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Laumonnier, H.
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1

CA 15-Les adénomes hépatocellulaires mutes â-caténine : exp..:

Zucman-Rossi, J. ; Blanc, J.F. ; Cunha, A.Sq....
Gastroentérologie Clinique et Biologique.  30 (2006)  8-9 - p. 1056 , 2006
Link: https://doi.org/10.1016/..
 
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2

CO-29 Traitement par vertébroplastie des traumatismes rachi..:

Barreau ; Laumonnier, H. ; Menegon, P...
Journal of Neuroradiology.  32 (2005)  2 - p. 82 , 2005
Link: https://doi.org/10.1016/..
 
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3

Ptchd1 deficiency induces excitatory synaptic and cognitive..:

Ung, D C ; Iacono, G ; Méziane, H...
Molecular Psychiatry.  23 (2017)  5 - p. 1356-1367 , 2017
Link: https://doi.org/10.1038/..
 
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4

X-exome sequencing of 405 unresolved families identifies se..:

Hu, H ; Haas, S A ; Chelly, J...
Molecular Psychiatry.  21 (2015)  1 - p. 133-148 , 2015
Link: https://doi.org/10.1038/..
 
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5

Disruption of TCA Cycle and Glutamate Metabolism Identified..:

Veyrat-Durebex, Charlotte ; Corcia, Philippe ; Piver, Eric...
Molecular Neurobiology.  53 (2015)  10 - p. 6910-6924 , 2015
Link: https://doi.org/10.1007/..
 
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6

Phenotypic spectrum associated withPTCHD1deletions and trun..:

Chaudhry, A. ; Noor, A. ; Degagne, B....
Clinical Genetics.  88 (2014)  3 - p. 224-233 , 2014
Link: https://doi.org/10.1111/..
 
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7

C5a receptor signalling in dendritic cells controls the dev..:

Schmudde, I ; Ströver, H A ; Vollbrandt, T...
Mucosal Immunology.  6 (2013)  4 - p. 807-825 , 2013
Link: https://doi.org/10.1038/..
 
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8

Advances in Cellular Models to Explore the Pathophysiology ..:

Veyrat-Durebex, C. ; Corcia, P. ; Dangoumau, A....
Molecular Neurobiology.  49 (2013)  2 - p. 966-983 , 2013
Link: https://doi.org/10.1007/..
 
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9

Mutation screening of ASMT, the last enzyme of the melatoni..:

Pagan, Cecile ; Botros, Hany Goubran ; Poirier, Karine...
BMC Medical Genetics.  12 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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10

Postpartum subestrus in dairy cows: comparison of treatment..:

Mialot, J.P. ; Laumonnier, G. ; Ponsart, C....
Theriogenology.  52 (1999)  5 - p. 901-911 , 1999
Link: https://doi.org/10.1016/..
 
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11

PSMC3 proteasome subunit variants are associated with neuro..:

Ebstein, Frédéric ; Küry, Sébastien ; Most, Victoria...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506367/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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12

Rare germline heterozygous missense variants in BRCA1-assoc..:

Küry, Sébastien ; Ebstein, Frédéric ; Mollé, Alice...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8874225/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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13

Missense variants in DPYSL5 cause a neurodevelopmental diso..:

Jeanne, Médéric ; Demory, Hélène ; Moutal, Aubin...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2021.04.004.  , 2021
Link: https://hal.science/hal-..
 
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14

Missense variants in DPYSL5 cause a neurodevelopmental diso..:

Jeanne, Médéric ; Demory, Hélène ; Moutal, Aubin...
qt9t75z0zj.  , 2021
Link: https://escholarship.org..
 
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15

Missense variants in DPYSL5 cause a neurodevelopmental diso..:

Jeanne, Médéric ; Demory, Hélène ; Moutal, Aubin...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2021.04.004.  , 2021
Link: https://hal.archives-ouv..
 
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