Pediatric Nephrology
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- 2024
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Ophthalmic manifestations in children with tuberous sclerosis complex
(
- Contribution to journal › Article
- 2023
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Complement dysregulation associated with a genetic variant in factor H-related protein 5 in atypical hemolytic uremic syndrome
(
- Contribution to journal › Article
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Arginase release in hemolytic uremic syndrome affects the vasculature
2023) 11th VTEC International Symposium on Shiga Toxin (Verocytotoxin) Producing Escherichia coli Infections(
- Contribution to conference › Abstract
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Mark
Childhood tuberous sclerosis complex in southern Sweden: A paradigm shift in diagnosis and treatment.
(
- Contribution to journal › Article
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Mark
Genetic investigation of Nordic patients with complement-mediated kidney diseases
(
- Contribution to journal › Article
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Complement-mediated kidney diseases: Genotype, phenotype and inhibition studies
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Development of an IgG-based treatment for enterohemorrhagic E. coli gastroenteritis
2023) 11th VTEC International Symposium on Shiga Toxin (Verocytotoxin) Producing Escherichia coli Infections(
- Contribution to conference › Abstract
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Mark
Is kidney biopsy necessary in children with idiopathic nephrotic syndrome?
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- Contribution to journal › Article
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Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome
(
- Contribution to journal › Article
- 2022
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A role for complement blockade in kidney transplantation
(
- Contribution to journal › Article
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Crosstalk between the renin–angiotensin, complement and kallikrein–kinin systems in inflammation
(
- Contribution to journal › Scientific review
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Immunologic Control of Disseminated Aichi Virus Infection in X-Linked Agammaglobulinemia by Transplantation of TcRαβ-Depleted Haploidentical Hematopoietic Cells
(
- Contribution to journal › Letter
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A link between Krüppel-like factor 4, complement activation, and kidney damage
(
- Contribution to journal › Debate/Note/Editorial
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Apyrase decreases phage induction and Shiga toxin release from E. coli O157:H7 and has a protective effect during infection
(
- Contribution to journal › Article
- 2021
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Hyponatraemia despite isotonic maintenance fluid therapy : A time series intervention study
(
- Contribution to journal › Article
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Novel in vivo therapeutic approaches to Escherichia coli O157:H7 infection
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Extracellular vesicles in Shiga toxin-mediated disease
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
MRTFA overexpression promotes conversion of human coronary artery smooth muscle cells into lipid-laden foam cells
(
- Contribution to journal › Article
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Isolation and Characterization of Shiga Toxin-Associated Microvesicles
(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Extracellular vesicles in renal inflammatory and infectious diseases
(
- Contribution to journal › Scientific review
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Factor D Inhibition Blocks Complement Activation Induced by Mutant Factor B Associated With Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis
(
- Contribution to journal › Article
- 2020
-
Mark
Mechanisms of Shiga toxin-mediated signaling and toxicity
2020) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Shiga Toxin-Bearing Microvesicles Exert a Cytotoxic Effect on Recipient Cells Only When the Cells Express the Toxin Receptor
(
- Contribution to journal › Article
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Mark
Shiga Toxin Uptake and Sequestration in Extracellular Vesicles Is Mediated by Its B-Subunit
(
- Contribution to journal › Article
- 2019
-
Mark
Exosomes and microvesicles in normal physiology, pathophysiology, and renal diseases
(
- Contribution to journal › Scientific review
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Blockade of the kallikrein-kinin system reduces endothelial complement activation in vascular inflammation
(
- Contribution to journal › Article
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Mark
Shiga toxin signals via ATP and its effect is blocked by purinergic receptor antagonism
(
- Contribution to journal › Article
- 2018
-
Mark
Upptäckt av reninsubstrat kan leda till ny behandling för njursjukdom
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Aliskiren inhibits renin-mediated complement activation
(
- Contribution to journal › Article
- 2017
-
Mark
Studies of the pathophysiology and epidemiology of vasculitis
2017)(
- Thesis › Doctoral thesis (compilation)
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Mark
Orphan drug policies and use in pediatric nephrology
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Haemolytic uraemic syndrome
(
- Contribution to journal › Scientific review
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Neutrophil Protease Cleavage of Von Willebrand Factor in Glomeruli - An Anti-thrombotic Mechanism in the Kidney
(
- Contribution to journal › Scientific review
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Mark
Microvesicle transfer of kinin B1-receptors is a novel inflammatory mechanism in vasculitis
(
- Contribution to journal › Article
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Mark
C1-inhibitor decreases the release of vasculitis-like chemotactic endothelial microvesicles
(
- Contribution to journal › Article
-
Mark
Extracellular vesicles in renal disease
(
- Contribution to journal › Scientific review
-
Mark
Microvesicle involvement in Shiga toxin-associated infection
(
- Contribution to journal › Scientific review
- 2016
-
Mark
An international consensus approach to the management of atypical hemolytic uremic syndrome in children
(
- Contribution to journal › Scientific review
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Mark
Complement contributes to the pathogenesis of Shiga toxin-associated hemolytic uremic syndrome
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Early terminal complement blockade and C6 deficiency are protective in enterohemorrhagic Escherichia coli-infected mice
(
- Contribution to journal › Article
- 2015
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Mark
Complement Interactions with Blood Cells, Endothelial Cells and Microvesicles in Thrombotic and Inflammatory Conditions.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome.
(
- Contribution to journal › Article
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Mark
A Novel Mechanism of Bacterial Toxin Transfer within Host Blood Cell-Derived Microvesicles.
(
- Contribution to journal › Article
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Mark
NT-rådets ställningstagande till eculizumab är oacceptabelt
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Slutreplik, Diana Karpman och medförfattare : - NT-rådet bör omedelbart återkalla sitt beslut om eculizumab
(
- Contribution to journal › Debate/Note/Editorial
- 2014
-
Mark
An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome
(
- Contribution to journal › Article
-
Mark
Eculizumab treatment for rescue of renal function in IgA nephropathy.
(
- Contribution to journal › Article
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Mark
Enterohemorrhagic Escherichia coli Pathogenesis and the Host Response
(
- Contribution to journal › Article
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Mark
23 läkare om omskärelse av små pojkar : Läkarförbundet bör inta en mer odmjuk hållning
(
- Contribution to journal › Debate/Note/Editorial
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Mark
The Combined Role of Galactose-Deficient IgA1 and Streptococcal IgA-Binding M Protein in Inducing IL-6 and C3 Secretion from Human Mesangial Cells: Implications for IgA Nephropathy.
(
- Contribution to journal › Article
- 2013
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Mark
Ouabain Protects against Shiga Toxin-Triggered Apoptosis by Reversing the Imbalance between Bax and Bcl-xL
(
- Contribution to journal › Article
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Mark
Complement activation in thrombotic microangiopathy.
(
- Contribution to journal › Scientific review
-
Mark
Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab
(
- Contribution to journal › Article
-
Mark
Eculizumab in an anephric patient with atypical haemolytic uraemic syndrome and advanced vascular lesions.
(
- Contribution to journal › Article
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Mark
Complement Activation Associated with ADAMTS13 Deficiency in Human and Murine Thrombotic Microangiopathy.
(
- Contribution to journal › Article
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Mark
Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic-Uremic Syndrome
(
- Contribution to journal › Article
- 2012
-
Mark
The Antimicrobial Peptide Cathelicidin Protects Mice from Escherichia coli O157:H7-Mediated Disease.
(
- Contribution to journal › Article
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Mark
Management of Shiga toxin-associated Escherichia coli-induced haemolytic uraemic syndrome: randomized clinical trials are needed
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Escherichia coli O104:H4 and Hemolytic Uremic Syndrome: The Analysis Begins
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
A Novel C3 Mutation Causing Increased Formation of the C3 Convertase in Familial Atypical Hemolytic Uremic Syndrome.
(
- Contribution to journal › Article
-
Mark
Shiga toxin pathogenesis : kidney complications and renal failure
(
- Contribution to journal › Article
- 2011
-
Mark
Kinin System Activation in Vasculitis.
(
- Contribution to journal › Article
-
Mark
Phenotypic Expression of ADAMTS13 in Glomerular Endothelial Cells
(
- Contribution to journal › Article
-
Mark
Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritis
(
- Contribution to journal › Article
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Mark
Cross-Reactive Protection against Enterohemorrhagic Escherichia coli Infection by Enteropathogenic Escherichia coli in a Mouse Model.
(
- Contribution to journal › Article
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Mark
Complement activation on platelet-leukocyte complexes and microparticles in enterohemorrhagic Escherichia coli-induced hemolytic uremic syndrome.
(
- Contribution to journal › Article
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Mark
Differential degeneration of the locus coeruleus in dementia subtypes.
(
- Contribution to journal › Article
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Successful management of a planned pregnancy in severe congenital thrombotic thrombocytopaenic purpura: the Upshaw-Schulman syndrome.
(
- Contribution to journal › Article
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Mark
Hyperfiltration evaluated by glomerular filtration rate at diagnosis in children with cancer.
(
- Contribution to journal › Article
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IgA nephropathy associated with a novel N-terminal mutation in factor H.
(
- Contribution to journal › Article
-
Mark
Intestinal damage in enterohemorrhagic Escherichia coli infection.
(
- Contribution to journal › Article
- 2010
-
Mark
Antibody response to IgA-binding streptococcal M proteins in children with IgA nephropathy
(
- Contribution to journal › Article
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Mark
Intestinal Damage in Enterohemorrhagic Escherichia coli (EHEC) Infection
2010) 15th Congress of the International Pediatric Nephrology Association In Pediatric Nephrology 25(9). p.1834-1834(
- Contribution to journal › Published meeting abstract
-
Mark
ADAMTS13 Expression in Glomerular Endothelial Cells
(
- Contribution to journal › Published meeting abstract
-
Mark
Complement Activation on Platelet-Leukocyte Complexes and Microparticles in Enterohemorrhagic Escherichia coli-Induced Hemolytic Uremic Syndrome
(
- Contribution to journal › Published meeting abstract
-
Mark
Pathophysiology of typical hemolytic uremic syndrome.
(
- Contribution to journal › Article
-
Mark
Biologically active ADAMTS13 is expressed in renal tubular epithelial cells.
(
- Contribution to journal › Article
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Pathogen specific, IRF3-dependent signaling and innate resistance to human kidney infection.
(
- Contribution to journal › Article
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Mark
Antibody response to IgA-binding streptococcal M proteins in children with IgA nephropathy.
2010) 15th Congress of the International Pediatric Nephrology Association In Pediatric Nephrology 25(9). p.1830-1830(
- Contribution to journal › Published meeting abstract
-
Mark
Tissue deposits of IgA-binding streptococcal M proteins in IgA nephropathy and Henoch-Schonlein purpura.
(
- Contribution to journal › Article
-
Mark
Toll-Like Receptor 4 Promoter Polymorphisms: Common TLR4 Variants May Protect against Severe Urinary Tract Infection.
(
- Contribution to journal › Article
- 2009
-
Mark
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Neutrophil-derived proteinase 3 induces kallikrein-independent release of a novel vasoactive kinin
(
- Contribution to journal › Published meeting abstract
-
Mark
Successful thrombolysis of neonatal bilateral renal vein thrombosis originating in the IVC.
(
- Contribution to journal › Article
-
Mark
A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.
(
- Contribution to journal › Article
-
Mark
Molecular basis of ADAMTS13 dysfunction in thrombotic thrombocytopenic purpura.
(
- Contribution to journal › Article
-
Mark
The contact/kinin and complement systems in vasculitis.
2009) In APMIS Acta Pathologica, Microbiologica et Immunologica Scandinavica. Supplementum 117. p.48-54(
- Contribution to journal › Article
-
Mark
Neutrophil-derived proteinase 3 induces kallikrein-independent release of a novel vasoactive kinin.
(
- Contribution to journal › Article
-
Mark
Shiga toxin and lipopolysaccharide induce platelet-leukocyte aggregates and tissue factor release, a thrombotic mechanism in hemolytic uremic syndrome.
(
- Contribution to journal › Article
- 2008
-
Mark
A novel mutation in the complement regulator clusterin in recurrent haemolytic uraemic syndrome
(
- Contribution to journal › Published meeting abstract
-
Mark
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.
(
- Contribution to journal › Article
-
Mark
TLR- and CXCR1-dependent innate immunity: insights into the genetics of urinary tract infections.
(
- Contribution to journal › Scientific review
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Mark
Hemolytiskt uremiskt syndrom och trombotisk trombocytopen purpura. Nya rön om EHEC, komplementmutationer och ADAMTS13.
(
- Contribution to journal › Scientific review
-
Mark
Shiga toxin-mediated disease in MyD88-deficient mice infected with Escherichia coli O157:H7.
(
- Contribution to journal › Article
-
Mark
An outbreak of Escherichia coli O157:H7 infection in southern Sweden associated with consumption of fermented sausage; aspects of sausage production that increase the risk of contamination.
(
- Contribution to journal › Article
- 2007
-
Mark
Anguish over angiopathy: Hemolytic uremic syndrome.
(
- Contribution to journal › Article
-
Mark
ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura.
(
- Contribution to journal › Article
-
Mark
A genetic basis of susceptibility to acute pyelonephritis.
(
- Contribution to journal › Article
-
Mark
Inherited susceptibility to acute pyelonephritis: a family study of urinary tract infection.
(
- Contribution to journal › Article
-
Mark
A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.
(
- Contribution to journal › Article