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MRI and ultrasound fusion imaging for prenatal diagnosis

American journal of obstetrics and gynecology, 2013-08, Vol.209 (2), p.148.e1-148.e9

2013

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Prenatal prognosis in isolated congenital diaphragmatic hernia

American journal of obstetrics and gynecology, 2008, Vol.198 (1), p.80.e1-80.e5

2008

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Retroperitoneal Approach for Ureteropelvic Junction Obstruction: Encouraging Preliminary Results With Robot-Assisted Laparoscopic Repair

Frontiers in pediatrics, 2019-05, Vol.7, p.209-209

2019

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MR imaging of fetal cerebral anomalies

Pediatric radiology, 1998-04, Vol.28 (4), p.212-222

1998

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Comparison between ultrasound and magnetic resonance imaging in assessment of fetal cytomegalovirus infection

Prenatal diagnosis, 2008-08, Vol.28 (8), p.753-758

2008

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Fetal MRI findings in a retrospective cohort of 26 cases of prenatally diagnosed CHARGE syndrome individuals

Prenatal diagnosis, 2019-08, Vol.39 (9), p.781-791

2019

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Performance of prenatal diagnosis in esophageal atresia

Prenatal diagnosis, 2015-09, Vol.35 (9), p.888-893

2015

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Glial Periorbital Heterotopia: A Rare Type of Ocular Mass

Journal of ultrasound in medicine, 2020-08, Vol.39 (8), p.1491-1496

2020

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Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway

Ultrasound in obstetrics & gynecology, 2022-04, Vol.59 (4), p.532-542

2022

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Glial Periorbital Heterotopia

Journal of ultrasound in medicine, 2020-08, Vol.39 (8), p.1491-1496

2020

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Fetal MRI compared with ultrasound for the diagnosis of obstructive genital malformations

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1138-1145

2017

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Ultrasound and Fetal MRI Complementary Contributions to Appropriate Counseling in Small Bowel Obstruction

Fetal diagnosis and therapy, 2021-10, Vol.48 (8), p.567-574

2021

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Authors’ reply re: Refining the prognosis of fetuses infected with cytomegalovirus in the first trimester of pregnancy by serial prenatal assessment: a single‐centre retrospective study

BJOG : an international journal of obstetrics and gynaecology, 2020-04, Vol.127 (5), p.647-648

2020

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Large Duplications Can Be Benign Copy Number Variants: A Case of a 3.6-Mb Xq21.33 Duplication

Cytogenetic and genome research, 2017, Vol.151 (3), p.115-118

2017

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Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation

Birth defects research. A Clinical and molecular teratology, 2016-01, Vol.106 (1), p.36-46

2016

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Prenatal cortical hyperostosis with COL1A1 gene mutation

American journal of medical genetics. Part A, 2008-07, Vol.146A (14), p.1820-1824

2008

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Fetal lung volume: estimation at MR imaging-initial results

Radiology, 2001-04, Vol.219 (1), p.236

2001

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Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria

Neurogenetics, 2013-11, Vol.14 (3-4), p.215-224

2013

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Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation

Birth defects research, 2021-11, Vol.113 (18), p.1324-1332

2021

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Biometric and morphological features of the fetal bladder in lower urinary tract obstruction on magnetic resonance imaging: new perspectives for fetal cystoscopy

Ultrasound in obstetrics & gynecology, 2019-04

2019

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A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern

Birth defects research, 2018-04, Vol.110 (7), p.598-602

2018

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Malformative intracranial cysts: diagnosis and outcome

Child's nervous system, 2003-08, Vol.19 (7-8), p.477-483

2003

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MRI and ultrasound fusion imaging for prenatal diagnosis

Prenatal prognosis in isolated congenital diaphragmatic hernia

Retroperitoneal Approach for Ureteropelvic Junction Obstruction: Encouraging Preliminary Results With Robot-Assisted Laparoscopic Repair

MR imaging of fetal cerebral anomalies

Comparison between ultrasound and magnetic resonance imaging in assessment of fetal cytomegalovirus infection

Fetal MRI findings in a retrospective cohort of 26 cases of prenatally diagnosed CHARGE syndrome individuals

Performance of prenatal diagnosis in esophageal atresia

Glial Periorbital Heterotopia: A Rare Type of Ocular Mass

Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway

Glial Periorbital Heterotopia

Fetal MRI compared with ultrasound for the diagnosis of obstructive genital malformations

Ultrasound and Fetal MRI Complementary Contributions to Appropriate Counseling in Small Bowel Obstruction

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

Authors’ reply re: Refining the prognosis of fetuses infected with cytomegalovirus in the first trimester of pregnancy by serial prenatal assessment: a single‐centre retrospective study

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

Large Duplications Can Be Benign Copy Number Variants: A Case of a 3.6-Mb Xq21.33 Duplication

Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation

Prenatal cortical hyperostosis with COL1A1 gene mutation

Fetal lung volume: estimation at MR imaging-initial results

In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses

Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria

Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation

Biometric and morphological features of the fetal bladder in lower urinary tract obstruction on magnetic resonance imaging: new perspectives for fetal cystoscopy

A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern

Malformative intracranial cysts: diagnosis and outcome

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