Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Apostolos, Makrantonakis"'
Autor:
Styliani Parpoudi, Ioannis Mantzoros, Anna Gkiouliava, Dimitrios Kyziridis, Apostolos Makrantonakis, Christos Chatzakis, Christos Gekas, Dimitrios Konstantaras, Orestis Ioannidis, Stefanos Bitsianis, Dimosthenis Miliaras, Stamatios Aggelopoulos
Publikováno v:
Asian Journal of Surgery, Vol 45, Iss 11, Pp 2191-2196 (2022)
Background: The use of prosthetic meshes in abdominal wall reconstruction is a well-established approach; however, in certain cases where a bowel resection coexists its application is disputed. Any underlying inflammatory process may augment adhesion
Externí odkaz:
https://doaj.org/article/7307ef0d39fb4d08885d6d180bfe13fe
Autor:
Orestis Ioannidis, Angeliki Cheva, George Paraskevas, Nikolaos Papadimitriou, Athina Konstantara, Stavros Chatzopoulos, Anastasios Kotronis, Apostolos Makrantonakis, Emmanouil Kakoutis
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 104, Iss 5, Pp 268-275 (2012)
Pseudomyxoma peritonei is a rare clinical condition that is characterized by the presence of mucinous ascitis. It is believed to originate predominately from a mucinous neoplasm of the appendix including a heterogeneous group of tumours ranging from
Externí odkaz:
https://doaj.org/article/e48134fddf2044f9819080c4b5416675
Autor:
Orestis Ioannidis, George Paraskevas, Stavros Chatzopoulos, Anastasios Kotronis, Nikolaos Papadimitriou, Athina Konstantara, Apostolos Makrantonakis, Emmanouil Kakoutis
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 104, Iss 3, Pp 146-150 (2012)
Familial adenomatous polyposis (FAP) is a rare syndrome characterized by the presence of hundreds to thousands of colorectal adenomas and is responsible for less than 1% of all colorectal cancers. The syndrome is also characterized by extra-colorecta
Externí odkaz:
https://doaj.org/article/51182d6097df4f59b957ffa646058dce
Autor:
Orestis Ioannidis, Styliani Papaemmanouil, George Paraskevas, Anastasios Kotronis, Stavros Chatzopoulos, Athina Konstantara, Nikolaos Papadimitriou, Apostolos Makrantonakis, Emmanouil Kakoutis
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 104, Iss 1, Pp 37-40 (2012)
Peutz-Jeghers syndrome is a rare hereditary autosomal dominant disease caused by a mutation of the tumor suppressor gene serine/threonine kinase 11 located in chromosome 19p13.3. It is characterized by the presence of extensive mucocutaneous pigmenta
Externí odkaz:
https://doaj.org/article/b2f967e25bf84f6eb64ac2e2a1225283
Autor:
Orestis Ioannidis, Argiro Sekouli, George Paraskevas, Anastasios Kotronis, Stavros Chatzopoulos, Nikolaos Papadimitriou, Athina Konstantara, Apostolos Makrantonakis, Emmanouil Kakoutis
Publikováno v:
Journal of Research in Medical Sciences, Vol 17, Iss 1, Pp 92-95 (2012)
Intra-abdominal heterotopic ossification is extremely rare with only approximately 30 cases having been reported. While most reported cases have involved the mesentery, ossification of the peritoneum is even rarer. The pathogenesis remains undetermin
Externí odkaz:
https://doaj.org/article/6296bc39e06e490b8ec9308875c8630c
Autor:
Orestis Ioannidis, George Paraskevas, Anastasios Kotronis, Stavros Chatzopoulos, Athina Konstantara, Nikolaos Papadimitriou, Apostolos Makrantonakis, Emmanouil Kakoutis
Publikováno v:
Acta Medica, Vol 55, Iss 1, Pp 47-49 (2012)
Acenocoumarol is a vitamin K antagonist that is used for the treatment of acquired and congenital, both arterial and venous, thrombotic diseases. Its use is complicated by the narrow therapeutic range. Bleeding following oral anticoagulation, despite
Externí odkaz:
https://doaj.org/article/b48c493f3b74450199b6938550bab8a5
Autor:
Orestis Ioannidis, Charis Chatzidelios, Ioannis Mantzoros, Dimitrios Tatsis, Loukiani Kitsikosta, Christos Chatzakis, Apostolos Makrantonakis, George Paraskevas, Efstathios Kotidis, Manousos G. Pramateftakis, Konstantinos Tsalis
Publikováno v:
Cirugia y cirujanos. 86(5)
Neuroendocrine carcinoma (NEC) of the colon is a rare and very aggressive tumor with poor prognosis. The current case report presents a 53-year-old male with a 6 cm × 10 cm ascending colon carcinoma, causing large intestine obstruction, with simulta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce1306b79744e8621698b6434ff081bd
https://pubmed.ncbi.nlm.nih.gov/30226488
https://pubmed.ncbi.nlm.nih.gov/30226488
Autor:
Dimitrios Tatsis, Orestis Ioannidis, Christos Chatzakis, Loukiani Kitsikosta, Konstantinos Tsalis, Manousos George Pramateftakis, Apostolos Makrantonakis, Charis Chatzidelios, Ioannis Mantzoros, George P. Paraskevas, Efstathios Kotidis
Publikováno v:
Cirugía y Cirujanos. 86
Neuroendocrine carcinoma (NEC) of the colon is a rare and very aggressive tumor with poor prognosis. The current case report presents a 53-year-old male with a 6 cm × 10 cm ascending colon carcinoma, causing large intestine obstruction, with simulta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09bd48bb06b6c14b2e8dd08d5c3b70e7
https://doi.org/10.24875/ciru.18000058
https://doi.org/10.24875/ciru.18000058
Autor:
Styliani Parpoudi, Dimitrios Patridas, Pavlos Iosifidis, Apostolos Makrantonakis, Ioannis Mantzoros, Konstantinos Tsalis, Dimitrios Kyziridis
Publikováno v:
The American Journal of Case Reports
Patient: Male, 77 Final Diagnosis: Pilonidal cyst Symptoms: Severe pain •bleeding mass Medication: — Clinical Procedure: Local radiation therapy • neoadjuvant chemotherapy • surgical resection Specialty: Surgery Objective: Rare disease Backgr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e16431d10ad427fb3044df3a74f822d
https://doi.org/10.12659/ajcr.892843
https://doi.org/10.12659/ajcr.892843
Autor:
Emmanouil Kakoutis, Angeliki Cheva, Anastasios Kotronis, Apostolos Makrantonakis, George Paraskevas, Stavros Chatzopoulos, Nikolaos Papadimitriou, Athina Konstantara, Orestis Ioannidis
Publikováno v:
Revista Española de Enfermedades Digestivas v.104 n.5 2012
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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Pseudomyxoma peritonei is a rare clinical condition that is characterized by the presence of mucinous ascitis. It is believed to originate predominately from a mucinous neoplasm of the appendix including a heterogeneous group of tumours ranging from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c46599565185772fbf64c68e59be8716
https://doi.org/10.4321/s1130-01082012000500009
https://doi.org/10.4321/s1130-01082012000500009