Results 131 to 140 of about 2,048 (238)
Congenital Primary Pachydermoperiostosis and Striate Palmoplantar Keratoderma - a Case Report [PDF]
Slobodan Stojanović+3 more
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Metasztatikus csontdaganatos esetek a római kori Pannóniából. [Skeletal metastases from the Roman Period of Pannonia.] [PDF]
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
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A Case of Hypertrophic Gastropathy and Early Gastric Cancer Associated with Pachydermoperiostosis [PDF]
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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Complete primary pachydermoperiostosis
Ananda Jayanaga+4 more
openaire +3 more sources
136 Non-invasive evaluation of pachydermia of pachydermoperiostosis by vital confocal microscopy [PDF]
Takashi Nomura+2 more
openalex +1 more source
Prathima, Munichandrappa+2 more
openaire +2 more sources
P03-020 - A novel 15-HPGD mutation in pachydermoperiostosis [PDF]
A Tolun+5 more
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Cutis verticis gyrata primitif essentiel, une affection cutanée rare: cas clinique et revue de la littérature [PDF]
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
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Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis
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
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