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Lorenzoni 2012 Lorenzoni PJ, Scola RH, Kay CSK, Werneck LC. Congenital myasthenic syndrome: a brief review. Congenital myasthenic syndrome and minicore-like myopathy with DOK7 mutation. Myasthenia gravis and atracurium: a case report. Presynaptic congenital myasthenic syndrome due to quantal release deficiency. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome.

Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction. Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE. Myasthenia gravis and Schmidt syndrome. Acetylcholinesterase inhibitor treatment for myasthenia gravis. Cochrane Database of Systematic Reviews 2014, Issue 10. Chapter 33: Geoepidemiology of myasthenia gravis. Pseudoephedrine- and ephedrine-containing medicines: 2012 review of actions to manage the risk of misuse.

Phenotypical spectrum of congenital myasthenic syndrome caused by mutations in COLQ gene. Mihaylova 2008b /ephedrine-sulfate-vs-ephedrine-hcl/ Ephedrine withdrawal, Muller J, Vilchez J, Salih M, Kabiraj M, D’Amico A, et al. Clinical and molecular genetic findings ephedrine withdrawal 22 COLQ-mutant Ephedrine withdrawal patients.

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes. Refinement ephedrine withdrawal the clinical phenotype in MUSK-related congenital myasthenic syndromes. Block of the endplate acetylcholine receptor channel by the sympathomimetic doses ephedrine for sale online try ephedrine withdrawal, pseudoephedrine and albuterol.

A multi-center, single-blind, randomized study comparing thymectomy to no ephedrine withdrawal in non-thymomatous myasthenia gravis (MG) patients receiving prednisone. Nelson 1935 Nelson Ephedrine withdrawal. Myasthenia gravis in a child: observations on the effect ephedrine withdrawal ephedrine visit web page. CrossRefNicole ephedrine withdrawal Nicole /ephedrine-appetite-suppressant/, Chaouch A, Torbergsen T, Bauche S, De Bruyckere E, Fontenille M-J, et al.

Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy. Clinical features of the DOK7 neuromuscular junction synaptopathy.

The congenital myasthenic syndromes. Clinical features in a series of fast channel congenital myasthenia syndrome. Transient neonatal myasthenia gravis. Multiple sclerosis associated with defects in neuromuscular transmission. Mary Broadfoot Walker (1888-1974): a historic discovery in myasthenia gravis. Anti-LRP4 autoantibodies in AChR- and MuSK-antibody negative myasthenia gravis.

Myasthenia gravis in mothers and their newborns. Chapter 13: Including non-randomized studies. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014. Robb 2010 Robb SA, Muntoni F, Simonds AK. Respiratory management of congenital myasthenic syndromes in childhood: Workshop 8th December 2009, UCL Institute of Neurology, London, UK. Beneficial effects of albuterol in congenital myasthenic syndrome with epsilon-subunit mutations.

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Six Things Every Chiropractor Should Know About OpioidsAn increase in addictions and deaths due to opioids has raised significant concern and media attention.

We offer this brief overview on this important public health problem for the practicing chiropractor. Why We Need to Fix the Mechanoreceptors (Part 2)The muscle spindle, a particular type of mechanoreceptor, is located deep within the muscle belly, encapsulated in fascia made up of intrafusal fibers, all within the extrafusal muscle fibers.

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