Results 41 to 50 of about 4,881 (207)

Thyroid function among women with gestational trophoblastic diseases. A cross-sectional study

open access: yesSão Paulo Medical Journal
BACKGROUND: Gestational trophoblastic diseases (GTDs) are treatable rare tumors with wide distribution. The estimated incidence of GTDs varies dramatically between different regions globally.
Harun Düğeroğlu, Murat Özgenoğlu
doaj   +1 more source

Reproductive Wastage in Recurrent Partial Hydatidiform Mole: A Clinical Dilemma. [PDF]

open access: yes, 2013
Recurrent partial Hydatidiform mole is an extremely rare clinical entity which represent a part of the gestational trophoblatic neoplasia spectrum. Since the first case was reported by Honore.
Ashmita, D   +3 more
core  

Variation in the Thyrotropic Activity of Human Chorionic Gonadotropin in Chinese Hamster Ovary Cells Arises from Differential Expression of the Human Thyrotropin Receptor and Microheterogeneity of the Hormone. [PDF]

open access: yes, 1995
The role of hCG as a stimulator of the human thyroid has been a subject of controversy, because discrepant results have been obtained in different in vitro assays.
Amir, S.M.   +4 more
core   +1 more source

Whole‐genome paternal uniparental disomy identified through prenatal single‐nucleotide polymorphism‐based cell‐free DNA screening

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 73-78, January 2026.
ABSTRACT Objective Prenatal single‐nucleotide polymorphism (SNP)‐based cell‐free DNA (cfDNA) screening can identify genome‐wide paternal uniparental disomy (GW‐UPDpat), including cases with complete hydatidiform mole with a coexisting fetus (CHMCF), those with placental mesenchymal dysplasia (PMD) and those with a mosaic/chimeric GW‐UPDpat syndrome ...
P. Benn   +5 more
wiley   +1 more source

Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome [PDF]

open access: yes, 2014
BackgroundAlthough the reference human genome sequence was declared finished in 2003, some regions of the genome remain incomplete due to their complex architecture.
Albracht, Derek   +12 more
core   +2 more sources

Early diagnosis and treatment of hydatidiform mole in adolescent pregnant woman [PDF]

open access: yes, 2021
Hydatidiform mole belongs to the spectrum of gestational trophoblastic disorders in which abnormal conception leads to excess placental tissue formation in the absence of fetal development. The incidence of hydatidiform mole is quite rare so that not all
Kaspan, Kaspan   +1 more
core   +2 more sources

Abdominal Hysterectomy Under Thoracic Epidural Anesthesia for Complete Molar Pregnancy in a Patient With Atypical Preeclampsia and Hyperthyroidism in a Resource‐Limited Setting: Case Report and Literature Review

open access: yesCase Reports in Anesthesiology, Volume 2026, Issue 1, 2026.
Background Hydatidiform mole is a rare gynecological disease arising from trophoblastic tissue. There is no standard anesthetic management for patients undergoing major abdominal surgery; the decision may be based on preoperative patient status, the presence of coexisting illnesses, the risk of aspiration, and the availability of advanced equipment ...
Mesay Milkias   +5 more
wiley   +1 more source

Molecular and immunohistochemical characteristics of complete hydatidiform moles [PDF]

open access: yesBalkan Journal of Medical Genetics, 2017
Abstract Molar pregnancy is a gestational trophoblastic disease that belongs to the category of precancerous lesions. On the other end of the spectrum are gestational trophoblastic neoplasms such as invasive mole, choriocarcinoma, placental site trophoblastic tumor and epithelioid trophoblastic tumor, which are considered malignant ...
Kubelka-Sabit, Katerina   +6 more
openaire   +4 more sources

Choriocarcinoma in the Cervix: Case Report of a Challenging Differential Diagnosis

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Background Primary cervical choriocarcinoma in abortion curettage tissue is extremely rare and represents a diagnostic challenge. It is a serious condition that requires prompt and targeted therapeutic management. This case report describes the diagnostic evaluation, taking into account relevant differential diagnoses and highlighting the importance of
Kristin Pfister   +6 more
wiley   +1 more source

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