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2. [Type I familial amyloidotic polyneuropathy. Corino Andrade's disease]. Munar-Qués M Med Clin (Barc); 1990 Jan; 94(2):53-5. PubMed ID: 2158604 [No Abstract] [Full Text] [Related]
3. [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]
4. [A case of spontaneous corneal perforation in De Andrade's Portuguese amyloidosis]. Abenhaim A; Hoang-Xuan T; Goichot-Bonnat L; Dhermy P; Pouliquen Y Bull Soc Ophtalmol Fr; 1988 Feb; 88(2):223, 226. PubMed ID: 3214895 [No Abstract] [Full Text] [Related]
5. [Corino Andrade's disease. Clinical and pathological study]. Curcio FI; Scornik JS; Ale JS; Curcio HF Prensa Med Argent; 1970 Oct; 57(34):1611-5. PubMed ID: 5487281 [No Abstract] [Full Text] [Related]
6. Familial amyloidotic polyneuropathy: ocular manifestations with clinicopathological observation. Futa R; Inada K; Nakashima H; Baba H; Kojima Y; Okamura R; Araki S Jpn J Ophthalmol; 1984; 28(3):289-98. PubMed ID: 6098757 [TBL] [Abstract][Full Text] [Related]
7. [Electroencephalographic changes in Corino de Andrade's paramyloidosis; preliminary note on four cases]. SILVA P; ANTUNES L; DO ROSARIO R Med Contemp; 1959 Feb; 77(2):69-80. PubMed ID: 13643289 [No Abstract] [Full Text] [Related]
8. [Familial amyloidosis of the Andrade disease type in a Greek family]. Laskaratos J; Fronimopoulos J Klin Monbl Augenheilkd; 1987 May; 190(5):439-41. PubMed ID: 3613447 [TBL] [Abstract][Full Text] [Related]
9. Conduction disturbances in 190 patients with familial amyloidotic polyneuropathy (Andrade's type). Falcão De Freitas A; Barbedo A Adv Cardiol; 1978; 21():206-9. PubMed ID: 202146 [No Abstract] [Full Text] [Related]
11. [Pulmonary involvement in familial amyloid polyneuropathy type I]. Díaz Lobato S; Guerrero E; González P; Crespo M; Esteban R; Villasante C Rev Clin Esp; 1991 Nov; 189(7):335-7. PubMed ID: 1767091 [TBL] [Abstract][Full Text] [Related]
12. [Portuguese-type familial amyloidotic polyneuropathy: presentation of a case]. Peinado Guerrero E; Hernández Gallego J; Calandre L; Cabello A; Bermejo F Med Clin (Barc); 1985 Feb; 84(5):191-4. PubMed ID: 2984487 [No Abstract] [Full Text] [Related]
13. [Peripheral neuropathy in familial primary amyloidosis, with special reference to 10 cases in one family and a review of the literature]. Araki S; Mawatari S; Oota M; Iwashita H; Kuroiwa Y No To Shinkei; 1968 Jan; 20(1):11-8. PubMed ID: 4298009 [No Abstract] [Full Text] [Related]
14. [Portuguese amyloid neuropathy (apropos of 3 further cases)]. Joyeux O; Girard PF; Trillet M; Carrier H; Michel D Rev Neurol (Paris); 1975 Dec; 131(12):867-71. PubMed ID: 183257 [No Abstract] [Full Text] [Related]
15. [Polyneuritic paramyloidosis of the Portuguese type (familial amyloid polyneuropathy). A differential diagnosis from ulcero-mutilating acropathy]. Poiares Baptista A; Trincão R Ann Dermatol Syphiligr (Paris); 1966; 93(4):374-82. PubMed ID: 4290883 [No Abstract] [Full Text] [Related]
16. [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]
17. [Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]. Adams D; Reilly M; Harding AE; Said G Rev Neurol (Paris); 1992; 148(12):736-41. PubMed ID: 1338934 [TBL] [Abstract][Full Text] [Related]
18. Primary amyloidosis with familial vitreous opacities: an unusual case and family. Okayama M; Goto I; Ogata J; Omae T; Yoshida I; Inomata H Arch Intern Med; 1978 Jan; 138(1):105-11. PubMed ID: 202208 [TBL] [Abstract][Full Text] [Related]