Biblio

11 resultats trouvés
Filtres: Auteur is Richard, Pascale  [Clear All Filters]
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Marey I, Fressart V, Rambaud C, Fornes P, Martin L, Grotto S, Alembik Y, Gorka H, Millat G, Gandjbakhch E et al..  2020.  Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy. OPEN MEDICINE. 15:435-446.
Tiberghien P, Toussirot E, Richard P, Morel P, Garraud O.  2021.  Convalescent plasma to treat COVID-19: Following the Argentinian lead. TRANSFUSION AND APHERESIS SCIENCE. 60:103161.
Gallian P, Le Cam S, Brisbarre N, Pastorino B, Amroun A, Malard L, de Lamballerie X, Bliem C, Richard P, Morel P et al..  Submitted.  COVID-19 convalescent plasma: Evolving strategies for serological screening in France. VOX SANGUINIS.
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Ader F, De Groote P, Reant P, Rooryck-Thambo C, Dupin-Deguine D, Rambaud C, Khraiche D, Perret C, Pruny JFrancois, Mathieu-Dramard M et al..  2019.  FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations. CLINICAL GENETICS. 96:317-329.
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Thevenon J, Laurent G, Ader F, Laforet P, Klug D, Pentiah ADuva, Gouya L, Maurage CAlain, Kacet S, Eicher J-C et al..  2017.  High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations. EUROPACE. 19:651-659.
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Cambon-Viala M, Gerard H, Nguyen K, Richard P, Ader F, Pruny J-F, Donal E, Eicher J-C, Huttin O, Selton-Suty C et al..  2021.  Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction Phenotype/Genotype of Noncompaction. JOURNAL OF CARDIAC FAILURE. 27:677-681.
Gallian P, de Lamballerie X, Salez N, Piorkowski G, Richard P, Paturel L, Djoudi R, Leparc-Goffart I, Tiberghien P, Chiaroni J et al..  2014.  Prospective detection of chikungunya virus in blood donors, Caribbean 2014 (vol 123, pg 3679, 2014). BLOOD. 124:1695-1696.
Bordet C, Brice S, Maupain C, Gandjbakhch E, Isidor B, Palmyre A, Moerman A, Toutain A, Akloul L, Brehin A-C et al..  2020.  Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study. JOURNAL OF CLINICAL MEDICINE. 9:1365.
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Richard P, Ader F, Roux M, Donal E, Eicher J-C, Aoutil N, Huttin O, Selton-Suty C, Coisne D, Jondeau G et al..  2019.  Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. CLINICAL GENETICS. 95:356-367.
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Nguyen K, Roche S, Donal E, Odent S, Eicher J-C, Faivre L, Millat G, Salgado D, Desvignes J-P, Lavoute C et al..  2019.  Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy Experience of a Multicentric Study of 200 French Patients. CIRCULATION-GENOMIC AND PRECISION MEDICINE. 12:e002500.
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Gallian P, Cabie A, Richard P, Paturel L, Charrel RN, Pastorino B, Leparc-Goffart I, Tiberghien P, de Lamballerie X.  2017.  Zika virus in asymptomatic blood donors in Martinique. BLOOD. 129:263-266.