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Expanding molecular and clinical spectrum of CPT1C‐associated hereditary spastic paraplegia (SPG73)—a case series

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52288Source: DataRank Database

Expanding molecular and clinical spectrum of CPT1C‐associated hereditary spastic paraplegia (SPG73)—a case series is a research paper published in Annals of Clinical and Translational Neurology (2024). On theSindex it has a DataRank of 0. It has been cited 3 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 0.57)OA: goldTopics (40)IDs (PubMed, PMC, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (6)

Vicente Quiroz ORCID,Luca Schierbaum ORCID,Amy Tam ORCID,Julian E. Alecu ORCID,Darius Ebrahimi‐Fakhari ORCID

Live enrichment

PubMed:39737739 PMC:PMC11920729 OpenAlex:https://openalex.org/W4405915459

Deutsche Forschungsgemeinschaft

Grant: 536105452

National Institute of Neurological Disorders and Stroke

Grant: K08NS123552

Deutsche Forschungsgemeinschaft

Grant: unidentified

unidentified

Spastic Paraplegia Foundation

Boston Children's Hospital Translational Research Program

International Parkinson and Movement Disorder Society

FWCI

0.57

Citation Percentile

0.6%

Citation Trend

2025

goldLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.52288

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.52288

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.52288

journalhttps://doi.org/10.1002/acn3.52288

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39737739

Fields of Study

Hereditary Neurological DisordersNeurological diseases and metabolismNeurogenetic and Muscular Disorders Research03 medical and health sciences0302 clinical medicine

MeSH Terms

Carnitine O-PalmitoyltransferaseChild, PreschoolHumansMaleSpastic Paraplegia, HereditaryCognitive Dysfunction

Keywords

Hereditary spastic paraplegiaSpasticityMedicineSpasticParaplegiaPhysical medicine and rehabilitationWeaknessPediatricsPhysical therapyNeuroscienceGeneGeneticsSurgeryPhenotypePsychiatryPsychologyCerebral palsySpinal cordMaleCarnitine O-PalmitoyltransferaseSpastic Paraplegia, HereditaryChild, PreschoolHumansNeurosciences. Biological psychiatry. NeuropsychiatryCognitive DysfunctionNeurology. Diseases of the nervous systemRC346-429Brief CommunicationRC321-571

Sustainable Development Goals

SDG 0: Good health and well-being