Zobrazeno 1 - 10
of 68
pro vyhledávání: '"S H, Appel"'
Autor:
R G, Miller, D H, Moore, D A, Forshew, J S, Katz, R J, Barohn, M, Valan, M B, Bromberg, K L, Goslin, M C, Graves, L F, McCluskey, A L, McVey, T, Mozaffar, J M, Florence, A, Pestronk, M, Ross, E P, Simpson, S H, Appel, Lauren, Elman
Publikováno v:
Neurology. 77:973-979
Objective: To use a historical placebo control design to determine whether lithium carbonate slows progression of amyotrophic lateral sclerosis (ALS). Methods: A phase II trial was conducted at 10 sites in the Western ALS Study Group using similar do
Autor:
A, Jawaid, M, Poon, A M, Strutt, L K, Rice, E J, McDowell, A R, Salamone, S U, Qureshi, E, Simpson, S H, Appel, M K, York, P E, Schulz
Publikováno v:
European journal of neurology. 18(4)
The presence of the apolipoprotein E (ApoE) 4 genotype is associated with an earlier age of onset for Alzheimer's disease (AD) and several other neurodegenerative disorders. The objective of this study was to investigate the effect of ApoE genotypes
Autor:
A, Jawaid, A R, Salamone, A M, Strutt, S B, Murthy, M, Wheaton, E J, McDowell, E, Simpson, S H, Appel, M K, York, P E, Schulz
Publikováno v:
European journal of neurology. 17(5)
Several metabolic derangements associated with diabetes mellitus type 2 (DM) have been associated with a better outcome in amyotrophic lateral sclerosis (ALS), including hyperlipidemia and obesity. Here, we tested the hypothesis that DM would have a
Autor:
R G, Smith, S H, Appel
Publikováno v:
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases. 1
Publikováno v:
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases. 1
Publikováno v:
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases. 2
Motor neuron dysfunction and loss in amyotrophic lateral sclerosis (ALS) have been attributed to several different mechanisms, including increased intracellular calcium, glutamate excitotoxicity, oxidative stress and free radical damage, mitochondria
Publikováno v:
Journal of neuroscience research. 60(1)
Experimental studies have suggested that increased calcium and inappropriate calcium handling by motoneurons might have a significant role in motoneuron degeneration. To further define the involvement of calcium in motoneuron loss we used the oxalate
Publikováno v:
Journal of neurochemistry. 73(5)
Mutation in the Nurr1 gene, a member of the nuclear receptor superfamily, causes selective agenesis of dopaminergic neurons in the midbrain of null mice. Homozygous Nurr1 knockout mice (Nurr1-/-) die 1 day after birth, but heterozygous mice (Nurr1 +/
Publikováno v:
Journal of neuroscience research. 56(6)
Heme oxygenase-1 (HO-1) is a stress protein induced in response to a variety of oxidative challenges. After treatment of the hybrid septal cells SN 56 with beta-amyloid peptide (beta-AP1-40) or hydrogen peroxide (H2O2), we detected high levels of rea
Publikováno v:
Journal of neuroscience research. 53(5)
To determine whether specific antibodies are present in PD, we used an enzyme-linked immunosorbant assay (ELISA) that identifies increased immunoglobulin (IgG) levels towards a synthetic substrate prepared by incubating ovalbumin with dopamine and co