نتایج جستجو برای: hungry bone syndrome

تعداد نتایج: 906164  

2012
Poramaporn Prasarttong-Osoth Pakpong Wathanaoran Waraporn Imruetaicharoenchoke Supakorn Rojananin

Primary hyperparathyroidism (PHPT) is not an uncommon disease in the western countries. In Thailand, on the contrary, PHPT was a rare condition with various clinical presentations. All 45 PHPT patients who underwent parathyroidectomy at the Department of Surgery, Siriraj Hospital during January 1997 and December 2007 were retrospectively reviewed. Demographic data, clinical presentation, locali...

2009
Vanessa Carroni Ancuţa Leahu Giancarlo Biliotti

AN UNEXPECTED HYPERPARATHYROIDISM AS A CONSEQUENCE OF RADICAL TREATMENT OF PRIMARY HYPERPARATHYROIDISM (Abstract): The possibility of a rebound of the parathyroid hormone (PTH) plasma level after a temporary return to the physiological range following the ablation of a parathyroid adenoma is a well known phenomenon; on the opposite, the pathogenesis until now is not completely clear. This resea...

Moein Mobini Rahim Vakili, Saba Vakili,

McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  We describe a girl patient with MAS having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. Clinical presentat...

Journal: :BMJ case reports 2013
Robert James Jessie James Amarjit Singh Vij Kamaljeet Kaur Vij

To cite: James R, James J, Vij AS, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013201994 DESCRIPTION We describe the case of a 30-year-old woman who presented with breathing difficulty and a history of spontaneous fractures. The possibility of primary hyperparathyroidism was kept in mind and the patient was evaluated. The initial laboratory assessment ...

2014

The four parathyroid glands, normally located behind the four poles of the thyroid gland, secrete parathyroid hormone (PTH), which regulates extracellular calcium levels. Hyperparathyroidism, which can be primary, secondary, tertiary or quaternary, results in excess production of PTH. Excessive PTH secretion may be due to hyper-function in the glands themselves, in which case it is referred to ...

Journal: :Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia 2011
A J Felsenfeld B S Levine C R Kleeman

The major contributions of Fuller Albright to our understanding of calcium and phosphorus regulation and primary hyperparathyroidism are highlighted. Albright was the first investigator to initiate a systematic study of mineral metabolism. With resources limited to the measurement of serum calcium and phosphorus and the infusion of parathyroid extract, Albright used balance studies to establish...

Mohadeseh Hashem Boroojerdi, Nasibeh Daneshvar, Noor Sabariah, Peyman Ghoraishizadeh, Rajesh Ramasamy, Seman Zainina,

Background: Myelodysplastic syndrome is a mixed clonal disorder of bone marrow progenitor cells. Understanding the pattern of the different lineage-specific, immature, and mature markers in myelodysplastic syndrome will help in setting-up the frame of reference to diagnose. Patients and Methods: We compared 60 bone marrow samples from 30 newly-diagnosed patients with myelodysplastic syndrome ...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی مشهد - دانشکده دندانپزشکی 1394

جایگزینی دندان های از دست رفته به وسیله ایمپلنت دندانی به فراوانی انجام میشود. برای اینکه ایمپلنت به طور بهینه جایگزین شود باید در استخوان ایده ال جایگذاری شود که البته این نقایص قابل ترمیم هستند، یکی از این روشها guided bone regeneration است.

Journal: :international journal of pediatrics 0
moein mobini department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. rahim vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. saba vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran.

mccune-albright syndrome (mas) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. the disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  we describe a girl patient with mas having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. clinical presentat...

Journal: :iranian journal of blood and cancer 0
mohadeseh hashem boroojerdi nasibeh daneshvar peyman ghoraishizadeh rajesh ramasamy seman zainina noor sabariah

background: myelodysplastic syndrome is a mixed clonal disorder of bone marrow progenitor cells. understanding the pattern of the different lineage-specific, immature, and mature markers in myelodysplastic syndrome will help in setting-up the frame of reference to diagnose. patients and methods: we compared 60 bone marrow samples from 30 newly-diagnosed patients with myelodysplastic syndrome an...

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