Page last updated: 2024-11-08

serine and Migraine with Aura

serine has been researched along with Migraine with Aura in 6 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Migraine with Aura: A subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)

Research Excerpts

ExcerptRelevanceReference
"Familial hemiplegic migraine is an episodic neurological disorder characterized by transient sensory and motor symptoms and signs."1.56Astrocyte deletion of α2-Na/K ATPase triggers episodic motor paralysis in mice via a metabolic pathway. ( Bice, AR; Bonni, A; Brier, LM; Bumstead, JR; Chen, X; Crowley, JR; Culver, JP; Dikranian, K; Haigis, MC; Ippolito, JE; Oldenborg, A; Papouin, T; Rensing, NR; Ringel, AE; Shin, H; Smith, SE; Wong, M; Zhao, G, 2020)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Smith, SE1
Chen, X1
Brier, LM1
Bumstead, JR1
Rensing, NR1
Ringel, AE1
Shin, H1
Oldenborg, A1
Crowley, JR1
Bice, AR1
Dikranian, K1
Ippolito, JE1
Haigis, MC1
Papouin, T1
Zhao, G1
Wong, M1
Culver, JP1
Bonni, A1
Inagaki, A1
Frank, CA1
Usachev, YM1
Benveniste, M1
Lee, A1
Cestèle, S1
Labate, A1
Rusconi, R1
Tarantino, P1
Mumoli, L1
Franceschetti, S1
Annesi, G1
Mantegazza, M1
Gambardella, A1
Tottene, A1
Pivotto, F1
Fellin, T1
Cesetti, T1
van den Maagdenberg, AM1
Pietrobon, D1
Gargus, JJ1
Tournay, A1
Chan, YC1
Burgunder, JM1
Wilder-Smith, E1
Chew, SE1
Lam-Mok-Sing, KM1
Sharma, V1
Ong, BK1

Reviews

1 review available for serine and Migraine with Aura

ArticleYear
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
    Epilepsia, 2013, Volume: 54, Issue:5

    Topics: Adolescent; Adult; Cell Line, Transformed; Computer Simulation; DNA Mutational Analysis; Electric St

2013

Other Studies

5 other studies available for serine and Migraine with Aura

ArticleYear
Astrocyte deletion of α2-Na/K ATPase triggers episodic motor paralysis in mice via a metabolic pathway.
    Nature communications, 2020, 12-02, Volume: 11, Issue:1

    Topics: Animals; Astrocytes; Ataxia; Brain; Disease Models, Animal; Electroencephalography; Female; Function

2020
Pharmacological correction of gating defects in the voltage-gated Ca(v)2.1 Ca²⁺ channel due to a familial hemiplegic migraine mutation.
    Neuron, 2014, Jan-08, Volume: 81, Issue:1

    Topics: Animals; Animals, Genetically Modified; Biophysical Phenomena; Biophysics; Calcium; Calcium Channels

2014
Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.
    The Journal of biological chemistry, 2005, May-06, Volume: 280, Issue:18

    Topics: Brain Edema; Calcium Channels, N-Type; Cell Line, Tumor; Craniocerebral Trauma; Humans; Leucine; Mig

2005
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
    Pediatric neurology, 2007, Volume: 37, Issue:6

    Topics: Adult; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Humans; Male; Migraine with

2007
Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2008, Volume: 15, Issue:8

    Topics: Adolescent; Adult; Calcium Channels; Child; DNA Mutational Analysis; Electroencephalography; Family

2008