Literature DB >> 13009934

[Distribution of the cholinesterase activity at the level of the myoneural synapse].

R COUTEAUX, J TAXI.   

Abstract

Entities:  

Keywords:  CHOLINESTERASE; MYONEURAL JUNCTION

Mesh：

Substances：

Year:  1952        PMID： 13009934

Source DB:  PubMed          Journal:  C R Hebd Seances Acad Sci        ISSN： 0001-4036


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  4 in total

1.  [Regeneration of the subneural apparatus of motor end-plates].

Authors:  B CSILLIK; G SAVAY
Journal:  Acta Neuroveg (Wien)       Date:  1958

2.  Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.

Authors:  Stéphanie Bauché; Geoffroy Vellieux; Damien Sternberg; Marie-Joséphine Fontenille; Elodie De Bruyckere; Claire-Sophie Davoine; Guy Brochier; Julien Messéant; Lucie Wolf; Michel Fardeau; Emmanuelle Lacène; Norma Romero; Jeanine Koenig; Emmanuel Fournier; Daniel Hantaï; Nathalie Streichenberger; Veronique Manel; Arnaud Lacour; Aleksandra Nadaj-Pakleza; Sylvie Sukno; Françoise Bouhour; Pascal Laforêt; Bertrand Fontaine; Laure Strochlic; Bruno Eymard; Frédéric Chevessier; Tanya Stojkovic; Sophie Nicole
Journal:  J Neurol       Date:  2017-07-15       Impact factor: 4.849

3.  Localization of butyrylcholinesterase at the neuromuscular junction of normal and acetylcholinesterase knockout mice.

Authors:  Brigitte Blondet; Gilles Carpentier; Arnaud Ferry; Arnaud Chatonnet; José Courty
Journal:  J Histochem Cytochem       Date:  2010-08-30       Impact factor: 2.479

4.  New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.

Authors:  Stéphanie Bauché; Alain Sureau; Damien Sternberg; John Rendu; Céline Buon; Julien Messéant; Myriam Boëx; Denis Furling; Julien Fauré; Xénia Latypova; Antoinette Bernabe Gelot; Michèle Mayer; Pierre Mary; Sandra Whalen; Emmanuel Fournier; Isabelle Cloix; Ganaelle Remerand; Fanny Laffargue; Marie-Christine Nougues; Bertrand Fontaine; Bruno Eymard; Arnaud Isapof; Laure Strochlic
Journal:  Neurol Genet       Date:  2020-12-03
  4 in total

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