نتایج جستجو برای: osteodystrophy

تعداد نتایج: 914  

Journal: :The Journal of bone and joint surgery. British volume 1957
E C LEHMANN

For many years intermittent attention has been paid to the aptly named phenomenon of leontiasis ossea. Numerous conditions affecting the appearance of the face have been included but the application of a reasonable definition, such as appears in Dorland’s Medical Dictionary, makes a considerable proportion of cases unworthy of the designation. Dorland declares the condition to be a bilateral an...

Journal: :Journal of Evolution of Medical and Dental Sciences 2016

Journal: :Kidney international 2007
E Cavalier P Delanaye A Carlisi J-M Krzesinski J-P Chapelle

The determination of intact parathyroid hormone levels is used for diagnosis and in the management of renal osteodystrophy. Pre-analytical and analytical conditions are important in the overall confidence of the assay. Unfortunately, there are no clear recommendations for the use of serum samples or samples anticoagulated with ethylenediaminotetraacetic acid (EDTA) for the best preservation of ...

Journal: :Brazilian Journal of Medical and Biological Research 2002

Journal: :Journal of Clinical Investigation 1974

Journal: :Journal 2007
Marc G DuVal Sarah Davidson Andrew Ho Rachale Cohen Michael Park Somayeh Nourian Gerald Baker George K B Sándor

Albright"s hereditary osteodystrophy (AHO) is a complex genetic disorder characterized by brachydactyly, gonadotropin resistance, hypothyroidism, pseudohypoparathyroid syndrome and heterotopic ossification. Heterotopic ossification rarely occurs in the maxillofacial region. In this article, we present such a case, describe the etiology, characteristics and treatment of AHO and suggest a potenti...

2003
Michael D. Brown

A patient with pseudohypoparathyroidism is presented. The phenotypic appearance, known as Albright heredity osteodystrophy includes: short stature, round face, brachydactylia, and ectopic calcifications in the soft tissues. Dental manifestations reported in the literature are enamel hypoplasia, hypodontia, malformed roots, enlarged pulp chambers, microdontia, and pulp calcifications. Additional...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1996
C Jarava J R Armas M Salgueira A Palma

Serum total alkaline phosphatase is the most commonly used biochemical marker of bone disease in renal patients, but alkaline phosphatase originates from different organs and sometimes lacks specificity. Bone isoenzyme measurement is considered superior to total alkaline phosphatase for the assessment of bone metabolism. We have studied the value of bone isoenzyme, determined by a new. IRMA (Ta...

2016
Renata C. Pereira Thomas L. Andersen Peter A. Friedman Navdeep Tumber Isidro B. Salusky Katherine Wesseling-Perry

Pediatric renal osteodystrophy (ROD) is characterized by changes in bone turnover, mineralization, and volume that are brought about by alterations in bone resorption and formation. The resorptive and formative surfaces on the cancellous bone are separated from the marrow cavity by canopies consisting of a layer of flat osteoblastic cells. These canopies have been suggested to play a key role i...

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