Polly J Ferguson

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Polly J



Publications in SciGraph latest 50 shown

  • 2018 Chronic Recurrent Multifocal Osteomyelitis (CRMO) in THE MICROBIOME IN RHEUMATIC DISEASES AND INFECTION
  • 2017-12 Chronic Recurrent Multifocal Osteomyelitis (CRMO): Presentation, Pathogenesis, and Treatment in CURRENT OSTEOPOROSIS REPORTS
  • 2017-04 Chronic Recurrent Multifocal Osteomyelitis and Related Diseases—Update on Pathogenesis in CURRENT RHEUMATOLOGY REPORTS
  • 2017-03 Treatment Advances in Chronic Non-Bacterial Osteomyelitis and Other Autoinflammatory Bone Conditions in CURRENT TREATMENT OPTIONS IN RHEUMATOLOGY
  • 2016-10-25 Nlrp12 mutation causes C57BL/6J strain-specific defect in neutrophil recruitment in NATURE COMMUNICATIONS
  • 2016-07 Proceedings of the 2016 Childhood Arthritis and Rheumatology Research Alliance (CARRA) Scientific Meeting in PEDIATRIC RHEUMATOLOGY
  • 2015-07 New discoveries in CRMO: IL-1β, the neutrophil, and the microbiome implicated in disease pathogenesis in Pstpip2-deficient mice in SEMINARS IN IMMUNOPATHOLOGY
  • 2014-06 Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction in MOLECULAR PSYCHIATRY
  • 2013-11 Exome Sequencing Reveals RAG1 Mutations in a Child with Autoimmunity and Sterile Chronic Multifocal Osteomyelitis Evolving into Disseminated Granulomatous Disease in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2013-10 Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction in MOLECULAR PSYCHIATRY
  • 2013-10 The non-canonical Wnt ligand Wnt5a rescues morphological deficits in Prickle2-deficient hippocampal neurons in MOLECULAR PSYCHIATRY
  • 2012-07 Developing juvenile localized scleroderma (jLS) consensus treatment regimens for comparative effectiveness studies in PEDIATRIC RHEUMATOLOGY
  • 2012-04 Current Understanding of the Pathogenesis and Management of Chronic Recurrent Multifocal Osteomyelitis in CURRENT RHEUMATOLOGY REPORTS
  • 2011-12 Novel mutation of the LPIN2 gene in Turkish brothers with Majeed syndrome. Response to IL-1 inhibition in PEDIATRIC RHEUMATOLOGY
  • 2009-12 Papular xanthomas and erosive arthritis in a 3 year old girl, is this a new MRH variant? in PEDIATRIC RHEUMATOLOGY
  • 2009 Monogenic Autoinflammatory Syndromes in A CLINICIAN'S PEARLS AND MYTHS IN RHEUMATOLOGY
  • 2008-12 Primary multifocal osseous lymphoma in a child in PEDIATRIC RADIOLOGY
  • 2001-01 The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 in NATURE GENETICS
  • 1997-04 Genetic control of resistance to insulin-dependent diabetes in NOD mice.• 382 in PEDIATRIC RESEARCH
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