Results
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Hyaluronectin is produced by oligodendrocytes and Schwann cells in vitro. [electronic resource] by
- Courel, M N
- Marret, S
- Girard, N
- Chauzy, C
- Olivier, A
- Bertrand, P
- Delpech, A
- Laquerriere, A
- Asou, H
- Delpech, B
Producer: 19980508
In:
Journal of neurocytology vol. 27
Availability: No items available.
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69.
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Valosin-containing protein gene mutations: clinical and neuropathologic features. [electronic resource] by
- Guyant-Maréchal, L
- Laquerrière, A
- Duyckaerts, C
- Dumanchin, C
- Bou, J
- Dugny, F
- Le Ber, I
- Frébourg, T
- Hannequin, D
- Campion, D
Producer: 20060913
In:
Neurology vol. 67
Availability: No items available.
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70.
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Molecular characteristics of multifocal brain histiocytic sarcoma. [electronic resource] by
- Marguet, F
- Piton, N
- Adle-Biassette, H
- Renaud, F
- Bohers, E
- Boyer, T
- Zarea, A
- Derrey, S
- Sabourin, J C
- Laquerrière, A
Producer: 20200819
In:
Neuropathology and applied neurobiology vol. 45
Availability: No items available.
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71.
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Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. [electronic resource] by
- Martinaud, O
- Laquerrière, A
- Guyant-Maréchal, L
- Ahtoy, P
- Vera, P
- Sergeant, N
- Camuzat, A
- Bourgeois, P
- Hauw, J J
- Campion, D
- Hannequin, D
Producer: 20051027
In:
Acta neuropathologica vol. 110
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72.
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Paradoxical inhibitory effect of serotonin on cortisol production from adrenocortical lesions causing Cushing's syndrome. [electronic resource] by
- Louiset, E
- Cartier, D
- Contesse, V
- Duparc, C
- Lihrmann, I
- Young, J
- Bertherat, J
- Reznik, Y
- Kuhn, J M
- Laquerrière, A
- Vaudry, H
- Lefebvre, Herve
Producer: 20050610
In:
Endocrine research vol. 30
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74.
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In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation. [electronic resource] by
- Sauvestre, F
- Moutton, S
- Badens, C
- Broussin, B
- Carles, D
- Houcinat, N
- Lacoste, C
- Marguet, F
- Pecheux, C
- Villard, L
- Pelluard, F
- Laquerrière, A
- André, G
Producer: 20190123
In:
Neuropathology and applied neurobiology vol. 43
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75.
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Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families. [electronic resource] by
- Bouchet, C
- Vuillaumier-Barrot, S
- Gonzales, M
- Boukari, S
- Bizec, C Le
- Fallet, C
- Delezoide, A-L
- Moirot, H
- Laquerriere, A
- Encha-Razavi, F
- Durand, G
- Seta, N
Producer: 20071206
In:
Molecular genetics and metabolism vol. 90
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76.
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Signaling switch of the urotensin II vasosactive peptide GPCR: prototypic chemotaxic mechanism in glioma. [electronic resource] by
- Lecointre, C
- Desrues, L
- Joubert, J E
- Perzo, N
- Guichet, P-O
- Le Joncour, V
- Brulé, C
- Chabbert, M
- Leduc, R
- Prézeau, L
- Laquerrière, A
- Proust, F
- Gandolfo, P
- Morin, F
- Castel, H
Producer: 20151215
In:
Oncogene vol. 34
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77.
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Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. [electronic resource] by
- Bevilacqua, J A
- Monnier, N
- Bitoun, M
- Eymard, B
- Ferreiro, A
- Monges, S
- Lubieniecki, F
- Taratuto, A L
- Laquerrière, A
- Claeys, K G
- Marty, I
- Fardeau, M
- Guicheney, P
- Lunardi, J
- Romero, N B
Producer: 20110620
In:
Neuropathology and applied neurobiology vol. 37
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78.
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Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease. [electronic resource] by
- Haïk, S
- Brandel, J P
- Sazdovitch, V
- Delasnerie-Lauprêtre, N
- Peoc'h, K
- Laplanche, J L
- Privat, N
- Duyckaerts, C
- Kemeny, J L
- Kopp, N
- Laquerrière, A
- Mohr, M
- Deslys, J P
- Dormont, D
- Hauw, J J
Producer: 20001222
In:
Neurology vol. 55
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79.
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Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): report of 16 fetal cases. [electronic resource] by
- Bessières-Grattagliano, B
- Foliguet, B
- Devisme, L
- Loeuillet, L
- Marcorelles, P
- Bonnière, M
- Laquerrière, A
- Fallet-Bianco, C
- Martinovic, J
- Zrelli, S
- Leticee, N
- Cayol, V
- Etchevers, H C
- Vekemans, M
- Attie-Bitach, T
- Encha-Razavi, F
Producer: 20100201
In:
European journal of medical genetics vol. 52
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80.
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Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease. [electronic resource] by
- Béhin, A
- Acquaviva-Bourdain, C
- Souvannanorath, S
- Streichenberger, N
- Attarian, S
- Bassez, G
- Brivet, M
- Fouilhoux, A
- Labarre-Villa, A
- Laquerrière, A
- Pérard, L
- Kaminsky, P
- Pouget, J
- Rigal, O
- Vanhulle, C
- Eymard, B
- Vianey-Saban, C
- Laforêt, P
Producer: 20170123
In:
Revue neurologique vol. 172
Availability: No items available.
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