Results 131 to 140 of about 4,842,655 (152)
Some of the next articles are maybe not open access.
Sir James Paget: Paget's Disease of the Nipple, Paget's Disease of Bone
Journal of Perioperative Practice, 2013Sir James Paget was one of the ‘great’ Victorians. Eminent as a surgeon, pathologist and teacher, his nobility of character and application to his work made him a leader in his profession in that age of great men.
openaire +2 more sources
Clinical Nuclear Medicine, 1999
A 69-year-old man who had an elevated prostate-specific antigen level and newly diagnosed biopsy-proved prostate cancer was referred for Tc-99m MDP bone scintigraphy for initial evaluation of skeletal metastases. He had no skeletal pain or deformities.
Z I, Assi, N I, Bohnen, B L, Shulkin
openaire +2 more sources
A 69-year-old man who had an elevated prostate-specific antigen level and newly diagnosed biopsy-proved prostate cancer was referred for Tc-99m MDP bone scintigraphy for initial evaluation of skeletal metastases. He had no skeletal pain or deformities.
Z I, Assi, N I, Bohnen, B L, Shulkin
openaire +2 more sources
Paget's disease of the esophagus
Diseases of the Esophagus, 2002We describe the case of a 72-year-old male patient who was suffering from Pagetoid spread to the esophageal mucosa from adenocarcinoma located in the distal esophagus and proximal stomach. Esophageal Paget's disease is rare. The histogenesis of extramammary Paget's disease has remained controversial.
M, Karakök +5 more
openaire +2 more sources
New England Journal of Medicine, 2017
An 89-year-old man presented with a 1-year history of a nonhealing groin rash that did not respond to antibiotics, antifungal agents, or glucocorticoids. A diagnosis of extramammary Paget’s disease was made by means of a skin biopsy.
Sarah H, Mehrtens, Sriramulu, Tharakaram
openaire +2 more sources
An 89-year-old man presented with a 1-year history of a nonhealing groin rash that did not respond to antibiotics, antifungal agents, or glucocorticoids. A diagnosis of extramammary Paget’s disease was made by means of a skin biopsy.
Sarah H, Mehrtens, Sriramulu, Tharakaram
openaire +2 more sources
Gerontologia Clinica, 2009
Paget's disease of bone is a focal bone disorder that is common among older people of Western European descent. It is an unusual disorder, for although we now have safe and highly effective treatment, there are many aspects of its pathogenesis and natural history that we do not yet understand.
Brya, Matthews, Tim, Cundy
openaire +4 more sources
Paget's disease of bone is a focal bone disorder that is common among older people of Western European descent. It is an unusual disorder, for although we now have safe and highly effective treatment, there are many aspects of its pathogenesis and natural history that we do not yet understand.
Brya, Matthews, Tim, Cundy
openaire +4 more sources
Bisphosphonates in Paget's disease
Bone, 2011Paget's disease is the best example of a common high turnover bone disease. A review of the early use of bisphosphonates in the treatment of this condition shows that many of the fundamental therapeutic issues were identified using drugs which by today's standards were far from ideal.
Ian R, Reid, D J, Hosking
openaire +2 more sources
2016
Paget’s disease of the breast is a rare breast tumor that was first identified by Sir James Paget in 1874. It is characterized by eczema-form changes accompanied with erosion and ulceration of the nipple and areolar epidermis. It is mostly correlated with ductal carcinoma in situ (DCIS); additionally, it can be accompanied by invasive ductal carcinoma (
Abdullah İğci +2 more
openaire +1 more source
Paget’s disease of the breast is a rare breast tumor that was first identified by Sir James Paget in 1874. It is characterized by eczema-form changes accompanied with erosion and ulceration of the nipple and areolar epidermis. It is mostly correlated with ductal carcinoma in situ (DCIS); additionally, it can be accompanied by invasive ductal carcinoma (
Abdullah İğci +2 more
openaire +1 more source
Metabolism, 2018
Juvenile Paget disease (JPD) is a rare disorder, mainly caused by mutations in the gene TNFRSF11B that encodes osteoprotegerin (OPG). Loss of OPG action causes generalized, extremely rapid bone turnover. The clinical manifestations are both skeletal - progressive skeletal deformity that develops in childhood - and extra-skeletal, including hearing loss,
Stergios A. Polyzos +2 more
openaire +2 more sources
Juvenile Paget disease (JPD) is a rare disorder, mainly caused by mutations in the gene TNFRSF11B that encodes osteoprotegerin (OPG). Loss of OPG action causes generalized, extremely rapid bone turnover. The clinical manifestations are both skeletal - progressive skeletal deformity that develops in childhood - and extra-skeletal, including hearing loss,
Stergios A. Polyzos +2 more
openaire +2 more sources
American Journal of Obstetrics and Gynecology, 2002
Our goal was to review our experience with Paget's disease of the vulva relative to initial examination, treatment, and oncologic outcome.Patients who were treated for extramammary Paget's disease of the vulva at the University of South Florida were identified in our vulvar cancer database for the period 1988 through 2000. The charts were reviewed, and
Stephen, Tebes +2 more
openaire +2 more sources
Our goal was to review our experience with Paget's disease of the vulva relative to initial examination, treatment, and oncologic outcome.Patients who were treated for extramammary Paget's disease of the vulva at the University of South Florida were identified in our vulvar cancer database for the period 1988 through 2000. The charts were reviewed, and
Stephen, Tebes +2 more
openaire +2 more sources