Results 81 to 90 of about 4,884 (208)
Internal Medicine Journal, Volume 54, Issue 7, Page 1056-1065, July 2024.Abstract Normal‐anion‐gap metabolic acidosis (NAGMA) is a common but often under‐recognised and poorly understood condition, especially by less‐experienced clinicians. In adults, NAGMA might be an initial clue to a more significant underlying pathology, such as autoimmune diseases, hypergammaglobulinemia or drug toxicities.
Ritesh Bhandari +2 more
wiley +1 more source
Hipouricemia con hipercalciuria. Estudio longitudinal y revisión del tema
NefrologíaResumen: Antecedentes y objetivo: La asociación de hipouricemia e hipercalciuria es poco frecuente. En 1974 se describió un nuevo síndrome nominado Hipouricemia con hipercalciuria y reducción de la densidad ósea.
Teresa Moraleda Mesa +5 more
doaj +1 more source
Kidney & Blood Pressure Research, 2015 Background/Aims: Hypercalcemia can result in nephrocalcinosis/nephrolithiasis and may lead to renal failure. Idiopathic infantile hypercalcemia is caused by mutations of the CYP24A1 gene, which regulates vitamin D activity.
Tilman Jobst-Schwan +5 more
doaj +1 more source
The effect of serum levels of vitamin D in stone recurrencein patients with urinary tract stone [PDF]
, 2018 Introduction: The role of vitamin D in kidney stone disease and its effect on stone formation is still controversial. Objectives: To find out the possible role of 25(OH) D3 as an intrinsic factor in urinary calcium stone formers (SFs; individuals with
Mohammad Ali Beigi, Faramarz. +2 more
core
Diagnostic and therapeutic aspects of recurrent renal stone disease
African Journal of Nephrology, 1998 Recurrent renal stones occur in 7.5% of Caucasian men and 3% of all women. Even with increasing urbanisation, renal calculi are reported in less than I% of black South African men and women.
Anthony Meyers +2 more
doaj +1 more source
P60 | Osteopoikylosis and secondary hyperparathyroidism: an unusual association of rare diseases
Italian Journal of MedicineBackground: Osteopoikilosis (OPK) is a rare bone disease with a prevalence of 1/50,000. It’s usually diagnosed incidentally by radiographic examinations. The etiopathogenesis is still unclear. In Literature OPK is described as frequently associated with
doaj +1 more source
Jornal de Pediatria, 2001 OBJETIVO: analisar a história clínica e evolução de crianças e adolescentes com HI, ressaltando peculiaridades próprias destes pacientes. MÉTODOS: 471 pacientes portadores de HI têm sido acompanhados em regime ambulatorial, sendo submetidos ao protocolo:
Maria Goretti M. G. Penido +6 more
doaj +1 more source
The Pathophysiology and Treatment of Hypertension in Patients With Cushing's Syndrome [PDF]
, 2019 When hypertension, a pathology that is frequently found in the general population, presents in a young patient, secondary causes such as Cushing's syndrome (CS), a rare disease characterized by long-term elevated cortisol levels, should be considered ...
Barbot, Mattia +2 more
core +1 more source
Idiopathic Hypercalciuria: Risk Factors for Symptomatic Forms in Children in the Fundación Cardioinfantil [PDF]
Revista Ciencias de la Salud, 2008 Idiopathic Hypercalciuria (IH) is a metabolicdisease, in most cases asymptomatic, but some patientsexpress complaints consistent with hematuria,polaquiuria, dysuria, urinary incontinence,enuresis and abdominal or back pain, that affectsactivities of ...
Carolina Ulloa Barón, MD, esp.
doaj