Antonio Orlacchio

University of Perugia — Italy

Medicine · Health Sciences

39h-index4.9kcitations266works2.12yr avg
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Research Topics

Lysosomal Storage Disorders Research(52), Hereditary Neurological Disorders(51), Neurological diseases and metabolism(36), Neurogenetic and Muscular Disorders Research(35), Alzheimer's disease research and treatments(32)

Publications260 total

Targeted plasma proteomics uncover proteins associated with KIF5A-linked SPG10 and ALS spectrum disorders
Human Genetics and Genomics Advances·2025Open Access
Targeted plasma proteomics uncover novel proteins associated with <i>KIF5A</i> -linked SPG10 and ALS spectrum disorders
2025Open Access
Biomarkers in Hereditary Spastic Paraplegias
International Journal of Molecular Sciences·2025· 2 citedOpen Access
Spastic paraplegia leading PSEN1‐related familial Alzheimer’s disease in Italy
Alzheimer s & Dementia·2024Open Access
Effects of APOE isoforms in diabetic nephropathy patients of South India
Acta Diabetologica·2024· 2 citedOpen Access
Experimental Cell Models for Investigating Neurodegenerative Diseases
International Journal of Molecular Sciences·2024· 11 citedOpen Access
Special Issue “Neurogenetics in Neurology”
International Journal of Molecular Sciences·2024Open Access
Mild cognitive impairment in novel SPG4/SPAST mutation‐related sporadic late onset hereditary spastic paraplegia: case series
Alzheimer s & Dementia·2023Open Access
Prevalence of Cardiovascular Diseases in South Asians: Scrutinizing Traditional Risk Factors and Newly Recognized Risk Factors Sarcopenia and Osteopenia/Osteoporosis
Current Problems in Cardiology·2023· 7 cited
Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanisms
Expert Review of Proteomics·2023· 12 cited
Hereditary spastic paraplegia: Genetic heterogeneity and common pathways
Experimental Neurology·2022· 45 citedOpen Access
The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment
International Journal of Molecular Sciences·2022· 37 citedOpen Access
Review of: "Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1"
2022Open Access
Hereditary Spastic Paraplegia: An Update
International Journal of Molecular Sciences·2022· 139 citedOpen Access
Nano- from nature to nurture: A comprehensive review on facets, trends, perspectives and sustainability of nanotechnology in the food sector
Energy·2021· 109 cited
Review for "Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder"
2021
Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network
Journal of the Neurological Sciences·2021
Transmission Jeopardy of Adenomatosis Polyposis Coli and Methylenetetrahydrofolate Reductase in Colorectal Cancer
Journal of the Renin-Angiotensin-Aldosterone System·2021· 6 citedOpen Access
Clinico‐genetic study of two Japanese pedigrees with hereditary spastic paraparesis and Alzheimer's disease
Alzheimer s & Dementia·2020Open Access
Recurrent de novo missense variant E210K in UBTF causes juvenile dystonia-parkinsonism
Neurological Sciences·2020· 16 cited
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Frequent Co-authors

Toshitaka Kawarai(12), Giorgio Bernardi(12), Peter St George‐Hyslop(9), Sabata Martino(9), Aldo Orlacchio(8), Carla Emiliani(7), Sandro Sorbi(6), Roberto Tiribuzi(5), Lucia Crispoltoni(5), Fabrizio Gaudiello(5), Ekaterina Rogaeva(4), Toshitaka Kawarai(4), Arun Meyyazhagan(4), Alessandro Stefani(4), Celeste Montecchiani(4), You‐Qiang Song(4), Filippo M. Santorelli(3), Carla Babalini(3), Valerio Chiurchiù(3), Mauro Maccarrone(3)