Effects of Sacubitril/Valsartan on Blood Pressure and Proteinuria in Hypertensive Patients With Chronic Kidney Disease [PDF]
Maki Murakoshi +5 more
openalex +1 more source
Significance of tonsillectomy combined with steroid pulse therapy for IgA nephropathy with mild proteinuria [PDF]
Hiroyuki Komatsu +8 more
openalex +1 more source
ABSTRACT The presence of excess weight is no longer a distinguishing feature between patients with type 1 diabetes (T1D) and those with type 2 diabetes (T2D). Obesity treatment in patients with T2D improves glycemic control and reduces or even eliminates medication burden.
Kathleen R. Ruddiman +2 more
wiley +1 more source
Childhood-onset primary Sjögren's Syndrome presenting as nephrotic syndrome: a case report and literature review. [PDF]
Song Y +5 more
europepmc +1 more source
Fibroblast‐specific palladin drives kidney fibrosis via MRTF–SRF signaling
Abstract Fibrosis is a common end‐stage pathway of progressive chronic kidney diseases. Previously we demonstrated that myocardin‐related transcription factor (MRTF)–serum response factor (SRF) signaling drives the expression of fibrosis‐related molecules through actin cytoskeleton dynamics in renal fibroblasts.
Naoki Yamamoto +27 more
wiley +1 more source
Spontaneous remission in primary membranous nephropathy: mechanisms, predictive factors, and implications for personalized management. [PDF]
Wu M, Chen Y, He Z, Jin Y.
europepmc +1 more source
FIXED AND REPRODUCIBLE ORTHOSTATIC PROTEINURIA. III. EFFECT OF INDUCED RENAL HEMODYNAMIC ALTERATIONS UPON URINARY PROTEIN EXCRETION* [PDF]
Roscoe R. Robinson +3 more
openalex +1 more source
Severity of foot process effacement is associated with proteinuria in patients with IgA nephropathy [PDF]
Ji‐Hye Lee +7 more
openalex +1 more source
Hypertension and its complications in a young man with autoimmune disease [PDF]
Basile, Jan N. +9 more
core +1 more source
Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions
ABSTRACT Objective We describe a series of pregnancies with autosomal dominant lymphedema and generalized lymphatic dysplasia in the fetus diagnosed with prenatal exome or genome sequencing. We focus on specific syndromes, fetal features, and parental symptoms to deepen our understanding of congenital lymphatic anomalies.
Sara G. Vargo +4 more
wiley +1 more source

