Man with rash on left hand

著者: Chimanji, Neeraj, Aboudan, Hassan, Mempin, Marion‐Vincent
出版年 J Am Coll Emerg Physicians Open (2020)

A Case Report: Co-presenting COVID-19 Infection and Acute Drug Intoxication

著者: Riekena, Jeremy, Lee, Irene, Lui, Anita, Mempin, Marion-Vincent
出版年 Clin Pract Cases Emerg Med (2020)

Postural Performance and Strategy in the Unipedal Stance of Soccer Players at Different Levels of Competition

著者: Paillard, Thierry, Noé, Frédéric, Rivière, Terence, Marion, Vincent, Montoya, Richard, Dupui, Philippe
出版事項 2006

Human Cytomegalovirus Carries a Cell-Derived Phospholipase A2 Required for Infectivity

著者: Allal, Cuider, Buisson-Brenac, Claire, Marion, Vincent, Claudel-Renard, Clotilde, Faraut, Thomas, Dal Monte, Paola, Streblow, Daniel, Record, Michel
出版事項 2004

Pharmacological Modulation of the Retinal Unfolded Protein Response in Bardet-Biedl Syndrome Reduces Apoptosis and Preserves Light Detection Ability

著者: Mockel, Anais, Obringer, Cathy, Hakvoort, Theodorus B. M., Seeliger, Mathias, Lamers, Wouter H., Stoetzel, Corinne, Dollfus, Hélène, Marion, Vincent
出版事項 2012

Hepatic Adaptation Compensates Inactivation of Intestinal Arginine Biosynthesis in Suckling Mice

著者: Marion, Vincent, Sankaranarayanan, Selvakumari, de Theije, Chiel, van Dijk, Paul, Hakvoort, Theo B. M., Lamers, Wouter H., Köhler, Eleonore S.
出版事項 2013

Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation

著者: Marion, Vincent, Stoetzel, Corinne, Schlicht, Dominique, Messaddeq, Nadia, Koch, Michael, Flori, Elisabeth, Danse, Jean Marc, Mandel, Jean-Louis, Dollfus, Hélène
出版事項 2009

Endothelial Arginine Resynthesis Contributes to the Maintenance of Vasomotor Function in Male Diabetic Mice

著者: Chennupati, Ramesh, Meens, Merlijn J. P. M. T., Marion, Vincent, Janssen, Ben J., Lamers, Wouter H., De Mey, Jo G. R., Köhler, S. Eleonore
出版事項 2014

Bardet-Biedl Syndrome: A Study of the Renal and Cardiovascular Phenotypes in a French Cohort

著者: Imhoff, Olivier, Marion, Vincent, Stoetzel, Corinne, Durand, Myriam, Holder, Muriel, Sigaudy, Sabine, Sarda, Pierre, Hamel, Christian P., Brandt, Christian, Dollfus, Hélène, Moulin, Bruno
出版事項 2011

Arginine Deficiency Causes Runting in the Suckling Period by Selectively Activating the Stress Kinase GCN2

著者: Marion, Vincent, Sankaranarayanan, Selvakumari, de Theije, Chiel, van Dijk, Paul, Lindsey, Patrick, Lamers, Marinus C., Harding, Heather P., Ron, David, Lamers, Wouter H., Köhler, S. Eleonore
出版事項 2011

Comparing the Bbs10 complete knockout phenotype with a specific renal epithelial knockout one highlights the link between renal defects and systemic inactivation in mice

著者: Cognard, Noëlle, Scerbo, Maria J, Obringer, Cathy, Yu, Xiangxiang, Costa, Fanny, Haser, Elodie, Le, Dane, Stoetzel, Corinne, Roux, Michel J, Moulin, Bruno, Dollfus, Hélène, Marion, Vincent
出版年 Cilia (2015)

Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects

著者: Bloch-Zupan, Agnès, Jamet, Xavier, Etard, Christelle, Laugel, Virginie, Muller, Jean, Geoffroy, Véronique, Strauss, Jean-Pierre, Pelletier, Valérie, Marion, Vincent, Poch, Olivier, Strahle, Uwe, Stoetzel, Corinne, Dollfus, Hélène
出版事項 2011

Relative Adipose Tissue Failure in Alström Syndrome Drives Obesity-Induced Insulin Resistance

著者: Geberhiwot, Tarekegn, Baig, Shanat, Obringer, Cathy, Girard, Dorothée, Dawson, Charlotte, Manolopoulos, Konstantinos, Messaddeq, Nadia, Bel Lassen, Pierre, Clement, Karine, Tomlinson, Jeremy W., Steeds, Richard P., Dollfus, Hélène, Petrovsky, Nikolai, Marion, Vincent
出版年 Diabetes (2021)

Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)

著者: Scheidecker, Sophie, Etard, Christelle, Pierce, Nathan W, Geoffroy, Véronique, Schaefer, Elise, Muller, Jean, Chennen, Kirsley, Flori, Elisabeth, Pelletier, Valérie, Poch, Olivier, Marion, Vincent, Stoetzel, Corinne, Strähle, Uwe, Nachury, Maxence V, Dollfus, Hélène
出版事項 2013

Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy

著者: Scheidecker, Sophie, Etard, Christelle, Haren, Laurence, Stoetzel, Corinne, Hull, Sarah, Arno, Gavin, Plagnol, Vincent, Drunat, Séverine, Passemard, Sandrine, Toutain, Annick, Obringer, Cathy, Koob, Mériam, Geoffroy, Véronique, Marion, Vincent, Strähle, Uwe, Ostergaard, Pia, Verloes, Alain, Merdes, Andreas, Moore, Anthony T., Dollfus, Hélène
出版年 Am J Hum Genet (2015)

Consensus clinical management guidelines for Alström syndrome

著者: Tahani, Natascia, Maffei, Pietro, Dollfus, Hélène, Paisey, Richard, Valverde, Diana, Milan, Gabriella, Han, Joan C., Favaretto, Francesca, Madathil, Shyam C., Dawson, Charlotte, Armstrong, Matthew J., Warfield, Adrian T., Düzenli, Selma, Francomano, Clair A., Gunay-Aygun, Meral, Dassie, Francesca, Marion, Vincent, Valenti, Marina, Leeson-Beevers, Kerry, Chivers, Ann, Steeds, Richard, Barrett, Timothy, Geberhiwot, Tarekegn
出版年 Orphanet J Rare Dis (2020)