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Items: 1 to 20 of 271

1.

Analysis of a large kindred with Blau syndrome for HLA, autoimmunity, and sarcoidosis.

Raphael SA, Blau EB, Zhang WH, Hsu SH.

Am J Dis Child. 1993 Aug;147(8):842-8.

PMID:
8394645
2.

Blau syndrome: a new kindred.

Alonso D, Elgart GW, Schachner LA.

J Am Acad Dermatol. 2003 Aug;49(2):299-302.

PMID:
12894082
3.

Pediatric granulomatous arthritis: an international registry.

Rosé CD, Wouters CH, Meiorin S, Doyle TM, Davey MP, Rosenbaum JT, Martin TM.

Arthritis Rheum. 2006 Oct;54(10):3337-44.

4.

NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.

Aróstegui JI, Arnal C, Merino R, Modesto C, Antonia Carballo M, Moreno P, García-Consuegra J, Naranjo A, Ramos E, de Paz P, Rius J, Plaza S, Yagüe J.

Arthritis Rheum. 2007 Nov;56(11):3805-13.

5.

A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members.

Milman N, Ursin K, Rødevand E, Nielsen FC, Hansen TV.

Scand J Rheumatol. 2009 May-Jun;38(3):190-7. doi: 10.1080/03009740802464194.

PMID:
19169908
6.

A comparison of Blau's syndrome and sarcoidosis.

James DG.

Sarcoidosis. 1994 Sep;11(2):100-1.

PMID:
7809491
7.

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

Okafuji I, Nishikomori R, Kanazawa N, Kambe N, Fujisawa A, Yamazaki S, Saito M, Yoshioka T, Kawai T, Sakai H, Tanizaki H, Heike T, Miyachi Y, Nakahata T.

Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134.

8.

Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16.

Tromp G, Kuivaniemi H, Raphael S, Ala-Kokko L, Christiano A, Considine E, Dhulipala R, Hyland J, Jokinen A, Kivirikko S, Korn R, Madhatheri S, McCarron S, Pulkkinen L, Punnett H, Shimoya K, Spotila L, Tate A, Williams CJ.

Am J Hum Genet. 1996 Nov;59(5):1097-107.

9.

[Blau syndrome or familial form of sarcoidosis with onset during infancy].

Moraillon I, Hayem F, Bourrillon A, Morel P, Rybojad M.

Ann Dermatol Venereol. 1996;123(1):29-30. French.

PMID:
8734114
10.
11.

Sporadic Blau syndrome with onset of widespread granulomatous dermatitis in the newborn period.

Stoevesandt J, Morbach H, Martin TM, Zierhut M, Girschick H, Hamm H.

Pediatr Dermatol. 2010 Jan-Feb;27(1):69-73. doi: 10.1111/j.1525-1470.2009.01060.x.

PMID:
20199415
12.

Familial rheumatoid arthritis: a kindred identified through a proband with seronegative juvenile arthritis includes members with seropositive, adult-onset disease.

Rossen RD, Brewer EJ, Sharp RM, Yunis EJ, Schanfield MS, Birdsall HH, Ferrell RE, Templeton JW.

Hum Immunol. 1982 Jun;4(3):183-96.

PMID:
6214529
13.

Autosomal dominant granulomatous arthritis, uveitis, skin rash, and synovial cysts.

Pastores GM, Michels VV, Stickler GB, Su WP, Nelson AM, Bovenmyer DA.

J Pediatr. 1990 Sep;117(3):403-8.

PMID:
2391595
14.

Co-existence of chronic renal failure, renal clear cell carcinoma, and Blau syndrome.

Akil I, Ozguven A, Canda E, Yilmaz O, Nese N, Ozkol M, May S, Franke A, Cirak S.

Pediatr Nephrol. 2010 May;25(5):977-81. doi: 10.1007/s00467-009-1413-5.

PMID:
20084402
15.

Blau syndrome associated with a CARD15/NOD2 mutation.

Snyers B, Dahan K.

Am J Ophthalmol. 2006 Dec;142(6):1089-92. Epub 2006 Aug 2.

PMID:
17157607
16.

Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review.

Punzi L, Furlan A, Podswiadek M, Gava A, Valente M, De Marchi M, Peserico A.

Autoimmun Rev. 2009 Jan;8(3):228-32. doi: 10.1016/j.autrev.2008.07.034. Epub 2008 Aug 19.

17.

Blau syndrome and related genetic disorders causing childhood arthritis.

Becker ML, Rose CD.

Curr Rheumatol Rep. 2005 Dec;7(6):427-33. Review.

PMID:
16303101
18.
19.

Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.

Rosé CD, Doyle TM, McIlvain-Simpson G, Coffman JE, Rosenbaum JT, Davey MP, Martin TM.

J Rheumatol. 2005 Feb;32(2):373-5.

PMID:
15693102
20.

[Familial uveitis. Forms and incidence in patients at the University Eye Hospital Tubingen].

Deuter CM, Stübiger N, Siepmann K, Derse M, Zierhut M.

Ophthalmologe. 2003 Sep;100(9):713-9. German.

PMID:
14504896

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