|1.||Cordat, Emmanuelle: 11 articles (08/2014 - 09/2004)|
|2.||Yenchitsomanus, Pa-Thai: 9 articles (08/2015 - 04/2004)|
|3.||Yenchitsomanus, Pa-thai: 9 articles (07/2014 - 07/2002)|
|4.||Reithmeier, Reinhart A F: 9 articles (10/2010 - 09/2004)|
|5.||Sawasdee, Nunghathai: 8 articles (08/2015 - 07/2002)|
|6.||Alper, Seth L: 7 articles (04/2011 - 01/2002)|
|7.||Akkarapatumwong, Varaporn: 5 articles (08/2015 - 04/2004)|
|8.||Wagner, Carsten A: 5 articles (04/2015 - 01/2007)|
|9.||Bruce, Lesley J: 5 articles (07/2013 - 07/2002)|
|10.||Malasit, Prida: 5 articles (09/2012 - 07/2002)|
|1.||Renal Tubular Acidosis (Distal Renal Tubular Acidosis)
01/01/2011 - "To investigate clinically and genetically all the distal renal tubular acidosis (dRTA) cases in Cyprus, to study one more family from Greece and to perform the first dRTA prenatal diagnosis. "
08/01/2009 - "In a study group of 40 surgically treated patients with posterior urethral valve (PUV) and normal estimated glomerular filtration rate, we evaluated the change in height standard deviation scores (SDSs) while they were on bicarbonate therapy in the presence of idRTA and complete distal renal tubular acidosis (dRTA). "
10/01/2008 - "This study investigated two naturally occurring point mutations in a4's COOH terminus that cause recessive distal renal tubular acidosis (dRTA), R807Q and G820R. "
06/01/2005 - "We suggest that all children with distal renal tubular acidosis (dRTA) should be subjected to an equilibrium study and audiological evaluation, as well as to a CT or MRI scan. "
11/01/1978 - "Renal biospy studies are reported from 10 patients with distal renal tubular acidosis (DRTA). "
|2.||Urinary Tract Infections (Urinary Tract Infection)
04/01/1993 - "In conclusion, the long-term efficacy of alkali therapy for prevention of recurrent stone formation with dRTA is confirmed when the patient takes enough alkali agents and the urinary tract infection is well controlled."
04/01/1996 - "In group 2, dRTA was present in 8/9 urolithiasis in 6/9, previous upper urinary tract infection (UTI) in 2/9 and TIN in 5/6 patients who were kidney biopsied. "
|3.||Sensorineural Hearing Loss
10/01/2013 - "Our study shows that rare and family-specific variants in ATP6V1B1 are responsible for DRTA and sensorineural hearing loss syndrome in Turkey. "
07/01/2010 - "This study indicated that a significant percentage of the children with DRTA had sensorineural hearing loss and mutation in ATP6V1B1 gene. "
06/01/2005 - "We report here a case of progressive sensorineural hearing loss with a large vestibular aqueduct and dRTA, and the results of audiological and equilibrium studies. "
06/01/2005 - "dRTA has been described in association with sensorineural hearing loss, but there are no reported cases that have been examined in detail using audiological and equilibrium studies. "
10/01/2013 - "The objective of this multicenter study is to screen DRTA patients with sensorineural hearing loss for ATP6V1B1 gene mutations and present genotype/phenotype correlation. "
12/01/2002 - "This study demonstrates that alkaline therapy corrects abnormal bone cell function and elevates bone mineral density in dRTA patients, indicating the causal role of acidosis in the alterations of bone cell functions and reduction in bone mineral density. "
05/01/2015 - "The prevalence of incomplete dRTA (urinary acidification defect without acidosis) was 25% (14/57). "
05/01/2015 - "The prevalence of complete dRTA (urinary acidification defect with acidosis) was 5% (3/57). "
06/01/2013 - "Additional analyses revealed normal anion gap metabolic acidosis with a positive urine anion gap and dRTA. "
07/01/2010 - "Diagnosis of DRTA was based on clinical manifestations and detection of normal anion gap metabolic acidosis, urine pH higher than 5.5, and positive urinary anion gap. "
01/01/2013 - "Autosomal dominant dRTA is less severe and appears during adolescence or adulthood and may or may not develop nephrocalcinosis. "
06/01/2012 - "Here, to emphasize the need for initiating investigations for pSS in any patient presenting with nephrocalcinosis due to dRTA, we report a 21-year-old woman presenting with nephrocalcinosis long before pSS was objectively diagnosed."
01/01/2008 - "Based on both clinical and biochemical assessment in combination with molecular genetics, we have shown that the etiology of nephrocalcinosis is different in each girl: one had FHHNC and her sister had dRTA."
04/01/2007 - "Patients with dRTA often present a radiographic picture of nephrocalcinosis. "
03/01/2002 - "Nephrocalcinosis might be one of the causal factors in the persistence of dRTA."
|2.||Ammonium Chloride (Sal Ammoniac)
|5.||Proton-Translocating ATPases (ATPase, H+)