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1
Androgenetic Complete Hydatidiform Moles With p57KIP2-Positive Immunostaining
Androgenetic Complete Hydatidiform Moles With p57KIP2-Positive Immunostaining
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Androgenetic Complete Hydatidiform Moles With p57KIP2-Positive Immunostaining

Usui, Hirokazu ; Sato, Asuka ; Ota, Masayuki ; Ikeda, Jun-ichiro ; Shozu, Makio

American journal of clinical pathology, 2020-12, Vol.154 (6), p.776-783 [Periódico revisado por pares]

US: Oxford University Press

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2
Diagnostic Utility of Twist1, Ki-67, and E-Cadherin in Diagnosing Molar Gestations and Hydropic Abortions
Diagnostic Utility of Twist1, Ki-67, and E-Cadherin in Diagnosing Molar Gestations and Hydropic Abortions
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Diagnostic Utility of Twist1, Ki-67, and E-Cadherin in Diagnosing Molar Gestations and Hydropic Abortions

Moussa, Rabab A ; Eesa, Ahmed N ; Abdallah, Zeinab F ; Abdelmeged, Ayman ; Mahran, Ahmed ; Bahaa, Haitham

American journal of clinical pathology, 2018-03, Vol.149 (5), p.442-455 [Periódico revisado por pares]

US: Oxford University Press

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3
Pathogenic role of Twist-1 protein in hydatidiform molar pregnancies and investigation of its potential diagnostic utility in complete moles
Pathogenic role of Twist-1 protein in hydatidiform molar pregnancies and investigation of its potential diagnostic utility in complete moles
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Pathogenic role of Twist-1 protein in hydatidiform molar pregnancies and investigation of its potential diagnostic utility in complete moles

Jahanbin, Behnaz ; Sarmadi, Soheila ; Ghasemi, Dorsa ; Nili, Fatemeh ; Moradi, Jafar-Ali ; Ghasemi, Soha

Diagnostic pathology, 2023-03, Vol.18 (1), p.40-40, Article 40 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Ethnic disparities in complete and partial molar pregnancy incidence: a retrospective analysis of arab and jewish women in single medical center
Ethnic disparities in complete and partial molar pregnancy incidence: a retrospective analysis of arab and jewish women in single medical center
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Ethnic disparities in complete and partial molar pregnancy incidence: a retrospective analysis of arab and jewish women in single medical center

Aiob, Ala ; Gumin, Dina ; Zilberfarb, Inna ; Naskovica, Karina ; Sgayer, Inshirah ; Mikhail, Susana Mustafa ; Sharon, Avishalom ; Lowenstein, Lior

BMC public health, 2024-05, Vol.24 (1), p.1440-7, Article 1440 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
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A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation

Demond, Hannah ; Anvar, Zahra ; Jahromi, Bahia Namavar ; Sparago, Angela ; Verma, Ankit ; Davari, Maryam ; Calzari, Luciano ; Russo, Silvia ; Jahromi, Mojgan Akbarzadeh ; Monk, David ; Andrews, Simon ; Riccio, Andrea ; Kelsey, Gavin

Genome medicine, 2019-12, Vol.11 (1), p.84-84, Article 84 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
The impact of pre-evacuation ultrasound examination in histologically confirmed hydatidiform mole in missed abortion
The impact of pre-evacuation ultrasound examination in histologically confirmed hydatidiform mole in missed abortion
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The impact of pre-evacuation ultrasound examination in histologically confirmed hydatidiform mole in missed abortion

Tang, Yunhui ; Zhu, Chenqi ; Zhu, Chen ; Liang, Feng ; Lee, Arier ; Yao, Xiaoying ; Chen, Qi

BMC women's health, 2020-09, Vol.20 (1), p.196-196, Article 196 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting
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Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting

Sanchez-Delgado, Marta ; Martin-Trujillo, Alejandro ; Tayama, Chiharu ; Vidal, Enrique ; Esteller, Manel ; Iglesias-Platas, Isabel ; Deo, Nandita ; Barney, Olivia ; Maclean, Ken ; Hata, Kenichiro ; Nakabayashi, Kazuhiko ; Fisher, Rosemary ; Monk, David Eggermann, Thomas

PLoS genetics, 2015-11, Vol.11 (11), p.e1005644-e1005644 [Periódico revisado por pares]

United States: Public Library of Science

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8
Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report
Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report
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Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report

Uemura, Nozomi ; Takai, Yasushi ; Mikami, Yukiko ; Ogasawara, Miwa ; Saitoh, Masahiro ; Baba, Kazunori ; Tamaru, Junichi ; Hara, Masaaki ; Seki, Hiroyuki

Journal of medical case reports, 2019-08, Vol.13 (1), p.256-256, Article 256 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Rapid progression from complete molar pregnancy to post-molar gestational trophoblastic neoplasia: a rare case report and literature review
Rapid progression from complete molar pregnancy to post-molar gestational trophoblastic neoplasia: a rare case report and literature review
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Rapid progression from complete molar pregnancy to post-molar gestational trophoblastic neoplasia: a rare case report and literature review

Qian, Jing ; Gracious, Kaoma ; Sun, Liping

Frontiers in oncology, 2023-12, Vol.13, p.1303249 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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10
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

Cubellis, Maria Vittoria ; Pignata, Laura ; Verma, Ankit ; Sparago, Angela ; Del Prete, Rosita ; Monticelli, Maria ; Calzari, Luciano ; Antona, Vincenzo ; Melis, Daniela ; Tenconi, Romano ; Russo, Silvia ; Cerrato, Flavia ; Riccio, Andrea

Clinical epigenetics, 2020-09, Vol.12 (1), p.139, Article 139 [Periódico revisado por pares]

Germany: BioMed Central Ltd

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