Výsledky vyhledávání - Françoise Müller
- Zobrazuji výsledky 1 - 12 z 12
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1
Early fetal megacystis between 11 and 15 weeks of gestation Autor R. Favre, M. Köhler, B. Gasser, Françoise Müller, I. Nisand
Vydáno 1999Artigo -
2
Contribution of fetal magnetic resonance imaging and amniotic fluid digestive enzyme assays to the evaluation of gastrointestinal tract abnormalities Autor Cathérine Garel, Sophie Dreux, Pascale Philippe‐Chomette, E. Vuillard, J.F. Oury, Françoise Müller
Vydáno 2006Artigo -
3
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4
Fetal urine biochemistry at 13-23 weeks of gestation in lower urinary tract obstruction: criteria for<i>in-utero</i>treatment Autor W. Abdennadher, G. E. Chalouhi, Sophie Dreux, Jonathan Rosenblatt, R. Favre, Fabien Guimiot, Laurent Salomon, J.-F. Oury, Y. Ville, Françoise Müller
Vydáno 2014Artigo -
5
Paradoxic Activation of the Renin-Angiotensin System in Twin-Twin Transfusion Syndrome: An Explanation for Cardiovascular Disturbances in the Recipient Autor D. Mahieu‐Caputo, A. Meulemans, Jéléna Martinovic, Marie‐Claire Gubler, Anne‐Lise Delezoide, Françoise Müller, Patrick Madélénat, Nicholas M. Fisk, Marc Dommergues
Vydáno 2005Artigo -
6
Overexpression of Copper Zinc Superoxide Dismutase Impairs Human Trophoblast Cell Fusion and Differentiation Autor Jean‐Louis Frendo, Patrice Thérond, Terry Bird, Nathalie Massin, Françoise Müller, Jean Guibourdenche, Dominique Luton, Michel Vidaud, Wayne B. Anderson, Danièle Evain‐Brion
Vydáno 2001Artigo -
7
Fetal serum β2-microglobulin predicts postnatal renal function in bilateral uropathies Autor Marc Dommergues, Françoise Müller, Sandrine Ngo, Patrick Hohlfeld, Jean‐François Oury, Laurent Bidat, D. Mahieu‐Caputo, Paul Sagot, G. Body, R. Favre, Yves Dumez
Vydáno 2000Artigo -
8
Defect of Villous Cytotrophoblast Differentiation into Syncytiotrophoblast in Down’s Syndrome<sup>1</sup> Autor 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
Vydáno 2000Artigo -
9
Analysis of blood from Zika virus-infected fetuses: a prospective case series Autor 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
Vydáno 2017Artigo -
10
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia Autor 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
Vydáno 1998Artigo -
11
Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome Autor 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
Vydáno 2017Artigo -
12
<i>ACTG2</i>variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome Autor 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
Vydáno 2015Artigo
Vyhledávací nástroje:
Související témata
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