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7. [A Portuguese case of primitive familial amyloidosis]. Becq-Giraudon B; de Giacomini P; Babin P; Gil R; Sudre Y Nouv Presse Med; 1974 Feb; 3(5):260. PubMed ID: 4819951 [No Abstract] [Full Text] [Related]
8. [Urinary organic acids in paramyloidosis of Corino de Andrade type (preliminary observations)]. da COSTA S; RELVAS ME; HALPERN MJ; da SILVA A Gaz Med Port; 1960; 13():609-13. PubMed ID: 13695797 [No Abstract] [Full Text] [Related]
9. [Familial amyloidotic polyneuropathy --Portuguese type-- clinical and neurophysiologic course]. Conceição I; Carvalho M; Alves M; Luís ML Acta Med Port; 1993 Jan; 6(1):15-7. PubMed ID: 8386429 [TBL] [Abstract][Full Text] [Related]
10. [Trials with "anti-serum specific" immune serum in cases of paramyloidosis of Corino de Andrade type (preliminary note)]. da COSTA S; SOARES AD; CAETANO JA; da SILVA J; da SILVA A Gaz Med Port; 1960; 13():614-6. PubMed ID: 13695804 [No Abstract] [Full Text] [Related]
11. [Familial amyloidosis, Finnish type with marked anhidrosis]. Ishiguchi H; Shimoya K; Ohnishi A; Murai Y; Nakazato M; Hoshii Y Rinsho Shinkeigaku; 1996 Mar; 36(3):436-41. PubMed ID: 8741346 [TBL] [Abstract][Full Text] [Related]
12. Corino Andrade (1906-2005): a clinical geneticist before its own time. Sequeiros J Clin Genet; 2006 Feb; 69(2):194-6. PubMed ID: 16433703 [No Abstract] [Full Text] [Related]
13. [Survey on the occurrence of para-amyloidosis of the Portuguese type. (Corino de Andrade's disease) in the vicinity of Portugal]. Juan-Cervera GM; Ramo SJ Rev Sanid Hig Publica (Madr); 1968; 42(5):321-33. PubMed ID: 5740505 [No Abstract] [Full Text] [Related]
14. [Ocular lesions in primary familial amyloidosis (a syndrome associating opacitieis of the vitreous body, vascular lesions of the retina and an amyloid neuropathy)]. Franceschetti AT; Rabinowicz T J Genet Hum; 1969 Oct; 17(3):349-66. PubMed ID: 4319009 [No Abstract] [Full Text] [Related]
15. [A familial observation of hereditary vitreal amyloidosis associated with glaucoma]. Limon S; Rousselie F; Joseph E Arch Ophtalmol Rev Gen Ophtalmol; 1973; 33(6):525-8. PubMed ID: 4274542 [No Abstract] [Full Text] [Related]
16. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies. Conceição I; Sales-Luis ML; De Carvalho M; Evangelista T; Fernandes R; Paunio T; Kangas H; Coutinho P; Neves C; Saraiva MJ Muscle Nerve; 2003 Dec; 28(6):715-21. PubMed ID: 14639586 [TBL] [Abstract][Full Text] [Related]
17. Primary familial amyloidosis of the cornea. Kirk HQ; Rabb M; Hattenhauer J; Smith R Trans Am Acad Ophthalmol Otolaryngol; 1973; 77(4):OP411-7. PubMed ID: 4126001 [No Abstract] [Full Text] [Related]
18. Scalloped pupils in familial amyloidosis. Lessell S; Wolf PA; Benson MD; Cohen AS N Engl J Med; 1975 Oct; 293(18):914-5. PubMed ID: 1177989 [No Abstract] [Full Text] [Related]
19. Periorbital ecchymoses are not pathognomonic of the light-chain type of amyloidosis. Outteryck O; Stojkovic T; Launay D; Meignie-Ramon B; Vermersch P Acta Derm Venereol; 2007; 87(6):544-5. PubMed ID: 17989898 [No Abstract] [Full Text] [Related]