{"doi":"10.1007/8904_2011_17","title":"Three Adult Siblings with Mucopolysaccharidosis Type II (Hunter Syndrome): A Report on Clinical Heterogeneity and 12 Months of Therapy with Idursulfase","abstract":null,"journal":"JIMD Reports","year":2011,"id":15803,"datarank":0.8314057461644415,"base_score":2.4849066497880004,"endowment":2.4849066497880004,"self_citation_contribution":0.37273599746820013,"citation_network_contribution":0.45866974869624144,"self_endowment_contribution":0.37273599746820013,"citer_contribution":0.45866974869624144,"corpus_percentile":null,"corpus_rank":null,"citation_count":11,"citer_count":11,"citers_with_citation_signal":10,"citers_with_endowment":10,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":119126,"name":"Kerry T. Devine","orcid":null,"position":1,"is_corresponding":false},{"id":119127,"name":"David O. Sillence","orcid":null,"position":2,"is_corresponding":false},{"id":119125,"name":"Michel C. Tchan","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"base_score":2.4849066497880004,"endowment":2.4849066497880004,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"23430829","pmcid":"PMC3509811","openalex_id":"https://openalex.org/W342980","authors":[],"funders":[],"total_grants":0,"fwci":0.0,"citation_percentile":0.0003427,"influential_citations":2,"citation_trend":[{"year":2015,"count":2},{"year":2017,"count":1},{"year":2018,"count":2},{"year":2020,"count":2},{"year":2021,"count":1},{"year":2022,"count":2},{"year":2024,"count":1}],"oa_status":"bronze","license":null,"oa_locations":[{"url":"https://link.springer.com/content/pdf/10.1007/8904_2011_17.pdf","host_type":"book series"},{"url":"https://europepmc.org/articles/pmc3509811?pdf=render","host_type":"GREEN"},{"url":"https://link.springer.com/content/pdf/10.1007/8904_2011_17.pdf","host_type":"publisher"},{"url":"http://link.springer.com/content/pdf/10.1007/8904_2011_17","host_type":"publisher"},{"url":"https://doi.org/10.1007/8904_2011_17","host_type":"book series"},{"url":"https://pubmed.ncbi.nlm.nih.gov/23430829","host_type":"repository"},{"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/3509811","host_type":"repository"}],"fields_of_study":["Lysosomal Storage Disorders Research","Neurogenetic and Muscular Disorders Research","Child Nutrition and Feeding Issues","Medicine"],"mesh_terms":[],"keywords":["Hunter syndrome","Mucopolysaccharidosis type II","Mucopolysaccharidosis","Enzyme replacement therapy","Medicine","Pediatrics","Disease","Internal medicine"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Affordable and clean energy"},{"sdg_number":0,"sdg_label":"Good health and well-being"}],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[{"name":"omim"}],"source":"live","citation_network_status":"fetched"},"created_at":"2026-06-01T19:02:21.105174Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}