Zobrazeno 1 - 10
of 5 662
pro vyhledávání: '"Renal tubular acidosis"'
Autor:
Francisco H. Negrete-Pedraza, Víctor Garcia-Nieto, Carlos A. Castro-Fuentes, Omar E. Valencia-Ledezma
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Altitude influences bicarbonate levels, it is a variable that is hardly considered in diagnosing Renal Tubular Acidosis (RTA), so it should be a factor to consider when diagnosing this pathology, especially at 2250 mts over the se
Externí odkaz:
https://doaj.org/article/670db1e24dc14d88b97fae40c18091c3
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-11 (2024)
Abstract Objective To investigate the risk factors of renal tubular acidosis (RTA) in patients with primary Sjögren’s syndrome (pSS) and create a personalized nomogram for predicting pSS-RTA patients. Method Data from 99 pSS patients who underwent
Externí odkaz:
https://doaj.org/article/1d24ccf931d64b8eac3f00d2512046f4
Autor:
Arianna Traunero, Francesco Baldo, Andrea Magnolato, Grazia Di Leo, Egidio Barbi, Irene Bruno
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-5 (2024)
Abstract Background Mitochondrial diseases (MDs) are systemic disorders that can affect multiple organs. Renal manifestations, including renal tubular acidosis, are common because kidneys are particularly vulnerable to energy deprivation. Treatment o
Externí odkaz:
https://doaj.org/article/7efdbb4efe7e440784aab698171ebda9
Autor:
Rayees Yousuf Sheikh, Nucksheeba Aziz Bhat, Farhat Mustafa, Puja Tripathi, Nidhi Johri, Imtiyaz Wani
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 36, Iss 1, Pp 1-7 (2024)
Abstract Hypokalemia is a common issue in clinical settings, often indicating underlying systemic conditions that require careful evaluation. This study presents three cases where hypokalemic paralysis served as the initial symptom of systemic diseas
Externí odkaz:
https://doaj.org/article/f203bc58ed094cba95fe2373997f5c61
Autor:
Rafael Coradin, Maria Lúcia Lemos Lopes, João Carlos Goldani, Pedro Enrico Ventura, Elizete Keitel
Publikováno v:
Advances in Rheumatology, Vol 64, Iss 1, Pp 1-7 (2024)
Abstract Introduction Sjögren’s disease (SD) is an immune-mediated chronic inflammatory disease that affects epithelial tissues, mainly salivary and lacrimal glands. It also presents extraglandular manifestations. The main renal manifestation is t
Externí odkaz:
https://doaj.org/article/e917587e620945829e473274f9df5b12
Autor:
Vijay Sundarsingh, R. Manoj Kumar, Manjunath Kulkarni, Firas Rauf Mammoo, Pramela Renisha Rodrigues, Y. M. Prashanth
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background Pregnancy imposes significant physiological changes, including alterations in electrolyte balance and renal function. This is especially important because certain disorders might worsen and make people more susceptible to electrol
Externí odkaz:
https://doaj.org/article/a9515f3a833f418f8874b3841ebd2b02
Autor:
Rana Bhattacharjee, Partha P. Chakraborty, Neeti Agrawal, Ajitesh Roy, Animesh Maiti, Subhankar Chowdhury
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 28, Iss 2, Pp 184-191 (2024)
Introduction: We aimed to describe the clinical, biochemical and etiological profile of patients referred with a provisional diagnosis of rickets in tertiary care centres. In addition, we tried to propose a diagnostic algorithm for the evaluation of
Externí odkaz:
https://doaj.org/article/495a077c965749c9b118611e8b8326db
Autor:
Teresa Antonia Kiener, Elena Moré, Michael Franzen, Janne Cadamuro, Christoph Schwarz, Carsten Bergmann, Hermann Salmhofer
Publikováno v:
Kidney & Blood Pressure Research, Vol 49, Iss 1, Pp 239-244 (2024)
Introduction: This study was designed to determine the mineral composition of calculi in nephrocalcinosis with nephrolithiasis, diagnose the underlying disease, and monitor the course of renal function in patients with nephrocalcinosis-nephrolithiasi
Externí odkaz:
https://doaj.org/article/903badd7ce5b4870b7dc3b2f886bcd8a
Autor:
Hugo Hernán Abarca-Barriga, María Cristina Laso-Salazar, Diego Orihuela-Tacuri, Jenny Chirinos-Saire, Anahí Venero-Nuñez
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Fanconi-Bickel syndrome is characterized by hepatorenal disease caused by anomalous glycogen storage. It occurs due to variants in the SLC2A2 gene. We present a male patient of 2 years 7 months old, with failure to thrive, hepatom
Externí odkaz:
https://doaj.org/article/20d5351d41b24c7cb1a7866292cc8dfd
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message In managing Sjogren's syndrome, a thorough patient history, proper lab tests, and imaging are crucial. Clinicians should prioritize checking electrolyte levels in cases of muscle weakness, as early detection of hypokalemia can pr
Externí odkaz:
https://doaj.org/article/e8d5756e8992420f98f73472492c2e48