Disease: Primary tubular proximal acidosis
- A case of severe osteomalacia caused by Tubulointerstitial nephritis with Fanconi syndrome in asymptomotic primary biliary cirrhosis
- A case report of nephrogenic diabetes insipidus with idiopathic Fanconi syndrome in a child who presented with vitamin D resistant rickets
- A Counterion-Free Strategy for Chronic Metabolic Acidosis Based on an Orally Administered Gut-Restricted Inorganic Adsorbent
- A mathematical model of the four cardinal acid-base disorders
- A monoclonal V kappa l light chain responsible for incomplete proximal tubulopathy
- A phase I trial of high-dose diaziquone and autologous bone marrow transplantation: an Illinois Cancer Council study
- A review of renal tubular acidosis
- Aetiological, clinical and metabolic profile of hypokalaemic periodic paralysis in adults: a single-centre experience
- Ambulatory diagnostic evaluation of 389 recurrent renal stone formers. A proposal for clinical classification and investigation
- Ammonium metabolism: emphasis on energy considerations
- Anti-carbonic anhydrase II antibody reflects urinary acidification defect especially in proximal renal tubules in patients with primary Sjogren syndrome
- Application of the disequilibrium pH method to investigate the mechanism of urinary acidification
- Association of Familial Hyperkalemia and Hypertension (FHHt) with proximal renal tubular acidosis and epileptic seizures
- Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures
- Atypical presentation of distal renal tubular acidosis in two siblings
- Autosomal recessive renal proximal tubulopathy and hypercalciuria: a new syndrome
- Bartter's syndrome presenting with features resembling renal tubular acidosis. Improvement of renal tubular defects by indomethacin
- Biochemical markers of renal disease in primary Sjogren's syndrome
- Biomarkers and Diagnostic Testing for Renal Disease in Sjogren's Syndrome
- Cadmium-induced osteopathy: clinical and autopsy findings of four patients
- Carbonic anhydrase II deficiency
- Cellular acidification occurs during anoxia in cultured, but not in freshly isolated, rabbit proximal tubular cells
- Clinical and Biochemical Characteristics of Patients with Renal Tubular Acidosis in Southern Part of West Bengal, India: A Retrospective Study
- Clinical and laboratory approaches in the diagnosis of renal tubular acidosis
- Clinical evaluation of Chinese patients with primary distal renal tubular acidosis
- Clinical features and recovery patterns of acquired non-thyrotoxic hypokalemic paralysis
- Clinical profile of distal renal tubular acidosis
- Cobalamin C deficiency complicated by an atypical glomerulopathy
- Comparison of growth in primary Fanconi syndrome and proximal renal tubular acidosis
- Dental features in congenital persistent renal tubular acidosis of proximal type
- Dental findings in Brazilian patients with Fanconi syndrome
- Diseases of renal adenosine triphosphatase
- Disorders of calcium-phosphate metabolism in primary renotubular dysfunction
- Disorders of distal nephron function
- Disorders of water and acid-base homeostasis
- Distal renal tubular acidosis and nephrolithiasis in 3 cases of primary Sjogren syndrome
- Distal renal tubular acidosis as a cause of osteomalacia in a patient with primary Sjogren's syndrome
- Distal Renal Tubular Acidosis due to Primary Sjogren's Syndrome: Presents as Hypoakalemic Paralysis with Hypokalemia-Induced Nephrogenic Diabetes Insipidus
- Distal Renal Tubular Acidosis Screening by Urinary Acidification Testing in Mexican Children
- Effect of chronic salt and water loading on the tubular defects of a child with Fanconi syndrome (cystinosis)
- Entry to "formula tunnel" revealed by SLC4A4 human mutation and structural model
- Exploration of renal tubular functions
- Fanconi syndrome with hepatorenal karyomegaly in a young Sphynx cat
- Fanconi's syndrome and distal (type 1) renal tubular acidosis in a patient with primary Sjogren's syndrome with monoclonal gammopathy of undetermined significance
- Genetic causes and mechanisms of distal renal tubular acidosis
- Hyperchloremic normal gap metabolic acidosis
- Hyperphosphatemia
- Hyperphosphatemia
- Hypokalemic Paralysis due to Primary Sjogren Syndrome: Case Report and Review of the Literature
- Hypopotassemic paralysis: a rare presentation of proximal renal tubular acidosis
- Idiopathic Fanconi's syndrome with nephrogenic diabetes insipidus in a child who presented as vitamin D resistant rickets--a case report and review of literature
- Impaired urinary acidification in the hypothyroid rat
- Improving outcomes for patients with distal renal tubular acidosis: recent advances and challenges ahead
- Inherited monogenic kidney stone diseases: recent diagnostic and therapeutic advances
- Markers of Kidney Tubule Dysfunction and Major Adverse Kidney Events
- Metabolic bone disease as a presenting manifestation of primary Sjogren's syndrome: Three cases and review of literature
- Natural history of primary distal renal tubular acidosis treated since infancy
- NBCe1-A Regulates Proximal Tubule Ammonia Metabolism under Basal Conditions and in Response to Metabolic Acidosis
- Nephrocalcinosis and proximal tubulopathy in Sjogren's Syndrome.
- Nephrogenic diabetes insipidus with idiopathic Fanconi's syndrome in a child who presented as vitamin D resistant rickets
- Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiency
- Osteomalacia secondary to renal tubular acidosis in a patient with primary Sjogren's syndrome
- Parathyroid hormone directly inhibits tubular reabsorption of bicarbonate in normocalcaemic rats with chronic hyperparathyroidism
- Pathophysiology and diagnosis of renal tubular acidosis
- Pediatric primary calcific band keratopathy with or without glaucoma from biallelic SLC4A4 mutations
- Primary proximal renal tubular acidosis; A therapeutical approach and long term follow-up
- Primary proximal tubular acidosis. Clinical and therapeutic considerations
- Primary Sjogren's syndrome manifesting as sclerotic metabolic bone disease
- Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal tubular cells
- Proximal renal tubular acidosis with and without Fanconi syndrome
- Proximal renal tubular dysfunction in primary distal renal tubular acidosis
- Proximal tubular dysfunction in primary Sjogren's syndrome: a clinicopathological study of 2 cases
- Proximal tubular renal dysfunction among HIV infected patients on Tenofovir versus Tenofovir sparing regimen in western Kenya
- Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease
- Randomized controlled trial: lisinopril reduces proteinuria, ammonia, and renal polypeptide tubular catabolism in patients with chronic allograft nephropathy
- Rare renal proximal tubular dysfunctions in primary biliary cholangitis
- Refractory rickets due to Fanconi's Syndrome secondary to Wilson's disease
- Regulation of kidney on potassium balance and its clinical significance
- Renal aspects of metabolic acid-base disorders in neonates
- Renal handling of water and sodium in children with proximal and distal renal tabular acidosis
- Renal Involvement in Primary Sjogren's Syndrome: A Case Series of Three Cases with Various Clinicopathological Presentations
- Renal tubular acidosis
- Renal Tubular Acidosis
- Renal tubular acidosis complicated with hypokalemic periodic paralysis
- Renal tubular acidosis in primary Sjogren's syndrome: study on the immunology and ultrastructure of EBV
- Renal Tubular Acidosis Manifesting as Severe Metabolic Bone Disease
- Renal Tubular Acidosis Presenting as Nephrogenic Diabetes Insipidus
- Renal tubular dysfunction in patients with primary Sjogren syndrome
- Review of the Pathophysiologic and Clinical Aspects of Hypokalemia in Children and Young Adults: an Update
- Rickets with hypophosphatemia, hypokalemia and normal anion gap metabolic acidosis: not always an easy diagnosis
- Stimulation of renal sulfate secretion by metabolic acidosis requires Na+/H+ exchange induction and carbonic anhydrase
- Successful Medical Therapy for Hypophosphatemic Rickets due to Mitochondrial Complex I Deficiency Induced de Toni-Debré-Fanconi Syndrome
- Symptomatic primary hyperparathyroidism: a retrospective analysis of fifty one cases from a single centre
- The spectrum of renal tubular acidosis in paediatric Sjogren syndrome
- Tubulointerstitial nephritis in primary Sjogren syndrome: clinical manifestations and response to treatment
- Two case studies from a family with primary Fanconi syndrome
- Understanding the Functional Expression of Na+-Coupled SLC4 Transporters in the Renal and Nervous Systems: A Review
- Unilateral nephrectomy and cisplatin as risk factors of ifosfamide-induced nephrotoxicity: analysis of 120 patients
- What is the underlying defect in patients with isolated, proximal renal tubular acidosis?
- Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study