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UnknownFive-year results of brentuximab vedotin in patients with relapsed or refractory systemic anaplastic large cell lymphoma.
Not available
S-EPMC5746164 | biostudies-literature
UnknownRare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Not available
S-EPMC9892767 | biostudies-literature
UnknownA MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.
Not available
S-EPMC8440635 | biostudies-literature
UnknownIncidence, management and outcomes in hepatic artery complications after paediatric liver transplantation: protocol of the retrospective, international, multicentre HEPATIC Registry.
Not available
S-EPMC11177692 | biostudies-literature
UnknownSolving unsolved rare neurological diseases-a Solve-RD viewpoint.
Not available
S-EPMC8440537 | biostudies-literature
UnknownComprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses.
Not available
S-EPMC11513043 | biostudies-literature
UnknownClinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14.
Not available
S-EPMC10064225 | biostudies-literature
UnknownAn interconnected data infrastructure to support large-scale rare disease research.
Not available
S-EPMC11413801 | biostudies-literature
UnknownPancreatic surgery outcomes: multicentre prospective snapshot study in 67 countries.
Not available
S-EPMC10771125 | biostudies-literature
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