156 related articles for article (PubMed ID: 10486324)
1. Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.
Cuisset L; Drenth JP; Berthelot JM; Meyrier A; Vaudour G; Watts RA; Scott DG; Nicholls A; Pavek S; Vasseur C; Beckmann JS; Delpech M; Grateau G
Am J Hum Genet; 1999 Oct; 65(4):1054-9. PubMed ID: 10486324
[TBL] [Abstract][Full Text] [Related]
2. Identification of a locus on chromosome 1q44 for familial cold urticaria.
Hoffman HM; Wright FA; Broide DH; Wanderer AA; Kolodner RD
Am J Hum Genet; 2000 May; 66(5):1693-8. PubMed ID: 10741953
[TBL] [Abstract][Full Text] [Related]
3. An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q.
McDermott MF; Aganna E; Hitman GA; Ogunkolade BW; Booth DR; Hawkins PN
Arthritis Rheum; 2000 Sep; 43(9):2034-40. PubMed ID: 11014353
[TBL] [Abstract][Full Text] [Related]
4. Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.
Aganna E; Martinon F; Hawkins PN; Ross JB; Swan DC; Booth DR; Lachmann HJ; Bybee A; Gaudet R; Woo P; Feighery C; Cotter FE; Thome M; Hitman GA; Tschopp J; McDermott MF
Arthritis Rheum; 2002 Sep; 46(9):2445-52. PubMed ID: 12355493
[TBL] [Abstract][Full Text] [Related]
5. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.
Kumar S; Deffenbacher K; Marres HA; Cremers CW; Kimberling WJ
Am J Hum Genet; 2000 May; 66(5):1715-20. PubMed ID: 10762556
[TBL] [Abstract][Full Text] [Related]
6. A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.
Cohn DH; Shohat T; Yahav M; Ilan T; Rechavi G; King L; Shohat M
Am J Hum Genet; 2000 Sep; 67(3):647-51. PubMed ID: 10930359
[TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant Muckle-Wells syndrome associated with cystinuria, ichthyosis, and aphthosis in a four-generation family.
Berthelot JM; Maugars Y; Robillard N; Pascal O; Stalder JF; David A; Prost A
Am J Med Genet; 1994 Oct; 53(1):72-4. PubMed ID: 7802040
[TBL] [Abstract][Full Text] [Related]
8. Muckle-Wells syndrome: clinical and histological skin findings compatible with cold air urticaria in a large kindred.
Haas N; Küster W; Zuberbier T; Henz BM
Br J Dermatol; 2004 Jul; 151(1):99-104. PubMed ID: 15270877
[TBL] [Abstract][Full Text] [Related]
9. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
Dodé C; Le Dû N; Cuisset L; Letourneur F; Berthelot JM; Vaudour G; Meyrier A; Watts RA; Scott DG; Nicholls A; Granel B; Frances C; Garcier F; Edery P; Boulinguez S; Domergues JP; Delpech M; Grateau G
Am J Hum Genet; 2002 Jun; 70(6):1498-506. PubMed ID: 11992256
[TBL] [Abstract][Full Text] [Related]
10. The arthropathy of the Muckle-Wells syndrome.
Watts RA; Nicholls A; Scott DG
Br J Rheumatol; 1994 Dec; 33(12):1184-7. PubMed ID: 8000753
[TBL] [Abstract][Full Text] [Related]
11. [Muckle-Wells syndrome].
Barriére H; Prost A; Wallex B
Ann Dermatol Venereol; 1977 Oct; 104(10):664-6. PubMed ID: 610522
[No Abstract] [Full Text] [Related]
12. [Muckle-Wells syndrome: 4 cases in three generations].
Buxtorf K; Cerottini JP; Fellrath JM; Debétaz LF; Guillod J; Panizzon RG
Ann Dermatol Venereol; 2000 Oct; 127(10):822-4. PubMed ID: 11060385
[TBL] [Abstract][Full Text] [Related]
13. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
14. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.
Hoffman HM; Mueller JL; Broide DH; Wanderer AA; Kolodner RD
Nat Genet; 2001 Nov; 29(3):301-5. PubMed ID: 11687797
[TBL] [Abstract][Full Text] [Related]
15. [Deafness, urticaria, arthritis, hypogonadism and renal insufficiency (syndrome of Muckle and Wells) (author's transl)].
Perrottet C; Mach RS; Fabre J
Schweiz Rundsch Med Prax; 1974 May; 63(21):651-9. PubMed ID: 4831496
[No Abstract] [Full Text] [Related]
16. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
Morlé L; Bozon M; Zech JC; Alloisio N; Raas-Rothschild A; Philippe C; Lambert JC; Godet J; Plauchu H; Edery P
Am J Hum Genet; 2000 Dec; 67(6):1592-7. PubMed ID: 11035633
[TBL] [Abstract][Full Text] [Related]
17. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
Desautels A; Turecki G; Montplaisir J; Sequeira A; Verner A; Rouleau GA
Am J Hum Genet; 2001 Dec; 69(6):1266-70. PubMed ID: 11704926
[TBL] [Abstract][Full Text] [Related]
18. [AA-amyloidosis in Muckle-Wells syndrome].
Kozlovskaia LV; Rameev VV; Ianushkevich TN; Proskurneva EP; Konovalov DV; Simonian AKh; Sarkisova IA
Ter Arkh; 2002; 74(6):69-72. PubMed ID: 12136491
[No Abstract] [Full Text] [Related]
19. The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.
Vollmer M; Jung M; Rüschendorf F; Ruf R; Wienker T; Reis A; Krapf R; Hildebrandt F
Am J Hum Genet; 1998 Dec; 63(6):1724-31. PubMed ID: 9837825
[TBL] [Abstract][Full Text] [Related]
20. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.
Beiraghi S; Miller-Chisholm A; Kimberling WJ; Sun CE; Wang YF; Russell LJ; Khoshnevisan M; Storm AL; Long RE; Witt PD; Mazaheri M; Diehl SR
J Craniofac Genet Dev Biol; 1999; 19(3):128-34. PubMed ID: 10589394
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
