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Pernicious anemia: what are the actual diagnosis criteria?

Cattan D.

World J Gastroenterol. 2011 Jan 28;17(4):543-4. doi: 10.3748/wjg.v17.i4.543.


Clinical features and outcomes in 348 patients with polyarteritis nodosa: a systematic retrospective study of patients diagnosed between 1963 and 2005 and entered into the French Vasculitis Study Group Database.

Pagnoux C, Seror R, Henegar C, Mahr A, Cohen P, Le Guern V, Bienvenu B, Mouthon L, Guillevin L; French Vasculitis Study Group.

Arthritis Rheum. 2010 Feb;62(2):616-26. doi: 10.1002/art.27240.


Characterization of new mutations in the 5'-flanking region of the familial Mediterranean fever gene.

Notarnicola C, Boizet-Bonhoure B, de Santa Barbara P, Osta MA, Cattan D, Touitou I.

Genes Immun. 2009 Apr;10(3):273-9. doi: 10.1038/gene.2009.8. Epub 2009 Mar 5.


ABCC6 is unlikely to be a modifier gene for familial Mediterranean fever severity.

Chassaing N, Touitou I, Cattan D, Calvas P.

J Genet. 2007 Dec;86(3):293-5. No abstract available.


Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever.

Touitou I, Sarkisian T, Medlej-Hashim M, Tunca M, Livneh A, Cattan D, Yalçinkaya F, Ozen S, Majeed H, Ozdogan H, Kastner D, Booth D, Ben-Chetrit E, Pugnère D, Michelon C, Séguret F, Gershoni-Baruch R; International Study Group for Phenotype-Genotype Correlation in Familial Mediterranean Fever.

Arthritis Rheum. 2007 May;56(5):1706-12.


Early and severe amyloidosis in a patient with concurrent familial Mediterranean fever and pseudoxanthoma elasticum.

Cattan D, Bouali B, Chassaing N, Martinez F, Dupont JM, Dode C, Martin L.

Br J Dermatol. 2006 Jun;154(6):1190-3.


Discussion on the effect of chronic hypergastrinemia on human enterochromaffin-like cells: insights from patients with sporadic gastrinomas.

Cattan D.

Gastroenterology. 2003 Aug;125(2):627; author reply 627-8. No abstract available.


CATSPER2, a human autosomal nonsyndromic male infertility gene.

Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, Zaizov R, Shalev H, Delaunay J, Fellous M, Lancet D, Beckmann JS.

Eur J Hum Genet. 2003 Jul;11(7):497-502.


Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.

Am J Hum Genet. 2002 Dec;71(6):1467-74. Epub 2002 Nov 14.


The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome.

Dodé C, André M, Bienvenu T, Hausfater P, Pêcheux C, Bienvenu J, Lecron JC, Reinert P, Cattan D, Piette JC, Szajnert MF, Delpech M, Grateau G; French Heraditary Recurrent Inflammatory Disorder Study Group.

Arthritis Rheum. 2002 Aug;46(8):2181-8.


Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks.

Dodé C, Hazenberg BP, Pêcheux C, Cattan D, Moulin B, Barthélémy A, Gubler MC, Delpech M, Grateau G.

Nephrol Dial Transplant. 2002 Jul;17(7):1212-7.


[Familial Mediterranean fever].

Cattan D, Dervichian M.

Rev Prat. 2002 Jan 15;52(2):149-54. Review. French.


[Hereditary hyperferritinemia syndrome and cataract].

Feys J, Nodarian M, Aygalenq P, Cattan D, Bouccara AS, Beaumont C.

J Fr Ophtalmol. 2001 Oct;24(8):847-50. French.


MEFV mutations and phenotype-genotype correlations in North African Jews and Armenians with familial Mediterranean fever.

Cattan D, Dervichian M, Thomas M, Dode C, Touitou I.

Isr Med Assoc J. 2001 Nov;3(11):803-4.


The MICA region determines the first modifier locus in familial Mediterranean fever.

Touitou I, Picot MC, Domingo C, Notarnicola C, Cattan D, Demaille J, Koné-Paut I.

Arthritis Rheum. 2001 Jan;44(1):163-9.


Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever.

Dodé C, Pêcheux C, Cazeneuve C, Cattan D, Dervichian M, Goossens M, Delpech M, Amselem S, Grateau G.

Am J Med Genet. 2000 Jun 5;92(4):241-6.


Clinical versus genetic diagnosis of familial Mediterranean fever.

Grateau G, Pêcheux C, Cazeneuve C, Cattan D, Dervichian M, Goossens M, Delpech M, Amselem S, Dodé C.

QJM. 2000 Apr;93(4):223-9.


Inflammatory bowel disease in non-Ashkenazi Jews with familial Mediterranean fever.

Cattan D, Notarnicola C, Molinari N, Touitou I.

Lancet. 2000 Jan 29;355(9201):378-9. Erratum in: Lancet 2000 Mar 18;355(9208):1020.


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