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American Journal of Human Genetics|June 12, 1999
Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 geneV Satre, N Monnier, F Berthoin, et al.
Analytical Chemistry|August 20, 2011
Combed single DNA molecules imaged by secondary ion mass spectrometryArmelle Cabin-Flaman, Anne-Françoise Monnier, Yannick Coffinier, et al.
Applied Optics|September 10, 2005
Robust determination of optical path difference: fringe tracking at the infrared optical telescope array interferometerEttore Pedretti, Wesley A Traub, John D Monnier, et al.
Early Human Development|August 9, 2014
Emotional and effortful control abilities in 42-month-old very preterm and full-term childrenArnaud Witt, Anne Theurel, Cristina Borradori Tolsa, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 1, 2006
Microbiological diagnosis of empyema in children: comparative evaluations by culture, polymerase chain reaction, and pneumococcal antigen detection in pleural fluidsAlban Le Monnier, Etienne Carbonnelle, Jean-Ralph Zahar, et al.
Pharmacy Practice|October 9, 2019
Role of community pharmacists in skin cancer screening: A descriptive study of skin cancer risk factors prevalence and photoprotection habits in Barcelona, Catalonia, SpainJoan F Mir, Maria Estrada-Campmany, Anna Heredia, et al.
Scientific Reports|October 5, 2023
Human peripheral blood mononuclear cells display a temporal evolving inflammatory profile after myocardial infarction and modify myocardial fibroblasts phenotypeElodie Miquelestorena-Standley, Ana Valéria Vinhais da Silva, Marina Monnier, et al.
Scientific Reports|January 22, 2020
Syntaxin-3 is dispensable for basal neurotransmission and synaptic plasticity in postsynaptic hippocampal CA1 neuronsShan Shi, Ke Ma, Na-Ryum Bin, et al.
BMJ Open|September 15, 2021
Early versus differed arterial catheterisation in critically ill patients with acute circulatory failure: a multicentre, open-label, pragmatic, randomised, non-inferiority controlled trial: the EVERDAC protocolGrégoire Muller, Toufik Kamel, Damien Contou, et al.
Human Mutation|October 30, 2010
From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypesHaifa Hichri, John Rendu, Nicole Monnier, et al.
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