Articles

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Our experience of anti-interleukin 1 therapy

Authors: N Gulez, B Sozeri and P Gulez

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P210

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Differential diagnosis of CRMO

Authors: A Kozlova, V Roshchin, D Abramov, N Bolshakov, A Roppelt, D Yuhacheva and A Shcherbina

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P208

Content type: Poster presentation Published on: 28 September 2015

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Interleukin 1 blockade withcanakinumab for Hyper IGD syndrome (HIDS)

Authors: J Brunnner, E Binder, D Karall, J Zschocke and C Fauth

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P206

Content type: Poster presentation Published on: 28 September 2015

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Clinical experiences with canakinumab as a treatment for autoinflammatory disorders

Authors: C Saperia, P McAuley, J Raffaghello, S Fazlul Haque and G Sussman

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P202

Content type: Poster presentation Published on: 28 September 2015

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Cryopyrin associated periodic syndromes (CAPS): immunological characterization of knock-in mouse model to exploit novel approaches for the modulation of the NLRP3 inflammasome.

Authors: A Bertoni, S Carta, E Balza, P Catellani, C Pellecchia, F Penco, F Schena, S Borghini, ML Trotta, C Pastorino, I Ceccherini, A Martini, A Rubartelli, M Gattorno and S Chiesa

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P200

Content type: Poster presentation Published on: 28 September 2015

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Beneficial effect of methotrexate on a case of Nakajo-Nishimura syndrome

Authors: K Kunimoto, F Ozaki, F Furukawa and N Kanazawa

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P199

Content type: Poster presentation Published on: 28 September 2015

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Interleukin-1-related cytokines as potential biomarkers in autoinflammatory skin diseases

Authors: H Bonnekoh, M Maurer and K Krause

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P197

Content type: Poster presentation Published on: 28 September 2015

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Pediatric chronic non-bacterial osteomyelitis in Goteborg, Sweden

Authors: S Berg, P Wekell, S Óskarsdóttir, J Martinell, R Rupröder, E Fridh, A Karlsson, T Backteman and A Fasth

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P180

Content type: Poster presentation Published on: 28 September 2015

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Chronic recurrent multifocal osteomyelitis in N. Greece: disease burden in pediatric patients

Authors: M Trachana, P Pratsidou-Gertsi, E Papadimitriou, A Anastasiou, E Karatza, G Pardalos and E Roilides

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P172

Content type: Poster presentation Published on: 28 September 2015

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Behcet Disease in pediatric Argentinian patients

Authors: S Meiorin, C Vega, E Macias, T Gonzalez Vargas and G Espada

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P170

Content type: Poster presentation Published on: 28 September 2015

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Cronic non-bacterial osteomyelitis (CNO) in a cohort of pediatric patients: clinical, biological and radiological response to treatment with Anakinra

Authors: M Pardeo, D Pires Marafon, V Messia, R Nicolai, C Bracaglia, F de Benedetti and A Insalaco

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P168

Content type: Poster presentation Published on: 28 September 2015

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The case of Schnitzler syndrome in one single rheumatologic center

Authors: S Salugina, E Fedorov, V Gorodetskiy, M Evsikova and N Lopatina

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P164

Content type: Poster presentation Published on: 28 September 2015

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The familial Mediterranean fever (FMF) 50 score: does it work in a controlled clinical trial? Re-analysis of the trial of rilonacept for patients with colchicine resistant or intolerant FMF

Authors: P Hashkes and B Huang

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P158

Content type: Poster presentation Published on: 28 September 2015

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Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene

Authors: H Girschick, C Wolf, H Morbach, C Hertzberg and MA Lee-Kirsch

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P141

Content type: Poster presentation Published on: 28 September 2015

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Comparison of the colchicine concentration between different matrix; plasma, leucocytes, ficoll solution measured by ESI LC-MS/MS

Authors: H Gul, E Demirkaya, B Eser, T Honca, FN Felek and D Simsek

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P137

Content type: Poster presentation Published on: 28 September 2015

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Anti-IL1ß-monoclonal antibody in two adult patients with PFAPA Syndrome - a single centre experience

Authors: B Kortus-Götze and J Hoyer

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P135

Content type: Poster presentation Published on: 28 September 2015

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Increased prevalence of attention deficit hyperactivity disorder in children with Familial Mediterranean Fever

Authors: E Lavi, I Berger, E Eisenstein and Y Berkun

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P131

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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MEFV gene mutation distrubution in Azerbaijan population

Authors: A Berdeli, G Mukhtarova, A Oz and S Musayev

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P127

Content type: Poster presentation Published on: 28 September 2015

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Identification of pyrin targets by CHiP-Seq

Authors: G Wood, Y Kanno, H Sun, G Gutierrez-Cruz, I Aksentijevich and D Kastner

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P125

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Coexistence of PFAPA syndrome and FMF in Armenian children

Authors: N Mkrtchyan, G Amaryan and T Sarkisian

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P102

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Genotype -phenotype correlation of MEFV mutations in Eastern / Central European population

Authors: N Toplak, M Debeljak and T Avcin

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P100

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Screening for inherited metabolic disorders in patients with Familial Mediterranean Fever

Authors: E Kiykim, AC Aktuglu-Zeybek, K Barut, T Zubarioglu, MS Cansever, A Aydin and O Kasapcopur

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P97

Content type: Poster presentation Published on: 28 September 2015

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Prevalence of CECR1 mutations in pediatric patients with polyarteritis nodosa, livedo reticularis and/or stroke

Authors: R Caorsi, A Grossi, A Insalaco, M Alessio, S Martino, E Cortis, A Morreale, F Caroli, A Martini, I Ceccherini and M Gattorno

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O87

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Toll like receptor 2 is overexpressed in FMF patients during attacks and inhibited by colchicine treatment

Authors: H Ben-David, V Hornung, T Ebert, A Livneh and I Ben-Zvi

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P74

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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The IL-1 inhibitor Canakinumab for Familial Mediterranean Fever: the Greek experience in 12 patients

Authors: K Laskari, P Boura, GN Dalekos, A Garyfallos, D Karokis, D Pikazis, L Settas, G Skarantavos, E Tsitsami and PP Sfikakis

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P72

Content type: Poster presentation Published on: 28 September 2015

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Empirical use of anakinra in AA amyloidosis of uncertain aetiology

Authors: T Lane, DM Rowczenio, JA Gilbertson, JD Gillmore, AD Wechalekar, PN Hawkins and HJ Lachmann

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O70

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Enlarging the clinical spectrum of SAVI syndrome

Authors: R Caorsi, G Rice, S Volpi, F Cardinale, A Buoncompagni, Y Crow, A Martini, M Gattorno and P Picco

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P70

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Effectiveness of canakinumab treatment in Schnitzler's syndrome: a multi-center randomized placebo-controlled study

Authors: K Krause, A Tsianakas, N Wagner, J Fischer, K Weller, M Metz and M Maurer

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O66

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Atypical manifestations in CAPS sydrome: not so unfrequent?

Authors: S Buján-Rivas, M Basagaña-Torrentó, C Modesto-Caballero, JI Aróstegui-Gorospe, M Vilardell-Tarrès and J Yagüe

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P66

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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CECR1 p.Gly47Arg mutations are not increased in frequency in Turkish Behçet's disease patients compared with healthy controls

Authors: B Erer, E Remmers, M Takeuchi, D Ustek, I Tugal-Tutkun, E Seyahi, Y Ozyazgan, A Gul, M Ombrello and D Kastner

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P64

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Familial chilblain lupus caused by an activating mutation in STING

Authors: N König, C Fiehn, H-M Lorenz and MA Lee-Kirsch

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O62

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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First case of somatic mosaicism in TRAPS caused by a novel 24 nucleotides deletion in the TNFRSF1A gene

Authors: D Rowczenio, E Omoyinmi, H Trojer, T Lane, P Brogan, P Hawkins and H Lachmann

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O60

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Long-term efficacy and safety of Canakinumab in active Hyper-IgD syndrome (HIDS): results from an open-label study

Authors: JI Aróstegui, J Anton, I Calvo, A Robles, A Speziale, Y Joubert, G Junge and J Yagüe

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O58

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Whole-Body MRI versus bone scintigraphy: which is the best diagnostic tool in patients with chronic recurrent multifocal osteomyelitis (CRMO)?

Authors: MF Villani, L Tanturri de Horatio, MC Garganese, I Casazza, S Savelli, M Pardeo, V Messia, F De Benedetti and A Insalaco

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P58

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Monocytes and neutrophils in the inflammatory cascade of systemic onset Juvenile Idiopathic Arthritis

Authors: N ter Haar, W de Jager, R Scholman, P Leliefeld, T Tak, B Vastert and S de Roock

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O54

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Late onset of the cryopyrin-associated periodic syndrome (CAPS) associated with low level of somatic mosaicism in six patients

Authors: D Rowczenio, S Melo Gomes, J Aróstegui, E Omoyinmi, E Gonzalez-Roca, A Standing, D Eleftheriou, N Klein, P Brogan, H Lachmann and P Hawkins

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P37

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Diagnostics of CAPS in Quebec thanks to teaching program

Authors: A-L Chetaille, A Albert, K Adams, P Fortin and L Michou

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P35

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Spontaneous Type I IFN response in SAMHD1-deficient mice requires both, functional intracellular RNA and DNA sensing pathways

Authors: R Behrendt, T Schumann, A Gerbaulet, S Wittmann, T Gramberg and A Roers

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O33

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Characterisation of human iPS cells harbouring the p.A329T variant of caspase-1

Authors: J Thiem and A Rösen-Wolff

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P33

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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A large family having Muckle Wells Syndrome

Authors: SS Kilic and S Cekic

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P31

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Neutralization of Interferon-gamma is efficacious in a mouse model of HLH secondary to chronic inflammation

Authors: G Prencipe, I Caiello, C Bracaglia, C de Min and F De Benedetti

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O29

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Development of the autoinflammatory disease damage index (ADDI)

Authors: K Annink, N ter Haar, M Gattorno, H Lachmann, J Kuemmerle-Deschner, S Ozen, R Goldbach-Mansky, K Durrant, O Della Casa Alberighi and J Frenkel

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P29

Content type: Poster presentation Published on: 28 September 2015

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A significant role for tumor necrosis factor in Nlrp3 inflammasomeopathies

Authors: M McGeough, A Wree, C Pena, M Inzaugarat, A Feldstein and H Hoffman

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O27

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Variant CAPS in an adult- the use of genetics

Authors: M Rozenbam, D Rimar, L Kaly, G Slobodin, A Awisat and I Rosner

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P27

Content type: Poster presentation Published on: 28 September 2015

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Genetic and phenotypic characteristics of 114 patients with mevalonate kinase deficiency

Authors: J Jeyaratnam, N ter Haar, H Lachmann, A Simon, P Brogan, M Doglio, M Cattalini, J Anton, C Modesto, P Quartier, J Frenkel and M Gattorno

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P25

Content type: Poster presentation Published on: 28 September 2015

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Clinical follow-up on a cohort of patients with deficiency of adenosine deaminase 2 (DADA2)

Authors: K Barron, A Ombrello, D Stone, P Hoffmann, I Aksentijevich, Q Zhou, A Jones and D Kastner

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O21

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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The intracellular signalling pathway signature (the signalome) in PBMCs in the presence of a common TRAPS-associated genetic variant, TNFRSF1A p.(Arg121Gln) (legacy p.R92Q) is distinct from normal PBMCs and from other pathogenic variants

Authors: A Bybee, O Negm, W Abduljabbar, L Fairclough, H Lachmann, T Lane, I Todd, P Hawkins and P Tighe

Citation: Pediatric Rheumatology 2015 13(Suppl 1):P19

Content type: Poster presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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NGS for the diagnosis of autoinflammatory diseases: the experience of Montpellier

Authors: G Sarrabay, G Tachon, D Mechin and I Touitou

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O17

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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First report of MEFV duplication in FMF patient

Authors: G Sarrabay, D Méchin, B Dumont, M André and I Touitou

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O15

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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Loss of function mutation in a mitochondrial chaperone protein leading to dyregulated ROS production, and autoinflammatory disease in a single kindred

Authors: A Standing, D Eleftheriou, C Paisan-Ruiz, D Rowcenzio, Y Hong, E Omoyinmi, P Woo, P Hawkins, H Lachmann, N Klein and P Brogan

Citation: Pediatric Rheumatology 2015 13(Suppl 1):O1

Content type: Oral presentation Published on: 28 September 2015

This article is part of a Supplement: Volume 13 Supplement 1
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