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 NCBI Filters

Results by year

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

Year Number of Results
1970 1
1974 2
1975 7
1976 4
1977 4
1978 8
1979 5
1980 7
1981 6
1982 6
1983 9
1984 12
1985 7
1986 15
1987 4
1988 4
1989 16
1990 23
1991 27
1992 25
1993 25
1994 42
1995 55
1996 34
1997 50
1998 63
1999 63
2000 66
2001 86
2002 65
2003 63
2004 75
2005 122
2006 86
2007 115
2008 119
2009 131
2010 120
2011 118
2012 117
2013 160
2014 135
2015 114
2016 98
2017 103
2018 87
2019 99
2020 78
2021 60
2022 40
2023 34
2024 10

Text availability

Article attribute

Article type

Publication date

Search Results

2,512 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal neuron morphology"
Page 1
Huntington's disease: from molecular pathogenesis to clinical treatment.
Ross CA, Tabrizi SJ. Ross CA, et al. Lancet Neurol. 2011 Jan;10(1):83-98. doi: 10.1016/S1474-4422(10)70245-3. Lancet Neurol. 2011. PMID: 21163446 Review.
Huntington's disease is a progressive, fatal, neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin gene, which encodes an abnormally long polyglutamine repeat in the huntingtin protein. Huntington's disease has served as a model for the study of ot …
Huntington's disease is a progressive, fatal, neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin gene, which enco …
Epigenetics in epilepsy.
Kobow K, Blümcke I. Kobow K, et al. Neurosci Lett. 2018 Feb 22;667:40-46. doi: 10.1016/j.neulet.2017.01.012. Epub 2017 Jan 19. Neurosci Lett. 2018. PMID: 28111355 Review.
However, progression of seizure activity as well as the development of drug-resistance remains difficult to predict, irrespective of the underlying epileptogenic condition, i.e., traumatic brain injury, developmental brain lesions, brain tumors or genetic inheritance. ...I …
However, progression of seizure activity as well as the development of drug-resistance remains difficult to predict, irrespective of …
The dark matter of the brain.
Ovsepian SV. Ovsepian SV. Brain Struct Funct. 2019 Apr;224(3):973-983. doi: 10.1007/s00429-019-01835-7. Epub 2019 Jan 18. Brain Struct Funct. 2019. PMID: 30659350 Review.
Herein, I review emerging data suggesting massive redundancy of nerve cells in mammalian nervous system, maintained in inhibited state at high energetic costs. Acquired in the course of evolution, these collections of dormant neurons and circuits evade routine funct …
Herein, I review emerging data suggesting massive redundancy of nerve cells in mammalian nervous system, maintained in inhibited state at hi …
Neuroprotective Effect of Antioxidants in the Brain.
Lee KH, Cha M, Lee BH. Lee KH, et al. Int J Mol Sci. 2020 Sep 28;21(19):7152. doi: 10.3390/ijms21197152. Int J Mol Sci. 2020. PMID: 32998277 Free PMC article. Review.
Overabundance and abnormal levels of ROS and/or overload of metals are regulated by cellular defense mechanisms, intracellular signaling, and physiological functions of antioxidants in the brain. ...Herein, we present a general analysis and overview of various antioxidants …
Overabundance and abnormal levels of ROS and/or overload of metals are regulated by cellular defense mechanisms, intracellular signal …
Familial dysautonomia.
Axelrod FB. Axelrod FB. Muscle Nerve. 2004 Mar;29(3):352-63. doi: 10.1002/mus.10499. Muscle Nerve. 2004. PMID: 14981733 Review.
The genetic error probably affects development, as well as maintenance, of neurons because there is neuropathological and clinical progression. Pathological alterations consist of decreased unmyelinated and small-fiber neurons. Clinical features reflect widespread i …
The genetic error probably affects development, as well as maintenance, of neurons because there is neuropathological and clinical pr …
Sensory neuron diseases.
Sghirlanzoni A, Pareyson D, Lauria G. Sghirlanzoni A, et al. Lancet Neurol. 2005 Jun;4(6):349-61. doi: 10.1016/S1474-4422(05)70096-X. Lancet Neurol. 2005. PMID: 15907739 Review.
Sensory neuron diseases (SND) are a distinct subgroup of peripheral-nervous-system diseases, first acknowledged in 1948. ...SND are commonly idiopathic but can be genetic diseases; the latter tend to involve subtypes of sensory neurons and are associated with certai …
Sensory neuron diseases (SND) are a distinct subgroup of peripheral-nervous-system diseases, first acknowledged in 1948. ...SND are c …
Spinal muscular atrophies.
Viollet L, Melki J. Viollet L, et al. Handb Clin Neurol. 2013;113:1395-411. doi: 10.1016/B978-0-444-59565-2.00010-1. Handb Clin Neurol. 2013. PMID: 23622363 Review.
Spinal muscular atrophies (SMA) are genetic disorders characterized by degeneration of lower motor neurons. The most frequent form is caused by mutations of the survival motor neuron 1 gene (SMN1). ...SMN plays a key role in metabolism of RNA. However, the link betw …
Spinal muscular atrophies (SMA) are genetic disorders characterized by degeneration of lower motor neurons. The most frequent form is …
Superior segmental optic nerve hypoplasia: A review.
Wu JH, Lin CW, Liu CH, Weinreb RN, Welsbie DS. Wu JH, et al. Surv Ophthalmol. 2022 Sep-Oct;67(5):1467-1475. doi: 10.1016/j.survophthal.2022.02.008. Epub 2022 Feb 18. Surv Ophthalmol. 2022. PMID: 35189184 Review.
Superior segmental optic nerve hypoplasia (SSONH) is a congenital condition characterized by developmental abnormalities of the superior optic disc and an underappreciated differential diagnosis for glaucoma. ...Optical coherence tomography can be helpful in disting …
Superior segmental optic nerve hypoplasia (SSONH) is a congenital condition characterized by developmental abnormalities of th …
Otopathologic Abnormalities in CHARGE Syndrome.
da Costa Monsanto R, Knoll RM, de Oliveira Penido N, Song G, Santos F, Paparella MM, Cureoglu S. da Costa Monsanto R, et al. Otolaryngol Head Neck Surg. 2022 Feb;166(2):363-372. doi: 10.1177/01945998211008911. Epub 2021 Apr 20. Otolaryngol Head Neck Surg. 2022. PMID: 33874787
RESULTS: Our study included 12 TBs from 6 donors. We found a high prevalence of abnormalities affecting the ears. The most frequent findings were stapes malformation (100%), aberrant course of the facial nerve (100%) with narrow facial recess (50%), sclerotic and hy …
RESULTS: Our study included 12 TBs from 6 donors. We found a high prevalence of abnormalities affecting the ears. The most frequent f …
Giant axonal neuropathy.
Hentati F, Hentati E, Amouri R. Hentati F, et al. Handb Clin Neurol. 2013;115:933-8. doi: 10.1016/B978-0-444-52902-2.00052-7. Handb Clin Neurol. 2013. PMID: 23931822 Review.
The prognosis is usually severe with death occurring during the second or third decade; nevertheless a less severe course is reported in some patients. ...Giant axons are also found in the central nervous system associated with Rosenthal fibers and a variable degree …
The prognosis is usually severe with death occurring during the second or third decade; nevertheless a less severe course is r …
2,512 results