Lista de obras - Claas Hinze - Dominio Público Uruguay

4.4 Different phenotype of anaemia in systemic juvenile idiopathic arthritis (s-JIA) compared to anaemia in other subtypes of JIA.

artículo científico publicado en 2008

Autoinflammatory diseases: New diagnostic criteria for CAPS - turning horses into zebras?

artículo científico publicado en 2016

B cell depletion: on the rise

artículo científico publicado en 2007

B-cell depletion in Wegener's granulomatosis.

artículo científico publicado en 2008

Calcium and zinc tune autoinflammatory Toll-like receptor 4 signaling by S100A12

artículo científico publicado en 2018

Challenges of Diagnosing Cognitive Dysfunction With Neuropsychiatric Systemic Lupus Erythematosus in Childhood.

artículo científico publicado en 2016

Combination of ofatumumab and fresh frozen plasma in hypocomplementemic systemic lupus erythematosus: a case report

artículo científico publicado en 2018

Combination of rituximab and abatacept as an exit strategy for repetitive B-cell depletion in children with severe autoimmune diseases: a report of three cases

artículo científico publicado en 2018

Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean Fever

artículo científico publicado en 2016

Current management of juvenile dermatomyositis in Germany and Austria: an online survey of pediatric rheumatologists and pediatric neurologists.

artículo científico publicado en 2018

Development of positive antinuclear antibodies and rheumatoid factor in systemic juvenile idiopathic arthritis points toward an autoimmune phenotype later in the disease course

artículo científico publicado en 2014

Development of practice and consensus-based strategies including a treat-to-target approach for the management of moderate and severe juvenile dermatomyositis in Germany and Austria.

artículo científico publicado en 2018

Effectiveness of dexamethasone iontophoresis for temporomandibular joint involvement in juvenile idiopathic arthritis.

artículo científico publicado en 2011

Evaluation of sedimentation rate methodology reveals an unusual pediatric subpopulation with lupus or lupus-like syndrome and hemolytic anemia

artículo científico publicado en 2012

Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets

artículo científico publicado en 2009

Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke ⬇️

artículo científico publicado el 14 de marzo de 2011

Impact of IL1RN Variants on Response to Interleukin-1 Blocking Therapy in Systemic Juvenile Idiopathic Arthritis

scientific article published on 28 January 2020

Inherited p40phox deficiency differs from classic chronic granulomatous disease

scientific article published on 06 August 2018

Kawasaki disease without fever

artículo científico publicado en 2009

Leukocyte adhesion deficiency type 1 presenting with recurrent pyoderma gangrenosum and flaccid scarring

artículo científico publicado en 2010

Management of juvenile idiopathic arthritis: hitting the target

artículo científico

Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature.

artículo científico publicado en 2017

PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype.

artículo científico publicado en 2013

Pediatric rheumatology--its own specialty

scientific article published on 01 June 2008

Practice and consensus-based strategies in diagnosing and managing systemic juvenile idiopathic arthritis in Germany

artículo científico publicado en 2018

Proinflammatory Cytokine Environments Can Drive Interleukin-17 Overexpression by γ/δ T Cells in Systemic Juvenile Idiopathic Arthritis

artículo científico publicado en 2017

Reply

Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations

artículo científico publicado en 2011

Rituximab therapy for severe refractory chronic Henoch-Schönlein purpura.

artículo científico publicado en 2009

Serum S100A8/A9 and S100A12 Levels in Children With Polyarticular Forms of Juvenile Idiopathic Arthritis: Relationship to Maintenance of Clinically Inactive Disease During Anti-Tumor Necrosis Factor Therapy and Occurrence of Disease Flare After Disc

scientific article published on 24 January 2019

Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases

artículo científico publicado en 2015

Subtype-specific peripheral blood gene expression profiles in recent-onset juvenile idiopathic arthritis

scientific article published on July 2009

Synergistic Signaling of TLR and IFNα/β Facilitates Escape of IL-18 Expression from Endotoxin Tolerance

scientific article published on 01 March 2020

Treatment with high-dose recombinant human hyaluronidase-facilitated subcutaneous immune globulins in patients with juvenile dermatomyositis who are intolerant to intravenous immune globulins: a report of 5 cases.

artículo científico publicado en 2016

Understanding the biology and use of TNF therapy in jia-clinical outcomes

artículo científico publicado en 2014

Varicella-zoster-virus vaccination in immunosuppressed children with rheumatic diseases using a pre-vaccination check list.

artículo científico publicado en 2018

[Back to school physical education despite rheumatism : Development and testing of a sport scientific-based physical education certification]

scientific article published on 01 October 2018

Lista de obras de Claas Hinze

4.4 Different phenotype of anaemia in systemic juvenile idiopathic arthritis (s-JIA) compared to anaemia in other subtypes of JIA.

Autoinflammatory diseases: New diagnostic criteria for CAPS - turning horses into zebras?

B cell depletion: on the rise

B-cell depletion in Wegener's granulomatosis.

Calcium and zinc tune autoinflammatory Toll-like receptor 4 signaling by S100A12

Challenges of Diagnosing Cognitive Dysfunction With Neuropsychiatric Systemic Lupus Erythematosus in Childhood.

Combination of ofatumumab and fresh frozen plasma in hypocomplementemic systemic lupus erythematosus: a case report

Combination of rituximab and abatacept as an exit strategy for repetitive B-cell depletion in children with severe autoimmune diseases: a report of three cases

Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean Fever

Current management of juvenile dermatomyositis in Germany and Austria: an online survey of pediatric rheumatologists and pediatric neurologists.

Development of positive antinuclear antibodies and rheumatoid factor in systemic juvenile idiopathic arthritis points toward an autoimmune phenotype later in the disease course

Development of practice and consensus-based strategies including a treat-to-target approach for the management of moderate and severe juvenile dermatomyositis in Germany and Austria.

Effectiveness of dexamethasone iontophoresis for temporomandibular joint involvement in juvenile idiopathic arthritis.

Evaluation of sedimentation rate methodology reveals an unusual pediatric subpopulation with lupus or lupus-like syndrome and hemolytic anemia

Gene expression signatures in polyarticular juvenile idiopathic arthritis demonstrate disease heterogeneity and offer a molecular classification of disease subsets

Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke ⬇️

Impact of IL1RN Variants on Response to Interleukin-1 Blocking Therapy in Systemic Juvenile Idiopathic Arthritis

Inherited p40phox deficiency differs from classic chronic granulomatous disease

Kawasaki disease without fever

Leukocyte adhesion deficiency type 1 presenting with recurrent pyoderma gangrenosum and flaccid scarring

Management of juvenile idiopathic arthritis: hitting the target

Munchausen by proxy syndrome mimicking systemic autoinflammatory disease: case report and review of the literature.

PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype.

Pediatric rheumatology--its own specialty

Practice and consensus-based strategies in diagnosing and managing systemic juvenile idiopathic arthritis in Germany

Proinflammatory Cytokine Environments Can Drive Interleukin-17 Overexpression by γ/δ T Cells in Systemic Juvenile Idiopathic Arthritis

Reply

Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations

Rituximab therapy for severe refractory chronic Henoch-Schönlein purpura.

Serum S100A8/A9 and S100A12 Levels in Children With Polyarticular Forms of Juvenile Idiopathic Arthritis: Relationship to Maintenance of Clinically Inactive Disease During Anti-Tumor Necrosis Factor Therapy and Occurrence of Disease Flare After Disc

Single amino acid charge switch defines clinically distinct proline-serine-threonine phosphatase-interacting protein 1 (PSTPIP1)-associated inflammatory diseases

Subtype-specific peripheral blood gene expression profiles in recent-onset juvenile idiopathic arthritis

Synergistic Signaling of TLR and IFNα/β Facilitates Escape of IL-18 Expression from Endotoxin Tolerance

Treatment with high-dose recombinant human hyaluronidase-facilitated subcutaneous immune globulins in patients with juvenile dermatomyositis who are intolerant to intravenous immune globulins: a report of 5 cases.

Understanding the biology and use of TNF therapy in jia-clinical outcomes

Varicella-zoster-virus vaccination in immunosuppressed children with rheumatic diseases using a pre-vaccination check list.

[Back to school physical education despite rheumatism : Development and testing of a sport scientific-based physical education certification]