Clinicopathological quiz. De novo membranous glomerulonephritis (MGN)

Dietary supplementation of cystinotic mice by lysine inhibits the megalin pathway and decreases kidney cystine content.

Scientific reports·2023

Disruption of pathways regulated by Integrator complex in Galloway-Mowat syndrome due to WDR73 mutations.

Scientific reports·2021

A mouse model suggests two mechanisms for thyroid alterations in infantile cystinosis: decreased thyroglobulin synthesis due to endoplasmic reticulum stress/unfolded protein response and impaired lysosomal processing.

Endocrinology·2015

The European renal genome project: an integrated approach towards understanding the genetics of kidney development and disease.

Organogenesis·2009

Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).

Journal of medical genetics·2009

Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation.

European journal of ophthalmology·2008

C-reactive protein as a potential effector molecule in the pathogenesis of acute post-streptococcal glomerulonephritis: a narrative review.

Pediatric nephrology (Berlin, Germany)·2026

Cystinosis-associated metabolic bone disease: pathogenesis and outcome.

Pediatric nephrology (Berlin, Germany)·2026

Safety and clinical outcomes of antithrombotic therapy in children and young adults with kidney failure on dialysis: a 10-year single-center retrospective cohort study.

Pediatric nephrology (Berlin, Germany)·2026

Immunosuppression in children with primary mitochondrial diseases after kidney transplantation: insight from case series of RMND1-related disease.

Pediatric nephrology (Berlin, Germany)·2026

Kidney transplantation in children with extended ilio-caval thrombosis.

Pediatric nephrology (Berlin, Germany)·2026

Clinical improvement of acquired partial lipodystrophy in an adolescent with C3 glomerulopathy treated with pegcetacoplan.

Pediatric nephrology (Berlin, Germany)·2026

AMETHYST: a Retrospective Cohort Study of Treatment Patterns and Outcomes in Patients With Glucocorticoid-refractory Macrophage Activation Syndrome Complicating Still's Disease.

Arthritis & rheumatology (Hoboken, N.J.)·2026

Diffuse large B-cell lymphoma mimicking musculoskeletal nontuberculous mycobacterial infection: A fatal diagnostic challenge.

IDCases·2026

Deep Mycobacterium marinum Infection of the Digit Presenting Without Cutaneous Lesions: A Case Report.

Cureus·2026

Progress and perspectives in primary mitochondrial myopathy: Highlights from the 2025 mitochondrial medicine masterclass with a focus on TK2 deficiency.

Therapeutic advances in rare disease·2026

Mycobacterial infections and recurrent osteomyelitis in a patient with an autosomal dominant mutation in IFN-gamma receptor 1 with overexpression of the receptor.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases·2026

T cell-derived CCL5 drives macrophage immunometabolic remodeling in chronic prostatitis via the CCR5-ERK-PKM2/HIF-1α axis.

Redox biology·2026

Related Experiment Videos

Clinicopathological quiz. De novo membranous glomerulonephritis (MGN)

Related Concept Videos

Dietary supplementation of cystinotic mice by lysine inhibits the megalin pathway and decreases kidney cystine content.

Disruption of pathways regulated by Integrator complex in Galloway-Mowat syndrome due to WDR73 mutations.

A mouse model suggests two mechanisms for thyroid alterations in infantile cystinosis: decreased thyroglobulin synthesis due to endoplasmic reticulum stress/unfolded protein response and impaired lysosomal processing.

The European renal genome project: an integrated approach towards understanding the genetics of kidney development and disease.

Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).

Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutation.

C-reactive protein as a potential effector molecule in the pathogenesis of acute post-streptococcal glomerulonephritis: a narrative review.

Cystinosis-associated metabolic bone disease: pathogenesis and outcome.

Safety and clinical outcomes of antithrombotic therapy in children and young adults with kidney failure on dialysis: a 10-year single-center retrospective cohort study.

Immunosuppression in children with primary mitochondrial diseases after kidney transplantation: insight from case series of RMND1-related disease.

Kidney transplantation in children with extended ilio-caval thrombosis.

Clinical improvement of acquired partial lipodystrophy in an adolescent with C3 glomerulopathy treated with pegcetacoplan.

AMETHYST: a Retrospective Cohort Study of Treatment Patterns and Outcomes in Patients With Glucocorticoid-refractory Macrophage Activation Syndrome Complicating Still's Disease.

Diffuse large B-cell lymphoma mimicking musculoskeletal nontuberculous mycobacterial infection: A fatal diagnostic challenge.

Deep Mycobacterium marinum Infection of the Digit Presenting Without Cutaneous Lesions: A Case Report.

Progress and perspectives in primary mitochondrial myopathy: Highlights from the 2025 mitochondrial medicine masterclass with a focus on TK2 deficiency.

Mycobacterial infections and recurrent osteomyelitis in a patient with an autosomal dominant mutation in IFN-gamma receptor 1 with overexpression of the receptor.

T cell-derived CCL5 drives macrophage immunometabolic remodeling in chronic prostatitis via the CCR5-ERK-PKM2/HIF-1α axis.

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Clinicopathological quiz. De novo membranous glomerulonephritis (MGN)

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