Page last updated: 2024-11-08

alanine and Nervous System Diseases

alanine has been researched along with Nervous System Diseases in 11 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Nervous System Diseases: Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle.

Research Excerpts

ExcerptRelevanceReference
"Although remdesivir (GS-5734) has recently demonstrated clinical benefits against the pandemic outbreak of coronavirus disease 2019 (COVID-19), neuropsychological adverse reactions (ADRs) remain to be examined in real-world settings."1.62Neuropsychological adverse drug reactions of Remdesivir: analysis using VigiBase, the WHO global database of individual case safety reports. ( Dragioti, E; Jacob, L; Jung, SY; Kang, HC; Kim, JH; Kim, MS; Kostev, K; Koyanagi, A; Lascu, A; Lee, S; Lee, SW; Salem, JE; Shin, JI; Smith, L; Tizaoui, K; Yang, JW; Yon, DK, 2021)
"Primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm and painful hands, and/or feet."1.33SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. ( Drenth, JP; Guillet, G; Jansen, JB; Kirby, RL; Taieb, A; te Morsche, RH, 2005)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19902 (18.18)18.7374
1990's2 (18.18)18.2507
2000's2 (18.18)29.6817
2010's2 (18.18)24.3611
2020's3 (27.27)2.80

Authors

AuthorsStudies
Lee, S1
Yang, JW1
Jung, SY1
Kim, MS1
Yon, DK1
Lee, SW1
Kang, HC1
Dragioti, E1
Tizaoui, K1
Jacob, L1
Koyanagi, A1
Salem, JE1
Kostev, K1
Lascu, A1
Shin, JI1
Kim, JH1
Smith, L1
Lee, CJ1
Qiu, TA1
Sweedler, JV1
Wasan, H1
Singh, D1
Kh, R1
McAninch, EA1
Jo, S1
Preite, NZ1
Farkas, E1
Mohácsik, P1
Fekete, C1
Egri, P1
Gereben, B1
Li, Y1
Deng, Y1
Patti, ME1
Zevenbergen, C1
Peeters, RP1
Mash, DC1
Bianco, AC1
Miki, T1
Zwingman, TA1
Wakamori, M1
Lutz, CM1
Cook, SA1
Hosford, DA1
Herrup, K1
Fletcher, CF1
Mori, Y1
Frankel, WN1
Letts, VA1
Yamamoto-Watanabe, Y1
Watanabe, M1
Jackson, M1
Akimoto, H1
Sugimoto, K1
Yasujima, M1
Wakasaya, Y1
Matsubara, E1
Kawarabayashi, T1
Harigaya, Y1
Lyndon, AR1
Shoji, M1
DEKABAN, A1
FIELD, JB1
STEVENS, H1
Drenth, JP1
te Morsche, RH1
Guillet, G1
Taieb, A1
Kirby, RL1
Jansen, JB1
Jones, LA1
Skare, JC1
Cohen, AS1
Harding, JA1
Milunsky, A1
Skinner, M1
Koeppen, AH1
Wallace, MR1
Benson, MD1
Altland, K1
Dunn, HG1
Perry, TL1
Dolman, CL1

Reviews

2 reviews available for alanine and Nervous System Diseases

ArticleYear
d-Alanine: Distribution, origin, physiological relevance, and implications in disease.
    Biochimica et biophysica acta. Proteins and proteomics, 2020, Volume: 1868, Issue:11

    Topics: Alanine; Animals; Diabetes Mellitus; Humans; Kidney Diseases; Liver Cirrhosis; Mental Disorders; Neo

2020
Safinamide in neurological disorders and beyond: Evidence from preclinical and clinical studies.
    Brain research bulletin, 2021, Volume: 168

    Topics: Alanine; Animals; Anticonvulsants; Antiparkinson Agents; Benzylamines; Humans; Monoamine Oxidase; Ne

2021

Other Studies

9 other studies available for alanine and Nervous System Diseases

ArticleYear
Neuropsychological adverse drug reactions of Remdesivir: analysis using VigiBase, the WHO global database of individual case safety reports.
    European review for medical and pharmacological sciences, 2021, Volume: 25, Issue:23

    Topics: Adenosine Monophosphate; Adverse Drug Reaction Reporting Systems; Alanine; Bayes Theorem; Cohort Stu

2021
Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
    The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3

    Topics: Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Cerebral Cortex; Gene Frequency; HEK2

2015
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
    Neuroscience, 2008, Jul-31, Volume: 155, Issue:1

    Topics: Alanine; Animals; Animals, Newborn; Calbindins; Calcium Channels, N-Type; Cells, Cultured; Cysteine;

2008
Quantification of cystatin C in cerebrospinal fluid from various neurological disorders and correlation with G73A polymorphism in CST3.
    Brain research, 2010, Nov-18, Volume: 1361

    Topics: Aged; Aged, 80 and over; Alanine; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Biomarkers; Case

2010
Familial idiopathic hypoglycemia: neurological complications.
    Archives of neurology, 1962, Volume: 7

    Topics: Alanine; Galactose; Glucagon; Glucose Tolerance Test; Humans; Hypoglycemia; Leucine; Nervous System

1962
SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.
    The Journal of investigative dermatology, 2005, Volume: 124, Issue:6

    Topics: Adult; Alanine; Conserved Sequence; Cysteine; Erythromelalgia; Female; Genes, Dominant; Heterozygote

2005
Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent.
    Clinical genetics, 1992, Volume: 41, Issue:2

    Topics: Adult; Alanine; Amyloid; Amyloidosis; Base Sequence; DNA; Female; Germany; Humans; Male; Molecular S

1992
Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
    Muscle & nerve, 1990, Volume: 13, Issue:11

    Topics: Adult; Aged; Alanine; Amyloidosis; Blotting, Southern; DNA; Female; Humans; Isoelectric Focusing; Ma

1990
A syndrome resembling Friedreich's ataxia with relapsing polyneuropathy and hyperalaninemia.
    Neurology, 1968, Volume: 18, Issue:3

    Topics: Alanine; Brain; Child; Child, Preschool; Chronic Disease; Demyelinating Diseases; Diagnosis, Differe

1968