neuronopathy

Common Name(s)

neuronopathy

Description for this condition is not yet available.
 

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "neuronopathy" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "neuronopathy" returned 37 free, full-text research articles on human participants. First 3 results:

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
 

Author(s): A Reghan Foley, Manoj P Menezes, Amelie Pandraud, Michael A Gonzalez, Ahmad Al-Odaib, Alexander J Abrams, Kumiko Sugano, Atsushi Yonezawa, Adnan Y Manzur, Joshua Burns, Imelda Hughes, B Gary McCullagh, Heinz Jungbluth, Ming J Lim, Jean-Pierre Lin, Andre Megarbane, J Andoni Urtizberea, Ayaz H Shah, Jayne Antony, Richard Webster, Alexander Broomfield, Joanne Ng, Ann A Mathew, James J O'Byrne, Eva Forman, Mariacristina Scoto, Manish Prasad, Katherine O'Brien, Simon Olpin, Marcus Oppenheim, Iain Hargreaves, John M Land, Min X Wang, Kevin Carpenter, Rita Horvath, Volker Straub, Monkol Lek, Wendy Gold, Michael O Farrell, Sebastian Brandner, Rahul Phadke, Kazuo Matsubara, Michael L McGarvey, Steven S Scherer, Peter S Baxter, Mary D King, Peter Clayton, Shamima Rahman, Mary M Reilly, Robert A Ouvrier, John Christodoulou, Stephan Züchner, Francesco Muntoni, Henry Houlden

Journal: Brain. 2014 Jan;137(Pt 1):44-56.

 

Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of disorders. A particularly severe subgroup first described in 1894, and subsequently called Brown-Vialetto-Van Laere syndrome, is characterized by progressive pontobulbar palsy, sensorineural ...

Last Updated: 15 Jan 2014

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Pattern-recognition approach to neuropathy and neuronopathy.
 

Author(s): Richard J Barohn, Anthony A Amato

Journal: Neurol Clin. 2013 May;31(2):343-61.

 

Neuropathic disorders encompass those that affect the neuron's cell body or neuronopathies, those affecting the peripheral process, or peripheral neuropathies. The peripheral neuropathies can be broadly subdivided into the myelinopathies and axonopathies, conditions which can be hereditary ...

Last Updated: 6 May 2013

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Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2.
 

Author(s): Sini Penttilä, Manu Jokela, Peter Hackman, Anna Maija Saukkonen, Jari Toivanen, Bjarne Udd

Journal: Eur. J. Hum. Genet.. 2012 Nov;20(11):1193-6.

 

Spinal muscular atrophies (SMAs) are hereditary disorders characterized by degeneration of lower motor neurons. Different SMA types are clinically and genetically heterogeneous and many of them show significant phenotypic overlap. We recently described the clinical phenotype of a ...

Last Updated: 18 Oct 2012

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "neuronopathy" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.