Results 71 to 80 of about 10,313 (226)
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]
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
core +1 more source
Idiopathic clubbing: A case report
Clubbing of the fingers and toes has been recognized as a clinical manifestation of intra thoracic disease from the earliest times. Hippocrates particularly described the condition as occurring with advanced phthisis and empyema and emphasized the ...
N S Neki +4 more
doaj +1 more source
Solitary fibrous tumor of the pleura: surgery and clinical course in 18 cases [PDF]
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
core +1 more source
Chromosome 4q deletion syndrome: Narrowing the cardiovascular critical region to 4q32.2–q34.3 [PDF]
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
core +1 more source
HemaSphere, Volume 7, Issue S3, August 2023.
Ganesh Kumar Viswanathan +6 more
wiley +1 more source
Primary Idiopathic Osteoarthropathy: Could It Be Related to Alcoholism?
Background. Hypertrophic osteoarthropathy (HOA) is a syndrome characterized by abnormal proliferation of the skin and bony structures at the distal extremities resulting in digital clubbing, periosteal bony reaction, and joint effusion. It can be primary
Yanal Alnimer +3 more
doaj +1 more source
Primary hypertrophic osteoarthropathy, autosomal recessive type 1 (PHOAR1, MIM259100) is caused by mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD, MIM601688) on chromosome 4q34.
Yue Li +8 more
doaj +1 more source
Thymic Carcinoma Associated with Cerebellar Degeneration [PDF]
We present the case of a 57-year-old man with ataxia and clinical and radiological features of cerebellar degeneration. A computed tomography showed a mediastinal mass. The patient was diagnosed of thymic carcinoma. paraneoplastic cerebellar degeneration
García Cuartero, Irene +3 more
core +2 more sources
A Rare Cause of Refractory Anaemia hidden between Folds
British Journal of Haematology, Volume 202, Issue 4, Page 712-712, August 2023.
Syna Hamani +3 more
wiley +1 more source
Reverse frontal lifting: alternative for the treatment of pachydermoperiostosis [PDF]
Introduction: Patient diagnosed with pachydermoperiostosis, presenting a strong cutaneous manifestation, making it impossible to correct the defect by the usual facial lifting techniques.
Ronaldo Pontes +4 more
doaj +1 more source

