Results 131 to 140 of about 2,048 (238)

Congenital Primary Pachydermoperiostosis and Striate Palmoplantar Keratoderma - a Case Report [PDF]

open access: gold, 2014
Slobodan Stojanović   +3 more
openalex   +1 more source

Metasztatikus csontdaganatos esetek a római kori Pannóniából. [Skeletal metastases from the Roman Period of Pannonia.] [PDF]

open access: yes, 2014
According to paleopathological literature, tumors have a great antiquity. The prevalence of tumor metastases in historical populations might have differed from that in modern humans, because of substantial differences in ...
Bernert, Zsolt   +10 more
core  

A Case of Hypertrophic Gastropathy and Early Gastric Cancer Associated with Pachydermoperiostosis [PDF]

open access: yes, 2000
Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal new bone formation of tubular bones, and hypertrophic skin changes (pachydermia).
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core  

Complete primary pachydermoperiostosis

open access: yesCeylon Medical Journal, 2020
Ananda Jayanaga   +4 more
openaire   +3 more sources

Pachydermoperiostosis

open access: yesIndian Journal of Dermatology, Venereology, and Leprology, 2016
Prathima, Munichandrappa   +2 more
openaire   +2 more sources

P03-020 - A novel 15-HPGD mutation in pachydermoperiostosis [PDF]

open access: yes, 2013
A Tolun   +5 more
core   +1 more source

Cutis verticis gyrata primitif essentiel, une affection cutanée rare: cas clinique et revue de la littérature [PDF]

open access: yes, 2014
Le cutis verticis gyrata (CVG), du cuir chevelu, est une maladie rare et évolutive de la peau du scalp. Elle est caractérisée par une hypertrophie et une hyperlaxité cutanée formant des plis semblables aux gyri du cortex cérébral.
Benchamkha Yassine   +5 more
core   +2 more sources

Pachydermoperiostosis - A case report.

open access: bronze, 1984
Seiya Jingushi   +5 more
openalex   +2 more sources

Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

open access: yesJPRAS Open, 2019
Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat   +1 more
doaj  

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