Results 21 to 30 of about 4,881 (207)
ABO Genotyping of Complete Hydatidiform Moles [PDF]
Disease Markers, 1993 It has been suggested that the ABO blood group of a patient and her partner influence the clinical outcome for patients having a pregnancy with a complete hydatidiform mole (CHM). Since CHM lack red blood Cells, it has not previously been possible to type CHM serologically and investigate the relationship between the blood group of the CHM and that of ...
R A, Fisher +4 more
openaire +4 more sources
, 2011 Complete mole, also known as “classic” hydatidiform mole, is the prototype of molar gestation bearing the traditional description of “hydatid,” for example, grape-like structures at the time of evacuation, a term that was used throughout the last century. The historical tale of “365 babies” of the Dutch’s Countess Margaret of Henneberg (Chap.
The Radswiki, Henry Knipe, Ammar Ashraf
+4 more sources
Perbandingan Imunoekspresi p53 dan Caspase-3 Pada Mola Hidatidosa Parsial, Mola Hidatidosa Komplit, dan Koriokarsinoma [PDF]
, 2014 Background: Partial hydatidiform mole, complete hydatidiform mole and choriocarcinoma are gestational trophoblastic diseases which have high incidence in Indonesia.
Agustina, Hasrayati +3 more
core +3 more sources
Telomerase activity in gestational trophoblastic disease [PDF]
, 1999 Aims - To investigate the pattern of telomerase activity in hydatidiform mole as compared with normal placenta and choriocarcinoma, and to determine the prognostic significance of telomerase activity in hydatidiform mole. Methods - Telomerase activity in
Cheung, ANY +5 more
core +1 more source
Stem Cell Research, 2021 Recurrent hydatidiform mole (RHM) is characterized by the occurrence of at least twice hydatidiform mole. Unlike sporadic complete hydatidiform moles (CHMs), which are androgenetic with 2 paternal chromosomes, CHMs associated with familial recurrence are
Tingyu Gong +5 more
doaj +1 more source
Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners [PDF]
, 2016 The supernumerary chromosome 21 in Down syndrome differentially affects the methylation statuses at CpG dinucleotide sites and creates genome-wide transcriptional dysregulation of parental alleles, ultimately causing diverse pathologies.
Alves da Silva, Antônio Francisco +12 more
core +3 more sources
Septic shock in a woman with a hydatidiform mole: A case report
Case Reports in Women's Health, 2022 Hydatidiform moles can be fatal because of the risk of massive bleeding or thyroid storm; however, they rarely occur concomitantly with sepsis. We present herein the case of a woman with a hydatidiform mole with septic shock.
Yuki Yoshimoto +5 more
doaj +1 more source
Molecular genotyping of placental site and epithelioid trophoblastic tumours; female predominance [PDF]
, 2016 OBJECTIVE: To investigate a large series of placental site trophoblastic tumours (PSTT) and epithelioid trophoblastic tumours (ETT) and determine the relationship between their development and the type and sex of both the immediately antecedent and ...
Fisher, RA +4 more
core +1 more source
Obstetrics and Gynecology International, 2018 Objective. We sought to determine the prevalence of and factors associated with hydatidiform molar gestations amongst patients undergoing uterine evacuation at Mbarara Regional Referral Hospital (MRRH), Mbarara, Uganda. Methods.
Olivier Mulisya +11 more
doaj +1 more source
Partial molar pregnancy with live fetus diagnosed on second trimester: a case report [PDF]
, 2016 Hydatidiform mole is part of a group of diseases classified as gestational trophoblastic disease, which results from an aberrant fertilization. They are associated with an increase risk for the development of neoplasm, specifically choriocarcinoma, a ...
Cardoso, Rosete Maria Amorim Novais Nogueira +4 more
core +1 more source