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Results 1 - 10 of 12 for Hereditary amyloidosis
  1. ... Registry: Amyloidosis, hereditary systemic 1 Familial transthyretin amyloidosis Hereditary amyloidosis National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
  2. ... Cerebral amyloid angiopathy, genetic HCHWA-D HCHWA-I Hereditary cerebral hemorrhage with amyloidosis-Dutch type Hereditary cerebral hemorrhage with amyloidosis-Icelandic ...
  3. ... responsible for some cases of a condition called hereditary renal amyloidosis, which causes impairment of kidney (renal) function and ... Liepnieks J, Uemichi T, Wheeler G, Correa R. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. Nat ...
  4. ... Frangione B. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med. 1990 Dec 1;172(6): ...
  5. ... Frangione B. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med. 1990 Dec 1;172(6): ...
  6. ... 6-phosphate dehydrogenase deficiency , also called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden ...
  7. ... HUMAN apolipoprotein A-I Tests of APOA1 PubMed AMYLOIDOSIS, HEREDITARY SYSTEMIC 2; AMYLD2 APOLIPOPROTEIN A-I; APOA1 NCBI ... Lohse P, Buttner J, Schmidt H, Rocken C. Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel ...
  8. ... 2007.05712.x. Citation on PubMed Saraiva MJ. Hereditary transthyretin amyloidosis: molecular basis and therapeutical strategies. Expert Rev Mol ...
  9. ... S, Younkin S, Roos R, Van Broeckhoven C. Hereditary cerebral hemorrhage with amyloidosis Dutch type (AbetaPP 693): decreased plasma amyloid-beta ... Maat-Schieman M, Roos R, van Duinen S. Hereditary cerebral hemorrhage with amyloidosis-Dutch type. Neuropathology. 2005 Dec;25(4):288- ...
  10. ... J, Jensson O, Frangione B. Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma- ...
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