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The Ceylon medical journal, 1975 Some of the next articles are maybe not open access.
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Best Practice and Research in Clinical Rheumatology, 2011
Manuel Martinez-lavin
exaly +4 more sources
Manuel Martinez-lavin
exaly +4 more sources
Pachydermoperiostosis Mimicking Acromegaly
Journal of the Royal Society of Medicine, 1992I R, Mahy, J, Wiggins
exaly +3 more sources
Acta Medica Scandinavica, 1970
Abstract. The report concerns pachydermoperiostosis in two women, mother and daughter, a relationship which has never before been noted. Another unusual aspect is that the characteristic features of the condition were noted already at the birth of the daughter. Moreover both have had symptoms of disturbed gonadal function.
G, Pietruschka +4 more
openaire +4 more sources
Abstract. The report concerns pachydermoperiostosis in two women, mother and daughter, a relationship which has never before been noted. Another unusual aspect is that the characteristic features of the condition were noted already at the birth of the daughter. Moreover both have had symptoms of disturbed gonadal function.
G, Pietruschka +4 more
openaire +4 more sources
The Journal of the Association of Physicians of India, 2018
A case of Pachydermoperiostosis (PDP) presented to us in rheumatology clinic with complaints of enlargement and broadening of bilateral hands and feet, grade IV digital clubbing, coarsening of facial features, excessive sweating of the palms, soles during summers.
Renu, Saigal +5 more
openaire +3 more sources
A case of Pachydermoperiostosis (PDP) presented to us in rheumatology clinic with complaints of enlargement and broadening of bilateral hands and feet, grade IV digital clubbing, coarsening of facial features, excessive sweating of the palms, soles during summers.
Renu, Saigal +5 more
openaire +3 more sources
Pachydermoperiostosis: an update
Clinical Genetics, 2005Pachydermoperiostosis (PDP) is a rare genodermatosis, characterized by pachydermia, digital clubbing, periostosis and an excess of affected males. Although an autosomal dominant model with incomplete penetrance and variable expression has been proved, both autosomal recessive and X‐linked inheritance have been suggested.
M, Castori +5 more
openaire +2 more sources