Influence of Genetic Polymorphisms in Prostaglandin E2 Pathway (COX-2/HPGD/SLCO2A1/ABCC4) on the Risk for Colorectal Adenoma Development and Recurrence after Polypectomy [PDF]
, 2016 OBJECTIVES: Deregulation of prostaglandin E2 (PGE2) levels reported in colorectal carcinogenesis contributes to key steps of cancer development. Our aim was to evaluate the influence of the genetic variability in COX-2/HPGD/SLCO2A1/ABCC4 PGE2 pathway ...
Brandão, C. +8 more
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A Unique Case Report of Hypertrophic Osteoarthropathy Associated With Endometrial Cancer and Literature Review. [PDF]
, 2017 Introduction: In this manuscript, we present an oncological case of hypertrophic osteoarthropathy (HOA) associated with endometrial cancer.Presentation of the case: A 46 year-old woman with a history of endometrial cancer (ER+/PR+) presented with ...
Hill, Ebone'D +2 more
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Revista Portuguesa de Pneumologia, 2009 A osteoartropatia hipertrófica secundária é uma alteração sistémica que acomete os ossos, as articulações e as partes moles, sendo secundária a alguma patologia intratorácica.
Angelo Ferreira da Silva Junior +5 more
doaj
Solitary fibrous tumor of the pleura: surgery and clinical course in 18 cases [PDF]
, 2009 Solitary fibrous tumors of the pleura are very rare neoplasms that can sometimes present with malignant features. Between 1984 and 2007, 18 cases were treated in our institution.
Bini, A +5 more
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Pachydermoperiostosis as a Rare Cause of Blepharoptosis
Türk Oftalmoloji Dergisi, 2014 A 37-year-old male patient diagnosed with pachydermoperiostosis at another center came to our clinic to rectify his blepharoptosis. The physical examination of the patient revealed skeleton and skin symptoms typical for pachydermoperiostosis.
Özlem Yalçın Tök +5 more
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Pachydermoperiostosis Masquerading as Acromegaly. [PDF]
, 2017 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
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Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2–q34.3 [PDF]
, 2012 The 4q deletion syndrome is a rare chromosome deletion syndrome with a wide range of clinical phenotypes. There is limited clinical phenotype and molecular correlation for congenital heart defects (CHDs) reported so far for this region primarily because ...
Baldwin +19 more
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Touraine-Solente-Gole Syndrome: A Rare Case Report
Delhi Journal of Ophthalmology, 2017 Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +1 more source
소아청소년기에서 SLCO2A1 gene 연관 만성 장병증 (CEAS) 의 임상 양상 [PDF]
, 2022 학위논문(석사) -- 서울대학교대학원 : 의과대학 임상의과학과, 2022.2. 고재성.Background and Aims: The incidence of inflammatory bowel disease (IBD) is increasing worldwide, and many atypical IBDs are being discovered.
임진규
core
The aetiology of clubbing and hypertrophic osteoarthropathy [PDF]
European Journal of Clinical Investigation, 1993 Abstract.The evidence is reviewed for the hypothesis that clubbing and hypertrophic osteoarthropathy are due to the peripheral impaction of megakaryocytes and platelet clumps in the fingers and toes, to which this particulate matter has passed in an axial stream.
openaire +3 more sources