First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination.

[1]  H. Chueh,et al.  Term delivery of a complete hydatidiform mole with a coexisting living fetus followed by successful treatment of maternal metastatic gestational trophoblastic disease. , 2014, Taiwanese journal of obstetrics & gynecology.

[2]  Chih-ping Chen,et al.  Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia. , 2014, Taiwanese journal of obstetrics & gynecology.

[3]  M. Sanchez-Ferrer,et al.  Uterine Rupture in Twin Pregnancy with Normal Fetus and Complete Hydatidiform Mole , 2013, Gynecologic and Obstetric Investigation.

[4]  K. Yoshiura,et al.  Identification of complete hydatidiform mole pregnancy-associated microRNAs in plasma. , 2013, Clinical chemistry.

[5]  Chih-ping Chen,et al.  Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction. , 2013, Taiwanese journal of obstetrics & gynecology.

[6]  O. Abdul-Rahman,et al.  Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7 , 2012, European Journal of Human Genetics.

[7]  Larissa V Furtado,et al.  Diagnostic utility of microsatellite genotyping for molar pregnancy testing. , 2013, Archives of pathology & laboratory medicine.

[8]  N. Montenegro,et al.  Complete mole in a dichorionic twin pregnancy after intracytoplasmic sperm injection. , 2013, Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia.

[9]  Nehal Mostafa,et al.  Twin pregnancy with complete hydatidiform mole and coexisting fetus following ovulation induction with a non-prescribed clomiphene citrate regimen: a case report , 2012, Journal of Medical Case Reports.

[10]  Colin A. Johnson,et al.  Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. , 2011, American journal of human genetics.

[11]  C. Huissoud,et al.  Grossesse gémellaire avec môle complète et fœtus vivant : à propos d’un cas non diagnostiqué en anténatal , 2011 .

[12]  P. Serhal,et al.  The nature and origin of binucleate cells in human preimplantation embryos: relevance to placental mesenchymal dysplasia. , 2011, Reproductive biomedicine online.

[13]  M. Peñaherrera,et al.  The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders , 2011, Clinical genetics.

[14]  P. Hui Molecular diagnosis of gestational trophoblastic disease , 2010, Expert review of molecular diagnostics.

[15]  P. Hui,et al.  Precise DNA Genotyping Diagnosis of Hydatidiform Mole , 2010, Obstetrics and gynecology.

[16]  K. Murphy,et al.  Molecular genotyping of hydatidiform moles: analytic validation of a multiplex short tandem repeat assay. , 2009, The Journal of molecular diagnostics : JMD.

[17]  K. Murphy,et al.  Diagnosis and Subclassification of Hydatidiform Moles Using p57 Immunohistochemistry and Molecular Genotyping: Validation and Prospective Analysis in Routine and Consultation Practice Settings With Development of an Algorithmic Approach , 2009, The American journal of surgical pathology.

[18]  A. Schott,et al.  Twin pregnancy with complete hydatidiform mole and coexistent fetus: obstetrical and oncological outcomes in a series of 14 cases. , 2009, European journal of obstetrics, gynecology, and reproductive biology.

[19]  E. González,et al.  Embarazo gemelar con mola completa y feto coexistente posterior a fertilización in vitro y transferencia de embriones complicado con placenta previa acreta. Reporte de un caso , 2009 .

[20]  Hodges,et al.  Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region , 2009, Journal of Medical Genetics.

[21]  G. Roshandel,et al.  Molar Pregnancy And Co-Existent Foetus: A Report Of Two Cases , 2009 .

[22]  S. Hakverdi,et al.  Twin pregnancy with a complete hydatidiform mole and co-existent live fetus: two case reports and review of the literature , 2009, Archives of Gynecology and Obstetrics.

[23]  P. Kuo,et al.  Triple genetic identities for the complete hydatidiform mole, placenta and co-existing fetus after transfer of a single in vitro fertilized oocyte: case report and possible mechanisms. , 2008, Human reproduction.

[24]  R. Kapur,et al.  Androgenetic/Biparental Mosaicism in an Infant with Hepatic Mesenchymal Hamartoma and Placental Mesenchymal Dysplasia , 2008, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

[25]  I. Lerer,et al.  Placental mesenchymal dysplasia associated with transient neonatal diabetes mellitus and paternal UPD6. , 2008, Placenta.

[26]  M. Gribaa,et al.  Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines. , 2008, Placenta.

[27]  C. Bifulco,et al.  Genotypic Analysis of Hydatidiform Mole: An Accurate and Practical Method of Diagnosis , 2008, The American journal of surgical pathology.

[28]  S. Dymarkowski,et al.  Complete hydatidiform mole with co-existing healthy fetus: A case report , 2008, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

[29]  U. Surti,et al.  P57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions. , 2008, Human pathology.

[30]  D. Dawson,et al.  Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia , 2007, Prenatal diagnosis.

[31]  W. Lam,et al.  Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5 , 2007, American journal of medical genetics. Part A.

[32]  L. Sunde,et al.  Evaluation of the risk of persistent trophoblastic disease after twin pregnancy with diploid hydatidiform mole and coexisting normal fetus. , 2007, American journal of obstetrics and gynecology.

[33]  A. Innes,et al.  Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. , 2007, Human reproduction.

[34]  Z. Parveen,et al.  Placental mesenchymal dysplasia. , 2007, Archives of pathology & laboratory medicine.

[35]  R. Kuick,et al.  Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans , 2006, Nature Genetics.

[36]  C. Livasy,et al.  Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia , 2005, Journal of Medical Genetics.

[37]  U. Surti,et al.  Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype , 2005, Prenatal diagnosis.

[38]  S. Weremowicz,et al.  Complete hydatidiform mole retaining a chromosome 11 of maternal origin: molecular genetic analysis of a case , 2004, Modern Pathology.

[39]  J. Blouin,et al.  Is genetic analysis useful in the routine management of hydatidiform mole? , 2003, Human reproduction.

[40]  N. Sebire,et al.  The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles. , 2002, Human molecular genetics.

[41]  M. Nakayama,et al.  Suspected involvement of the X chromosome in placental mesenchymal dysplasia , 2002, Congenital anomalies.

[42]  N. Sebire,et al.  Outcome of twin pregnancies with complete hydatidiform mole and healthy co-twin , 2002, The Lancet.

[43]  P. Hohlfeld,et al.  Molar pregnancy with a coexistent fetus after intracytoplasmic sperm injection. A case report. , 2001, Journal of reproductive medicine.

[44]  A. Yuzpe,et al.  Partial hydatidiform mole following transfer of a cryopreserved-thawed blastocyst. , 2000, Fertility and sterility.

[45]  Anthony F. Shaker,et al.  Twin pregnancy with a complete hydatidiform mole and co-existing fetus following in-vitro fertilization: case report. , 1999, Human reproduction.

[46]  D. Leonard,et al.  Molecular genetic testing from paraffin-embedded tissue distinguishes nonmolar hydropic abortion from hydatidiform mole. , 1999, Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology.

[47]  T. Hassold,et al.  Determinants of villous trophoblastic hyperplasia in spontaneous abortions. , 1998, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

[48]  R. Fisher,et al.  A prospective genetic study of complete and partial hydatidiform moles. , 1991, American journal of obstetrics and gynecology.

[49]  K. Ohama,et al.  Androgenetic origin of hydatidiform mole , 1977, Nature.