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Author/Creator David, V

1. 2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?. Issue 12 (23rd September 2008)

Authors:
Jaillard, S; Dubourg, C; Gérard-Blanluet, M; Delahaye, A; Pasquier, L; Dupont, C; Henry, C; Tabet, A-C; Lucas, J; Aboura, A; David, V; Benzacken, B; Odent, S; Pipiras, E
Journal:
Journal of medical genetics
Issue:
Volume 46:Issue 12(2009)
Page Start:
847
Record Type:
Journal Article
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4. First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations. Issue 1 (5th January 2005)

Authors:
Pasquier, L; Dubourg, C; Gonzales, M; Lazaro, L; David, V; Odent, S; Encha-Razavi, F
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 1(2005)
Page Start:
e4
Record Type:
Journal Article
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6. MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Issue 1 (9th July 2009)

Authors:
Le Meur, N; Holder-Espinasse, M; Jaillard, S; Goldenberg, A; Joriot, S; Amati-Bonneau, P; Guichet, A; Barth, M; Charollais, A; Journel, H; Auvin, S; Boucher, C; Kerckaert, J-P; David, V; Manouvrier-Hanu, S; Saugier-Veber, P; Frébourg, T; Dubourg, C; Andrieux, J; Bonneau, D
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 1(2010)
Page Start:
22
Record Type:
Journal Article
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7. Meta-analysis of individual-patient data from EVAR-1, DREAM, OVER and ACE trials comparing outcomes of endovascular or open repair for abdominal aortic aneurysm over 5 years. Issue 3 (3rd February 2017)

Authors:
Powell, J T; Sweeting, M J; Ulug, P; Blankensteijn, J D; Lederle, F A; Becquemin, J-P; Greenhalgh, R M; Greenhalgh, R M; Beard, J D; Buxton, M J; Brown, L C; Harris, P L; Powell, J T; Rose, J D G; Russell, I T; Sculpher, M J; Thompson, S G; Lilford, R J; Bell, P R F; Greenhalgh, R M
Journal:
British journal of surgery
Issue:
Volume 104:Issue 3(2017)
Page Start:
166
Record Type:
Journal Article
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8. O-218 Single-cell RNA sequencing reveals that Ashermańs syndrome is caused by chronic inflammation that induces differential molecular and cellular cartography in the human endometrium. (30th June 2022)

Authors:
Santamaria Costa, X; Beatriz, R; Nanda, K; Estefania, F; Raul, P; David, V; Luciano, R; Sergi, Q; Juan José, T; Ramon, A; Julio, H; Inmaculada, M; Felip, V; Carlos, S
Journal:
Human reproduction
Issue:
Volume 37(2022)Supplement 1
Page Start:
Record Type:
Journal Article
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9. One year prospective survey of azole resistance in Aspergillus fumigatus at a French cystic fibrosis reference centre: prevalence and mechanisms of resistance. (30th April 2019)

Authors:
Lavergne, R -A; Morio, F; Danner-Boucher, I; Horeau-Langlard, D; David, V; Hagen, F; Meis, J F; Le Pape, P
Journal:
Journal of antimicrobial chemotherapy
Issue:
Volume 74:Number 7(2019)
Page Start:
1884
Record Type:
Journal Article
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10. The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading. Issue 1 (16th January 2004)

Authors:
Livesey, K J; Wimhurst, V L C; Carter, K; Worwood, M; Cadet, E; Rochette, J; Roberts, A G; Pointon, J J; Merryweather-Clarke, A T; Bassett, M L; Jouanolle, A-M; Mosser, A; David, V; Poulton, J; Robson, K J H
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 1(2004)
Page Start:
6
Record Type:
Journal Article
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