نتایج جستجو برای: osteodystrophy

تعداد نتایج: 914  

Journal: :Journal of Japanese Society for Dialysis Therapy 1981

Journal: :Journal of Japanese Society for Dialysis Therapy 1985

Journal: :Research, Society and Development 2020

Journal: :Cukurova Medical Journal 2022

Pseudohypoparathyroidism is a rare inherited metabolic disorder that associated with parathormone resistance. Low serum calcium, high phosphates and raised levels suggesting resistance are biochemical characteristic features of . type 1 known as Albright’s hereditary osteodystrophy characterized by typical phenotype. This syndrome encompasses multiple clinical findings such brachydactyly, round...

Journal: :Seminars in dialysis 2003
David Trueba B Peter Sawaya Hanna Mawad Hartmut H Malluche

Bone biopsy is the gold standard for diagnosing the type and severity of renal osteodystrophy (ROD) in end-stage renal disease (ESRD) patients. In this article we review the indications, techniques, and complications of this minimally invasive procedure. The importance of careful preparation is emphasized.

Journal: :Journal of clinical pathology 1988
M Kaye J Henderson

Fifty two of 63 patients with renal osteodystrophy had one or more mononuclear cells positive for acid phosphatase in the marrow. These cells are also tartrate resistant and non-specific esterase negative, and are believed to be precursors to osteoclasts and other acid phosphatase positive cells resorbing bone on the trabecular surface.

2012
Sarah Tankersley Jim Cooley Erica Baravik-Munsell Erin Brinkman-Ferguson

Renal secondary hyperparathyroidism is a common sequela of chronic renal failure in the dog, but is not commonly observed in juvenile patients. A 6 month old female Labrador retriever with juvenile nephropathy and associated renal osteodystrophy is presented. Older dogs with this condition typically have highly pliable facial bones due to increased parathormone-induced osteoclastic activity sub...

Journal: :The American journal of medicine 1991
R W Watts S H Morgan C J Danpure P Purkiss R Y Calne K Rolles L R Baker M A Mansell L H Smith R M Merion

PURPOSE AND PATIENTS AND METHODS The purpose of this article is to report the experience of three centers with combined hepatic and renal transplantation for pyridoxine-resistant primary hyperoxaluria type I (alanine:glyoxylate aminotransferase [EC 2.6.1.44] deficiency), with particular emphasis on the selection criteria and timing of the operation. Nine patients with this inherited disease wer...

Journal: :Clinical Journal of the American Society of Nephrology 2010

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