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44. [Muckle-Wells syndrome associated with idiopathic interstitial pneumopathy]. Gómez Rodríguez F; Muñoz Lucena F; Peña Griñán N; Umbria Domínguez S An Med Interna; 1991 Feb; 8(2):85-6. PubMed ID: 1893010 [TBL] [Abstract][Full Text] [Related]
45. A variant Muckle-Wells syndrome with a novel mutation in CIAS1 gene responding to anakinra. Dalgic B; Egritas O; Sari S; Cuisset L Pediatr Nephrol; 2007 Sep; 22(9):1391-4. PubMed ID: 17486372 [TBL] [Abstract][Full Text] [Related]
46. [Syndrome of Muckle-Wells and autoinflammatory familiar syndrome induced by cold]. Calvo Penadés I; López Montesinos B; Marco Puche A Med Clin (Barc); 2011 Jan; 136 Suppl 1():16-21. PubMed ID: 21596182 [TBL] [Abstract][Full Text] [Related]
48. Amyloid goiter and arthritides after kidney transplantation in a patient with systemic amyloidosis and Muckle-Wells syndrome. Schwarz RE; Dralle H; Linke RP; Nathrath WB; Neumann KH Am J Clin Pathol; 1989 Dec; 92(6):821-5. PubMed ID: 2589249 [TBL] [Abstract][Full Text] [Related]
49. A case of Muckle-Wells syndrome caused by a novel H312P mutation in NALP3 (cryopyrin). Koike R; Kubota T; Hara Y; Ito S; Suzuki K; Yanagisawa K; Uchibori K; Miyasaka N Mod Rheumatol; 2007; 17(6):496-9. PubMed ID: 18084703 [TBL] [Abstract][Full Text] [Related]
50. [A contribution to the syndrome of hereditary hematuria, nephropathy and deafness]. NIETH H Verh Dtsch Ges Inn Med; 1959; 65():664-7. PubMed ID: 14427127 [No Abstract] [Full Text] [Related]
52. Hereditary renal disease associated with deafness; Alport's syndrome. Van Buchem FS; Beetstra A Proc K Ned Akad Wet C; 1965; 68(5):350-9. PubMed ID: 4221522 [No Abstract] [Full Text] [Related]
53. [Congenital nephritis with nerve deafness in a family. (3 cases of Alport's syndrome]. Valdés Ruiz M; Pascual-Leone Pascual A; Ciges Juan M; Abella Llácer A Rev Clin Esp; 1966 Aug; 102(3):197-204. PubMed ID: 5997883 [No Abstract] [Full Text] [Related]
54. Hereditary nephritis witj h perceptive deafness (Alport's syndrome). Lachhein L; Büttner H; Kennitz P; Thal W; Witkowski R Ger Med Mon; 1969 May; 14(5):218-22. PubMed ID: 5807504 [No Abstract] [Full Text] [Related]
55. Genetic factors in amyloidosis. Thomas PK J Med Genet; 1975 Dec; 12(4):317-26. PubMed ID: 176361 [TBL] [Abstract][Full Text] [Related]
56. [Familial hematuric nephropathy with deafness (Alport's syndrome). Apropos of 2 series of cases]. Chaptal J; Jean R; Pages A; Bonnet H Pediatrie; 1965 Sep; 20(6):649-64. PubMed ID: 5852220 [No Abstract] [Full Text] [Related]