Early onset chronic arthritis associated with chromosome deletion 22 q11.2 syndrome. Is it juvenile idiophatic arthritis?

Early onset chronic arthritis associated with chromosome deletion 22 q11.2 syndrome. Is it juvenile idiophatic arthritis?

Bibliographic Details
Main Authors:	Galindo Rocio, Diaz Gisela, De Cabo Pablo, Nuñez Esmeralda, Urda Antonio
Format:	Article
Language:	English
Published:	BMC 2011-09-01
Series:	Pediatric Rheumatology Online Journal

Similar Items

FAMILIAL CASE OF CHROMOSOME 22q11.2 DELETION SYNDROME
by: I. A. Tuzankina, et al.
Published: (2017-01-01)

Dopaminergic neurons in chromosome 22q11.2 deletion syndrome
by: Haruhisa Inoue
Published: (2021-01-01)

Immune Defects in Chromosome 22q11.2 Deletion Syndromes
by: Bobey, Nicola A.
Published: (2010)

The Development of Cognitive Control in Children with Chromosome 22q11.2 Deletion Syndrome
by: Heather M Shapiro, et al.
Published: (2014-06-01)

Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons
by: Yuko Arioka, et al.
Published: (2021-01-01)

CLINICAL CASE OF CHROMOSOME 22Q11.2 DELETION SYNDROME (DI-GEORGIE SYNDROME)
by: Ирина Анатольевна Никитина, et al.
Published: (2020-02-01)

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
by: Cabaral Margarita H, et al.
Published: (2012-04-01)

Thrombocytopenia and Postpartum Hemorrhage in a Woman with Chromosome 22q11.2 Deletion Syndrome
by: Sarah L. Pachtman, et al.
Published: (2016-01-01)

Chromosome 22q11.2 deletion: world definition criteria, standards for diagnosis and monitoring
by: M.A. Gonchar, et al.
Published: (2018-02-01)

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
by: Halder Ashutosh, et al.
Published: (2012-03-01)

Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features
by: Sira Korpaisarn, et al.
Published: (2013-01-01)

Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome
by: Gloria Colarusso, et al.
Published: (2010-06-01)

Hematological abnormalities and 22q11.2 deletion syndrome
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-01-01)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
by: Qiumei Du, et al.
Published: (2020-02-01)

The developmental cognitive trajectory of the 22q11.2 deletion
by: Jacobson, Clare Elizabeth Harvey
Published: (2012)

Temporomandibular joint involvement (TMJ), a silent disease with severe alterations in young adulthood patients affected by juvenile idiophatic arthritis (JIA)
by: Mario Bosco, et al.
Published: (2011-09-01)

Brain, behaviour and cognition in 22q11.2 deletion syndrome (22qDS)
by: Campbell, Linda Elisabet
Published: (2006)

Síndrome de deleção 22q11.2: compreendendo o CATCH22 22q11.2 deletion syndrome: catching the CATCH22
by: Rafael Fabiano M. Rosa, et al.
Published: (2009-06-01)

Structural connectivity and immunological correlates of emotion processing in children with chromosome 22q11.2 deletion syndrome
by: Sanders, Ashley F. P.
Published: (2019)

Specific differences in temporal binding aspects of the attentional blink in Chromosome 22q11.2 Deletion Syndrome
by: Antshel, K.M, et al.
Published: (2018)

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment
by: Lee Aaron, et al.
Published: (2007-10-01)

Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology
by: Sanders, Ashley F. P.
Published: (2016)

22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment
by: Leyla S. Namazova-Baranova, et al.
Published: (2016-12-01)

Psychiatric disorders associated with 22q11.2 deletion syndrome
by: Orsola Gambini
Published: (2016-06-01)

Neuropsychological and Language Deficits in 22q11.2 Deletion Syndrome
by: J Gordon Millichap, et al.
Published: (2014-07-01)

Disrupted anatomic networks in the 22q11.2 deletion syndrome
by: J. Eric Schmitt, MD PhD, et al.
Published: (2016-01-01)

Visual processing deficits in 22q11.2 Deletion Syndrome
by: Marjan Biria, et al.
Published: (2018-01-01)

Genotype-phenotype correlation in 22q11.2 deletion syndrome
by: Michaelovsky Elena, et al.
Published: (2012-12-01)

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
by: Gee James C, et al.
Published: (2008-06-01)

Sinus of Valsalva Aneurysm Rupture: An Unusual Presentation of Chromosome 22q11.2 Deletion: A Case Report
by: Eda-Cristina Abuchaibe, et al.
Published: (2012-01-01)

A cross-sectional analysis of the development of response inhibition in children with Chromosome 22q11.2 Deletion Syndrome
by: Heather M Shapiro, et al.
Published: (2013-08-01)

Síndrome de deleção 22q11.2 e cardiopatias congênitas 22q11.2 deletion syndrome and congenital heart defects
by: Rafael Fabiano M. Rosa, et al.
Published: (2011-06-01)

22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT
by: Leyla S. Namazova-Baranova, et al.
Published: (2017-11-01)

Acute dystonia in a patient with 22q11.2 deletion syndrome
by: Konstantinos Kontoangelos, et al.
Published: (2015-09-01)

The 22q11.2 Deletion Syndrome: A Gene Dosage Perspective
by: Antonio Baldini
Published: (2006-01-01)

Hypocalcemia due to 22q11.2 deletion syndrome diagnosed in adulthood
by: Maria Cabrer, et al.
Published: (2018-01-01)

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance
by: Nicole E Spruijt, et al.
Published: (2014-07-01)

Familial 22q11.2 deletion syndrome with autosomal dominant inheritance
by: Bahar Gokturk, et al.
Published: (2016-06-01)

Subcortical Myoclonus and Associated Dystonia in 22q11.2 Deletion Syndrome
by: Vincent Van Iseghem, et al.
Published: (2020-01-01)

Predictors of Velopharyngeal Dysfunction for Individuals with 22q11.2 Deletion Syndrome
by: Giordullo, Alyxis M.
Published: (2017)

Cannot write session to /tmp/vufind_sessions/sess_mphjuml947lifsp9elqgoosnnu