PubRank

Hiroshi Kaito

Author PubWeight™ 27.57‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Acute renal failure due to obstructive uric acid stones associated with acute gastroenteritis. Pediatr Nephrol 2009 2.09
2 A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome. Pediatr Res 2009 1.57
3 Rituximab treatment combined with methylprednisolone pulse therapy and immunosuppressants for childhood steroid-resistant nephrotic syndrome. Pediatr Nephrol 2014 1.46
4 Biopsy timing and Oxford classification variables in childhood/adolescent IgA nephropathy. Pediatr Nephrol 2014 1.43
5 Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity. Pediatr Nephrol 2011 1.39
6 Renal biopsy criterion in children with asymptomatic constant isolated proteinuria. Nephrol Dial Transplant 2012 1.38
7 Validity of the Oxford classification of IgA nephropathy in children. Pediatr Nephrol 2011 1.17
8 The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies. J Clin Endocrinol Metab 2010 1.07
9 Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR. Pediatr Res 2007 1.00
10 Natural history of genetically proven autosomal recessive Alport syndrome. Pediatr Nephrol 2014 0.96
11 Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation. Pediatrics 2011 0.92
12 Enamel-renal syndrome associated with hypokalaemic metabolic alkalosis and impaired renal concentration: a novel syndrome? Nephrol Dial Transplant 2006 0.89
13 Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation. Pediatr Nephrol 2010 0.86
14 A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism. Pediatr Nephrol 2007 0.86
15 Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: medical therapy. Clin Exp Nephrol 2015 0.85
16 Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome. Nephrol Dial Transplant 2008 0.85
17 Pretransplantation combined therapy with plasmapheresis and rituximab in a second living-related kidney transplant pediatric recipient with a very high risk for focal segmental glomerulosclerosis recurrence. Pediatr Transplant 2011 0.83
18 In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation. Hum Genet 2009 0.83
19 SLC26A3 gene analysis in patients with Bartter and Gitelman syndromes and the clinical characteristics of patients with unidentified mutations. Kobe J Med Sci 2013 0.81
20 Spontaneous remission in children with IgA nephropathy. Pediatr Nephrol 2012 0.81
21 Prognosis and pathological characteristics of five children with non-Shiga toxin-mediated hemolytic uremic syndrome. Pediatr Int 2007 0.80
22 Risk factors for developing severe clinical course in HUS patients: a national survey in Japan. Pediatr Int 2008 0.80
23 Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients. Pediatr Nephrol 2008 0.79
24 The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids. Pediatr Nephrol 2010 0.78
25 Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method. Early Hum Dev 2012 0.78
26 Renal biopsy criterion in idiopathic nephrotic syndrome with microscopic hematuria at onset. Pediatr Nephrol 2014 0.76
27 Clinical practice guideline for pediatric idiopathic nephrotic syndrome 2013: general therapy. Clin Exp Nephrol 2015 0.76
28 Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene. BMC Nephrol 2009 0.75
29 ABO-incompatible renal transplantation in Epstein syndrome. Clin Transplant 2010 0.75
30 Alport-like glomerular basement membrane changes with renal-coloboma syndrome. Pediatr Nephrol 2012 0.75
31 Acute kidney injury after acute gastroenteritis in an infant with hereditary hypouricemia. Eur J Pediatr 2013 0.75
32 Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency. Endocr J 2014 0.75
33 Long-term follow-up of juvenile acute nonproliferative glomerulitis (JANG). Pediatr Nephrol 2007 0.75