Results 71 to 80 of about 944 (190)
Bone Research Society 2021 Abstracts
, 2021 JBMR Plus, Volume 5, Issue S5, November 2021.
wiley +1 more source
Pachydermoperiostosis-critical analysis with report of five unusual cases [PDF]
, 2020 Pachydermoperiostosis (idiopathic hypertrophic arthropathy) {MIM 167100} is an uncommon disease characterized by unique phenotype (digital clubbing and pachydermia) and distinctive radiographic appearances (periostosis).
Anna Latos-Bielenska +5 more
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Chloride channels in astrocytes: structure, roles in brain homeostasis and implications in disease [PDF]
, 2020 Astrocytes are the most abundant cell type in the CNS (central nervous system). They exert multiple functions during development and in the adult CNS that are essential for brain homeostasis.
Elorza-Vidal, Xabier +2 more
core +1 more source
Metasztatikus csontdaganatos esetek a római kori Pannóniából. [Skeletal metastases from the Roman Period of Pannonia.] [PDF]
, 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
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A Case Report of Pachydermoperiostosis by Multidisciplinary Diagnosis and Treatment
罕见病研究A 20-year-old male patient presented to the Department of Dermatology of Peking Union Medical College Hospital with complaints of an 8-year history of facial scarring, swelling of the lower limbs, and a 4-year history of scalp thickening.
ZHANG Jie +16 more
doaj +1 more source
Nepal Journal of Dermatology, Venereology & Leprology, 2016 Pachydermoperiostosis, ( PDP), a rare hereditary disorder that is characterized by digital clubbing, pachydermia, subperiosteal new bone formation, associated with pain, polyarthritis, cutis verticis gyrata, seborrhoea and hyperhidrosis.
S Das, S Chakraborty, NS Sarkar
doaj +3 more sources
Ayurveda management of Touraine–Solente–Gole syndrome: A clinical experience
Journal of Ayurveda Case ReportsTouraine–Solente–Gole syndrome, also known as pachydermoperiostosis (PDP) or primary osteoarthropathy, is a rare genetic disorder characterized by a distinctive triad: pachydermia (skin thickening), digital clubbing, and periostosis (excessive bone ...
T. Shrilatha Kamath, Anchumol Joseph
doaj +1 more source
Crohn’s disease associated with pachydermoperiostosis [PDF]
, 1999 Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal change, pachydermia and autonomic nervous system symptoms such as facial flushing and hy perhidrosis.
김원호
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Pseudoacromegaly in pachydermoperiostosis [PDF]
BMJ Case Reports, 2016 A 19-year-old male patient presented with a year-long history of progressive painful enlargement of his hands and feet associated with excessive sweating and greasiness of the face, palms and soles. He also noticed pain over his wrists and ankles without any symptoms suggestive of raised intracranial tension and no recent increase in height.
Partha Pratim, Chakraborty +3 more
openaire +2 more sources