Results 91 to 100 of about 740 (177)

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

open access: yes, 2012
Pachydermoperiostosis, or primary hypertrophic osteoarthropathy (PHO), is an inherited multisystem disorder, whose features closely mimic the reactive osteoarthropathy that commonly accompanies neoplastic and inflammatory pathologies.
A. Superti-Furga   +107 more
core   +1 more source

Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report. [PDF]

open access: yesPan Afr Med J, 2023
Hlaing SS   +8 more
europepmc   +1 more source

A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids

open access: yes, 2016
Pachydermoperiostosis (PDP) is a multisystem disorder of mesenchymal origin. It is a form of hypertrophic osteoarthropathy. The typical clinical features include pachydermia, cutis verticus gyrata, digital clubbing, and periostosis. Patients present with
Bipasha Mukherjee, Md. Shahid Alam
core   +1 more source

Pachydermoperiostosis and Work Restrictions: A Case Report. [PDF]

open access: yesCureus, 2023
Chinichian M   +3 more
europepmc   +1 more source

Pachydermoperiostosis: a case report of initial improvement with etoricoxib. [PDF]

open access: yesAnn Med Surg (Lond), 2023
Vaidya N   +4 more
europepmc   +1 more source

Pachydermoperiostosis.

open access: yesIndian journal of dermatology, venereology and leprology, 2012
I, Hassan   +3 more
openaire   +3 more sources

Identification of three novel mutations in <i>SLCO2A1</i> in Asian-Indians with Pachydermoperiostosis. [PDF]

open access: yesIndian J Med Res, 2023
Pasumarthi D   +5 more
europepmc   +1 more source

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