Resultados da pesquisa - Françoise Müller
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1
Early fetal megacystis between 11 and 15 weeks of gestation Por R. Favre, M. Köhler, B. Gasser, Françoise Müller, I. Nisand
Publicado em 1999Artigo -
2
Contribution of fetal magnetic resonance imaging and amniotic fluid digestive enzyme assays to the evaluation of gastrointestinal tract abnormalities Por Cathérine Garel, Sophie Dreux, Pascale Philippe‐Chomette, E. Vuillard, J.F. Oury, Françoise Müller
Publicado em 2006Artigo -
3
Development of human fetal kidney in obstructive uropathy: Correlations with ultrasonography and urine biochemistry Por Farida Daïkha-Dahmane, Marc Dommergues, Françoise Müller, Françoise Narcy, Mireille Lacoste, A Beziau, Yves Dumez, Marie‐Claire Gubler
Publicado em 1997Artigo -
4
Fetal urine biochemistry at 13-23 weeks of gestation in lower urinary tract obstruction: criteria for<i>in-utero</i>treatment Por W. Abdennadher, G. E. Chalouhi, Sophie Dreux, Jonathan Rosenblatt, R. Favre, Fabien Guimiot, Laurent Salomon, J.-F. Oury, Y. Ville, Françoise Müller
Publicado em 2014Artigo -
5
Paradoxic Activation of the Renin-Angiotensin System in Twin-Twin Transfusion Syndrome: An Explanation for Cardiovascular Disturbances in the Recipient Por D. Mahieu‐Caputo, A. Meulemans, Jéléna Martinovic, Marie‐Claire Gubler, Anne‐Lise Delezoide, Françoise Müller, Patrick Madélénat, Nicholas M. Fisk, Marc Dommergues
Publicado em 2005Artigo -
6
Overexpression of Copper Zinc Superoxide Dismutase Impairs Human Trophoblast Cell Fusion and Differentiation Por Jean‐Louis Frendo, Patrice Thérond, Terry Bird, Nathalie Massin, Françoise Müller, Jean Guibourdenche, Dominique Luton, Michel Vidaud, Wayne B. Anderson, Danièle Evain‐Brion
Publicado em 2001Artigo -
7
Fetal serum β2-microglobulin predicts postnatal renal function in bilateral uropathies Por Marc Dommergues, Françoise Müller, Sandrine Ngo, Patrick Hohlfeld, Jean‐François Oury, Laurent Bidat, D. Mahieu‐Caputo, Paul Sagot, G. Body, R. Favre, Yves Dumez
Publicado em 2000Artigo -
8
Defect of Villous Cytotrophoblast Differentiation into Syncytiotrophoblast in Down’s Syndrome<sup>1</sup> Por Jean‐Louis Frendo, Michel Vidaud, Jean Guibourdenche, D. Luton, Françoise Müller, Daniel Bellet, Y. Giovagrandi, Anne Couturier‐Tarrade, Dominique Porquet, Philippe Blot, D. Evain‐Brion
Publicado em 2000Artigo -
9
Analysis of blood from Zika virus-infected fetuses: a prospective case series Por Bruno Schaub, Manon Vouga, Fatiha Najioullah, M. Gueneret, Alice Monthieux, Caroline Harte, Françoise Müller, Eugénie Jolivet, Clara Adenet, Sophie Dreux, Isabelle Leparc-Goffart, Raymond Césaire, Jean-Luc Voluménie, David Baud
Publicado em 2017Artigo -
10
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia Por Étienne Mornet, A. Taillandier, S Peyramaure, Fiona Kaper, Françoise Müller, Rolf E. Brenner, P Bussière, Peter Freisinger, J. Godard, M. Le Merrer, J.F. Oury, H Plauchu, Roberta Puddu, Rival Jm, Andrea Superti‐Furga, R. Touraine, JL Serre, Brigitte Simon‐Bouy
Publicado em 1998Artigo -
11
Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome Por Danny Halim, Erwin Brosens, Françoise Müller, Michael F. Wangler, Arthur L. Beaudet, James R. Lupski, Zeynep H. Coban Akdemir, Michael Doukas, Hans Stoop, Bianca M. de Graaf, Rutger W. W. Brouwer, Wilfred F. J. van IJcken, Jean‐François Oury, Jonathan Rosenblatt, Alan J. Burns, Dick Tibboel, Robert M.W. Hofstra, Maria M. Alves
Publicado em 2017Artigo -
12
<i>ACTG2</i>variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome Por Danny Halim, Robert M.W. Hofstra, Luca Signorile, Robert M. Verdijk, Christine S. van der Werf, Yunia Sribudiani, Rutger W. W. Brouwer, Wilfred F. J. van IJcken, Niklas Dahl, Joanne Verheij, Clarisse Baumann, John A. Kerner, Yolande van Bever, Niels Galjart, René Wijnen, Dick Tibboel, Alan J. Burns, Françoise Müller, Alice S. Brooks, Maria M. Alves
Publicado em 2015Artigo
Ferramentas de pesquisa:
Assuntos relacionados
Biology
Genetics
Medicine
Fetus
Pregnancy
Internal medicine
Endocrinology
Urinary system
Gene
Kidney
Renal function
Amniotic fluid
Andrology
Biochemistry
Cytotrophoblast
Gastroenterology
Gestation
Gestational age
Hydronephrosis
In utero
Missense mutation
Molecular biology
Mutation
Obstetrics
Obstructive uropathy
Oligohydramnios
Pathology
Placenta
Syncytiotrophoblast
Urinary tract obstruction