Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 34
2010 318
2011 50
2013 1
2015 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

318 results

Results by year

Filters applied: . Clear all
Page 1
Motor neuron diversity in development and disease.
Kanning KC, Kaplan A, Henderson CE. Kanning KC, et al. Annu Rev Neurosci. 2010;33:409-40. doi: 10.1146/annurev.neuro.051508.135722. Annu Rev Neurosci. 2010. PMID: 20367447 Review.
Although often considered as a group, spinal motor neurons are highly diverse in terms of their morphology, connectivity, and functional properties and differ significantly in their response to disease. ...In multiple degenerative contexts including ALS, spinal m …
Although often considered as a group, spinal motor neurons are highly diverse in terms of their morphology, connectivity, and functio …
TRPV4-mediated channelopathies.
Verma P, Kumar A, Goswami C. Verma P, et al. Channels (Austin). 2010 Jul-Aug;4(4):319-28. doi: 10.4161/chan.4.4.12905. Epub 2010 Jul 6. Channels (Austin). 2010. PMID: 20676052 Free article. Review.
Recently it gained immense medical and clinical interest as several independent studies have demonstrated that mutations in the TRPV4 gene can results in genetic disorders like Brachyolmia, Charcot-Marie-Tooth disease type 2C, Spinal Muscular Atrophy and Here …
Recently it gained immense medical and clinical interest as several independent studies have demonstrated that mutations in the TRPV4 gene c …
Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model.
Hua Y, Sahashi K, Hung G, Rigo F, Passini MA, Bennett CF, Krainer AR. Hua Y, et al. Genes Dev. 2010 Aug 1;24(15):1634-44. doi: 10.1101/gad.1941310. Epub 2010 Jul 12. Genes Dev. 2010. PMID: 20624852 Free PMC article.
Increasing survival of motor neuron 2, centromeric (SMN2) exon 7 inclusion to express more full-length SMN protein in motor neurons is a promising approach to treat spinal muscular atrophy (SMA), a genetic neurodegenerative disease. Previously, we identified …
Increasing survival of motor neuron 2, centromeric (SMN2) exon 7 inclusion to express more full-length SMN protein in motor neurons is a pro …
Causes of camptocormia.
Finsterer J, Strobl W. Finsterer J, et al. Disabil Rehabil. 2011;33(17-18):1702-3. doi: 10.3109/09638288.2010.543750. Epub 2010 Dec 23. Disabil Rehabil. 2011. PMID: 21182366 Review.
Other causes include dystonia, multisystem atrophy, Alzheimer's disease, myopathy, motor neuron disease, myasthenia or chronic inflammatory demyelinating polyneuropathy. Rare causes include adverse reactions of drugs, disc herniation, arthritis, spinal trauma, paran …
Other causes include dystonia, multisystem atrophy, Alzheimer's disease, myopathy, motor neuron disease, myasthenia or chronic inflam …
[Catastrophic neuromuscular diseases].
Muñoz Blanco JL. Muñoz Blanco JL. Neurologia. 2010 Oct;25 Suppl 1:37-45. doi: 10.1016/S0213-4853(10)70049-9. Neurologia. 2010. PMID: 21129596 Free article. Review. Spanish.
This situation is more common in ventilated patients with associated muscular weakness, acute neuropathies or motor neuron disease, and 3) inappropriate medical intervention in patients with neuromuscular disease with a definitive diagnosis but longstanding disease (amyotr …
This situation is more common in ventilated patients with associated muscular weakness, acute neuropathies or motor neuron disease, a …
High throughput screening for SMA.
Titus S, Marugan J, Southall N, Inglese J, Austin C, Zheng W, Androphy E. Titus S, et al. 2009 May 18 [updated 2010 Sep 2]. In: Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010–. 2009 May 18 [updated 2010 Sep 2]. In: Probe Reports from the NIH Molecular Libraries Program [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2010–. PMID: 21433373 Free Books & Documents. Review.
Spinal muscular atrophy (SMA) is caused by insufficient levels of the survival motor neuron protein SMN. ...
Spinal muscular atrophy (SMA) is caused by insufficient levels of the survival motor neuron protein SMN. ...
Clinical features and molecular mechanisms of spinal and bulbar muscular atrophy (SBMA).
Katsuno M, Banno H, Suzuki K, Adachi H, Tanaka F, Sobue G. Katsuno M, et al. Adv Exp Med Biol. 2010;685:64-74. doi: 10.1007/978-1-4419-6448-9_6. Adv Exp Med Biol. 2010. PMID: 20687495 Review.
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset neurodegenerative disease characterized by slowly progressive muscle weakness and atrophy. ...Lower motor neurons in the anterior horn of the spinal cord and those in the brainstem moto …
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset neurodegenerative disease characterized by slowly progressi …
Perspectives and diagnostic considerations in spinal muscular atrophy.
Prior TW. Prior TW. Genet Med. 2010 Mar;12(3):145-52. doi: 10.1097/GIM.0b013e3181c5e713. Genet Med. 2010. PMID: 20057317 Free article. Review.
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease and the most common genetic cause of infant mortality. The disease results in motor neuron loss and skeletal muscle atrophy. Spinal muscular atrophy is cau …
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease and the most common genetic cause of infant …
Hirayama disease.
Tynan J, Frangou E, Voll C, Otani R, Harder S. Tynan J, et al. Can J Neurol Sci. 2010 Sep;37(5):703-5. doi: 10.1017/s0317167100010969. Can J Neurol Sci. 2010. PMID: 21059525 No abstract available.
Spinal muscular atrophy: mechanisms and therapeutic strategies.
Lorson CL, Rindt H, Shababi M. Lorson CL, et al. Hum Mol Genet. 2010 Apr 15;19(R1):R111-8. doi: 10.1093/hmg/ddq147. Epub 2010 Apr 13. Hum Mol Genet. 2010. PMID: 20392710 Free PMC article. Review.
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder and a leading genetic cause of infantile mortality. ...The clinical features of the disease are caused by specific degeneration of alpha-motor neurons in the spinal cord …
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder and a leading genetic cause of infan …
318 results