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microform
Mémoires sur la maniere d'élever les vers à soie [microform] : et sur la culture du mûrier blanc, lus à la Société royale d'agriculture de Lyon / par M. T**** de la même société.
Author / Creator:Thomé, C.-J., -approximately 1780.
Publisher:Paris : Chez Vallat-la-Chapelle, 1767.
Date:1767.
Call Numbers:T/RAV/FM4/2
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Microglia-neuron interaction at nodes of Ranvier depends on neuronal activity through potassium release and contributes to remyelination
Author / Creator:Ronzano, R. ; Roux, T. ; Thetiot, M. ; Aigrot, M. S. ; Richard, L. ; Lejeune, F. X. ; Mazuir, E. ; Vallat, J. M. ; Lubetzki, C. ; Desmazières, A.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2021-09, Vol.12 (1), p.5219-18, Article 5219
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Cell culture evidence for neuronal degeneration in amyotrophic lateral sclerosis being linked to glutamate AMPA/kainate receptors
Author / Creator:Couratier, P. ; Sindou, P. ; Hugon, J. ; Couratier, P. ; Hugon, J. ; Vallat, J.-M. ; Dumas, M.
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 1993-01, Vol.341 (8840), p.265-268
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Identification of seven novel mutations in the GAN gene
Author / Creator:Bomont, P. ; Ioos, C. ; Yalcinkaya, C. ; Korinthenberg, R. ; Vallat, JM ; Assami, S. ; Munnich, A. ; Chabrol, B. ; Kurlemann, G. ; Tazir, M. ; Koenig, M.
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2003-04, Vol.21 (4), p.446-446
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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)
Author / Creator:Carrié, A ; Piccolo, F ; Leturcq, F ; de Toma, C ; Azibi, K ; Beldjord, C ; Vallat, J M ; Merlini, L ; Voit, T ; Sewry, C ; Urtizberea, J A ; Romero, N ; Tomé, F M ; Fardeau, M ; Sunada, Y ; Campbell, K P ; Kaplan, J C ; Jeanpierre, M
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 1997-06, Vol.34 (6), p.470-475
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Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations
Author / Creator:De Sandre-Giovannoli, A ; Chaouch, M ; Boccaccio, I ; Bernard, R ; Delague, V ; Grid, D ; Vallat, J M ; Lévy, N ; Mégarbané, A
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2003-07, Vol.40 (7), p.e87-87
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A randomised double blind trial versus placebo does not confirm the benefit of α-interferon in polyneuropathy associated with monoclonal IgM
Author / Creator:MARIETTE, XAVIER ; BROUET, JEAN-CLAUDE ; CHEVRET, SYLVIE ; LEGER, JEAN-MARC ; CLAVELOU, PIERRE ; POUGET, JEAN ; VALLAT, JEAN-MARC ; VIAL, CHRISTOPHE
Publisher:England: BMJ Group
Journal title:Journal of neurology, neurosurgery and psychiatry, 2000-08, Vol.69 (2), p.279-280
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Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study
Author / Creator:De Armas, R. ; Sindou, P. ; Gelot, A. ; Routon, M. C. ; Ponsot, G. ; Vallat, J. M.
Publisher:Germany: Springer Nature B.V
Journal title:Acta neuropathologica, 2004-10, Vol.108 (4), p.341-344
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Expression of myelin proteins in the adult heterozygous Trembler mouse
Author / Creator:Vallat, J. M. ; Sindou, P. ; Garbay, B. ; Preux, P. M. ; Anani, T. ; Richard, L. ; Diot, M.
Publisher:Berlin: Springer
Journal title:Acta neuropathologica, 1999-09, Vol.98 (3), p.281-287
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Dominantly Inherited Peripheral Neuropathies
Author / Creator:VALLAT, JEAN-MICHEL
Publisher:Hagerstown, MD: Oxford University Press (OUP)
Journal title:Journal of Neuropathology & Experimental Neurology, 2003-07, Vol.62 (7), p.699-714
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Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families
Author / Creator:Rouger, H ; LeGuern, E ; Birouk, N ; Gouider, R ; Tardieu, S ; Plassart, E ; Gugenheim, M ; Vallat, J-M ; Louboutin, J-P ; Bouche, P ; Agid, Y ; Brice, A
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 1997, Vol.10 (6), p.443-450
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Autosomal-Recessive Charcot-Marie-Tooth Diseases
Author / Creator:Vallat, Jean-Michel ; Tazir, Meriem ; Magdelaine, Corinne ; Sturtz, Franck ; Grid, Djamel
Publisher:Hagerstown, MD: Lippincott Williams & Wilkins
Journal title:Journal of neuropathology and experimental neurology, 2005-05, Vol.64 (5), p.363-370
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Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis
Author / Creator:Hahn, Angelika F. ; Ainsworth, Peter J. ; Bolton, Charles F. ; Bilbao, Juan M. ; Vallat, Jean-Michel
Publisher:Berlin: Springer
Journal title:Acta neuropathologica, 2001-02, Vol.101 (2), p.129-139
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Recommendations on diagnostic strategies for chronic inflammatory demyelinating polyradiculoneuropathy
Author / Creator:French CIDP Study Group
Publisher:England: The Fellowship of Postgraduate Medicine
Journal title:Journal of neurology, neurosurgery and psychiatry, 2008-02, Vol.84 (993), p.378
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Autosomal recessive forms of Charcot-Marie-Tooth disease
Author / Creator:Vallat, J. M. ; Grid, D. ; Magdelaine, C. ; Sturtz, F. ; Tazir, M.
Publisher:United States: Springer Nature B.V
Journal title:Current neurology and neuroscience reports, 2004-09, Vol.4 (5), p.413-419
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IgG Neuropathy: An Immunoelectron Microscopic Study
Author / Creator:Vallat, Jean-Michel ; Magy, Laurent ; Sindou, Philippe ; Magdelaine, Corinne ; Cros, Didier
Publisher:Hagerstown, MD: Lippincott Williams & Wilkins
Journal title:Journal of neuropathology and experimental neurology, 2005-05, Vol.64 (5), p.386-390
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Low prevalence of HTLV-1 antibodies in the serum of patients with tropical spastic paraplegia from the Ivory Coast
Author / Creator:Hugon, J ; Vallat, J M ; Dumas, M ; Verdier, M ; Denis, F ; Akani, F ; Boa, Y F ; Giordano, C
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 1990-03, Vol.53 (3), p.269-269
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Epidemics and outbreaks of peripheral nervous system disorders: II. Toxic and nutritional causes
Publisher:Heidelberg: Springer Nature B.V
Journal title:Journal of neurology, 2021-03, Vol.268 (3), p.892-902
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Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes
Publisher:Heidelberg: Springer Nature B.V
Journal title:Journal of neurology, 2021-03, Vol.268 (3), p.879-890
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Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families
Author / Creator:Rouger, H ; LeGuern, E ; Birouk, N ; Gouider, R ; Tardieu, S ; Plassart, E ; Gugenheim, M ; Vallat, J M ; Louboutin, J P ; Bouche, P ; Agid, Y ; Brice, A
Publisher:United States
Journal title:Human mutation, 1997, Vol.10 (6), p.443
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Mémoires sur la maniere d'élever les vers à soie [microform] : et sur la culture du mûrier blanc, lus à la Société royale d'agriculture de Lyon / par M. T**** de la même société.

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Microglia-neuron interaction at nodes of Ranvier depends on neuronal activity through potassium release and contributes to remyelination

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Cell culture evidence for neuronal degeneration in amyotrophic lateral sclerosis being linked to glutamate AMPA/kainate receptors

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Identification of seven novel mutations in the GAN gene

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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

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Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

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A randomised double blind trial versus placebo does not confirm the benefit of α-interferon in polyneuropathy associated with monoclonal IgM

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Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study

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Expression of myelin proteins in the adult heterozygous Trembler mouse

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Dominantly Inherited Peripheral Neuropathies

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Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families

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Autosomal-Recessive Charcot-Marie-Tooth Diseases

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Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis

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Recommendations on diagnostic strategies for chronic inflammatory demyelinating polyradiculoneuropathy

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Autosomal recessive forms of Charcot-Marie-Tooth disease

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IgG Neuropathy: An Immunoelectron Microscopic Study

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Low prevalence of HTLV-1 antibodies in the serum of patients with tropical spastic paraplegia from the Ivory Coast

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Epidemics and outbreaks of peripheral nervous system disorders: II. Toxic and nutritional causes

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Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes

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Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families

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