同: GAMT

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1. 先天性代謝異常：個々の障害の発見 inborn errors of metabolism identifying the specific disorder
2. 先天性代謝異常：代謝性救急疾患 inborn errors of metabolism metabolic emergencies
3. 新生児における筋緊張低下を引き起こす末梢神経および筋肉の障害に関する概要 overview of peripheral nerve and muscle disorders causing hypotonia in the newborn

English Journal

The role of L-arginine/L-homoarginine/nitric oxide pathway for aortic distensibility and intima-media thickness in stroke patients.

Haghikia A1,2, Yanchev GR3, Kayacelebi AA3, Hanff E3, Bledau N1, Widera C1,4, Sonnenschein K1, Haghikia A5, Weissenborn K6, Bauersachs J1, Bavendiek U1, Tsikas D7.
Amino acids.Amino Acids.2017 Mar 11. doi: 10.1007/s00726-017-2409-2. [Epub ahead of print]
PMID 28285332

Guanidinoacetate Methyltransferase Activity in Lymphocytes, for a Fast Diagnosis.

Berends LM1, Struys EA1, Roos B1, Holwerda U1, Jansen EE1, Salomons GS1, Wamelink MM2.
JIMD reports.JIMD Rep.2017 Feb 21. doi: 10.1007/8904_2017_4. [Epub ahead of print]
PMID 28220408

Creatine Enhances Mitochondrial-Mediated Oligodendrocyte Survival After Demyelinating Injury.

Chamberlain KA1,2, Chapey KS1, Nanescu SE1, Huang JK3,2.
The Journal of neuroscience : the official journal of the Society for Neuroscience.J Neurosci.2017 Feb 8;37(6):1479-1492. doi: 10.1523/JNEUROSCI.1941-16.2016. Epub 2017 Jan 9.
PMID 28069926

Japanese Journal

Cytochemical and cytological properties of perineuronal oligodendrocytes in the mouse cortex

Takasaki Chihiro,Yamasaki Miwako,Uchigashima Motokazu,Konno Kohtarou,Yanagawa Yuchio,Watanabe Masahiko
European Journal of Neuroscience 32(8), 1326-1336, 2010-10
… Instead, almost all perineuronal oligodendrocytes expressed glia-specific or glia-enriched metabolic enzymes, i.e. the creatine synthetic enzyme S-adenosylmethionine:guanidinoacetate N-methyltransferase and L-serine biosynthetic enzyme 3-phosphoglycerate dehydrogenase. …
NAID 120003370661

Guanidinoacetate methyltransferase deficiency (GAMT)

GORDON Neil
Brain & development 32(2), 79-81, 2010-02-01
NAID 10027212575

クレアチンの網膜移行性と生合成 (第26回生体膜と薬物の相互作用シンポジウム講演要旨集)

細谷健一,中島寿久,立川正憲 [他]
薬学雑誌 124(-), 85-88, 2004-11-25
NAID 40006893518

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Guanidinoacetate methyltransferase deficiency - Genetics ...

Guanidinoacetate methyltransferase deficiency is an inherited disorder that primarily affects the brain and muscles. Without early treatment, people with this disorder have neurological problems that are usually severe.

Guanidinoacetate methyltransferase (GAMT) deficiency

Guanidinoacetate methyltransferase deficiency and epilepsy. Epilepsia (submitted). 6. Applegarth DA, Hardwick DF, Ross PM. Creatinine excretion in children and usefulness of creatinine equivalents in amino acid 134. 7. a new8. ...