eponyms-2.json

{
    "date": "2016-11-06",
    "documents": [
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Anatomy"
            },
            "tag": "anat",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Dermatology"
            },
            "tag": "derm",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Hematology"
            },
            "tag": "heme",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Neurology"
            },
            "tag": "neuro",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Oncology"
            },
            "tag": "onc",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Pediatrics"
            },
            "tag": "peds",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Renal"
            },
            "tag": "renal",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": "Syndromes"
            },
            "tag": "synd",
            "type": "tag"
        },
        {
            "author": "ajyee",
            "date": "2005-01-17",
            "dateUpdated": "2005-01-17",
            "localized": {
                "en": {
                    "text": "Congenital anomaly of the splanchnic vasculature, arises from defects in vitelline vein formation; in type 1, portal vein completely diverted into IVC and complete absence of formation of intrahepatic portal vein; in type 2, portal venous system is formed, but there is an abnormal communication with systemic veins, usually IVC; associated with hepatic encephalopathy and hepatopulmonary syndrome; more common in dogs, particularly Yorkshire terriers.",
                    "title": "Abernethy malformation"
                }
            },
            "tags": [
                "anat",
                "peds"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "2007-04-05",
            "localized": {
                "en": {
                    "text": "Rare entity of spontaneous or mechanically-induced hematomas on the volar aspect of fingers associated with burning pain and swelling of the digits.",
                    "title": "Achenbach's syndrome"
                }
            },
            "tags": [
                "synd",
                "derm"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "dateUpdated": "1998-03-21",
            "localized": {
                "en": {
                    "text": "Artery that when severed, can lead to anterior spinal syndrome; can be severed in abdominal aortic aneurysm repair.",
                    "title": "Adamkiewicz, artery of"
                }
            },
            "tags": [
                "anat"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "2006-07-19",
            "dateUpdated": "2006-07-19",
            "localized": {
                "en": {
                    "text": "Sex-linked hydrocephalus, aqueductal stenosis, mental deficiency, and flexion deformities and spasticity of the extremities.  Most common inherited forms of inherited hydrocephalus.  X-linked (Xq28), due to mutation in L1CAM.",
                    "title": "Bickers-Adams syndrome"
                }
            },
            "tags": [
                "synd",
                "neuro",
                "peds"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "2000-03-12",
            "dateUpdated": "2000-03-12",
            "localized": {
                "en": {
                    "text": "Brain stem encephalitis.  Has features of Miller Fisher syndrome, but with encephalopathy and hyperreflexia.  Associated with anti-GQ1b antibodies; can be te treated with IVIG and plasma exchange.",
                    "title": "Bickerstaff's encephalitis"
                }
            },
            "tags": [
                "neuro",
                "synd"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "localized": {
                "en": {
                    "text": "The angle made by the proximal nail fold and the nail plate.",
                    "title": "Lovibond's angle"
                }
            },
            "tags": [
                "derm",
                "anat"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "2000-07-15",
            "localized": {
                "en": {
                    "text": "In deep vein thrombosis, two calves are wrapped with cuffs to see if there is asymetry in tolerance to pressure of 180 mm Hg.",
                    "title": "Lowenberg's sign"
                }
            },
            "tags": [
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "2000-02-28",
            "dateUpdated": "2000-02-28",
            "localized": {
                "en": {
                    "text": "Wilms's tumor, Anirida, Genital anomalies, and mental Retardation; 33% chance of developing Wilms's tumor; associated with mutation in WT1 gene.",
                    "title": "WAGR"
                }
            },
            "tags": [
                "renal",
                "synd",
                "onc",
                "peds"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "dateUpdated": "1998-03-21",
            "localized": {
                "en": {
                    "text": "A subset of lymphoplasmacytic lymphoma (a malignancy involving small B lymphocytes, plasmactyoid lymphocytes, and plasma cells) with bone marrow involvement and IgM monoclonal gammopathy in the blood.  Characterized by macroglobulinemia and associated with visual impairment, neurologic problems, bleeding, cryoglobulinemia, and hyperviscosity.",
                    "title": "Waldenström's macroglobulinemia"
                }
            },
            "tags": [
                "heme",
                "onc"
            ],
            "type": "main"
        },
        {
            "author": "ajyee",
            "date": "1998-03-21",
            "dateUpdated": "1998-03-21",
            "localized": {
                "en": {
                    "text": "The broken ring of lymphoid tissue, formed of the lingual, facial, and pharyngeal tonsils, commonly involved in non-Hodgkin's lymphoma and rarely in Hodgkin's disease.",
                    "title": "Waldeyer's throat ring"
                }
            },
            "tags": [
                "heme",
                "onc",
                "anat"
            ],
            "type": "main"
        }
    ]
}