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Genetic variants in the NOD2/CARD15 gene are associated with early mortality in sepsis patientsBRENMOEHL, Julia; HERFARTH, Hans; HOLLER, Ernst et al.Intensive care medicine (Print). 2007, Vol 33, Num 9, issn 0342-4642, 1541-1548 [8 p.]Article

CARD15/NOD2 in a Tunisian population with Crohn's diseaseZOUITEN-MEKKI, Lilia; ZAOUALI, Habib; BOUBAKER, Jalel et al.Digestive diseases and sciences. 2005, Vol 50, Num 1, pp 130-135, issn 0163-2116, 6 p.Article

Crohn's disease and the NOD2 gene: A role for Paneth cellsLALA, Sanjay; OGURA, Yasunori; OSBORNE, Caroline et al.Gastroenterology (New York, NY. 1943). 2003, Vol 125, Num 1, pp 47-57, issn 0016-5085, 11 p.Article

Flore intestinale et maladie de Crohn = Intestinal flora and Crohn's diseaseDESREUMAUX, P; COLOMBEL, J.-F.Annales pharmaceutiques françaises. 2003, Vol 61, Num 4, pp 276-281, issn 0003-4509, 6 p.Conference Paper

Response to Medical Treatment in Patients with Crohn's Disease: The Role of NOD2/CRAD15, Disease Phenotype, and Age of DiagnosisWEISS, B; LEBOWITZ, O; FIDDER, H. H et al.Digestive diseases and sciences. 2010, Vol 55, Num 6, pp 1674-1680, issn 0163-2116, 7 p.Article

Effect of NOD2/CARD15 variants in T-cell depleted allogeneic stem cell transplantationGRANELL, Miquel; URBANO-ISPIZUA, Alvaro; TALARN, Carme et al.Haematologica (Roma). 2006, Vol 91, Num 10, pp 1372-1376, issn 0390-6078, 5 p.Article

Functional expression of NOD2, a novel pattern recognition receptor for bacterial motifs, in primary murine astrocytesSTERKA, David; RATI, Dana M; MARRIOTT, Ian et al.Glia (New York, NY. Print). 2006, Vol 53, Num 3, pp 322-330, issn 0894-1491, 9 p.Article

NOD2/CARD15 mutations in Croatian patients with Crohn's disease : prevalence and genotype-phenotype relationshipCUKOVIC-CAVKA, Silvija; VERMEIRE, Severine; JADRESIN, Oleg et al.European journal of gastroenterology & hepatology. 2006, Vol 18, Num 8, pp 895-899, issn 0954-691X, 5 p.Article

Génétique des maladies inflammatoires cryptogénétiques de l'intestin = Genetic of inflammatory bowel diseaseZOUITEN MEKKI, Lilia; KHALFAOUI, Taoufik; BOUBAKER, Jalel et al.Tunisie médicale. 2004, Vol 82, Num 7, pp 635-641, issn 0041-4131, 7 p.Article

Mieux comprendre pour mieux traiter la maladie de Crohn : Gastro-entérologie = From a better understanding to a better therapy of Crohn's diseaseMICHETTI, P.Médecine et hygiène. 2004, Vol 62, Num 2498, pp 1872-1879, issn 0025-6749, 6 p.Article

NOD2/CARD15 genotype and common gastrointestinal diseases in 43 600 individualsYAZDANYAR, S; NORDESTGAARD, B. G.Journal of internal medicine. 2010, Vol 267, Num 2, pp 228-236, issn 0954-6820, 9 p.Article

Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian populationBIANCHI, Vera; MACONI, Giovanni; ARDIZZONE, Sandro et al.European journal of gastroenterology & hepatology. 2007, Vol 19, Num 3, pp 217-223, issn 0954-691X, 7 p.Article

Plasma carnitine ester profiles in crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypesBENE, Judit; KOMLOSI, Katalin; MELEGH, Béla et al.British journal of nutrition. 2007, Vol 98, Num 2, pp 345-350, issn 0007-1145, 6 p.Article

Gastroduodenal Crohn's disease is associated with NOD2/CARD15 gene polymorphisms, particularly L1007P homozygosityMARDINI, Houssam E; GREGORY, Kalvin J; NASSER, Munira et al.Digestive diseases and sciences. 2005, Vol 50, Num 12, pp 2316-2322, issn 0163-2116, 7 p.Article

What are the major arguments in favour of the genetic susceptibility for inflammatory bowel disease?TAMBOLI, Cyrus P; CORTOT, Antoine; COLOMBEL, Jean-Frédéric et al.European journal of gastroenterology & hepatology. 2003, Vol 15, Num 6, pp 587-592, issn 0954-691X, 6 p.Article

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's diseaseTOMER, Gitit; CEBALLOS, Clare; CONCEPCION, Erlinda et al.The American journal of gastroenterology. 2003, Vol 98, Num 11, pp 2479-2484, issn 0002-9270, 6 p.Article

The relation between NOD2/CARD15 mutations and the prevalence and phenotypic heterogeneity of Crohn's disease : Lessons from the Israeli Arab Crohn's disease cohortKARBAN, Amir; ATIA, Oren; ELIAKIM, Rami et al.Digestive diseases and sciences. 2005, Vol 50, Num 9, pp 1692-1697, issn 0163-2116, 6 p.Article

Maladies inflammatoires chroniques de l'intestin (Paris, 14 mars 2003, résumés) = Chronic inflammatory disease of the bowel (Paris, March 14 2003, abstracts)French workshop of medicineJournée française de médecine. 2003, 23 p.Conference Proceedings

NOD2/CARD15 Gene Mutations in Patients with Familial Mediterranean FeverBERKUN, Yackov; KARBAN, Amir; PADEH, Shai et al.Seminars in arthritis and rheumatism. 2012, Vol 42, Num 1, pp 84-88, issn 0049-0172, 5 p.Article

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15^- Crohn's disease patientsMARQUEZ, Ana; VARADE, Jezabel; DE LA CONCHA, Emilio G et al.European journal of human genetics. 2009, Vol 17, Num 10, pp 1304-1308, issn 1018-4813, 5 p.Article

Relationship between clinical features of Crohn's disease and the risk of developing extraintestinal manifestationsBARREIRO-DE ACOSTA, Manuel; ENRIQUE DOMINGUEZ-MUNOZ, J; NUNEZ-PARDO DE VERA, M. Concepcion et al.European journal of gastroenterology & hepatology. 2007, Vol 19, Num 1, pp 73-78, issn 0954-691X, 6 p.Article

A sporadic case of early-onset sarcoidosis resembling Blau syndrome due to the recurrent R334W missense mutation on the NOD2 geneCOTO-SEGURA, P; MALLO-GARCIA, S; COSTA-ROMERO, M et al.British journal of dermatology (1951). 2007, Vol 157, Num 6, pp 1257-1259, issn 0007-0963, 3 p.Article

Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish populationZHIFENG ZHOU; LIN, Xing-Yu; AKOLKAR, Pradip N et al.The American journal of gastroenterology. 2002, Vol 97, Num 12, pp 3095-3101, issn 0002-9270, 7 p.Article

Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycanBONEN, Denise K; OGURA, Yasunori; CHO, Judy H et al.Gastroenterology (New York, NY. 1943). 2003, Vol 124, Num 1, pp 140-146, issn 0016-5085, 7 p.Article