PW02-017 - New tools for the ISSAID society website

Por Touitou, I, Milhavet, F
Publicado em 2013

Excess PCR primers may dramatically affect SSCP efficiency.

Por Cai, Q Q, Touitou, I
Publicado em 1993

Familial Mediterranean Fever (FMF) before the age of one year

Por Delion, F, Touitou, I, Kone-Paut, I
Publicado em 2008

Aortoarteritis and cardiomyopathy in a child with Blau Syndrome

Por Khubchandani, RP, Hasija, RP, Touitou, I, Khemani, C
Publicado em 2011

Experience with pediatric sarcoidosis at a centre in Mumbai, India

Por Khubchandani, RP, Hasija, RP, Touitou, I, Khemani, C
Publicado em 2011

NGS for the diagnosis of autoinflammatory diseases: the experience of Montpellier

Por Sarrabay, G, Tachon, G, Mechin, D, Touitou, I
Publicado no Pediatr Rheumatol Online J (2015)

Paediatric Behçet's disease in France

Por Kone-Paut, I, Gorchakoff-Molina..., A, Weschler, B, Touitou, I
Publicado em 2002

Refractory auto‐inflammatory syndrome associated with digenic transmission of low‐penetrance tumour necrosis factor receptor‐associated periodic syndrome and cryopyrin‐associated p...

Por Touitou, I, Perez, C, Dumont, B, Federici, L, Jorgensen, C
Publicado em 2006

First report of MEFV duplication in FMF patient

Por Sarrabay, G, Méchin, D, Dumont, B, André, M, Touitou, I
Publicado no Pediatr Rheumatol Online J (2015)

The chicken ovalbumin promoter is under negative control which is relieved by steroid hormones.

Por Gaub, M P, Dierich, A, Astinotti, D, Touitou, I, Chambon, P
Publicado em 1987

The clinical spectrum of 94 French patients carrying a single mutated MEFV allele

Por Koné-Paut I, Hentgen V, Guillaume-Czitrom S, Lacassagne S, Tran TA, Touitou I
Publicado em 2008-09-01

Autoinflammatory gene mutations in Behçet's disease

Por Koné‐Paut, I, Sanchez, E, Quellec, A Le, Manna, R, Touitou, I
Publicado em 2007

An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement

Por Touitou, I, Rittore, C, Philibert, L, Yagüe, J, Shinar, Y, Aksentijevich, I
Publicado em 2009

The clinical spectrum of 94 French patients carrying a single mutated MEFV allele

Por Koné-Paut, I, Hentgen, V, Guillaume-Czitrom, S, Lacassagne, S, Tran, TA, Touitou, I
Publicado em 2008

Characterization of the TNFR1-d2 protein: Implication in TNF receptor associated periodic syndrome (TRAPS)?

Por Rittore, C, Sanchez, E, Soler, S, Ea, V, Genevieve, D, Touitou, I, Grandemange, S
Publicado no Pediatr Rheumatol Online J (2015)

NLRP1 mutations cause autoinflammatory diseases in human

Por Grandemange, S, Sanchez, E, Louis-Plence, P, Rittore, C, Reed, JC, Touitou, I, Geneviève, D
Publicado no Pediatr Rheumatol Online J (2015)

OR10-002 - A novel TNFR1 transcript of TRAPS gene

Por Rittore, C, Sanchez, E, Soler, S, Albers, M, Obici, L, McDermott, MF, Touitou, I, Grandemange, S
Publicado em 2013

Identification of three ADA2 deficiency families with novel CECR1 mutations

Por Sarrabay, G, Insalaco, A, Uettwiller, F, Tieulié, N, Quartier-dit-maire, P, Melki, J, Touitou, I
Publicado no Pediatr Rheumatol Online J (2015)

A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients

Por Federici, L, Rittore‐Domingo, C, Koné‐Paut, I, Jorgensen, C, Rodière, M, Quellec, A Le, Touitou, I
Publicado em 2006

P03-010 - IL10 SNPs associated with BD in Western Algeria

Por Khaib Dit Naib, O, Aribi, M, Idder, A, Chiali, A, Sairi, H, Touitou, I, Lefranc, G, Barat-Houari, M
Publicado em 2013