The Experts below are selected from a list of 3537 Experts worldwide ranked by ideXlab platform
Kunihiko Akagi - One of the best experts on this subject based on the ideXlab platform.
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrate
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Kunimasa Yan, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrated by abdominal computed tomography scans. Renal histology revealed calcinosis of renal tubules in 2 patients. Computed tomography is a reliable method for the detection of Nephrocalcinosis in this disorder. Hypercalciuria was also seen in 6 patients. A calcium-loading test performed in 2 patients suggested that hypercalciuria was of renal origin. Although the true pathogenesis is still not known, hypercalciuria and Nephrocalcinosis appear to be a common complication in patients with idiopathic LMW proteinuria. These complications and clinical features suggest that idiopathic LMW proteinuria in Japan is likely to be identical to Dent's disease in the United Kingdom.
Takashi Igarashi - One of the best experts on this subject based on the ideXlab platform.
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrate
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Kunimasa Yan, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrated by abdominal computed tomography scans. Renal histology revealed calcinosis of renal tubules in 2 patients. Computed tomography is a reliable method for the detection of Nephrocalcinosis in this disorder. Hypercalciuria was also seen in 6 patients. A calcium-loading test performed in 2 patients suggested that hypercalciuria was of renal origin. Although the true pathogenesis is still not known, hypercalciuria and Nephrocalcinosis appear to be a common complication in patients with idiopathic LMW proteinuria. These complications and clinical features suggest that idiopathic LMW proteinuria in Japan is likely to be identical to Dent's disease in the United Kingdom.
Michael A Linshaw - One of the best experts on this subject based on the ideXlab platform.
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a novel compound heterozygous romk mutation presenting as late onset bartter syndrome associated with Nephrocalcinosis and elevated 1 25 oh 2 vitamin d levels
Clinical and Experimental Nephrology, 2011Co-Authors: Amita Sharma, Michael A LinshawAbstract:Bartter syndrome (BS) is a rare renal tubular disorder presenting with hypokalemic metabolic alkalosis, which is classified into five types. KCNJ1 mutations usually cause the neonatal form of BS, type II BS (OMIM 241200). However, this report concerns a female patient with a novel, compound heterozygous KCNJ1 mutation that causes late-onset BS. The unique clinical findings of this case include persistently elevated 1,25(OH)2 vitamin D levels, possibly due to increase prostaglandin E2 levels, and medullary Nephrocalcinosis. Treatment with COX-2 inhibitors resolved her hypercalciuria and improved her height and weight; renal function remains stable and there is no progression of Nephrocalcinosis.
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a novel compound heterozygous romk mutation presenting as late onset bartter syndrome associated with Nephrocalcinosis and elevated 1 25 oh 2 vitamin d levels
Clinical and Experimental Nephrology, 2011Co-Authors: Amita Sharma, Michael A LinshawAbstract:Bartter syndrome (BS) is a rare renal tubular disorder presenting with hypokalemic metabolic alkalosis, which is classified into five types. KCNJ1 mutations usually cause the neonatal form of BS, type II BS (OMIM 241200). However, this report concerns a female patient with a novel, compound heterozygous KCNJ1 mutation that causes late-onset BS. The unique clinical findings of this case include persistently elevated 1,25(OH)2 vitamin D levels, possibly due to increase prostaglandin E2 levels, and medullary Nephrocalcinosis. Treatment with COX-2 inhibitors resolved her hypercalciuria and improved her height and weight; renal function remains stable and there is no progression of Nephrocalcinosis.
Tatsuhiro Yamanaka - One of the best experts on this subject based on the ideXlab platform.
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrate
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Kunimasa Yan, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrated by abdominal computed tomography scans. Renal histology revealed calcinosis of renal tubules in 2 patients. Computed tomography is a reliable method for the detection of Nephrocalcinosis in this disorder. Hypercalciuria was also seen in 6 patients. A calcium-loading test performed in 2 patients suggested that hypercalciuria was of renal origin. Although the true pathogenesis is still not known, hypercalciuria and Nephrocalcinosis appear to be a common complication in patients with idiopathic LMW proteinuria. These complications and clinical features suggest that idiopathic LMW proteinuria in Japan is likely to be identical to Dent's disease in the United Kingdom.
Hiroshi Hayakawa - One of the best experts on this subject based on the ideXlab platform.
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrate
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hypercalciuria and Nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in japan is the disease identical to dent s disease in united kingdom
Nephron, 1995Co-Authors: Takashi Igarashi, Hiroshi Hayakawa, Hiroshi Shiraga, Hidehiko Kawato, Kunimasa Yan, Haruo Kawaguchi, Tatsuhiro Yamanaka, Shinya Tsuchida, Kunihiko AkagiAbstract:Idiopathic low-molecular-weight (LMW) proteinuria is a newly described renal disease in Japan and Italy. We report on 7 patients who manifested bilateral or unilateral Nephrocalcinosis, as demonstrated by abdominal computed tomography scans. Renal histology revealed calcinosis of renal tubules in 2 patients. Computed tomography is a reliable method for the detection of Nephrocalcinosis in this disorder. Hypercalciuria was also seen in 6 patients. A calcium-loading test performed in 2 patients suggested that hypercalciuria was of renal origin. Although the true pathogenesis is still not known, hypercalciuria and Nephrocalcinosis appear to be a common complication in patients with idiopathic LMW proteinuria. These complications and clinical features suggest that idiopathic LMW proteinuria in Japan is likely to be identical to Dent's disease in the United Kingdom.