Gian Nicola Gallus - Concepedia

Author

Gian Nicola Gallus

University of Siena ORCID

Also Known As

G. N. Gallus, G.N. Gallus, GN Gallus, Gian Nicola Gallus, GianNicola Gallus, Guido Primiano

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

University of Siena University of Milano-Bicocca Azienda Ospedaliera Universitaria Senese German Center for Neurodegenerative Diseases University of Pisa

About

Gian Nicola Gallus is an author at University of Siena specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	254
2	Health Sciences	2	2	80
3	Natural Sciences	1	1	19
4	Genetic Medicine	1	1	20
5	Hepatology	1	1	56

Gian Nicola Gallus

Publications

669

Citations

H-Index

Page 1

	Year	Citations
A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis Andrea Mignarri, Gian Nicola Gallus, Maria Teresa Dotti, Journal of Inherited Metabolic Disease	2014	158
Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis Andrea Mignarri, Alessandro Magni, Marina Del Puppo, Journal of Inherited Metabolic Disease	2015	67
Two novel <i>HTRA1</i> mutations in a European CARASIL patient Silvia Bianchi, Chiara Di Palma, Gian Nicola Gallus, Neurology GeneticsImmunologyPathologyMolecular GeneticsVitamin K	2014	56
Heterozygous mutations of <i><scp>HTRA</scp>1</i> gene in patients with familial cerebral small vessel disease Ilaria Di Donato, Silvia Bianchi, Gian Nicola Gallus, CNS Neuroscience & Therapeutics	2017	51
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid Federica Ginanneschi, Andrea Mignarri, Mauro Mondelli, Journal of Neurology Cerebrotendinous XanthomatosisChenodeoxycholic AcidNeurologyNeuropathologyMedicine	2012	46
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy. Gian Nicola Gallus, Elena Cardaioli, Alessandra Rufa, PubMed	2010	41
Clinical relevance and neurophysiological correlates of spasticity in cerebrotendinous xanthomatosis Andrea Mignarri, Símone Rossi, Michele Ballerini, Journal of Neurology Clinical RelevanceRadiology	2010	34
A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency Paola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, European Journal of Human Genetics Mendelian DisorderGenetic DisorderRetinitis PigmentosaGeneticsLate-onset Ataxia	2009	30
A second MNGIE patient without typical mitochondrial skeletal muscle involvement Elena Cardaioli, Paola Da Pozzo, Edoardo Malfatti, Neurological Sciences Mitochondrial MyopathyKinesiologyMuscle InjuryMitochondrial FunctionSkeletal Muscle	2010	24
Four novel CYP27A1 mutations in seven Italian patients with CTX Gian Nicola Gallus, Maria Teresa Dotti, Andrea Mignarri, European Journal of Neurology	2010	24

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