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10.1007/s00198-015-3090-5 http://scihub22266oqcxt.onion/10.1007/s00198-015-3090-5 C4483244!4483244!25906239     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25906239&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Osteoporos+Int 2015 ; 26 (7): 2039-42 Nephropedia Template TP {{tp|p=25906239|t=2015. Hypophosphatemic osteomalacia: an unusual clinical presentation of multiple myeloma |pdf=|usr=}}{{25906239}} gab.com Text Hypophosphatemic osteomalacia: an unusual clinical presentation of multiple myeloma JO: Osteoporos Int http://www.kidney.de/pget.php?&tw=1&pmid=25906239 #FOAvip An unusual case of a 75-year-old man is presented who had multiple stress fractures due to adult onset hypophosphatemic osteomalacia, which was the result of Fanconi syndrome, with light chain cast proximal tubulopathy due to multiple myeloma. A 75-year-old man presented with diffuse pain and muscle weakness. He had multiple stress fractures, low serum phosphate, decreased renal tubular reabsorption of phosphate, and normal PTH and FGF23, indicating adult onset hypophosphatemic osteomalacia. Phosphate supplements with calcitriol resulted in clinical recovery and healing of stress fractures. Because of proteinuria, a renal biopsy was performed that revealed Fanconi syndrome with light chain cast proximal tubulopathy and light kappa chains were found in serum and urine. A bone biopsy confirmed the diagnosis of multiple myeloma, and treatment with chemotherapy resulted in cytological and clinical recovery. Twit Text FOAVip Hypophosphatemic osteomalacia: an unusual clinical presentation of multiple myeloma ????Osteoporos Int http://www.kidney.de/pget.php?&tw=1&pmid=25906239 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25906239 #FOAvip English Wikipedia <ref>{{Cite pmid|25906239}}</ref> Hypophosphatemic osteomalacia: an unusual clinical presentation of multiple myeloma #MMPMID25906239 Reyskens M; Sleurs K; Verresen L; Janssen M; van den Berg J; Geusens P Osteoporos Int 2015[]; 26 (7): 2039-42 PMID25906239show ga An unusual case of a 75-year-old man is presented who had multiple stress fractures due to adult onset hypophosphatemic osteomalacia, which was the result of Fanconi syndrome, with light chain cast proximal tubulopathy due to multiple myeloma. A 75-year-old man presented with diffuse pain and muscle weakness. He had multiple stress fractures, low serum phosphate, decreased renal tubular reabsorption of phosphate, and normal PTH and FGF23, indicating adult onset hypophosphatemic osteomalacia. Phosphate supplements with calcitriol resulted in clinical recovery and healing of stress fractures. Because of proteinuria, a renal biopsy was performed that revealed Fanconi syndrome with light chain cast proximal tubulopathy and light kappa chains were found in serum and urine. A bone biopsy confirmed the diagnosis of multiple myeloma, and treatment with chemotherapy resulted in cytological and clinical recovery. äHypophosphatemic osteomalacia: an unusual clinical presentation of mul(epmc).pdf DeepDyve Pubget Overpricing