A. Laquérrière - Concepedia

Author

A. Laquérrière

Also Known As

A Laquerriere, A Laquerrière, A. LAQUERRIERE, A. Laquerriere, A. Laquerrière, A. Laquerrière, A. Laquerriére, A. Laquérrière, A. Laquerriere, A. Laquerrière

129

Publications

2.7K

Citations

H-Index

127

Concepts

All Affiliations

Université de Rouen Normandie Inserm Centre Hospitalier Universitaire de Rouen Hôpital Charles-Nicolle Centre National de la Recherche Scientifique

About

A. Laquérrière is an author at Université de Rouen Normandie specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	28	1.2K
2	Health Sciences	6	6	139
3	Social Sciences	4	4	204
4	Engineering	1	1	56
5	Anatomy	1	1	20

A. Laquérrière

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Phenotype associated with APP duplication in five families L. Cabrejo, Lucie Guyant‐Maréchal, A. Laquérrière, Brain GeneticsAlzheimer's DiseaseGenotype-phenotype AssociationApp LocusNeurology	2006	331
Valosin-containing protein gene mutations Lucie Guyant‐Maréchal, A. Laquérrière, Charles Duyckaerts, Neurology	2006	147
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization Jorge A. Bevilacqua, Nicole Monnier, Marc Bitoun, Neuropathology and Applied Neurobiology	2010	116
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease Isabelle Le Ber, A. Camuzat, E. Berger, Neurology	2009	95
Ontogeny of somatostatin receptors in the rat brain: Biochemical and autoradiographic study Bruno J. Gonzalez, Philippe Leroux, Corinne Bodénant, Neuroscience NeurophysiologyNeuroanatomyMedicinePhysiologySomatostatin Receptors	1989	84
Experimental evaluation of bilayered human collagen as a dural substitute A. Laquérrière, Jin Yun, Jérôme Tiollier, Journal of neurosurgery	1993	72
Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt–Jakob disease J.P. Brandel, V. Sazdovitch, N. Delasnerie–Lauprêtre, Neurology	2000	70
Molecular heterogeneity in fetal forms of type II lissencephaly C Bouchet, M. Gonzalés, Sandrine Vuillaumier‐Barrot, Human Mutation	2007	63
INTRAFAMILIAL DIVERSITY OF PHENOTYPE ASSOCIATED WITH <i>APP</i> DUPLICATION I. Guyant-Marechal, Éric Berger, A. Laquérrière, Neurology	2008	62
Intraadrenal Adrenocorticotropin Production in a Case of Bilateral Macronodular Adrenal Hyperplasia Causing Cushing’s Syndrome Hervé Lefèbvre, Céline Duparc, Nicolas Chartrel, The Journal of Clinical Endocrinology & Metabolism Adrenal GlandChromaffin CellsPituitary GlandIntraadrenal Adrenocorticotropin ProductionGrowth Hormone	2003	61

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