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Françoise Muller

Showing results (1-10 of 72) with videos related to

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 16, 2003
Prenatal biochemical screening for neural tube defectsFrançoise Muller
Prenatal Diagnosis|March 29, 2002
Hyperechogenic fetal bowel and Down syndrome. Results of a French collaborative study based on 680 prospective casesBrigitte Simon-Bouy, Françoise Muller,
Prenatal Diagnosis|October 16, 2002
Second trimester trisomy 21 maternal serum marker screening. Results of a countrywide study of 854,902 patientsFrançoise Muller, François Forestier, Bernard Dingeon, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 6, 2010
Screening for adverse pregnancy outcome at early gestational ageSophie Hourrier, Laurent J Salomon, Sophie Dreux, et al.
Prenatal Diagnosis|May 10, 2002
Detection and false-positive rates of maternal serum markers for Down syndrome screening according to maternal age in women over 35 years of age. A study of the agreement of eight dedicated software packagesFrançoise Muller, Jean-Christophe Thalabard, Sandrine Ngo, et al.
Prenatal Diagnosis|January 11, 2008
Nonvisualization of the fetal gallbladder by second-trimester ultrasound scan: strategy of clinical management based on four examplesMathias Boughanim, Alexandra Benachi, Sophie Dreux, et al.
Prenatal Diagnosis|October 15, 2003
First-trimester screening for Down syndrome in France combining fetal nuchal translucency measurement and biochemical markersFrançoise Muller, Clarisse Benattar, François Audibert, et al.
Prenatal Diagnosis|November 13, 2008
Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnanciesAurélie Garchet-Beaudron, Sophie Dreux, Nathalie Leporrier, et al.
Prenatal Diagnosis|September 29, 2011
Sonographic measurement of corpus spongiosum in male fetusesEdith Vuillard, Yvon Chitrit, Sophie Dreux, et al.
Pediatric Nephrology (Berlin, Germany)|June 12, 2016
Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutationLeire Gondra, Stéphane Décramer, Gihad E Chalouhi, et al.
Pageof 8

Showing results (1-10 of 72) with videos related to

Sort By:
Pageof 8
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 16, 2003
Prenatal biochemical screening for neural tube defectsFrançoise Muller
Prenatal Diagnosis|March 29, 2002
Hyperechogenic fetal bowel and Down syndrome. Results of a French collaborative study based on 680 prospective casesBrigitte Simon-Bouy, Françoise Muller,
Prenatal Diagnosis|October 16, 2002
Second trimester trisomy 21 maternal serum marker screening. Results of a countrywide study of 854,902 patientsFrançoise Muller, François Forestier, Bernard Dingeon, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 6, 2010
Screening for adverse pregnancy outcome at early gestational ageSophie Hourrier, Laurent J Salomon, Sophie Dreux, et al.
Prenatal Diagnosis|May 10, 2002
Detection and false-positive rates of maternal serum markers for Down syndrome screening according to maternal age in women over 35 years of age. A study of the agreement of eight dedicated software packagesFrançoise Muller, Jean-Christophe Thalabard, Sandrine Ngo, et al.
Prenatal Diagnosis|January 11, 2008
Nonvisualization of the fetal gallbladder by second-trimester ultrasound scan: strategy of clinical management based on four examplesMathias Boughanim, Alexandra Benachi, Sophie Dreux, et al.
Prenatal Diagnosis|October 15, 2003
First-trimester screening for Down syndrome in France combining fetal nuchal translucency measurement and biochemical markersFrançoise Muller, Clarisse Benattar, François Audibert, et al.
Prenatal Diagnosis|November 13, 2008
Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnanciesAurélie Garchet-Beaudron, Sophie Dreux, Nathalie Leporrier, et al.
Prenatal Diagnosis|September 29, 2011
Sonographic measurement of corpus spongiosum in male fetusesEdith Vuillard, Yvon Chitrit, Sophie Dreux, et al.
Pediatric Nephrology (Berlin, Germany)|June 12, 2016
Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutationLeire Gondra, Stéphane Décramer, Gihad E Chalouhi, et al.
Pageof 8