Y. Dumez

发表

Prenatal diagnosis of a satellited non‐acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature

A. Munnich, L. Faivre, M. Vekemans, 1999, Prenatal diagnosis.

Predicting perinatal outcome in isolated congenital diaphragmatic hernia using fetal pulmonary artery diameters.

A. Benachi, D. Mitanchez, R. Ruano, 2008, Journal of pediatric surgery.

Antenatal manifestations of mitochondrial respiratory chain deficiency.

A. Munnich, F. Brunelle, P. Rustin, 2003, The Journal of pediatrics.

Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience

D. Rabier, A. Chabli, B. Chadefaux-Vekemans, 2006, Prenatal diagnosis.

Impact of formaldehyde on the in vitro proportion of fetal DNA in maternal plasma and serum.

A. Benachi, Jean‐Marc Costa, Y. Dumez, 2005, Clinical chemistry.

Prenatal diagnosis of cardiac rhabdomyomas: incidence of associated cerebral lesions of tuberous sclerosis complex

P. Sonigo, A. Benachi, J. Martinovic, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

PRENATAL DIAGNOSIS OF HARLEQUIN FETUS

A. Bernheim, R. Henrion, M. Lutzner, 1983, The Lancet.

Prenatal sonographic diagnosis of congenital hiatal hernia

A. Benachi, J. Bernard, R. Ruano, 2004, Prenatal diagnosis.

Three‐dimensional ultrasonographic measurements of the fetal lungs for prediction of perinatal outcome in isolated congenital diaphragmatic hernia

A. Benachi, R. Ruano, M. Aubry, 2009, The journal of obstetrics and gynaecology research.

Predicting neonatal deaths and pulmonary hypoplasia in isolated congenital diaphragmatic hernia using the sonographic fetal lung volume-body weight ratio.

A. Benachi, R. Ruano, M. Zugaib, 2008, AJR. American journal of roentgenology.

Twin-to-twin transfusion syndrome. Role of the fetal renin-angiotensin system.

M. Gonzalès, M. Gubler, M. Dommergues, 2000, The American journal of pathology.

Fetal hypertension: an insight into the pathogenesis of the twin–twin transfusion syndrome

L. Salomon, P. Jouvet, J. Le Bidois, 2003, Prenatal diagnosis.

Efficacy of second-trimester selective termination for fetal abnormalities: international collaborative experience among the world's largest centers.

C. Rodeck, R. Wapner, M. Evans, 1994, American journal of obstetrics and gynecology.

Embryo reduction in multifetal pregnancies after infertility therapy: obstetrical risks and perinatal benefits are related to operative strategy.

L. Mandelbrot, I. Nisand, M. Dommergues, 1991, Fertility and sterility.

Evaluation of postnatal renal function in fetuses with bilateral obstructive uropathies by proton nuclear magnetic resonance spectroscopy.

L. Le Moyec, F. Muller, M. Dommergues, 1994, American journal of obstetrics and gynecology.

Risk evaluation of CVS

B. Brambati, W. Holzgreve, A. Kuliev, 1993, Prenatal diagnosis.

Transabdominal versus transcervical and transvaginal multifetal pregnancy reduction: international collaborative experience of more than one thousand cases.

Mark Johnson, K. Nicolaides, I. Timor-Tritsch, 1994, American journal of obstetrics and gynecology.

Three‐dimensional Ultrasonographic Appearance of the Fetal Akinesia Deformation Sequence

R. Ruano, M. Dommergues, Y. Dumez, 2003, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination

J. Dausset, J. Oury, D. Cohen, 1986, Human Genetics.

Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair

G. Renault, A. Lehmann, C. Arlett, 1992, The British journal of dermatology.

Fetal DNA in maternal serum: does it persist after pregnancy?

A. Benachi, J. Steffann, P. Ernault, 2003, Human Genetics.

First‐trimester fetal sex determination in maternal serum using real‐time PCR

A. Benachi, J. Jouannic, P. Ernault, 2001, Gynecologie, obstetrique & fertilite.

Fetal supraventricular tachycardia: a role for amiodarone as second‐line therapy?

E. Villain, J. Le Bidois, S. Delahaye, 2003, Prenatal diagnosis.

INTRAUTERINE INFECTION WITH HUMAN PARVOVIRUS

J. Lefrère, E. Caul, A. Couroucé, 1986, The Lancet.

Volume Contrast Imaging

A. Benachi, R. Ruano, M. Dommergues, 2004, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

TRANSFER OF NUCLEATED MATERNAL CELLS INTO FETAL CIRCULATION DURING THE SECOND TRIMESTER OF PREGNANCY

G. Socié, E. Gluckman, O. Brison, 1998 .

Sensitivity and Specificity of Prenatal Features of Physiological Shunts to Predict Neonatal Clinical Status in Transposition of the Great Arteries

D. Bonnet, D. Sidi, P. Vouhé, 2004, Circulation.

Fetal Niemann-Pick disease type C: Ultrastructural and lipid findings in liver and spleen

F. Dijoud, M. Vanier, C. Dumontel, 2005, Virchows Archiv A.

Development of human fetal kidney in obstructive uropathy: correlations with ultrasonography and urine biochemistry.

M. Gubler, F. Muller, M. Dommergues, 1997, Kidney international.

Impaired mitochondrial pyruvate importation in a patient and a fetus at risk.

S. Lyonnet, À. García‐Cazorla, A. Legrand, 2003, Molecular genetics and metabolism.

Rapid and early determination of sex using trophoblast biopsy specimens and Y chromosome specific DNA probes.

J. Weissenbach, R. Berger, G. Guellaen, 1984, British medical journal.

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

A. Munnich, P. Rustin, A. Rötig, 2000 .

Niemann‐Pick disease type B: first‐trimester prenatal diagnosis on chorionic villi and biochemical study of a foetus at 12 weeks of development

M. Vanier, J. Boué, Y. Dumez, 1985, Clinical genetics.

Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the Renin-Angiotensin system.

M. Gonzalès, M. Gubler, R. Bouvier, 2006, Journal of the American Society of Nephrology : JASN.

Genetic characterisation of circulating fetal cells allows non‐invasive prenatal diagnosis of cystic fibrosis

A. Munnich, A. Benachi, B. Lacour, 2006, Prenatal diagnosis.

Prenatal testing for inherited immune deficiencies by fetal blood sampling

C. Griscelli, A. Durandy, R. Henrion, 1982, Prenatal diagnosis.

Fetal serum beta2-microglobulin predicts postnatal renal function in bilateral uropathies.

R. Favre, P. Hohlfeld, P. Sagot, 2000, Kidney international.

Omphalocele in the first trimester: prediction of perinatal outcome

A. Benachi, C. Elie, F. Perrotin, 2013, Prenatal diagnosis.

Lung growth and maturation after tracheal occlusion in diaphragmatic hernia.

F. Brunelle, A. Benachi, J. Bourbon, 1998, American journal of respiratory and critical care medicine.

Tracheal obstruction in experimental diaphragmatic hernia: an endoscopic approach in the fetal lamb

A. Benachi, J. Bourbon, M. Dommergues, 1997, Prenatal diagnosis.

First Trimester Diagnosis of Genetic Diseases by DNA Analysis of Chorionic Villi: Preliminary Experience

P. Duquesnoy, M. Goossens, Y. Dumez, 1985 .

Prenatal diagnosis of spinal muscular atrophy by genetic analysis of circulating fetal cells

C. Béroud, A. Benachi, P. Paterlini-Bréchot, 2003, The Lancet.

Detection of maternal cells in human fetal blood during the third trimester of pregnancy using allele‐specific PCR amplification

G. Socié, E. Gluckman, O. Brison, 1997, British journal of haematology.

Expression of surfactant proteins and thyroid transcription factor 1 in an ovine model of congenital diaphragmatic hernia.

A. Benachi, J. Bourbon, B. Chailley-Heu, 2002, Journal of pediatric surgery.

Fetal enteroviral infection with cerebral ventriculomegaly and cardiomyopathy.

C. Fallet-Bianco, P. Lebon, J. Petitjean, 1994, Fetal diagnosis and therapy.

ANTENATAL PLAl TYPING AND DETECTION OF GP IIb‐IIIa COMPLEX

A. Kesseler, J. Muller, C. Kaplan, 1985, British journal of haematology.

First‐trimester diagnosis of osteogenesis imperfecta associated with encephalocele by conventional and three‐dimensional ultrasound

A. Benachi, J. Martinovic, R. Ruano, 2003, Prenatal diagnosis.

Stability of the m.8993T→G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome

A. Munnich, R. Frydman, J. Steffann, 2007, Journal of Medical Genetics.

Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development

A. Munnich, A. Rötig, A. Benachi, 2006, Journal of Medical Genetics.

Quantitative analysis of fetal pulmonary vasculature by 3-dimensional power Doppler ultrasonography in isolated congenital diaphragmatic hernia.

A. Benachi, D. Mitanchez, R. Ruano, 2006, American journal of obstetrics and gynecology.

Three‐dimensional ultrasonographic assessment of fetal lung volume as prognostic factor in isolated congenital diaphragmatic hernia

J. Thalabard, A. Benachi, R. Ruano, 2004, BJOG : an international journal of obstetrics and gynaecology.

Assay for Sjögren – Larsson Syndrome Based on a Deficiency of Phytol Degradation

A. Benachi, Jean‐Marc Costa, Y. Dumez, 2004 .

First-trimester prenatal diagnosis of mucolipidosis II (I-cell disease) by chorionic biopsy.

F. Thépot, L. Poenaru, L. Castelnau, 1984, American journal of human genetics.

Prenatal diagnosis of atypical tay‐sachs disease by chorionic villi sampling

L. Poenaru, L. Castelnau, Y. Dumez, 1984, Prenatal diagnosis.

FIRST TRIMESTER DIAGNOSIS OF HUNTER SYNDROME ON CHORIONIC VILLI

H. Galjaard, W. Kleijer, O. Diggelen, 1984, The Lancet.

Prenatal diagnosis of pyloric atresia‐junctional epidermolysis bullosa syndrome in a fetus not known to be at risk

F. Muller, C. Blanchet‐Bardon, P. Descamps, 2000, Prenatal diagnosis.

Prenatally diagnosed sacrococcygeal teratoma: a prognostic classification.

A. Benachi, M. Dommergues, M. Aubry, 2006, Journal of pediatric surgery.

Pericardial teratoma complicated by hydrops: successful fetal therapy by thoracoamniotic shunting

A. Benachi, D. Mitanchez, P. Vouhé, 2003, Prenatal diagnosis.

Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis

J. Oury, F. Muller, J. Boué, 1986, Human Genetics.

SRY-negative XX fetus with complete male phenotype

E. Vilain, M. Fellous, K. McElreavey, 1994, The Lancet.

Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy

L. Poenaru, L. Castelnau, Y. Dumez, 1985, Clinical genetics.

Antenatal manifestations of Smith‐Lemli‐Opitz (RSH) syndrome: A retrospective survey of 30 cases

A. Munnich, A. Benachi, F. Chevy, 2004, American journal of medical genetics. Part A.

Correlation between ultrasound and anatomical findings in fetuses with lower urinary tract obstruction in the first half of pregnancy

Y. Ville, A. Benachi, R. Robyr, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal prediction of renal function in fetal obstructive uropathies.

L. Mandelbrot, F. Muller, M. Dommergues, 1991, Journal of perinatal medicine.

Serum hCG assay: A method for detection of contamination of fetal blood samples

L. Mandelbrot, F. Muller, M. Dommergues, 1993, Prenatal diagnosis.

Development of human renal function: reference intervals for 10 biochemical markers in fetal urine.

L. Bussières, P. Aegerter, Y. Aigrain, 1996, Clinical chemistry.

Successful intrauterine shunting of a sacrococcygeal teratoma (SCT) causing fetal bladder obstruction

M. Dommergues, F. Auber, J. Jouannic, 2001, Prenatal diagnosis.

Percutaneous nephrostomy in utero.

R. Henrion, G. Vallancien, M. Aubry, 1982, Urology.

Systemic arteriovenous fistula leads to pulmonary artery remodeling and abnormal vasoreactivity in the fetal lamb.

J. Martinovic, A. Dinh-Xuan, S. Lanone, 2003, American journal of physiology. Lung cellular and molecular physiology.

Nonimmune fetal ascites: a series of 79 cases.

D. Luton, J. Oury, R. Favre, 2004, American journal of obstetrics and gynecology.

Prenatal management of congenital cystic adenomatoid malformation of the lung.

Y. Révillon, P. Sonigo, L. Mandelbrot, 1993, Journal of pediatric surgery.

Congenital cystic adenomatoid malformation of the lung: prenatal management and prognosis.

Y. Révillon, P. Sonigo, L. Mandelbrot, 1993, Journal of pediatric surgery.

Microvillar enzyme assays in amniotic fluid and fetal tissues at different stages of development

J. Oury, F. Muller, J. Boué, 1988, Prenatal diagnosis.

Congenital adenomatoid malformation of the lung: when is active fetal therapy indicated?

Y. Révillon, L. Mandelbrot, P. Jarreau, 1997, American journal of obstetrics and gynecology.

Prenatal diagnosis and confirmation of Infantile Refsum's disease

R. Wanders, R. Schutgens, B. Poll-The, 1987, Journal of Inherited Metabolic Disease.

Early prenatal diagnosis of inherited severe immunodeficiencies linked to enzyme deficiencies.

C. Griscelli, A. Durandy, F. Freycon, 1987, The Journal of pediatrics.

FETAL SERUM INTERFERON‐ALPHA SUGGESTS VIRAL INFECTION AS THE AETIOLOGY OF UNEXPLAINED LATERAL CEREBRAL VENTRICULOMEGALY

C. Fallet-Bianco, P. Lebon, M. Dommergues, 1996, Prenatal diagnosis.

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

J. Weissenbach, A. Munnich, C. Cruaud, 2005, Journal of Medical Genetics.

Prenatal diagnosis of sickle-cell anemia in the first trimester of pregnancy.

R. Henrion, M. Goossens, J. Rosa, 1983, The New England journal of medicine.

Trisomy 15 in chorionic villi and Prader‐Willi syndrome at birth

M. Vekemans, N. Morichon‐Delvallez, Y. Dumez, 1993, Prenatal diagnosis.

First‐trimester fetal sex determination in maternal serum using real‐time PCR. Jean‐Marc Costa, Alexandra Benachi, Evelyne Gautier, Jean‐Marie Jouannic, Pauline Ernault, Yves Dume. Prenatal Diagnosis 21(12): 1070–1074

A. Benachi, J. M. Costa, J. Jouannic, 2002, Prenatal diagnosis.

[Vascular Ehlers-Danlos syndrome].

É. Mousseaux, P. Boutouyrie, X. Jeunemaître, 2006, Presse medicale.

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up

A. Munnich, S. Lyonnet, M. Vekemans, 2000, Journal of medical genetics.

Three‐dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasia

P. Sonigo, F. Brunelle, A. Benachi, 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Keyhole sign: how specific is it for the diagnosis of posterior urethral valves?

A. Benachi, C. Elie, J. Saada, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti

A. Smahi, A. Munnich, S. Kenwrick, 2004, Prenatal diagnosis.

Second- and Third-Trimester Therapeutic Terminations of Pregnancy in Cases with Complete Placenta previa – Does Feticide Decrease Postdelivery Maternal Hemorrhage?

D. Cabrol, R. Ruano, M. Dommergues, 2004, Fetal Diagnosis and Therapy.

Thyroid function in fetus and mother during the second half of normal pregnancy.

L. Mandelbrot, M. Dommergues, Y. Dumez, 1991, Biology of the neonate.

Feticide during Second- and Third-Trimester Termination of Pregnancy: Opinions of Health Care Professionals

M. Garel, M. Dommergues, D. Mahieu‐Caputo, 2003, Fetal Diagnosis and Therapy.

Enrichment, immunomorphological, and genetic characterization of fetal cells circulating in maternal blood.

Bernard Lacour, Christophe Béroud, C. Béroud, 2002, The American journal of pathology.

Is the route of delivery a meaningful issue in triplets and higher order multiples?

M. Dommergues, D. Mahieu‐Caputo, Y. Dumez, 1998, Clinical obstetrics and gynecology.

Delivery of uncomplicated triplet pregnancies: is the vaginal route safer? A case-control study.

L. Mandelbrot, M. Dommergues, C. Huon, 1995, American journal of obstetrics and gynecology.

Prenatal diagnosis of megacystis‐microcolon‐intestinal hypoperistalsis syndrome: contribution of amniotic fluid digestive enzyme assay and fetal urinalysis

Y. Ville, J. Guibourdenche, P. Vaast, 2005, Prenatal diagnosis.

Accuracy of fetal lung volume assessed by three‐dimensional sonography

A. Benachi, J. Martinovic, R. Ruano, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Thoracoamniotic shunting for fetal pleural effusions with hydrops.

A. Benachi, L. Mandelbrot, R. Ruano, 2004, American journal of obstetrics and gynecology.

Congenital chylothorax with hydrops: postnatal care and outcome following antenatal diagnosis

L. Mandelbrot, M. Dommergues, G. Moriette, 1995, Acta paediatrica.

Reversal of fetal distress by emergency in utero decompression of hydrothorax.

L. Mandelbrot, M. Dommergues, M. Aubry, 1992, American journal of obstetrics and gynecology.

Factors associated with partial and complete regression of fetal lung lesions

C. Delacourt, Y. Révillon, A. Benachi, 2011, Ultrasound in Obstetrics and Gynecology.

Fetal lung volume measurement by magnetic resonance imaging in congenital diaphragmatic hernia

P. Sonigo, F. Brunelle, J. Thalabard, 2001, BJOG : an international journal of obstetrics and gynaecology.

Congenital diaphragmatic hernia: can prenatal ultrasonography predict outcome?

M. Gamerre, J. Oury, L. Mandelbrot, 1996, American journal of obstetrics and gynecology.

A Nomogram of Fetal Lung Volumes Estimated by 3‐Dimensional Ultrasonography Using the Rotational Technique (Virtual Organ Computer‐Aided Analysis)

J. Thalabard, A. Benachi, R. Ruano, 2006, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Efficacy of Transabdominal Multifetal Pregnancy Reduction: Collaborative Experience Among the World's Largest Centers

K. Nicolaides, R. Berkowitz, R. Wapner, 1993, Obstetrics and gynecology.

Prenatal diagnosis of pulmonary sequestration using three‐dimensional power Doppler ultrasound

Y. Révillon, A. Benachi, R. Ruano, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis of chronic granulomatous disease (CGD) in four high risk male fetuses

A. Durandy, J. Boué, Y. Dumez, 1987, Prenatal diagnosis.

Prenatal diagnosis of severe combined immunodeficiency with defective synthesis of HLA molecules

C. Griscelli, A. Durandy, N. Cerf-Bensussan, 1987, Prenatal diagnosis.

Prenatal diagnosis of severe combined immunodeficiency.

C. Griscelli, A. Durandy, R. Henrion, 1982, The Journal of pediatrics.

ANTENATAL DIAGNOSIS OF SEVERE COMBINED IMMUNODEFICIENCY FROM FETAL CORD BLOOD

C. Griscelli, A. Durandy, J. Frézal, 1982, The Lancet.

Ipsilateral Lung Volumes Assessed by Three-Dimensional Ultrasonography in Fetuses with Isolated Congenital Diaphragmatic Hernia

A. Benachi, R. Ruano, M. Zugaib, 2008, Fetal Diagnosis and Therapy.

Fetal Lung Volume Estimated by 3‐Dimensional Ultrasonography and Magnetic Resonance Imaging in Cases With Isolated Congenital Diaphragmatic Hernia

P. Sonigo, F. Brunelle, J. Thalabard, 2004, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Can Three-Dimensional Ultrasound Be Used for the Assessment of the Fetal Lung Volume in Cases of Congenital Diaphragmatic Hernia?

A. Benachi, J. Martinovic, R. Ruano, 2003, Fetal Diagnosis and Therapy.

Three‐dimensional sonographic measurement of contralateral lung volume in fetuses with isolated congenital diaphragmatic hernia

A. Benachi, R. Ruano, M. Zugaib, 2008, Journal of clinical ultrasound : JCU.

Predicting Neonatal Outcome in Isolated Congenital Diaphragmatic Hernia Using Ultrasonographic Pulmonary Measurements

A. Benachi, R. Ruano, M. Zugaib, 2007 .

Predicting pulmonary hypoplasia using the sonographic fetal lung volume to body weight ratio — how precise and accurate is it?

A. Benachi, J. Martinovic, R. Ruano, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Fetal serum ß2‐microglobulin and cystatin C in the prediction of post‐natal renal function in bilateral hypoplasia and hyperechogenic enlarged kidneys

M. Gubler, F. Audibert, F. Muller, 2004, Prenatal diagnosis.

Determination of the anatomical location of an antenatal intestinal occlusion by magnetic resonance imaging

Y. Révillon, P. Sonigo, F. Brunelle, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature

A. Munnich, L. Faivre, M. Vekemans, 1999, Prenatal diagnosis.

Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome.

Colin A. Johnson, A. Munnich, E. Génin, 2007, American journal of human genetics.

Sonography in prenatal diagnosis of congenital adrenal hyperplasia

A. Benachi, A. Rafii, J. Saada, 2004, Prenatal diagnosis.

Is complex gastroschisis predictable by prenatal ultrasound?

Y. Ville, L. Salomon, N. Khen-dunlop, 2012, BJOG : an international journal of obstetrics and gynaecology.

Fetal home monitoring for the prenatal management of gastroschisis

A. Benachi, L. Salomon, P. Jouvet, 2004, Acta obstetricia et gynecologica Scandinavica.

Serial transabdominal amnioinfusion in the management of gastroschisis with severe oligohydramnios.

M. Dommergues, M. Aubry, Y. Dumez, 1996, Journal of pediatric surgery.

[Prenatal diagnosis and management of foetal lung lesions].

Y. Ville, L. Salomon, S. Hourrier, 2011, Revue des maladies respiratoires.

International, Collaborative Experience of 1789 Patients Having Multifetal Pregnancy Reduction: A Plateauing of Risks and Outcomes

K. Nicolaides, R. Berkowitz, I. Timor-Tritsch, 1995, The Journal of the Society for Gynecologic Investigation: JSGI.

First‐trimester diagnosis of nuchal anomalies: significance and fetal outcome

R. Frydman, Y. Ville, Y. Dumez, 1992, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Congenital Erythropoietic Porphyria: Prenatal Diagnosis and Autopsy Findings in Two Sibling Fetuses

M. Gubler, Y. Nordmann, F. Muller, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Pathogenesis of Twin-Twin Transfusion Syndrome: The Renin-Angiotensin System Hypothesis

M. Gubler, D. Joly, F. Muller, 2001, Fetal Diagnosis and Therapy.

Diminutive fetal left ventricle at mid‐gestation associated with persistent left superior vena cava and coronary sinus dilatation

J. Martinovic, D. Bonnet, O. Picone, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The effect of a systemic arteriovenous fistula on the pulmonary arterial blood pressure in the fetal sheep

F. Laborde, J. Martinovic, R. Roussin, 2002, Prenatal diagnosis.

Extrathoracic heart (ectopia cordis). Report of two cases and review of the literature.

F. Laborde, Y. Dumez, F. Leca, 1989, International journal of cardiology.

Prenatal Diagnosis of Sporadic Apert Syndrome: A Sequential Diagnostic Approach Combining Three-Dimensional Computed Tomography and Molecular Biology

P. Sonigo, J. Amiel, M. Dommergues, 2000, Fetal Diagnosis and Therapy.

Middle cerebral artery Doppler in fetuses with transposition of the great arteries

A. Benachi, D. Bonnet, J. Le Bidois, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis of mucolipidosis type II on first‐trimester amniotic fluid

J. Oury, C. Mézard, J. Boué, 1990, Prenatal diagnosis.

First Trimester Prenatal Diagnosis of Metabolic Diseases

F. Thépot, J. Boué, L. Poenaru, 1985 .

Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

J. Melki, N. Philip, P. Burlet, 1992, Journal of medical genetics.

Meckel‐Gruber syndrome: Prenatal diagnosis at 10 menstrual weeks using embryoscopy

R. Berkowitz, M. Gubler, L. Mandelbrot, 1994, Prenatal diagnosis.

The value of daily fetal heart rate home monitoring in addition to serial ultrasound examinations in pregnancies complicated by fetal gastroschisis

Y. Ville, L. Salomon, G. Benoist, 2012, Prenatal diagnosis.

The association of gastroschisis with other congenital anomalies: how important is it?

A. Benachi, J. Martinovic, R. Ruano, 2011, Prenatal diagnosis.

Clinical course and outcome of antenatally detected atrioventricular block: experience of a single tertiary centre and review of the literature

Y. Ville, N. Costedoat-Chalumeau, L. Salomon, 2015, Prenatal diagnosis.

Prenatal diagnosis of bilateral isolated fetal hyperechogenic kidneys. Is it possible to predict long term outcome?

V. Tsatsaris, M. Dommergues, M. Gubler, 2002, BJOG : an international journal of obstetrics and gynaecology.

Method for first trimester selective abortion in multiple pregnancy.

Y. Dumez, J. Oury, 1986, Contributions to gynecology and obstetrics.

Fetal expressed gene analysis in maternal blood: a new tool for noninvasive study of the fetus.

A. Benachi, M. Vidaud, Jean‐Marc Costa, 2003, Clinical chemistry.

Hidden mortality of prenatally diagnosed vein of Galen aneurysmal malformation: retrospective study and review of the literature

Y. Ville, P. Sonigo, F. Brunelle, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Perinatal Three‐dimensional Color Power Doppler Ultrasonography of Vein of Galen Aneurysms

Francis Brunelle, F. Brunelle, A. Benachi, 2003, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Chorionic villi sampling using rigid forceps under ultrasound control.

M. Dommergues, Y. Dumez, 1986, Contributions to gynecology and obstetrics.

Chorionic villus sampling (CVS): World health organization european regional office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis

B. Brambati, W. Holzgreve, A. Kuliev, 1992, Journal of Assisted Reproduction and Genetics.

Prenatal Ultrasound May Predict Fetal Response to Therapy in Non-Hydropic Fetuses with Supraventricular Tachycardia

E. Villain, J. Le Bidois, M. Dommergues, 2002, Fetal Diagnosis and Therapy.

Twin-to-twin transfusion syndrome: selective feticide by embolization of the hydropic fetus.

L. Mandelbrot, M. Dommergues, A. Delezoide, 1995, Fetal diagnosis and therapy.

Rendering in fetal cardiac scanning: the intracardiac septa and the coronal atrioventricular valve planes

S. Yagel, A. Benachi, D. Valsky, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome

P. Bénit, A. Munnich, P. Rustin, 2003, Human Genetics.

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl‐containing subunit of the human pyruvate dehydrogenase complex

F. Fouque, J. Saudubray, B. Aral, 1999, Prenatal diagnosis.

[MRI and fetal multidetector CT in the diagnosis of fetal malformations].

N. Boddaert, P. Sonigo, F. Brunelle, 2008, Bulletin de l'Academie nationale de medecine.

[Antenatal diagnosis of hereditary epidermolysis bullosa].

C. Blanchet‐Bardon, Y. Dumez, A. Puissant, 1987, Annales de dermatologie et de vénéréologie.

Multifetal pregnancy reduction and selective termination

M. Evans, M. Dommergues, Y. Dumez, 1995, Current opinion in obstetrics & gynecology.

Neonatal effects of maternal administration of acebutolol.

C. Amiel‐Tison, C. Tchobroutsky, Y. Dumez, 1981, British medical journal.

Prenatal screening for Down syndrome: should first trimester ultrasound replace maternal serum screening?

L. Bussières, P. Aegerter, S. Uzan, 1996, Early human development.

Maternal-fetal folate status and neural tube defects: a case control study.

J. Zittoun, J. Marquet, F. Muller, 1995, Biology of the neonate.

Extraction of RNA from Dried Blood on Filter Papers after Long-Term Storage

A. Benachi, M. Vidaud, Jean‐Marc Costa, 2003 .

Molecular forms and solubility of acetylcholinesterase during the embryonic development of rat and human brain

Y. Dumez, F. Muller, J. Massoulie´, 1985, Brain Research.

Hematopoiesis in the human yolk sac: quantitation of erythroid and granulopoietic progenitors between 3.5 and 8 weeks of development.

A. Durandy, L. Coulombel, M. Dommergues, 1992, Bone marrow transplantation.

[Fetal renal impairment syndrome].

Y. Dumez, 2004, Annales d'urologie.

Amniotic fluid β-endorphin: A prognostic marker for gastroschisis?

J. Thalabard, P. Jouvet, F. Muller, 2002 .

[Prenatal diagnosis of a harlequin fetus using electron microscopy].

A. Bernheim, C. Blanchet‐Bardon, Y. Dumez, 1983, Annales de Pathologie.

Maternal and fetal serum and red blood cell folate levels in pregnancies complicated by neural tube defects

M. Dommergues, M. Zugaib, Y. Dumez, 1998 .

Prenatal diagnosis of the fragile‐X in male monozygotic twins: Discordant expression of the fragile site in amniocytes

N. Archidiacono, M. Rocchi, G. Monni, 1985, Prenatal diagnosis.

[A new prostaglandin E1 analog in late interruption of pregnancy, in utero deaths and very premature ruptures of the membranes. Apropos of 117 cases].

R. Henrion, P. Vige, Y. Dumez, 1984, Journal de gynecologie, obstetrique et biologie de la reproduction.

[Contribution of genetics].

A. Munnich, S. Lyonnet, M. Vekemans, 1999, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Fetal Urinary Biochemistry Predicts Postnatal Renal Function in Children With Bilateral Obstructive Uropathies

L. Mandelbrot, F. Muller, M. Dommergues, 1993, Obstetrics and gynecology.

[Primary intestinal lymphangiectasis with antenatal manifestation].

J. Navarro, A. Munck, P. Foucaud, 1986, Archives francaises de pediatrie.

[Bilateral Leydig cell tumor of the ovary in a woman with congenital adrenal hyperplasia. The first reported case].

M. Vacher-Lavenu, J. Luton, A. Bonnin, 1991, Presse medicale.

[Embryo reduction in multiple pregnancies. A French multicenter study].

M. Evans, I. Nisand, M. Dommergues, 1994, Journal de gynecologie, obstetrique et biologie de la reproduction.

Prepartum transabdominal amnio‐infusion for severe oligohydramnios

L. Mandelbrot, M. Dommergues, Y. Dumez, 1992, Acta obstetricia et gynecologica Scandinavica.

Omphalocele: beyond the size issue.

A. Benachi, L. Salomon, F. Auber, 2002, Journal of pediatric surgery.

Amniotic fluid digestive enzymes: Diagnostic value in fetal gastrointestinal obstructions

Y. Ville, F. Bargy, M. Dommergues, 1994, Prenatal diagnosis.

Twin-to-twin transfusion syndrome. Role of the fetal renin-angiotensin system.

M. Gonzalès, M. Gubler, M. Dommergues, 2000, American Journal of Pathology.

Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin

C. Rodeck, Y. Beuzard, Y. Blouquit, 1982, British journal of haematology.

Arthrogryposis multiplex congenita and Cerebellopontine Ischemic Lesions in Sibs: Recurrence of Prenatal Disruptive Brain Lesions with Different Patterns of Expression?

P. Sonigo, F. Encha-Razavi, L. Salomon, 2002, Fetal Diagnosis and Therapy.

[Results of prenatal management of fetuses with supraventricular tachycardia. A series of 66 cases].

E. Villain, J. Le Bidois, S. Delahaye, 2003, Journal de gynecologie, obstetrique et biologie de la reproduction.

New techniques for the prenatal diagnosis of hemoglobinopathies.

U. Testa, P. Rouyer‐Fessard, Y. Beuzard, 1981, Progress in clinical and biological research.

Enrichment, immunomorphological, and genetic characterization of fetal cells circulating in maternal blood.

A. Benachi, B. Lacour, G. Vona, 2002, The American journal of pathology.

Predicting neonatal deaths and pulmonary hypoplasia in isolated congenital diaphragmatic hernia using the sonographic fetal lung volume-body weight ratio.

A. Benachi, R. Ruano, M. Zugaib, 2008, AJR. American journal of roentgenology.

Three‐dimensional ultrasonographic measurements of the fetal lungs for prediction of perinatal outcome in isolated congenital diaphragmatic hernia

A. Benachi, R. Ruano, M. Aubry, 2009, The journal of obstetrics and gynaecology research.

Prenatal diagnosis of a satellited non‐acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature

A. Munnich, L. Faivre, M. Vekemans, 1999, Prenatal diagnosis.

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe

A. Moser, R. Heilig, J. Mandel, 1985, Human Genetics.