Item talk:Q317724

{

 "OpenAlex": {
   "id": "https://openalex.org/T12199",
   "display_name": "Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia",
   "description": "This cluster of papers focuses on the diagnosis and management of hereditary hemorrhagic telangiectasia (HHT), a genetic disorder characterized by vascular malformations. It covers topics such as genetics, pulmonary arteriovenous malformations, embolization, epistaxis, liver involvement, SMAD4 mutations, and vascular anomalies.",
   "keywords": [
     "Hereditary Hemorrhagic Telangiectasia",
     "Diagnosis",
     "Management",
     "Genetics",
     "Pulmonary Arteriovenous Malformations",
     "Embolization",
     "Epistaxis",
     "Liver Involvement",
     "SMAD4 Mutations",
     "Vascular Anomalies"
   ],
   "ids": {
     "openalex": "https://openalex.org/T12199",
     "wikipedia": "https://en.wikipedia.org/wiki/Hereditary_hemorrhagic_telangiectasia"
   },
   "subfield": {
     "id": "https://openalex.org/subfields/2716",
     "display_name": "Genetics"
   },
   "field": {
     "id": "https://openalex.org/fields/27",
     "display_name": "Medicine"
   },
   "domain": {
     "id": "https://openalex.org/domains/4",
     "display_name": "Health Sciences"
   },
   "siblings": [
     {
       "id": "https://openalex.org/T13738",
       "display_name": "CHARGE Syndrome and Related Genetic Disorders"
     },
     {
       "id": "https://openalex.org/T12400",
       "display_name": "Gene Therapy for Spinal Muscular Atrophy"
     },
     {
       "id": "https://openalex.org/T10554",
       "display_name": "Genetic and Clinical Aspects of Hemoglobin Disorders"
     },
     {
       "id": "https://openalex.org/T11157",
       "display_name": "Genomic Aberrations and Treatment of Chronic Lymphocytic Leukemia"
     },
     {
       "id": "https://openalex.org/T10129",
       "display_name": "Gliomas"
     },
     {
       "id": "https://openalex.org/T11917",
       "display_name": "Hereditary Angioedema: Molecular Mechanisms and Clinical Management"
     },
     {
       "id": "https://openalex.org/T11628",
       "display_name": "Molecular Pathogenesis of Myeloproliferative Disorders"
     },
     {
       "id": "https://openalex.org/T10176",
       "display_name": "Multipotent Mesenchymal Stem Cells"
     }
   ],
   "works_count": 23060,
   "cited_by_count": 196642,
   "updated_date": "2024-08-26T05:50:10.143808",
   "created_date": "2024-01-23"
 }

}