Results 51 to 60 of about 3,384 (157)

Henoch-Schonlein Purpura Successfully Treated with Dexamethasone: A Case Report of Six-Year-Old Female [PDF]

open access: yes, 2017
Henoch-Schonlein Purpura (HSP) is one of the most common causes of small vessel vasculitis in children.  A six-year-old female presented with abdominal pain, swelling and rashes over both the legs associated with multiple episodes of vomiting for ...
Adhikari, Purushottam
core   +2 more sources

Continuous Exposure to Environmental Endocrine Disruptors on the Prognosis of Children With Nephritis: An Observational Cohort Study

open access: yesReproductive, Female and Child Health, Volume 4, Issue 4, December 2025.
ABSTRACT Objective Explore the impact of partial urinary environmental endocrine disruptors (EEDs) on the pathogenesis and renal function in paediatric patients diagnosed with Henoch‐Schönlein purpura nephritis (HSPN). Methods This was an observational cohort study.
Hongjun Peng   +6 more
wiley   +1 more source

Oxford Classification of IgA Nephropathy Is Applicable to Predict Long-Term Outcomes of Henoch-Schönlein Purpura Nephritis

open access: yesIranian Journal of Allergy, Asthma and Immunology, 2014
Henoch-Schönlein purpura nephritis and IgA nephropathy are currently considered to be different clinical presentations of the same disease. There is need for a reliable proven, morphologic classification that can help clinicians more accurately formulate
Hamid Nasri
doaj  

Incidence of Autoimmune Diseases in 30,340 Danish Women With Polycystic Ovary Syndrome (PCOS) Compared to 151,520 Controls. A National Cohort Study

open access: yesClinical Endocrinology, Volume 103, Issue 6, Page 863-872, December 2025.
ABSTRACT Objective Autoimmunity can be part of the pathogenesis of polycystic ovary syndrome (PCOS), but prospective studies on autoimmune disease in population based cohorts are lacking. This study aimed to investigate incidence rates of autoimmune disease in Danish women with PCOS before and after PCOS diagnosis compared to controls.
Dorte Glintborg   +4 more
wiley   +1 more source

Genetics of immunoglobulin-A vasculitis (Henoch-Schönlein purpura): An updated review [PDF]

open access: yes, 2018
Immunoglobulin-A vasculitis (IgAV) is classically a childhood small-sized blood vessel vasculitis with predominant involvement of the skin. Gastrointestinal and joint manifestations are common in patients diagnosed with this condition.
A Benrick   +309 more
core   +4 more sources

Collapsing Glomerulopathy in Brazil: A Nationwide Descriptive Study

open access: yesNephrology, Volume 30, Issue 12, December 2025.
This multicenter study describes the characterization and outcomes of a retrospective cohort of collapsing glomerulopathy cases conducted in Brazil. These findings reinforce the understanding of this rare glomerulopathy. ABSTRACT Aim Collapsing glomerulopathy (CG) is a glomerular disease that progresses rapidly to renal replacement therapy (RRT ...
Marcos Adriano Garcia Campos   +26 more
wiley   +1 more source

Presentation of a patient with palpable purpuric rash [PDF]

open access: yes, 2009
Henoch Shonlein purpura (HSP) is a form of systemic vasculitis characterized by deposition of IgA dominant immune complexes in the small vessels. The triad of palpable purpuric rash on lower extremities, abdominal or renal involvement and arthritis is ...
Khalid, Safoorah, Khurshid, Mohammad
core   +1 more source

Immunoglobulin A Vasculitis Nephritis in Children: Experience from a Tertiary Care Hospital, Bangladesh [PDF]

open access: yes, 2020
Background and Aim: Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura (HSP),is the most common vasculitis in children with multiorgan involvement.
Afroze, Sharmin   +6 more
core   +2 more sources

HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schonlein purpura nephritis in Finnish pediatric population : a genome-wide association study [PDF]

open access: yes, 2021
Background The pathophysiology of Henoch-Schonlein purpura (HSP) is still unclear, but several findings suggest that genetic factors may influence disease susceptibility.
Jahnukainen, Timo   +6 more
core   +2 more sources

Fibromatous periorchitis [PDF]

open access: yes, 2009
We report a case of diffuse fibrous pseudotumour/fibromatous periorchitis, in a 43 year old male, that completely encased the right testis and was adjacent to a hydrocoele cavity.
Barakzai, Abrar   +2 more
core   +1 more source

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