X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
spg7 (35) 35
index medicus (34) 34
humans (33) 33
hereditary spastic paraplegia (27) 27
metalloendopeptidases - genetics (27) 27
atpases associated with diverse cellular activities (26) 26
clinical neurology (23) 23
spastic paraplegia, hereditary - genetics (20) 20
male (19) 19
mutation (18) 18
neurosciences (18) 18
paraplegin (18) 18
female (17) 17
middle aged (17) 17
phenotype (15) 15
spastic paraplegia (15) 15
adult (14) 14
ataxia (13) 13
spg7 mutations (13) 13
mitochondria (12) 12
m-aaa protease (11) 11
aged (10) 10
genetic aspects (10) 10
mutation - genetics (10) 10
genetics & heredity (9) 9
genotype (9) 9
neurology (9) 9
paralysis, spastic (9) 9
paraplegia - genetics (9) 9
pedigree (9) 9
adolescent (8) 8
analysis (8) 8
disease (8) 8
paraplegia (8) 8
abridged index medicus (7) 7
gene (7) 7
genetic research (7) 7
paralysis (7) 7
cerebellar ataxia (6) 6
child (6) 6
cohort studies (6) 6
nervous system diseases (6) 6
paraparesis (6) 6
spastic paraplegia, hereditary - diagnosis (6) 6
spastic paraplegia, hereditary - physiopathology (6) 6
young adult (6) 6
age of onset (5) 5
article (5) 5
child, preschool (5) 5
gene mutations (5) 5
genes (5) 5
genetic testing (5) 5
magnetic resonance imaging (5) 5
mutations (5) 5
neurodegenerative diseases (5) 5
research (5) 5
spastic ataxia (5) 5
spastic paraplegia 7 (5) 5
adenosine triphosphatases - genetics (4) 4
afg3l2 (4) 4
base sequence (4) 4
biochemistry & molecular biology (4) 4
cell biology (4) 4
dna mutational analysis (4) 4
dna sequencing (4) 4
electron transport (4) 4
genetic association studies (4) 4
genomics (4) 4
heat shock proteins (4) 4
homozygote (4) 4
medicine & public health (4) 4
molecular sequence data (4) 4
neuroradiology (4) 4
nucleotide sequencing (4) 4
spasticity (4) 4
spg7 gene (4) 4
spinocerebellar ataxia (4) 4
aged, 80 and over (3) 3
amyotrophic-lateral-sclerosis (3) 3
ataxia - genetics (3) 3
autosomal-dominant (3) 3
brain (3) 3
brain - pathology (3) 3
cell death (3) 3
cerebellar ataxia - genetics (3) 3
dna mutational analysis - methods (3) 3
exome - genetics (3) 3
family (3) 3
genetics (3) 3
identification (3) 3
impairment (3) 3
maps (3) 3
mechanisms (3) 3
membrane (3) 3
metalloendopeptidases - metabolism (3) 3
nervous system (3) 3
next generation sequencing (3) 3
optic nerve diseases - genetics (3) 3
paraplegia - diagnosis (3) 3
patients (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain, ISSN 0006-8950, 2012, Volume 135, Issue 10, pp. 2980 - 2993
Journal Article
Journal of Neurogenetics, ISSN 0167-7063, 01/2019, Volume 33, Issue 1, pp. 27 - 32
Hereditary spastic paraplegias (HSPs) are a diverse group of genetic conditions with variable severity and onset age. From a neurogenetic clinic, we identified... 
paraplegin | SPAST | SPG7 | primary lateral sclerosis | hereditary spastic paraplegia | late-onset | SPG7 MUTATIONS | GENETICS & HEREDITY | PARAPLEGIA | SQSTM1 | NEUROSCIENCES
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2016, Volume 98, Issue 6, pp. 1067 - 1076
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2019, Volume 26, Issue 1, pp. 80 - 86
Journal Article
BBA - Molecular Cell Research, ISSN 0167-4889, 10/2016, Volume 1863, Issue 10, pp. 2515 - 2530
Journal Article
European Neurology, ISSN 0014-3022, 06/2019, Volume 81, Issue 1-2, pp. 87 - 93
Background: Primary lateral sclerosis (PLS) is considered a rare variant of motor neuron disease (MND) characterized by selective upper motor neuron... 
Clinical Neurology: Research Article | Spastic paraplegia 7 | Primary lateral sclerosis | Mutation | PROTEIN | FORM | ALSIN | SPG7 | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 364, pp. 116 - 121
Journal Article
Frontiers in Physiology, 11/2015, Volume 6
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 08/2018, Volume 31, Issue 4, pp. 462 - 471
Purpose of review This review aims at updating the clinical and genetic aspects of hereditary spastic paraplegias (HSPs) and hereditary cerebellar ataxias... 
Spastic paraplegia | Spastic ataxia | Cerebellar ataxia | INFANTILE ONSET | cerebellar ataxia | spastic ataxia | PHENOTYPE | NEUROSCIENCES | CLINICAL NEUROLOGY | spastic paraplegia | NETWORK ANALYSIS | MUTATIONS CAUSE | SPG7 MUTATIONS | RECESSIVE ATAXIA | EARLY-ONSET | PERIPHERAL NEUROPATHY | DOMINANT CEREBELLAR-ATAXIA
Journal Article
Brain, ISSN 0006-8950, 5/2014, Volume 137, Issue 5, pp. 1323 - 1336
Journal Article