Zobrazeno 1 - 10
of 85
pro vyhledávání: '"T Vogiatzaki"'
Publikováno v:
Central nerve blocks.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e87ec9e74155c6c436d6c27b87f84a1a
https://doi.org/10.1136/rapm-2022-esra.499
https://doi.org/10.1136/rapm-2022-esra.499
Publikováno v:
Central nerve blocks.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::364bd610ecb1e1b3c3a01c3122d68fed
https://doi.org/10.1136/rapm-2022-esra.503
https://doi.org/10.1136/rapm-2022-esra.503
Autor:
Panagiotis Tsikouras, M Bachar, George Galazios, T Tsoleridis, Liberis A, T. Vogiatzaki, C Christofis
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology. 44:337-340
Homer's syndrome (HS) is based on dysfunction of symphathetic nervous system at the cervical canal. The signs of the syndrome occur on the same side as the lesion of the sympathetic trunk and include: a constricted pupil, a weak-droopy eyelid, appare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be227312f7a251a5d1068573ef87f2c1
https://doi.org/10.12891/ceog3590.2017
https://doi.org/10.12891/ceog3590.2017
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
T, Vogiatzaki, P, Tsikouras, T, Tsoleridis, M, Bachar, C, Christofis, A, Liberis, G, Galazios
Publikováno v:
Clinical and experimental obstetricsgynecology. 44(3)
Homer's syndrome (HS) is based on dysfunction of symphathetic nervous system at the cervical canal. The signs of the syndrome occur on the same side as the lesion of the sympathetic trunk and include: a constricted pupil, a weak-droopy eyelid, appare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e03ab277cda1a07070e18f069c9b91e4
https://pubmed.ncbi.nlm.nih.gov/29949268
https://pubmed.ncbi.nlm.nih.gov/29949268
Autor:
M, Stavrati, T, Vogiatzaki, C, Christofis, T, Tsoleridis, G, Tsatsanidis, Th, Papadopoulos, P, Chloropoulou, C, Iatrou
Publikováno v:
Khirurgiia. 82(1)
The use of ultrasound (US) guidance in regional anaesthesia has evolved in the last then years and has even been considered the fatest and safest way to identify peripheral nerves and vascular structures thus eliminating the risk of injuring them. Pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5628bce081f116c0e4cbaa559553ec71
https://pubmed.ncbi.nlm.nih.gov/29383901
https://pubmed.ncbi.nlm.nih.gov/29383901
Publikováno v:
Hippokratia. 19(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8e86c29c0b8489eac6a0292a10641ee
https://pubmed.ncbi.nlm.nih.gov/27703319
https://pubmed.ncbi.nlm.nih.gov/27703319
Publikováno v:
European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 43(1)
Objective The optimal treatment of patients with T3 laryngeal carcinoma is controversially challenged by open partial laryngectomies (OPL), transoral laser microsurgery (TLM) and radiation therapy alone (RT) or combined with chemotherapy (ChRT). Trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab454d292dd1825b65521f08e714cd10
https://pubmed.ncbi.nlm.nih.gov/27320417
https://pubmed.ncbi.nlm.nih.gov/27320417
Autor:
Alexandros Polychronidis, A. G. Spyridonidou, A. K. Alexoudis, T. Vogiatzaki, Constantinos Simopoulos, C. Iatrou
Publikováno v:
Anaesthesia. 65:74-77
Hereditary angioedema is a rare genetic disorder resulting from an inherited deficiency or dysfunction of the C1-esterase inhibitor of the classic complement pathway. It is characterised by recurrent episodes of angioedema, without urticaria or pruri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c37a1c684f9d061bb7efc9072614ba8
https://doi.org/10.1111/j.1365-2044.2009.06130.x
https://doi.org/10.1111/j.1365-2044.2009.06130.x
Publikováno v:
Anaesthesia. 64:73-78
Arrhythmogenic right ventricular dysplasia, also called right ventricular cardiomyopathy, is a genetically determined heart muscle disease, characterised by life-threatening ventricular arrhythmias in apparently healthy young people. The primary myoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e73ff87859d34d2052be0c7aae1dcf4
https://doi.org/10.1111/j.1365-2044.2008.05660.x
https://doi.org/10.1111/j.1365-2044.2008.05660.x