FERNANDO SCAGLIA's research topics

FERNANDO SCAGLIA

Concepts (745)

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Concepts are derived automatically from a person's publications.

The timeline below shows the dates (blue tick marks) of publications associated with FERNANDO SCAGLIA's top concepts. The average publication date for each concept is shown as a red circle, illustrating changes in the primary topics that FERNANDO SCAGLIA has written about over time.

Carnitine, 9 publications between 1998 and 2015, average publication date June 2007. Metabolism, Inborn Errors, 10 publications between 1999 and 2019, average publication date December 2008. Developmental Disabilities, 13 publications between 2000 and 2020, average publication date June 2009. Mitochondrial Encephalomyopathies, 7 publications between 2001 and 2023, average publication date February 2011. DNA, Mitochondrial, 25 publications between 2001 and 2022, average publication date August 2011. Mitochondrial Myopathies, 9 publications between 2002 and 2023, average publication date May 2012. Nitric Oxide, 7 publications between 2004 and 2017, average publication date March 2013. Citrulline, 7 publications between 2007 and 2023, average publication date July 2013. Mutation, 49 publications between 2002 and 2024, average publication date July 2013. Acidosis, Lactic, 5 publications between 2005 and 2023, average publication date December 2013. Arginine, 9 publications between 2004 and 2023, average publication date June 2014. MELAS Syndrome, 9 publications between 2006 and 2023, average publication date July 2014. Mitochondrial Diseases, 32 publications between 2003 and 2024, average publication date December 2014. Cardiomyopathies, 6 publications between 2004 and 2024, average publication date January 2015. Leigh Disease, 6 publications between 2005 and 2021, average publication date October 2015. Phenotype, 28 publications between 2004 and 2024, average publication date May 2016. Mitochondrial Proteins, 14 publications between 2008 and 2023, average publication date July 2016. Mitochondria, 21 publications between 2005 and 2024, average publication date August 2016. Congenital Disorders of Glycosylation, 6 publications between 2005 and 2024, average publication date April 2019. Brain Diseases, Metabolic, Inborn, 2 publications between 2019 and 2021, average publication date April 2020.

Carnitine
Metabolism, Inborn Errors
Developmental Disabilities
Mitochondrial Encephalomyopathies
DNA, Mitochondrial
Mitochondrial Myopathies
Nitric Oxide
Citrulline
Mutation
Acidosis, Lactic
Arginine
MELAS Syndrome
Mitochondrial Diseases
Cardiomyopathies
Leigh Disease
Phenotype
Mitochondrial Proteins
Mitochondria
Congenital Disorders of Glycosylation
Brain Diseases, Metabolic, Inborn

To see the data from this visualization as text, click here.

Name	Number of Publications	First Publication Year	Most Recent Publication Year	Average Publication Date
Carnitine	9	1998	2015	June 2007
Metabolism, Inborn Errors	10	1999	2019	December 2008
Developmental Disabilities	13	2000	2020	June 2009
Mitochondrial Encephalomyopathies	7	2001	2023	February 2011
DNA, Mitochondrial	25	2001	2022	August 2011
Mitochondrial Myopathies	9	2002	2023	May 2012
Nitric Oxide	7	2004	2017	March 2013
Citrulline	7	2007	2023	July 2013
Mutation	49	2002	2024	July 2013
Acidosis, Lactic	5	2005	2023	December 2013
Arginine	9	2004	2023	June 2014
MELAS Syndrome	9	2006	2023	July 2014
Mitochondrial Diseases	32	2003	2024	December 2014
Cardiomyopathies	6	2004	2024	January 2015
Leigh Disease	6	2005	2021	October 2015
Phenotype	28	2004	2024	May 2016
Mitochondrial Proteins	14	2008	2023	July 2016
Mitochondria	21	2005	2024	August 2016
Congenital Disorders of Glycosylation	6	2005	2024	April 2019
Brain Diseases, Metabolic, Inborn	2	2019	2021	April 2020

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