Lista de obras -

A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations

artículo científico publicado en 2019

A case of progressive breathlessness post partum.

artículo científico publicado en 2016

ABC-transporter upregulation mediates resistance to the CDK7 inhibitors THZ1 and ICEC0942

artículo científico publicado en 2019

Abnormal villous morphology mimicking a hydatidiform mole associated with paternal trisomy of chromosomes 3,7,8 and unipaternal disomy of chromosome 11

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Atypical placental site nodule (APSN) and association with malignant gestational trophoblastic disease; a clinicopathologic study of 21 cases.

artículo científico publicado en 2015

Circulating Cell Free DNA in the Diagnosis of Trophoblastic Tumors

artículo científico publicado en 2015

Clinical utility of selective molecular genotyping for diagnosis of partial hydatidiform mole; a retrospective study from a regional trophoblastic disease unit.

artículo científico publicado en 2014

Conserved gene sequences for species identification: PCR analysis of the 3′ UTR of the SON gene distinguishes human and other mammalian DNAs ⬇️

artículo científico publicado el 21 de junio de 1995

Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes

artículo científico publicado en 2018

Do we need post-pregnancy screening with human chorionic gonadotrophin after previous hydatidiform mole to identify patients with recurrent gestational trophoblastic disease?

scientific article published on 06 January 2019

EMA/CO for high-risk gestational trophoblastic neoplasia: good outcomes with induction low-dose etoposide-cisplatin and genetic analysis.

artículo científico publicado en 2012

Evaluation of deletions in 7q11.2 and 8p12–p21 as prognostic indicators of tumour development following molar pregnancy

article

Heterogeneity in recurrent complete hydatidiform mole: Presentation of two new Turkish families with different genetic characteristics ⬇️

artículo científico publicado el 26 de septiembre de 2010

Histopathological and immunohistochemical features of early hydatidiform mole in relation to subsequent development of persistent gestational trophoblastic disease

artículo científico publicado en 2014

Histopathological features of biparental complete hydatidiform moles in women with NLRP7 mutations

artículo científico publicado en 2012

Intensified therapies improve survival and identification of novel prognostic factors for placental-site and epithelioid trophoblastic tumours

scientific article published on 22 February 2019

Management and survival of patients with FIGO high-risk gestational trophoblastic neoplasia: the U.K. experience, 1995-2010.

artículo científico publicado en 2014

Molecular genotyping of placental site and epithelioid trophoblastic tumours; female predominance

artículo científico publicado en 2016

Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype on digynic triploid conceptions.

artículo científico publicado en 2012

Pembrolizumab is effective for drug-resistant gestational trophoblastic neoplasia.

artículo científico publicado en 2017

Risk of recurrent molar pregnancies following complete and partial hydatidiform moles.

artículo científico

Sensitive screening of single nucleotide polymorphisms in cell free DNA for diagnosis of gestational tumours

artículo científico publicado en 2022

The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

article

The results of treatment with high-dose chemotherapy and peripheral blood stem cell support for gestational trophoblastic neoplasia

artículo científico publicado en 2019

Lista de obras de

A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations

A case of progressive breathlessness post partum.

ABC-transporter upregulation mediates resistance to the CDK7 inhibitors THZ1 and ICEC0942

Abnormal villous morphology mimicking a hydatidiform mole associated with paternal trisomy of chromosomes 3,7,8 and unipaternal disomy of chromosome 11

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

Atypical placental site nodule (APSN) and association with malignant gestational trophoblastic disease; a clinicopathologic study of 21 cases.

Circulating Cell Free DNA in the Diagnosis of Trophoblastic Tumors

Clinical utility of selective molecular genotyping for diagnosis of partial hydatidiform mole; a retrospective study from a regional trophoblastic disease unit.

Conserved gene sequences for species identification: PCR analysis of the 3′ UTR of the SON gene distinguishes human and other mammalian DNAs ⬇️

Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes

Do we need post-pregnancy screening with human chorionic gonadotrophin after previous hydatidiform mole to identify patients with recurrent gestational trophoblastic disease?

EMA/CO for high-risk gestational trophoblastic neoplasia: good outcomes with induction low-dose etoposide-cisplatin and genetic analysis.

Evaluation of deletions in 7q11.2 and 8p12–p21 as prognostic indicators of tumour development following molar pregnancy

Heterogeneity in recurrent complete hydatidiform mole: Presentation of two new Turkish families with different genetic characteristics ⬇️

Histopathological and immunohistochemical features of early hydatidiform mole in relation to subsequent development of persistent gestational trophoblastic disease

Histopathological features of biparental complete hydatidiform moles in women with NLRP7 mutations

Intensified therapies improve survival and identification of novel prognostic factors for placental-site and epithelioid trophoblastic tumours

Management and survival of patients with FIGO high-risk gestational trophoblastic neoplasia: the U.K. experience, 1995-2010.

Molecular genotyping of placental site and epithelioid trophoblastic tumours; female predominance

Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype on digynic triploid conceptions.

Pembrolizumab is effective for drug-resistant gestational trophoblastic neoplasia.

Risk of recurrent molar pregnancies following complete and partial hydatidiform moles.

Sensitive screening of single nucleotide polymorphisms in cell free DNA for diagnosis of gestational tumours

The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

The results of treatment with high-dose chemotherapy and peripheral blood stem cell support for gestational trophoblastic neoplasia