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Françoise Muller

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Physiology

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Amniotic Fluid

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Newborn Infant

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TOP 3
Garchet-Beaudron Aurélie; Dreux Sophie; Leporrier Nathalie; Oury Jean-François; Muller Françoise;
Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnancies.
Dreux Sophie; Olivier Camille; Dupont Jean-Michel; Leporrier Nathalie; Oury Jean-François; Muller Françoise
Maternal serum screening in cases of mosaic and translocation Down syndrome.
Benoist Jean-François; Imbard Apolline; Dreux Sophie; Garel Catherine; Haddad Georges; Hoffet Méderic; Biou Daniel; Muller Françoise
Antenatal biochemical expression of cystinuria and relation to fetal hyperechogenic colon.

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2008: Garchet-Beaudron Aurélie; Dreux Sophie; Leporrier Nathalie; Oury Jean-François; Muller Françoise;
Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnancies.
Prenatal diagnosis 2008;28(12):1105-9.
2008: Dreux Sophie; Olivier Camille; Dupont Jean-Michel; Leporrier Nathalie; Oury Jean-François; Muller Françoise
Maternal serum screening in cases of mosaic and translocation Down syndrome.
Prenatal diagnosis 2008;28(8):699-703.
2007: Benoist Jean-François; Imbard Apolline; Dreux Sophie; Garel Catherine; Haddad Georges; Hoffet Méderic; Biou Daniel; Muller Françoise
Antenatal biochemical expression of cystinuria and relation to fetal hyperechogenic colon.
Clinical chemistry 2007;53(1):149-50.
2006: Garel C; Dreux S; Philippe-Chomette P; Vuillard E; Oury J-F; Muller F
Contribution of fetal magnetic resonance imaging and amniotic fluid digestive enzyme assays to the evaluation of gastrointestinal tract abnormalities.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2006;28(3):282-91.
2006: Gonin Julie; Dreux Sophie; Guimiot Fabien; Menez Françoise; Guibourdenche Jean; Biou Daniel; Muller Françoise
Neural tube defects cannot be diagnosed prenatally by electrophoresis of amniotic fluid transferrin isoforms.
Clinical chemistry 2006;52(8):1618-9.
2006: Dreux Sophie; Rousseau Thierry; Gerber Stefan; Col Jean-Yves; Dommergues Marc; Muller Françoise
Fetal serum beta2-microglobulin as a marker for fetal infectious diseases.
Prenatal diagnosis 2006;26(5):471-4.
2006: Azarian Madeleine; Dreux Sophie; Vuillard Edith; Meneguzzi Guerrino; Haber Saranda; Guimiot Fabien; Muller Françoise
Prenatal diagnosis of inherited epidermolysis bullosa in a patient with no family history: a case report and literature review.
Prenatal diagnosis 2006;26(1):57-9.
2005: Talabani Hana; Dreux Sophie; Luton Dominique; Simon-Bouy Brigitte; Le Fiblec Bernard; Col Jean-Yves; Guibourdenche Jean; Oury Jean-François; Muller Françoise
Fetal anal incontinence evaluated by amniotic fluid digestive enzyme assay in myelomeningocele spina bifida.
Pediatric research 2005;58(4):766-70.
2005: Muller Françoise; Dreux Sophie; Vaast Pascal; Dumez Yves; Nisand Israel; Ville Yves; Boulot Pierre; Guibourdenche Jean; Althusser Marc; Blin Gérard; Gautier Evelyne; Lespinard Catherine; Perrotin Franck; Poulain Patrice; Sarramon Marie-France;
Prenatal diagnosis of megacystis-microcolon-intestinal hypoperistalsis syndrome: contribution of amniotic fluid digestive enzyme assay and fetal urinalysis.
Prenatal diagnosis 2005;25(3):203-9.
2004: Forestier F; Sault C; Muller F; Gaucherand P; Gil S; Oger J L
False-positive amniotic fluid acetylcholinesterase PAGE due to contamination by the AFP diluent of an automated instrument.
Prenatal diagnosis 2004;24(6):478-9.
2004: Muller Françoise; Dreux Sophie; Audibert François; Chabaud Jean-Jacques; Rousseau Thierry; D'Hervé Dominique; Dumez Yves; Ngo Sandrine; Gubler Marie-Claire; Dommergues Marc
Fetal serum ss2-microglobulin and cystatin C in the prediction of post-natal renal function in bilateral hypoplasia and hyperechogenic enlarged kidneys.
Prenatal diagnosis 2004;24(5):327-32.
2004: Favre Romain; Dreux Sophie; Dommergues Marc; Dumez Yves; Luton Dominique; Oury Jean-François; Fiblec Bernard Le; Nisand Israel; Muller Françoise
Nonimmune fetal ascites: a series of 79 cases.
American journal of obstetrics and gynecology 2004;190(2):407-12.
2003: Muller Françoise; Dreux Sophie; Lemeur Alain; Sault Corinne; Desgrès Jean; Bernard Marguerite-Anne; Giorgetti Claude; Lemay Catherine; Mirallié Sophie; Beauchet Alain;
Medically assisted reproduction and second-trimester maternal serum marker screening for Down syndrome.
Prenatal diagnosis 2003;23(13):1073-6.
2003: Muller Françoise; Benattar Clarisse; Audibert François; Roussel Nathalie; Dreux Sophie; Cuckle Howard
First-trimester screening for Down syndrome in France combining fetal nuchal translucency measurement and biochemical markers.
Prenatal diagnosis 2003;23(10):833-6.
2003: Simon-Bouy B; Satre V; Ferec C; Malinge M C; Girodon E; Denamur E; Leporrier N; Lewin P; Forestier F; Muller F;
Hyperechogenic fetal bowel: a large French collaborative study of 682 cases.
American journal of medical genetics. Part A 2003;121A(3):209-13.
2003: Muller Françoise
Prenatal biochemical screening for neural tube defects.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2003;19(7-8):433-5.
2003: Muller Françoise; Dreux Sophie; Sault Corinne; Galland Armelle; Puissant Hugues; Couplet Gisèle; Lemay Catherine; Larcher Marie-Estelle; Renom Gilles;
Very low alpha-fetoprotein in Down syndrome maternal serum screening.
Prenatal diagnosis 2003;23(7):584-7.
2003: Kesrouani Assaad K; Guibourdenche Jean; Muller Françoise; Denamur Eric; Vuillard Edith; Garel Catherine; Delezoide Anne Lise; Eydoux Patrice; Tachdjian Gerard; Lebon Pierre; de Lagausie Pascal; Sibony Olivier; Bauman Clarisse; Oury Jean-François; Luton Dominique
Etiology and outcome of fetal echogenic bowel. Ten years of experience.
Fetal diagnosis and therapy 2003;18(4):240-6.
2003: Serre J-L; Feingold J; Simon-Bouy B; Muller F
[Towards an improved antenatal screening for cystic fibrosis]
Revue d'épidémiologie et de santé publique 2003;51(2):245-53.
2003: Muller Françoise; Dreux Sophie; Dupoizat Henry; Uzan Serge; Dubin Marie-Françoise; Oury Jean-François; Dingeon Bernard; Dommergues Marc
Second-trimester Down syndrome maternal serum screening in twin pregnancies: impact of chorionicity.
Prenatal diagnosis 2003;23(4):331-5.
2002: Muller Françoise; Thibaud Didier; Poloce Françoise; Gelineau Marie-Christine; Bernard Marguerite; Brochet Christine; Millet Christine; Réal Jean-Yves; Dommergues Marc
Risk of amniocentesis in women screened positive for Down syndrome with second trimester maternal serum markers.
Prenatal diagnosis 2002;22(11):1036-9.
2002: Muller Françoise; Dreux Sophie; Oury Jean-François; Luton Dominique; Uzan Serge; Uzan Michèle; Levardon Michel; Dommergues Marc
Down syndrome maternal serum marker screening after 18 weeks' gestation.
Prenatal diagnosis 2002;22(11):1001-4.
2002: Muller Françoise; Forestier François; Dingeon Bernard;
Second trimester trisomy 21 maternal serum marker screening. Results of a countrywide study of 854,902 patients.
Prenatal diagnosis 2002;22(10):925-9.
2002: Muller Françoise; Sault Corinne; Lemay Catherine; Roussel-Mizon Nathalie; Forestier François; Frendo Jean-Louis;
Second trimester two-step trisomy 18 screening using maternal serum markers.
Prenatal diagnosis 2002;22(7):605-8.
2002: Muller F; Simon-Bouy B; Girodon E; Monnier N; Malinge M C; Serre J L;
Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: results of a French molecular collaborative study based on 641 prospective cases.
American journal of medical genetics 2002;110(2):109-15.
2002: Simon-Bouy Brigitte; Muller Françoise;
Hyperechogenic fetal bowel and Down syndrome. Results of a French collaborative study based on 680 prospective cases.
Prenatal diagnosis 2002;22(3):189-92.
2001: Lia-Baldini A S; Muller F; Taillandier A; Gibrat J F; Mouchard M; Robin B; Simon-Bouy B; Serre J L; Aylsworth A S; Bieth E; Delanote S; Freisinger P; Hu J C; Krohn H P; Nunes M E; Mornet E
A molecular approach to dominance in hypophosphatasia.
Human genetics 2001;109(1):99-108.
2001: Taillandier A; Lia-Baldini A S; Mouchard M; Robin B; Muller F; Simon-Bouy B; Serre J L; Bera-Louville A; Bonduelle M; Eckhardt J; Gaillard D; Myhre A G; Körtge-Jung S; Larget-Piet L; Malou E; Sillence D; Temple I K; Viot G; Mornet E
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia.
Human mutation 2001;18(1):83-4.
2000: Muller F; Rebiffé M; Taillandier A; Oury J F; Mornet E
Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21.
Human genetics 2000;106(3):340-4.
2000: Taillandier A; Cozien E; Muller F; Merrien Y; Bonnin E; Fribourg C; Simon-Bouy B; Serre J L; Bieth E; Brenner R; Cordier M P; De Bie S; Fellmann F; Freisinger P; Hesse V; Hennekam R C; Josifova D; Kerzin-Storrar L; Leporrier N; Zabot M T; Mornet E
Fifteen new mutations (-195C>T, L-12X, 298-2A>G, T117N, A159T, R229S, 997+2T>A, E274X, A331T, H364R, D389G, 1256delC, R433H, N461I, C472S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with hypophosphatasia.
Human mutation 2000;15(3):293.
1999: Muller F; Bernard M A; Benkirane A; Ngo S; Lortat-Jacob S; Oury J F; Dommergues M
Fetal urine cystatin C as a predictor of postnatal renal function in bilateral uropathies.
Clinical chemistry 1999;45(12):2292-3.
1999: Muller F; Ngo S; Rebiffé M; Oury J F; Uzan S; Satgé D
Maternal serum s100b protein is ineffective for Down syndrome screening.
Prenatal diagnosis 1999;19(11):1086.
1999: Mornet E; Muller F; Ngo S; Taillandier A; Simon-Bouy B; Maire I; Oury J F
Correlation of alkaline phosphatase (ALP) determination and analysis of the tissue non-specific ALP gene in prenatal diagnosis of severe hypophosphatasia.
Prenatal diagnosis 1999;19(8):755-7.
1999: Muller F; Aegerter P; Ngo S; Fort A; Beauchet A; Giraudet P; Dommergues M
Software for prenatal down syndrome risk calculation: a comparative study of six software packages.
Clinical chemistry 1999;45(8 Pt 1):1278-80.
1999: Zurutuza L; Muller F; Gibrat J F; Taillandier A; Simon-Bouy B; Serre J L; Mornet E
Correlations of genotype and phenotype in hypophosphatasia.
Human molecular genetics 1999;8(6):1039-46.
1999: Muller F; Doche C; Ngo S; Faïna S; Charvin M A; Rebiffé M; Taguel V; Dingeon B
Stability of free beta-subunit in routine practice for trisomy 21 maternal serum screening.
Prenatal diagnosis 1999;19(1):85-6.
1999: Taillandier A; Zurutuza L; Muller F; Simon-Bouy B; Serre J L; Bird L; Brenner R; Boute O; Cousin J; Gaillard D; Heidemann P H; Steinmann B; Wallot M; Mornet E
Characterization of eleven novel mutations (M45L, R119H, 544delG, G145V, H154Y, C184Y, D289V, 862+5A, 1172delC, R411X, E459K) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with severe hypophosphatasia. Mutations in brief no. 217. Online.
Human mutation 1999;13(2):171-2.
1998: Muller F; Ngo S; Aegerter P; Le Bourdellès S; Taguel V; Rebiffé M; Faïna S; Giraudet P
Evaluation of the Abbott system in maternal serum screening for Down syndrome: the AxSym analyzer, AFP and hCG reagents and Maciel Prenatal Interpretive Software.
Clinica chimica acta; international journal of clinical chemistry 1998;277(1):65-75.
1998: Muller F; Dommergues M; Simon-Bouy B; Ferec C; Oury J F; Aubry M C; Bessis R; Vuillard E; Denamur E; Bienvenu T; Serre J L
Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index case.
Journal of medical genetics 1998;35(8):657-60.
1998: Mornet E; Taillandier A; Peyramaure S; Kaper F; Muller F; Brenner R; Bussière P; Freisinger P; Godard J; Le Merrer M; Oury J F; Plauchu H; Puddu R; Rival J M; Superti-Furga A; Touraine R L; Serre J L; Simon-Bouy B
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia.
European journal of human genetics : EJHG 1998;6(4):308-14.
1997: Dingeon B; Doche C; Doche L; Eynard J C; Mercier S; Muller F
[For a new approach of comprehensive quality control in clinical biology. Application to prenatal markers of trisomy risks]
Annales de biologie clinique 1997;55(6):637-8.
1997: Mornet E; Muller F; Lenvoisé-Furet A; Delezoide A L; Col J Y; Simon-Bouy B; Serre J L
Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects.
Human genetics 1997;100(5-6):512-4.
1996: Savey L; Muller F; Ndayizamba G; Lefiblec B; Serra B; Colau J C
[Maternal serum hCG at 15 weeks. Its value for detecting risk of pre-eclampsia or fetal hypotrophy]
Presse médicale (Paris, France : 1983) 1996;25(40):2049.
1996: Muller F; Dommergues M; Bussières L; Aegerter P; Le Fiblec B; Uzan S; Oury J F; Colau J C; Dumez Y
Prenatal screening for Down syndrome: should first trimester ultrasound replace maternal serum screening?
Early human development 1996;47 Suppl():S37-9.
1996: Muller F; Dommergues M; Bussières L; Lortat-Jacob S; Loirat C; Oury J F; Aigrain Y; Niaudet P; Aegerter P; Dumez Y
Development of human renal function: reference intervals for 10 biochemical markers in fetal urine.
Clinical chemistry 1996;42(11):1855-60.
1996: Muller F; Savey L; Le Fiblec B; Bussières L; Ndayizamba G; Colau J C; Giraudet P
Maternal serum human chorionic gonadotropin level at fifteen weeks is a predictor for preeclampsia.
American journal of obstetrics and gynecology 1996;175(1):37-40.
1996: Muller F; Bussières L
Maternal serum markers for fetal trisomy 21 screening.
European journal of obstetrics, gynecology, and reproductive biology 1996;65(1):3-6.
1995: Muller F; Bussières L; Chevallier B
[Maternal serum markers of fetal trisomy 21]
Presse médicale (Paris, France : 1983) 1995;24(27):1265-9.
1995: Muller F; Dommergues M; Aubry M C; Simon-Bouy B; Gautier E; Oury J F; Narcy F
Hyperechogenic fetal bowel: an ultrasonographic marker for adverse fetal and neonatal outcome.
American journal of obstetrics and gynecology 1995;173(2):508-13.
1994: Muller F; Dommergues M; Ville Y; Lewin F; Delvalez-Morichon N; Nihoul-Fekete C; Bargy F; Dumez Y; Boue A
Amniotic fluid digestive enzymes: diagnostic value in fetal gastrointestinal obstructions.
Prenatal diagnosis 1994;14(10):973-9.
1994: Muller F; Bussières L; Pèlissier M C; Oury J F; Boué C; Uzan S; Boué A
Do racial differences exist in second-trimester maternal hCG levels? A study of 23,369 patients.
Prenatal diagnosis 1994;14(7):633-6.
1994: Decoret E; Sibony O; Vuillard E; Bedu A; Faure O; Mandelbrot L; Muller F; Oury J F; Blot P
Prenatal diagnosis of in utero fetal gastrointestinal bleeding.
Fetal diagnosis and therapy 1994;9(4):252-5.
1994: Muller F; Parvy P; Dommergues M; Lortat-Jacob S; Dumez Y; Kamoun P
[Free amino acids in fetal urine and prognosis of renal function in bilateral obstructive uropathies]
Annales de biologie clinique 1994;52(9):651-5.
1993: Muller F; Dommergues M; Mandelbrot L; Aubry M C; Nihoul-Fekete C; Dumez Y
Fetal urinary biochemistry predicts postnatal renal function in children with bilateral obstructive uropathies.
Obstetrics and gynecology 1993;82(5):813-20.
1993: Duchatel F; Muller F; Oury J F; Mennesson B; Boue J; Boue A
Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestation.
Fetal diagnosis and therapy 1993;8(1):28-36.
1992: Muller F; Simon-Bouy B; Aubry M C; Duchatel F; Bessis R; Boué J
[Accidental ultrasonographic disclosure of isolated intra-abdominal fetal hyperechogenicity. Apropos of a series of 87 cases]
Journal de radiologie 1992;73(12):699-704.
1991: Muller F; Oury J F; Bussière P; Lewin F; Boué J
First-trimester diagnosis of hypophosphatasia. Importance of gestational age and purity of CV samples.
Prenatal diagnosis 1991;11(9):725-30.
1991: Muller F; Simon-Bouy B; Aubry M C; Duchatel F; Bessis R; Boué J
[Fortuitous discovery in echography of an isolated fetal intra-abdominal hyperechogenic mass. 87 cases]
Journal de gynécologie, obstétrique et biologie de la reproduction 1991;20(8):1115-21.
1990: Muller F; Boué A
A single chorionic gonadotropin assay for maternal serum screening for Down's syndrome.
Prenatal diagnosis 1990;10(6):389-98.
1990: Muller F; Pantin G; Normand N; Bucheton D; Der Sarkissian H; Boué J; Giraudet P; Henrion R; Boué A
[Does systemic determination of maternal serum alpha-1-fetoprotein have any value?]
Archives françaises de pédiatrie 1990;47(6):473-4.
1990: Lortat-Jacob S; Fekete C N; Dumez Y; Muller F; Aubry M C; Aubry J P
[Prenatal diagnosis and neonatal management of posterior urethral valves: apropos of 33 case reports]
Acta urologica Belgica 1990;58(1):29-37.
1990: Dumez Y; Muller F; Dommergues M; Nihoul-Fekete C
[Antenatal diagnosis of obstructive uropathies]
Chirurgie; mémoires de l'Académie de chirurgie 1990;116(6-7):517-22.
1989: Muller F; Oury J F; Boue A
First-trimester amniotic fluid acetylcholinesterase electrophoresis.
Prenatal diagnosis 1989;9(3):173-5.
1989: Mornet E; Simon-Bouy B; Serre J L; Muller F; Taillandier A; Martinez M; Boue J; Boue A
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes.
Clinical genetics 1989;35(2):81-7.
1988: Boue A; Muller F; Briard M L; Boue J
Interest of biology in the management of pregnancies where a fetal malformation has been detected by ultrasonography.
Fetal therapy 1988;3(1-2):14-23.
1986: Boué A; Muller F; Nezelof C; Oury J F; Duchatel F; Dumez Y; Aubry M C; Boué J
Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis.
Human genetics 1986;74(3):288-97.
1986: Muller F; Rebiffé M; Der Sarkissian H; Boué J; Boué A
[Decrease of various enzyme activities in the amniotic fluid of the fetuses with chromosomal anomalies]
Annales de génétique 1986;29(1):27-31.
1985: Muller F; Aubry M C; Gasser B; Duchatel F; Boué J; Boué A
Prenatal diagnosis of cystic fibrosis. II. Meconium ileus in affected fetuses.
Prenatal diagnosis 1985;5(2):109-17.
1984: Muller F; Frot J C; Aubry M C; Boue J; Boue A
Meconium ileus in cystic fibrosis fetuses.
Lancet 1984;2(8396):223.

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Françoise Muller

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