Blau syndrome: A new kindred

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

2001 • 5,526 citations

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

2001 • 4,997 citations

Nod2, a Nod1/Apaf-1 Family Member That Is Restricted to Monocytes and Activates NF-κB

2001 • 1,331 citations

CARD15 mutations in Blau syndrome

2001 • 945 citations

Familial granulomatous arthritis, iritis, and rash

1985 • 401 citations

Familial granulomatous synovitis, uveitis, and cranial neuropathies

1985 • 162 citations

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

1996 • 128 citations

Blau syndrome of granulomatous arthritis, iritis, and skin rash: A new family and review of the literature

1998 • 87 citations

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

1990 • 71 citations

Analysis of a Large Kindred With Blau Syndrome for HLA, Autoimmunity, and Sarcoidosis

1993 • 66 citations

Liver involvement in familial granulomatous arthritis (Blau syndrome).

1996 • 63 citations

Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions

1998 • 54 citations

Sarcoidosis in children

2000 • 46 citations

The Blau syndrome gene is not a major risk factor for sarcoidosis.

1999 • 45 citations

Histologic, ultrastructural, and immunocytochemical features of the granulomas seen in a child with the syndrome of familial granulomatous arthritis, uveitis, and rash.

1993 • 31 citations

Familial juvenile systemic granulomatosis (Blau's syndrome)

1996 • 27 citations

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

1996 • 8 citations