S. Berg

发表

Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

Mark S. Anderson, J. Casanova, L. Notarangelo, 2021, The Journal of experimental medicine.

Population‐based study of multisystem inflammatory syndrome associated with COVID‐19 found that 36% of children had persistent symptoms

B. Månsson, P. Brodin, C. Nordenhäll, 2021, Acta paediatrica.

Increased intracellular oxygen radical production in neutrophils during febrile episodes of periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis syndrome.

D. Foell, K. Brown, A. Karlsson, 2013, Arthritis and rheumatism.

Familial mediterranean fever – an increasingly important childhood disease in Sweden

P. Wekell, A. Fasth, S. Berg, 2013, Acta paediatrica.

Increased intracellular oxygen radical production in neutrophils during febrile episodes of PFAPA syndrome

D. Foell, K. Brown, A. Karlsson, 2013 .

Development and Validation of a Targeted Next-Generation Sequencing Gene Panel for Children With Neuroinflammation

E. Wassmer, T. Cullup, H. Ahlfors, 2019, JAMA network open.

Towards a new set of classification criteria for PFAPA syndrome

C. Wouters, S. Ozen, B. Neven, 2018, Pediatric Rheumatology.

Profile of blood cells and inflammatory mediators in periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome

K. Brown, A. Karlsson, P. Wekell, 2010, BMC pediatrics.

Epidemiology and clinical features of PFAPA: a retrospective cohort study of 336 patients in western Sweden

P. Wekell, A. Fasth, S. Berg, 2022, Pediatric Rheumatology.

Review of autoinflammatory diseases, with a special focus on periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis syndrome

A. Karlsson, P. Wekell, A. Fasth, 2016, Acta paediatrica.

Neutrophils from patients with SAPHO syndrome show no signs of aberrant NADPH oxidase-dependent production of intracellular reactive oxygen species

A. Karlsson, P. Wekell, A. Fasth, 2016, Rheumatology.

Recurrent Febrile Episodes and Abdominal Pain

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Rash and Fever since Two Weeks of Age

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Irregular Recurrent Fever

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases

N. Klein, K. Gilmour, S. Jolles, 2016, Arthritis & rheumatology.

Toward an Inclusive, Congruent, and Precise Definition of Autoinflammatory Diseases

A. Karlsson, P. Wekell, A. Fasth, 2017, Front. Immunol..

Skeletal Pain in Knee and Clavicle

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Recurrent Chest Pain

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

International periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome cohort: description of distinct phenotypes in 301 patients.

C. Wouters, I. Touitou, B. Neven, 2014, Rheumatology.

Profiles and treatment of attempted suicide by self-immolation.

S. Berg, K. J. Farrell, L. H. Taylor, 1997, General hospital psychiatry.

Concise report International periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome cohort: description of distinct phenotypes in 301 patients RHEUMATOLOGY

C. Wouters, I. Touitou, B. Neven, 2014 .

Anti-tumour necrosis factor treatment for the prevention of ischaemic events in patients with deficiency of adenosine deaminase 2 (DADA2).

S. Cooray, K. Armon, R. Goel, 2021, Rheumatology.

Deficiency of Adenosine Deaminase Type 2 (DADA2)

Standing, N. Klein, K. Gilmour, 2020 .

Recurrent Fever and Sore Throat

P. Wekell, S. Berg, Karin Rydenman, 2019, Pediatric Immunology.

From uncertainty to gradually managing and awaiting recovery of a periodic condition- a qualitative study of parents´ experiences of PFAPA syndrome

A. Karlsson, P. Wekell, C. Sparud-Lundin, 2019, BMC Pediatrics.

International PFAPA syndrome registry: cohort of 214 patients

I. Touitou, B. Bader-Meunier, D. Rigante, 2008, Pediatric Rheumatology Online Journal.

Periodic Fever Syndrome and Developmental Delay

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Genetic and phenotypic spectrum associated with IFIH1 gain-of-function

A. Vanderver, Y. Crow, D. Lev, 2020, Human mutation.

Efficacy of Moderately Dosed Etoposide in Macrophage Activation Syndrome–Hemophagocytic Lymphohistiocytosis

U. Andersson, A. Horne, J. Henter, 2021, The Journal of Rheumatology.

Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations

L. Truedsson, P. Garred, S. Berg, 2011, Genes and Immunity.

Severe COVID-19 in an APS1 patient with interferon autoantibodies treated with plasmapheresis

K. Blennow, C. Wennerås, H. Zetterberg, 2021, Journal of Allergy and Clinical Immunology.

Long Episodes of Rash and Fever

P. Wekell, A. Fasth, S. Berg, 2019, Pediatric Immunology.

Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency.

T. Huizinga, L. Trouw, L. Truedsson, 2015, Journal of autoimmunity.

Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations

L. Truedsson, P. Garred, S. Berg, 2011, Genes and Immunity.

MPO deficiency confers impaired processing of neutrophil reactive oxygen species in a patient with severe CRMO

A. Karlsson, P. Wekell, S. Berg, 2015, Pediatric Rheumatology.