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Accuracy of ultrasonography and magnetic resonance imaging in the diagnosis of placenta accreta

PloS one, 2014-04, Vol.9 (4), p.e94866-e94866

2014

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Cardiac rhabdomyoma with hydrops fetalis: Prenatal management by abdominal drainage

Taiwanese journal of obstetrics & gynecology, 2021-05, Vol.60 (3), p.551-553

2021

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Can a Predetermined Grid and Multidisciplinary Consultation Improve the Description of Cleft lip with or Without Cleft Palate?

The Cleft palate-craniofacial journal, 2024-07, Vol.61 (7), p.1143-1148

2024

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A Gardos channelopathy associated with nonimmune hydrops and fetal loss

Clinical genetics, 2022-12, Vol.102 (6), p.543-547

2022

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Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis

Clinical genetics, 2023-05, Vol.103 (5), p.560-565

2023

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The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome

Clinical genetics, 2021-10, Vol.100 (4), p.462-467

2021

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First trimester uterine artery Doppler, sFlt-1 and PlGF to predict preeclampsia in a high-risk population

The journal of maternal-fetal & neonatal medicine, 2017-07, Vol.30 (13), p.1514-1519

2017

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Allo-immunisation materno-fœtale par anticorps atypiques à propos de deux cas cliniques

La Presse médicale (1983), 2015-10, Vol.44 (10), p.1078-1082

2015

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Two cases of unusual allo-immunization caused by atypical antibodies

La Presse médicale (1983), 2015-10, Vol.44 (10), p.1078

2015

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Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations

American journal of medical genetics. Part A, 2014-07, Vol.164A (7), p.1821-1825

2014

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A Pilot Study Comparing 2- and 3-dimensional Ultrasound Imaging for Confirmation of Essure Fallopian Tube Pregnancy Prevention Implants

Journal of minimally invasive gynecology, 2019-09, Vol.26 (6), p.1117-1124

2019

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Prenatal Diagnosis of Myhre Syndrome in Two Cases: Further Delineation of the Cardiac and External Phenotype

Prenatal diagnosis, 2024-08

2024

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Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions: About a series of 178 cases

Placenta (Eastbourne), 2016-08, Vol.44, p.104-108

2016

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Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography

Journal of ultrasound in medicine, 2018-02, Vol.37 (2), p.531-534

2018

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R ubinstein‐ T aybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography

Journal of ultrasound in medicine, 2018-02, Vol.37 (2), p.531-534

2018

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Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Genetics in medicine, 2024-04, Vol.26 (4), p.101057, Article 101057

2024

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Monozygotic heterocaryotic twins: prenatal diagnosis and management

La Presse médicale (1983), 2009-07, Vol.38 (7-8), p.1170-1173

2009

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Prenatal Diagnosis of a ‘Minor’ Form of Brachmann-de Lange Syndrome by Three-Dimensional Sonography and Three-Dimensional Computed Tomography

Fetal diagnosis and therapy, 2004-03, Vol.19 (2), p.155-159

2004

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Grossesses gémellaires monozygotes hétérocaryotes : diagnostic et prise en charge prénatale

La Presse médicale (1983), 2009-07, Vol.38 (7), p.1170-1173

2009

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Prenatal Sonographic Patterns in Six Cases of Wolf-Hirschhorn (4p–) Syndrome

Fetal diagnosis and therapy, 2004-09, Vol.19 (5), p.421-430

2004

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Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases: Isolated polyhydramnios and amniotic fluid biochemistry

Prenatal diagnosis, 2015-12, Vol.35 (13), p.1331-1335

2015

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Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases

Prenatal diagnosis, 2015-12, Vol.35 (13), p.1331-1335

2015

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Monozygotic triplet pregnancies after single blastocyst transfer: two cases and literature review

Reproductive biomedicine online, 2010-09, Vol.21 (3), p.283-289

2010

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Accuracy of ultrasonography and magnetic resonance imaging in the diagnosis of placenta accreta

Cardiac rhabdomyoma with hydrops fetalis: Prenatal management by abdominal drainage

Can a Predetermined Grid and Multidisciplinary Consultation Improve the Description of Cleft lip with or Without Cleft Palate?

A Gardos channelopathy associated with nonimmune hydrops and fetal loss

Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis

Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series

The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome

First trimester uterine artery Doppler, sFlt-1 and PlGF to predict preeclampsia in a high-risk population

Allo-immunisation materno-fœtale par anticorps atypiques à propos de deux cas cliniques

Two cases of unusual allo-immunization caused by atypical antibodies

Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations

A Pilot Study Comparing 2- and 3-dimensional Ultrasound Imaging for Confirmation of Essure Fallopian Tube Pregnancy Prevention Implants

Prenatal Diagnosis of Myhre Syndrome in Two Cases: Further Delineation of the Cardiac and External Phenotype

Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions: About a series of 178 cases

Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography

R ubinstein‐ T aybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Monozygotic heterocaryotic twins: prenatal diagnosis and management

Prenatal Diagnosis of a ‘Minor’ Form of Brachmann-de Lange Syndrome by Three-Dimensional Sonography and Three-Dimensional Computed Tomography

Grossesses gémellaires monozygotes hétérocaryotes : diagnostic et prise en charge prénatale

Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series

Prenatal Sonographic Patterns in Six Cases of Wolf-Hirschhorn (4p–) Syndrome

Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases: Isolated polyhydramnios and amniotic fluid biochemistry

Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases

Monozygotic triplet pregnancies after single blastocyst transfer: two cases and literature review

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