Zobrazeno 1 - 10
of 60
pro vyhledávání: '"F. Maassarani"'
Autor:
Vincent Demesmaker, F Maassarani, Faouzi Abou-Messaoud, Konstantinos Kothonidis, Bernard Vanhoute, Muriel Parent
Publikováno v:
Journal of Surgical Case Reports
Although many types of pancreatic tumors exist, pancreatic solid serous cystadenoma stand as the most rare. Despite advances in medical imaging, definitive diagnosis remains complex. Here, we report a case of a 63-year-old man with a suspicious lesio
Publikováno v:
Journal of Surgical Case Reports
Anorectal melanoma is a rare disorder. There have only been a few cases reported and there is no consensus of treatment. We report a case of 50-year-old Caucasian man presenting intermittent prolapse of an anorectal mass during 6 months with occasion
Publikováno v:
Archives de Pédiatrie. 17:175-178
Autor:
Tom Devine, Tarek F. Maassarani
A Step-by-Step Guide to Blowing the Whistle—and Surviving the Storm That FollowsCorporate whistleblowers save lives, prevent fraud, and preserve the environment. But these results come through a long, difficult, draining, and often frightening proc
Publikováno v:
Acta Chirurgica Belgica. 103:230-232
Emphysematous cholecystitis is a relatively rare variant of acute cholecystitis with infection by gas-producing organisms. Diagnosis involves the demonstration of gas within the lumen or wall of the gallbladder by ultrasound or CT scan. In contrast t
Publikováno v:
Journal of Organometallic Chemistry. 466:265-271
The iodo-bridged or cationic cyclopalladated complexes 1b and 1c derived from N -phenyl-2-pyridylamine and 4b derived from phenyl-2-pyridylketone reacted with internal alkynes to yield five-membered heterocyclic 3 and carbocyclic products 6 with high
Publikováno v:
Acta Chirurgica Belgica. 102:345-347
Mirizzi syndrome is a partial obstruction of the biliary tree caused by a stone impacted in the cystic duct, with or without development of a cholecystobiliary fistula. Clinical signs are non-specific and suggest at first an obstructive jaundice. We
Publikováno v:
Acta chirurgica Belgica. 110(6)
Splenogonodal fusion is a rare congenital abnormality. We present the case of a continuous splenogonadal fusion diagnosed in the course of a laparoscopy for left non-palpable testis in a 1-year-old boy. This case illustrates that even though testicul
Publikováno v:
ChemInform. 25
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 17(2)