about
Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humansArginine and glycine stimulate creatine synthesis in creatine transporter 1-deficient lymphoblasts.Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene.Similar increases in extracellular lactic acid in the limbic system during epileptic and/or olfactory stimulation.Brief and repeated noise exposure produces different morphological and biochemical effects in noradrenaline and adrenaline cells of adrenal medulla.beta,beta'-Iminodipropionitrile-induced persistent dyskinetic syndrome in mice is transiently modified by MPTP.Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease.Reversible brain creatine deficiency in two sisters with normal blood creatine levelA Nervous System-Specific Model of Creatine Transporter Deficiency Recapitulates the Cognitive Endophenotype of the Disease: a Longitudinal StudyStriatal dopamine metabolism in monoamine oxidase B-deficient mice: a brain dialysis studyThe influence of dosage, age, and comedication on steady state plasma lamotrigine concentrations in epileptic children: a prospective study with preliminary assessment of correlations with clinical responseModulation of dihydroxyphenylacetaldehyde extracellular levels in vivo in the rat striatum after different kinds of pharmacological treatment
P50
Q24536125-D5512CE5-B4C0-4F1D-B8BC-E5854BE6558AQ40015525-E56B3588-60B6-4043-8FA6-A3E7A155C605Q43458982-86810DDE-9FEF-4890-A947-6992F2C8997FQ43503566-A20D18EA-C1B9-43C3-8603-6A406C805CACQ43918090-F703062A-9AE7-4F19-AB22-C9B8FDF04C75Q48321187-56B2F7B0-A245-45EC-87A6-F0EEB1D818E2Q51916119-251EDD58-0561-488F-9FC4-43B5E8894A8BQ59461785-58AB84F7-B9E6-4D4E-A9B1-9990CFE65730Q60912216-5C45A5E8-F2BF-4E9B-A599-126682530B70Q73229629-E0B3CBFD-5764-4600-9F46-62E97A0357FEQ73453674-C31829F2-7644-4F00-B740-9C7B1C17CECCQ73634982-0DB06E1E-6DCD-46E3-9151-41468920B877
P50
description
researcher ORCID ID = 0000-0003-3467-8648
@en
wetenschapper
@nl
name
Maria Grazia Alessandrì
@ast
Maria Grazia Alessandrì
@en
Maria Grazia Alessandrì
@es
Maria Grazia Alessandrì
@nl
type
label
Maria Grazia Alessandrì
@ast
Maria Grazia Alessandrì
@en
Maria Grazia Alessandrì
@es
Maria Grazia Alessandrì
@nl
prefLabel
Maria Grazia Alessandrì
@ast
Maria Grazia Alessandrì
@en
Maria Grazia Alessandrì
@es
Maria Grazia Alessandrì
@nl
P1153
7005233799
P31
P496
0000-0003-3467-8648