Francesco Emma
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View article: #1876 Time to diagnosis in patients with rare kidney diseases: findings form the European Rare Kidney Disease Registry
#1876 Time to diagnosis in patients with rare kidney diseases: findings form the European Rare Kidney Disease Registry Open
Background and Aims Limited expertise of healthcare professionals and late referral to specialist care may cause delays in establishing the correct diagnosis and initiate appropriate treatment in rare diseases. The European Rare Kidney Dis…
View article: #3150 Metabolic control affects growth in dRTA: findings from the ESPN–ERKNet dRTA sub-registry
#3150 Metabolic control affects growth in dRTA: findings from the ESPN–ERKNet dRTA sub-registry Open
Background and Aims Primary distal renal tubular acidosis (dRTA) is an inherited disease characterized by metabolic acidosis resulting from the inability of the distal nephron to secrete hydrogen ions. Recognized disease gene include ATP6V…
View article: Effects of Mango (Mangifera indica) Leaf Powder Supplementation on Growth Performance and Carcass Characteristics of Broiler Chickens (Gallus gallus domesticus)
Effects of Mango (Mangifera indica) Leaf Powder Supplementation on Growth Performance and Carcass Characteristics of Broiler Chickens (Gallus gallus domesticus) Open
This study evaluated the effects of Mangifera indica (mango) leaf powder (MLP) on the growth performance and carcass characteristics of broiler chickens. A total of 90 ROSS 308 broiler chicks (male and female), aged 21 days, with an averag…
View article: Cystinosis metabolic bone disease: inflammatory profile in human peripheral blood mononuclear cells and derived osteoclasts
Cystinosis metabolic bone disease: inflammatory profile in human peripheral blood mononuclear cells and derived osteoclasts Open
Cystinosis metabolic bone disease (CMBD) is an emerging concept in infantile nephropathic cystinosis, patients presenting with bone pains, fractures, and deformations during teenage or early adulthood. The underlying mechanisms remain uncl…
View article: Application of the updated International IgA Nephropathy Prediction Tool in children one or two years post-biopsy
Application of the updated International IgA Nephropathy Prediction Tool in children one or two years post-biopsy Open
The pediatric International IgA Nephropathy (IgAN) Prediction Tool comprises two models with and without ethnicity and is the first method to predict the risk of a 30% decline in estimated glomerular filtration rate (eGFR) or kidney failur…
View article: The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility
The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility Open
Pathological classifications in current use for the assessment of glomerular disease have been typically opinion-based and built on the expert assumptions of renal pathologists about lesions historically thought to be relevant to prognosis…
View article: The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults
The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults Open
To study the predictive value of biopsy lesions in IgA nephropathy in a range of patient ages we retrospectively analyzed the cohort that was used to derive a new classification system for IgA nephropathy. A total of 206 adults and 59 chil…
View article: Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update
Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update Open
Background It is unknown whether renal pathology lesions in immunoglobulin A nephropathy (IgAN) correlate with renal outcomes over decades of follow-up. Methods In 1130 patients of the original Validation Study of the Oxford Classification…
View article: The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy
The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy Open
NCT02090959.