Results 121 to 130 of about 10,313 (226)
Pachydermoperiostosis Masquerading as Acromegaly. [PDF]
Context: Acromegaly usually is suspected on clinical grounds. Biochemical confirmation is required to optimize therapy, but there are other differential diagnoses.
Cranston, T +5 more
core +1 more source
Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel <b><i>SLCO2A1</i></b> Mutation and Imaging Findings [PDF]
Murat Torğutalp +6 more
openalex +1 more source
Changes in life-style after liver transplantation [PDF]
Sixty-five pediatric patients who received liver transplants between May 1981 and May 1984 were observed for as many as 5 years and examined for changes in life-style.
Belle, SH +8 more
core
Pachydermoperiostosis (primary hypertrophic osteoarthropathy): report of a case with evidence of endothelial and connective tissue involvement. [PDF]
Marco Matucci‐Cerinic +8 more
openalex +1 more source
Background and aims Chronic enteropathy associated with SLCO2A1 gene is a rare intestinal disease caused by loss-of-function SLCO2A1 mutations, with clinical and genetic characteristics remaining largely unknown, especially in Chinese patients.
Qing Shang +8 more
doaj +1 more source
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenLung cancer is the second most common cancer in Iceland and the most frequent cause of cancer related deaths.
Agnes Smáradóttir +8 more
core
Feline Hypertrophic Osteopathy Associated with Congenital Megaesophagus: Two Case Reports and Literature Review [PDF]
ΔΕΝ ΔΙΑΤΙΘΕΤΑΙ ΠΕΡΙΛΗΨΗThis report describes two cases of feline hypertrophic osteopathy (HO) associated with congenital megaesophagus (ME). The diagnosis was based upon case history, physical examination, radiography and laboratory investigations.
ABU-SEIDA, A.M. +3 more
core +1 more source
[Pachydermoperiostosis (primary hypertrophic osteoarthropathy)].
Pachydermoperiostosis or primary hypertrophic osteoarthropathy is a rare disease characterized by cutaneous and osteoarthicular involvement. We describe two patients with finger clubbing, watch crystal nails, bones thickenings, arthritis and different grades of skin affection, without other clinical manifestations. Both did not know of having relatives
Javier A, Cavallasca +4 more
openaire +1 more source
[Pachydermoperiostosis (primary hypertrophic osteoarthropathy)].
A case of pachydermaperiostosis in a 16 year old male is presented. The main clinical features were bilateral mechanical gonalgia, acropachy, bilateral palpebral ptosis and hyperhydrosis. The diagnosis was confirmed by X-ray, showing a wide, symmetric periostosis. The literature is reviewed and the differential diagnosis is commented on.
N, Gómez Rodríguez +5 more
openaire +1 more source

