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Page 1
Juvenile segmental muscular atrophy.
Neufeld MY, Inzelberg R, Nisipeanu P, Korczyn AD. Neufeld MY, et al. Funct Neurol. 1991 Oct-Dec;6(4):405-10. Funct Neurol. 1991. PMID: 1810840 Review.
Unilateral upper limb atrophy is a rare entity that has been described mainly in Asia. Isolated cases were reported in the Western countries but never in the Middle East. ...The clinical and EMG features were consistent with a localized anterior horn cell lesion in the cer …
Unilateral upper limb atrophy is a rare entity that has been described mainly in Asia. Isolated cases were reported in the Western co …
[Advances in research of cervical spondylotic amyotrophy].
Ye X, Sun Y. Ye X, et al. Zhonghua Wai Ke Za Zhi. 2019 Sep 1;57(9):717-720. doi: 10.3760/cma.j.issn.0529-5815.2019.09.015. Zhonghua Wai Ke Za Zhi. 2019. PMID: 31474064 Review. Chinese.
Cervical spondylotic amyotrophy (CSA) has attracted more and more attention in recent years, according to early studies, it is based on cervical degeneration, and mainly characterized by segmental, asymmetric and stable muscular atrophy of upper extremities, …
Cervical spondylotic amyotrophy (CSA) has attracted more and more attention in recent years, according to early studies, it is based on cerv …
AAV gene delivery to the spinal cord: serotypes, methods, candidate diseases, and clinical trials.
Hardcastle N, Boulis NM, Federici T. Hardcastle N, et al. Expert Opin Biol Ther. 2018 Mar;18(3):293-307. doi: 10.1080/14712598.2018.1416089. Epub 2017 Dec 18. Expert Opin Biol Ther. 2018. PMID: 29249183 Review.
Phase 1 clinical trials using AAV gene therapy for pediatric disorders - spinal muscular atrophy (SMA) and giant axonal neuropathy (GAN) - are now underway. AREAS COVERED: This review addresses the latest progress in the field of AAV gene delivery to the s
Phase 1 clinical trials using AAV gene therapy for pediatric disorders - spinal muscular atrophy (SMA) and giant axonal …
The future of motor neuron disease: the challenge is in the genes.
Veldink JH, Van den Berg LH, Wokke JH. Veldink JH, et al. J Neurol. 2004 Apr;251(4):491-500. doi: 10.1007/s00415-004-0322-6. J Neurol. 2004. PMID: 15083302 Review.
Adult-onset motor neuron disease (MND) includes sporadic and familial forms of amyotrophic lateral sclerosis (ALS), lower motor neuron disease including progressive and segmental spinal muscular atrophy (LMND) and primary lateral sclerosis (PLS). ...
Adult-onset motor neuron disease (MND) includes sporadic and familial forms of amyotrophic lateral sclerosis (ALS), lower motor neuron disea …
Anatomic features of the paramedian muscle-splitting approaches to the lumbar spine.
Hoh DJ, Wang MY, Ritland SL. Hoh DJ, et al. Neurosurgery. 2010 Mar;66(3 Suppl Operative):13-24; discussion 24-5. doi: 10.1227/01.NEU.0000350866.25760.33. Neurosurgery. 2010. PMID: 20124927 Review.
BACKGROUND: Intermuscular approaches can expose the lumbar spine and minimize muscular trauma and injury. The segmental anatomy of the posterior lumbar musculature allows surgical access through separation of muscle groups and fascicles and provides one to develop i …
BACKGROUND: Intermuscular approaches can expose the lumbar spine and minimize muscular trauma and injury. The segmental anatom …
Transient receptor potential genes and human inherited disease.
Everett KV. Everett KV. Adv Exp Med Biol. 2011;704:1011-32. doi: 10.1007/978-94-007-0265-3_52. Adv Exp Med Biol. 2011. PMID: 21290338 Review.
This chapter aims to summarise those associations and focuses on the following diseases: focal segmental glomerulosclerosis; polycystic kidney disease; brachyolmia; spondylometaphyseal dysplasia; metatropic dysplasia; hereditary motor and sensory neuropathy; spinal
This chapter aims to summarise those associations and focuses on the following diseases: focal segmental glomerulosclerosis; polycyst …
Sporadic lower motor neuron disease with adult onset: classification of subtypes.
van den Berg-Vos RM, Visser J, Franssen H, de Visser M, de Jong JM, Kalmijn S, Wokke JH, van den Berg LH. van den Berg-Vos RM, et al. Brain. 2003 May;126(Pt 5):1036-47. doi: 10.1093/brain/awg117. Brain. 2003. PMID: 12690044 Review.
Group 3 could be subdivided into patients with weakness in predominantly the distal (group 3a) or the proximal (group 3b) muscle groups, both with disease progression to adjacent spinal cord segments. Distinctive features of group 1 were an older age at onset, more severe …
Group 3 could be subdivided into patients with weakness in predominantly the distal (group 3a) or the proximal (group 3b) muscle groups, bot …
[Physical medicine in the diagnosis and treatment of functional disorders of the spinal column].
Németh E. Németh E. Med Pregl. 1999 Jun-Aug;52(6-8):233-6. Med Pregl. 1999. PMID: 10518378 Review. Croatian.
Functional disorders are caused by direct or indirect injury (muscular spasm), inflammation, sudden movements etc. Functional disorders in regard to decreased joint volume are also called segmental or peripheral joint dysfunction, somatic dysfunction and function bl …
Functional disorders are caused by direct or indirect injury (muscular spasm), inflammation, sudden movements etc. Functional disorde …
Brachial amyotrophic diplegia in a patient with human immunodeficiency virus infection: widening the spectrum of motor neuron diseases occurring with the human immunodeficiency virus.
Berger JR, Espinosa PS, Kissel J. Berger JR, et al. Arch Neurol. 2005 May;62(5):817-23. doi: 10.1001/archneur.62.5.817. Arch Neurol. 2005. PMID: 15883271 Review.
Although amyotrophic lateral sclerosis and progressive spinal muscular atrophy have been recognized to occur in association with human immunodeficiency virus infection, to our knowledge, brachial amyotrophic diplegia, a form of segmental motor neuron d …
Although amyotrophic lateral sclerosis and progressive spinal muscular atrophy have been recognized to occur in associa …
11 results