Results 61 to 70 of about 7,575 (173)

Impaired Renal Base Excretion in Secretin Receptor Knock‐Out Mice During Prolonged Base‐Loading

Acta Physiologica, Volume 242, Issue 9, September 2026.
ABSTRACT Aim Secretin was recently found to play a pivotal role in the renal adaptation to acute base excess. Here, secretin increases pendrin‐dependent HCO3− secretion from the beta‐intercalated cells in the cortical collecting ducts. Whether secretin and its receptor play a role during prolonged base‐loading remains unknown.
Tobias Jensen, Jesper Frank Andersen, Laura Woidemann Trans, Ida Marie Modvig, Helga Vitzthum, Jens Juul Holst, Bolette Hartman, Samuel L. Svendsen, Mads Vaarby Sørensen, Jens Leipziger, Peder Berg   +10 more
wiley   +1 more source

Renally Generated Ammonia as a Cause of Hyperammonaemic Non‐Hepatic Encephalopathy

Nephrology, Volume 31, Issue 9, September 2026.
ABSTRACT Encephalopathy with high ammonia levels is most commonly associated with cirrhosis or urea cycle disorders, but it can also result from renal ammoniagenesis when renal excretion of ammonium is impaired. In the literature, this has been shown to occur in the presence of (1) urinary diversion to a segment of intestine; (2) urea‐splitting ...
Victoria E. Nkunu, Kevin Y. L. Mak, Kuldeep Dodia, Fraulein D. Morales, Alicia K. J. Chan, R. Todd Alexander, Peter M. Hwang   +6 more
wiley   +1 more source

Pathological Proximal Femur Fracture in a Patient with Distal Renal Tubular Acidosis: A Case Report

Journal of Bone and Joint Diseases
The incidence of pathological fractures is on the rise, resulting in significant morbidity for patients and their families, while also imposing a considerable burden on the healthcare system.
Lyakat Khan, Pulak Sharma, Himanshu J. Ashtankar, Ujjwala Raina   +3 more
doaj   +1 more source

Itching for a diagnosis: Dysesthesias as an atypical presentation of Wilson disease in an adolescent—Case report

JPGN Reports, Volume 7, Issue 3, Page 383-386, August 2026.
Abstract Wilson disease (WD) is an autosomal recessive disorder of hepatic copper metabolism with varied clinical presentations. We describe a 15‐year‐old male referred for elevated aminotransferases, burning facial pruritis, scalp dysesthesias, and chronic bilateral lower extremity edema.
Tierra L. R. Mosher, John Hicks, Krupa R. Mysore   +2 more
wiley   +1 more source

Importance of early audiologic assessment in distal renal tubular acidosis

International Medical Case Reports Journal, 2010
Anand P Swayamprakasam1, Elizabeth Stover1, Elizabeth Norgett1, Katherine G Blake-Palmer1, Michael J Cunningham2, Fiona E Karet11Department of Medical Genetics, Cambridge Institute for Medical Research, Cambridge, UK; 2Department of Otolaryngology ...
Elizabeth Norgett, Elizabeth Stover, P Swayamprakasam, An, et al   +4 more
doaj  

Sporadic hypothyroidism-related hypokalemic paralysis: Diagnosis in a resource-poor setting

Journal of Family Medicine and Primary Care, 2017
Hypothyroidism and distal renal tubular acidosis causing hypokalemic paralysis (HP) have been described only in four female patients. HP as the initial manifestation of uncomplicated diabetes has been reported only in three young males.
Nadasha Kadeeja, Nivetha Senthilnathan, Stalin Viswanathan, Rajeswari Aghoram   +3 more
doaj   +1 more source

Acidosis tubular renal distal y parálisis hipopotasémica. Presentación de un caso y revisión de la literatura

Revista Finlay, 2016
La acidosis tubular renal distal o tipo 1 es una entidad muy poco frecuente. Cursa con parálisis hipopotasémica. Puede ser autosómica dominante o recesiva. La autosómica dominante es menos severa y aparece en la adolescencia o en la etapa adulta.
Miguel Ángel Serra Valdés, Dinorah Oliva Venereo, Alain Landrián Davis, Jorge Luis Valdés Fúster   +3 more
doaj   +2 more sources

Two unusual cases of severe recalcitrant hypocalcemia due to aminoglycoside-induced hypomagnesemia

Indian Journal of Endocrinology and Metabolism, 2013
Aminoglycoside (AMG)-induced renal toxicity is well-known and may manifest with non-oliguric renal failure or renal tubular dysfunction like Fanconi-like syndrome, Barter syndrome-like syndrome or distal renal tubular acidosis (RTA). These phenomena have
Tarun Varma, Ashish Saini, Roopal Panchani, Nitin R Gupta   +3 more
doaj   +1 more source

Nephrolithiasis Associated with Nephrocalcinosis Is Primarily Composed of Carbonate Apatite

Kidney & Blood Pressure Research
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-nephrolithiasis ...
Teresa Antonia Kiener, Elena Moré, Michael Franzen, Janne Cadamuro, Christoph Schwarz, Carsten Bergmann, Hermann Salmhofer   +6 more
doaj   +1 more source

Abstracts

Molecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source