF]

open access: yesVojnosanitetski Pregled, 2016
Background/Aim. Recurrent or habitual missed abortions (RMA) are defined as three or more consecutive abortions. In the first trimester of pregnancy habitual missed abortions occur in about 1% of population.
Radović-Janošević Dragana   +5 more
doaj   +1 more source

Predictors of miscarriage: a matched case-control study [PDF]

open access: yesEpidemiology and Health, 2014
OBJECTIVES: The risk factors for miscarriage vary across communities and countries. This study was conducted to investigate the predictors of miscarriage in the west of Iran. METHODS: This matched case-control study was conducted in Hamadan Province from
Jalal Poorolajal   +4 more
doaj   +1 more source

Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal [PDF]

open access: yes, 2008
BACKGROUND: The prevalence of congenital uterine anomalies in women with reproductive failure remains unclear, largely due to methodological bias. The aim of this review is to assess the diagnostic accuracy of different methodologies and estimate the ...
Cocksedge, K.A.   +2 more
core   +1 more source

Maternal methyltetrahydrofolate reductase gene mutation in patients with missed abortions

open access: yesJournal of Taibah University Medical Sciences, 2018
Background: Missed abortions are a common problem, often caused by thrombophilia in both recurring and non-recurring cases. Aim: To determine whether the presence of a mutation in the methyltetrahydrofolate reductase (Mthfr) gene correlates with missed ...
Helmy A. Rady, MD
doaj   +1 more source

Reproductive outcome in pregnant women with recurrent pregnancy loss [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2015
PURPOSE: To estimate the future pregnancy success rate in women with a history of recurrent pregnancy loss. METHODS: A retrospective cohort study including 103 women seen at a clinic for recurrent pregnancy loss (loss group) between January 2006 and ...
Olivia Lúcia Nunes Costa   +3 more
doaj   +1 more source

In Situ Hybridization for the Identification of Karyotype Anomalies in the Histological Analysis of Early Spontaneous Abortion

open access: yesJournal of Biological Research, 2003
An estimated 15% of known pregnancies terminate in spontaneous abortion, the majority (90% circa) within the XII° week of gestation: early spontaneous abortion (ESA).
F. Grillo, C. Ivaldi, M. Curto
doaj   +1 more source

Fenótipo de subfertilidade, polimorfismos cromossômicos e falhas de concepção Subfertility phenotype, chromosome polymorphism and conception failures

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2011
OBJETIVO: avaliar a prevalência de alterações citogenéticas e polimorfismos cromossômicos em casais com fenótipo de subfertilidade em uma população brasileira.
Cássia de Lourdes Campanho   +3 more
doaj   +1 more source

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