G. Vaudour

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.

D. Scott, L. Cuisset, J. Berthelot, 2002, American journal of human genetics.

Membranous nephropathy associated with ovarian tumour in a young girl: recovery after removal

M. Lévy, P. Beauvais, G. Vaudour, 1989, European Journal of Pediatrics.

[Creutzfeldt-Jakob disease in 4 children treated with growth hormone].

D. Dormont, T. Billette de Villemeur, P. Beauvais, 1992, Revue neurologique.

Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

J. Beckmann, D. Scott, David Steven Scott, 1999, American journal of human genetics.

The Muckle-Wells syndrome and the major histocompatibility complex.

J. Muller, C. Kaplan, G. Vaudour, 2008, Tissue antigens.

[Primary intestinal lymphangiectasis with antenatal manifestation].

J. Navarro, A. Munck, P. Foucaud, 1986, Archives francaises de pediatrie.