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5. [The importance of TTR met 30 in the diagnosis of familial amyloidotic polyneuropathy in the absence of a positive family history]. Santos M; Dias L; Esperança P Rev Neurol; 2000 May 16-31; 30(10):929-31. PubMed ID: 10919188 [TBL] [Abstract][Full Text] [Related]
6. [Amyloid neuropathy resulting from an unknown protein]. Younsi R; Birouk N; Kissani N Rev Med Interne; 2009 Mar; 30(3):277-8. PubMed ID: 18584922 [TBL] [Abstract][Full Text] [Related]
7. [Hereditary amyloid neuropathies]. Adams D; Said G Ann Med Interne (Paris); 1995; 146(3):157-65. PubMed ID: 7653916 [No Abstract] [Full Text] [Related]
8. Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France. Lucotte G; Berriche S; David F; Rouquet H; Turpin JC Genet Couns; 1993; 4(4):285-7. PubMed ID: 8110416 [TBL] [Abstract][Full Text] [Related]
9. A case of atypical amyloid polyneuropathy with predominant upper-limb involvement with the diagnosis unexpectedly found at lung operation. Shirota Y; Iwata A; Ishiura H; Hashimoto M; Goto J; Shimizu J; Hanajima R; Nakajima J; Takazawa Y; Tsuji S Intern Med; 2010; 49(15):1627-31. PubMed ID: 20686303 [TBL] [Abstract][Full Text] [Related]
11. A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser). Patel K; Tagoe C; Bieri P; Weidenheim K; Tauras JM Amyloid; 2018 Sep; 25(3):211-212. PubMed ID: 30039724 [No Abstract] [Full Text] [Related]
12. Simple detection of abnormal serum transthyretin from patients with familial amyloidotic polyneuropathy by high-performance liquid chromatography/electrospray ionization mass spectrometry using material precipitated with specific antiserum. Kishikawa M; Nakanishi T; Miyazaki A; Shimizu A; Nakazato M; Kangawa K; Matsuo H J Mass Spectrom; 1996 Jan; 31(1):112-4. PubMed ID: 8799265 [No Abstract] [Full Text] [Related]