Alport syndrome with type I membranoproliferative glomerulonephritis

ARID1B-related disorder in 87 adults: Natural history and self-sustainability.

Genetics in medicine open·2024

A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling.

Heliyon·2024

Non-collagen genes role in digenic Alport syndrome.

BMC nephrology·2019

Low rate of return to pre-injury sport level in athletes after cartilage surgery: a 10-year follow-up study.

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA·2018

Alport syndrome: impact of digenic inheritance in patients management.

Clinical genetics·2016

Polyurethane-based cell-free scaffold for the treatment of painful partial meniscus loss.

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA·2016

Elevated Intraocular Pressure Independently Predicts Long-Term Progression to Advanced Chronic Kidney Disease: A 20-Year Longitudinal Cohort Study.

Nephron·2026

Human Organoids as Drug Development Tools for Polycystic Kidney Disease.

Nephron·2026

Sustained terminal complement inhibition on the endothelium with ravulizumab in patients with atypical Haemolytic Uremic Syndrome.

Nephron·2026

Clinical and Genetic Epidemiology of Autosomal Dominant Polycystic Kidney Disease among Patients Incident on First Kidney Replacement Therapy between 1990 and 2023, in a Major Hospital in the Northwest of Portugal.

Nephron·2026

Dietary Potassium and Blood Pressure.

Nephron·2026

The Impact of High-Altitude Acclimatization on Frontal Lobe Executive Function: The Mediating Effect of Creatinine.

Nephron·2026

One-step immunoassay of RNase A based on Fv-antibodies and switching peptides.

Chemical communications (Cambridge, England)·2026

MxA expression in systemic lupus erythematosus -associated myocarditis indicates type I interferon pathway activation.

Immunological medicine·2026

Amiodarone-induced thyrotoxicosis in a child with congenital heart disease.

Endocrinology, diabetes & metabolism case reports·2026

[Advances in the study of sialic acid-binding immunoglobulin-like lectins in ocular diseases].

Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology·2026

Coexisting mild autonomous cortisol secretion and isolated adrenocorticotropic hormone deficiency in a patient with an adrenal incidentaloma.

JCEM case reports·2026

Double autoimmune endocrinopathies: concurrent presentation of latent autoimmune diabetes in adults and Graves disease.

JCEM case reports·2026

Related Experiment Videos

Alport syndrome with type I membranoproliferative glomerulonephritis

Related Concept Videos

ARID1B-related disorder in 87 adults: Natural history and self-sustainability.

A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling.

Non-collagen genes role in digenic Alport syndrome.

Low rate of return to pre-injury sport level in athletes after cartilage surgery: a 10-year follow-up study.

Alport syndrome: impact of digenic inheritance in patients management.

Polyurethane-based cell-free scaffold for the treatment of painful partial meniscus loss.

Elevated Intraocular Pressure Independently Predicts Long-Term Progression to Advanced Chronic Kidney Disease: A 20-Year Longitudinal Cohort Study.

Human Organoids as Drug Development Tools for Polycystic Kidney Disease.

Sustained terminal complement inhibition on the endothelium with ravulizumab in patients with atypical Haemolytic Uremic Syndrome.

Clinical and Genetic Epidemiology of Autosomal Dominant Polycystic Kidney Disease among Patients Incident on First Kidney Replacement Therapy between 1990 and 2023, in a Major Hospital in the Northwest of Portugal.

Dietary Potassium and Blood Pressure.

The Impact of High-Altitude Acclimatization on Frontal Lobe Executive Function: The Mediating Effect of Creatinine.

One-step immunoassay of RNase A based on Fv-antibodies and switching peptides.

MxA expression in systemic lupus erythematosus -associated myocarditis indicates type I interferon pathway activation.

Amiodarone-induced thyrotoxicosis in a child with congenital heart disease.

[Advances in the study of sialic acid-binding immunoglobulin-like lectins in ocular diseases].

Coexisting mild autonomous cortisol secretion and isolated adrenocorticotropic hormone deficiency in a patient with an adrenal incidentaloma.

Double autoimmune endocrinopathies: concurrent presentation of latent autoimmune diabetes in adults and Graves disease.

Related Experiment Videos

Alport syndrome with type I membranoproliferative glomerulonephritis

Related Concept Videos

Related Articles