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Amyotrophic Lateral Sclerosis 4, Juvenile
Known as:
ALS4
, NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES
National Institutes of Health
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Related topics
Related topics
4 relations
Broader (1)
Amyotrophic Lateral Sclerosis
Autosomal dominant inheritance
Distal amyotrophy
Upper motor neuron signs
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Structural modulation induced by MIIIA metals in Ba3MQ4X (M = Al, Ga, In; Q = S, Se; X = Cl, Br): an experimental and computational analysis.
Abudukadi Tudi
,
Shujuan Han
,
Ailijiang Abudurusuli
,
Haohai Yu
,
Zhihua Yang
,
S. Pan
Dalton Transactions
2019
Corpus ID: 199469319
Four new chalcohalides Ba3AlQ4X (Q = S, Se; X = Cl, Br) have been discovered by a conventional high-temperature method. All of…
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2017
2017
[A amyotrophic lateral sclerosis (ALS) 4 family misdiagnosed as hereditary spastic paraplegia-a case report].
T. Taniguchi
,
Y. Hokezu
,
+4 authors
H. Takashima
Rinshō shinkeigaku Clinical neurology
2017
Corpus ID: 43229801
We report a 44 years old man with slowly progressive muscular atrophy of the extremities for over 30 years. He experienced…
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2016
2016
Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci
Fang He
,
Julie M. Jones
,
+6 authors
Peter K. Todd
Neurology: Genetics
2016
Corpus ID: 1813300
Objective: To determine whether GGGGCC (G4C2) repeat expansions at loci other than C9orf72 serve as common causes of amyotrophic…
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2014
2014
Association of genetic variants in senataxin and Alzheimer's disease in a Chinese Han population in Taiwan.
Che-Piao Shen
,
Wei-Yong Lin
,
+6 authors
F. Tsai
Chinese journal of physiology
2014
Corpus ID: 37109342
Development of Alzheimer's disease (AD) is characterized by progressive neuronal death and a decline in learning and memory…
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2012
2012
Inflammatory radiculoneuropathy in an ALS4 patient with a novel SETX mutation
T. Saiga
,
T. Tateishi
,
+8 authors
J. Kira
Journal of Neurology Neurosurgery & Psychiatry
2012
Corpus ID: 39345420
Amyotrophic lateral sclerosis 4 (ALS4), a rare form of autosomal dominant juvenile-onset ALS characterised by slow progression…
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Review
2011
Review
2011
[Gene mutations in familial amyotrophic lateral sclerosis].
M. Oda
,
Y. Izumi
,
R. Kaji
Brain and nerve = Shinkei kenkyu no shinpo
2011
Corpus ID: 43276554
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscle weakness that reflects…
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2005
2005
[Comparison of ALS gene mRNA between sessile and planktonic Candida albicans of oral cavities].
Q. Qi
,
T. Hu
,
Chun-hua Fu
,
Xue-dong Zhou
Hua xi kou qiang yi xue za zhi = Huaxi kouqiang…
2005
Corpus ID: 7312846
OBJECTIVE To observe the different mRNA levels of Candida albicans ALS gene family between planktonic and biofilm-grown cells…
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2003
2003
CMT with pyramidal features. Charcot-Marie-Tooth.
S. Vucic
,
M. Kennerson
,
D. Zhu
,
E. Miedema
,
C. Kok
,
G. Nicholson
Neurology
2003
Corpus ID: 28896537
To determine whether Charcot-Marie-Tooth (CMT) with pyramidal features is genetically distinct from other dominantly inherited…
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2002
2002
Arabidopsis Mutants with lncreased Sensitivity to Aluminum'
Paul
,
B.
,
Larsen
,
C. Tai
,
L. Kochian
,
S. Howell
2002
Corpus ID: 32961641
AI-sensitive (als) mutants of Arabidopsis were isolated and characterized with the aim of defining mechanisms of AI toxicity and…
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2000
2000
Cloning and Functional Analysis of ALS Family Genes from Candida albicans.
Xi Chen
,
J. Chen
Sheng wu hua xue yu sheng wu wu li xue bao Acta…
2000
Corpus ID: 37329241
With a 0.5 kb probe of CX2, distribution of CX2 tandem repeats was studied in different C.albicans strains. Results suggest that…
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