Zobrazeno 1 - 10
of 17
pro vyhledávání: '"J. B. Kovács"'
Autor:
Ákos P. Deák, Erika Hartmann, Gergely Kiss, Gyula Végső, J. B. Kovács, András Bibok, Szilárd Török, Attila Doros, László Piros, Dávid Korda, Á. Farkas
Publikováno v:
Transplantation Proceedings. 51:1281-1285
Introduction Following renal transplantation, the incidence of malignancies is 3–5 times higher than that of healthy individuals. Among other type of cancers, the risk of urological tumors is also elevated. However, only a few cases of de novo tran
Autor:
Robert M. Langer, László Piros, Gyula Végso, Attila Doros, Éva Toronyi, Szabolcs Tóth, J. B. Kovács, Z.-S. Lovró, P. Á. Deák
Publikováno v:
Transplantation Proceedings. 43:1230-1232
Among the several vascular variation those concerning the venous system of the kidneys show the most significant variability. They often play an important role when it comes to choosing the kidney to be removed for transplantation. Based on our prior
Publikováno v:
Transplantation proceedings. 44(7)
Between March 2008 and March 2011, hand-assisted laparoscopic donor nephrectomles were performed on 70 patients. Following the first 26 cases undertaken based on guidelines in the literature, we modified the procedure to avoid barotrauma to the kidne
Autor:
Jenő Járay, J. B. Kovács, É. Juhász, László Piros, G. Branstetter, Attila Doros, P. Á. Deák, Z.-S. Lovró
Publikováno v:
Transplantation proceedings. 42(6)
A key aspect in planning laparoscopic living-donor nephrectomy is mapping of vascular variations. Lumbar veins and early-branching renal arteries are of utmost importance. To date, 43 candidates including 18 men and 25 women aged 25 to 67 years have
Autor:
J. B. Kovács, Sarolta Kárpáti, Miklós Tóth, Judit Hársing, Zsolt Tulassay, Attila Zalatnai, Márta Marschalkó, Agnes I. Otto
Publikováno v:
Journal of the American Academy of Dermatology. 65:458-459
Publikováno v:
Orvosi hetilap. 132(17)
Publikováno v:
Orvosi hetilap. 127(34)
Publikováno v:
Orvosi hetilap. 130(48)
Seven patients with congenital sucrase-isomaltase deficiency corresponding to the known diagnostic criteria and five patients having combined disaccharidase deficiencies with unusual pattern characterized by more pronounced sucrase than lactase defic
Publikováno v:
Orvosi hetilap. 123(42)
Publikováno v:
Orvosi hetilap. 126(15)