• 1334 Citations
  • 17 h-Index
1986 …2019
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Fingerprint Dive into the research topics where Maria Grazia Alessandrì is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Creatine Medicine & Life Sciences
Corpus Striatum Medicine & Life Sciences
Dopamine Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Brain Medicine & Life Sciences
Amikacin Medicine & Life Sciences
Gentamicins Medicine & Life Sciences
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Medicine & Life Sciences

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Research Output 1986 2019

  • 1334 Citations
  • 17 h-Index
  • 50 Article

Brain mitochondrial proteome alteration driven by creatine deficiency suggests novel therapeutic venues for creatine deficiency syndromes

Giusti, L., Molinaro, A., Alessandrì, M. G., Boldrini, C., Ciregia, F., Lacerenza, S., Ronci, M., Urbani, A., Cioni, G., Mazzoni, M. R., Pizzorusso, T., Lucacchini, A. & Baroncelli, L., Jun 15 2019, In : Neuroscience. 409, p. 276-289 14 p.

Research output: Contribution to journalArticle

Creatine
Proteome
Brain
Energy Metabolism
Therapeutics

A Nervous System-Specific Model of Creatine Transporter Deficiency Recapitulates the Cognitive Endophenotype of the Disease: a Longitudinal Study

Molinaro, A., Alessandrì, M. G., Putignano, E., Leuzzi, V., Cioni, G., Baroncelli, L. & Pizzorusso, T., Nov 15 2018, (Accepted/In press) In : Scientific Reports. 9, 1, 1 p.

Research output: Contribution to journalArticle

Endophenotypes
Creatine
Nervous System
Longitudinal Studies
Phenotype
4 Citations (Scopus)

Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review

Mari, F., Berti, B., Romano, A., Baldacci, J., Rizzi, R., Grazia Alessandrì, M., Tessa, A., Procopio, E., Rubegni, A., Lourenḉo, C. M., Simonati, A., Guerrini, R. & Santorelli, F. M., May 1 2018, In : Neurogenetics. 19, 2, p. 123-130 8 p.

Research output: Contribution to journalArticle

Neuroimaging
Dysarthria
Mutation
Dystonia
Hydrolases

Four years follow up of ACY1 deficient patient and pedigree study

Alessandrì, M. G., Milone, R., Casalini, C., Nesti, C., Cioni, G. & Battini, R., Aug 1 2018, In : Brain and Development. 40, 7, p. 570-575 6 p.

Research output: Contribution to journalArticle

Pedigree
Language Development Disorders
Inborn Errors Metabolism
Intellectual Disability
Psychiatry
Creatine
Magnetic Resonance Spectroscopy
Therapeutics
Arginine:Glycine Amidinotransferase Deficiency
Kidney Calculi