[HTML][HTML] Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy

P Navon Elkan, SB Pierce, R Segel… - … England Journal of …, 2014 - Mass Medical Soc
Background Polyarteritis nodosa is a systemic necrotizing vasculitis with a pathogenesis
that is poorly understood. We identified six families with multiple cases of systemic and …

Seasonal variation in systemic onset juvenile rheumatoid arthritis in Israel.

Y Uziel, A Pomeranz, R Brik, P Navon… - The Journal of …, 1999 - europepmc.org
Objective To determine whether there is a seasonal peak onset of systemic juvenile
rheumatoid arthritis (SOJRA) suggestive of an infectious etiology. We examined the seasonal …

Lupus around the World: Outcome of a national Israeli cohort of pediatric systemic lupus erythematosus

…, Y Berkun, T Tauber, J Press, L Harel, P Navon… - Lupus, 2007 - journals.sagepub.com
The aim of this study was to describe the clinical manifestations and outcomes of a national
cohort of childhood systemic lupus erythematosus (cSLE). All cases of cSLE registered in the …

Pleural fluid characteristics in pulmonary brucellosis.

E Kerem, O Diav, P Navon, D Branski - Thorax, 1994 - thorax.bmj.com
Although pulmonary symptoms accompany up to 16% of cases of infection with Brucella
melitensis, pleural effusion has rarely been reported. A 12 year old girl had brucellosis with …

Hyperostosis–Hyperphosphatemia Syndrome: A Congenital Disorder of O‐Glycosylation Associated With Augmented Processing of Fibroblast Growth Factor 23

…, S Feinstein, I Urakawa, P Navon‐Elkan… - Journal of Bone and …, 2007 - academic.oup.com
Two hyperphosphatemic patients with mutations in GALNT3 showed low intact FGF23
levels with marked increase of processed C‐terminal fragments. FGF23 protein has three O‐…

Desensitization to hydroxychloroquine--experience of 4 patients.

M Mates, S Zevin, GS Breuer, P Navon… - The Journal of …, 2006 - jrheum.org
… Zevin, MD, Senior Lecturer, Department of Internal Medicine; GS Breuer, MD, Lecturer,
Department of Internal Medicine and Rheumatology Clinic; P. Navon, MD, Department of …

Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNALeu (UUR) gene (A3243T)

A Shaag, A Saada, A Steinberg, P Navon… - Biochemical and …, 1997 - Elsevier
We report a new mutation, an A→T transition at nt 3243 in the mitochondrial tRNA leu(UUR)
gene, in a 9-year-old girl who presented with muscle weakness of 3 years duration …

Dent's disease manifesting as focal glomerulosclerosis: is it the tip of the iceberg?

…, C Rinat, S Feinstein, P Navon-Elkan… - Pediatric …, 2009 - Springer
… All three mutations are pathogenic: two are novel (p.Asp727fs and p.Trp122X), and one
is a recurrent mutation, p.R648X. Given the atypical phenotype of these patients with Dent’s …

Acute rheumatic fever associated with Henoch‐Schönlein purpura: report of three cases and review of the literature

EM Eisenstein, P Navon‐Elkan - Acta Paediatrica, 2002 - Wiley Online Library
Aim: To describe a possible relationship between Henoch‐Schönlein purpura and rheumatic
fever. Methods: Patients with features of both diseases were identified by reviewing the …

Differentation of post-streptococcal reactive arthritis from acute rheumatic fever

J Barash, E Mashiach, P Navon-Elkan, Y Berkun… - The Journal of …, 2008 - Elsevier
… to 33% of the patients in the PSRA group (P = .004). The distribution of involved … (P = .0002).
Arthritis was symmetrical in 40% of patients with ARF and 22% of the patients with PSRA (P