Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sara Zakarias"'
Autor:
Marta Lange, Szabolcs Bozsányi, Ilze Lihacova, Alexey Lihachev, Luca Fésűs, Norbert Kiss, Antal Jobbágy, K. Farkas, Kende Lőrincz, Márta Medvecz, András Bánvölgyi, Norbert Wikonkál, Dmitrijs Bliznuks, Sara Zakarias, Pálma Anker
Publikováno v:
Diagnostics
Diagnostics, Vol 11, Iss 1315, p 1315 (2021)
Diagnostics; Volume 11; Issue 8; Pages: 1315
Diagnostics, Vol 11, Iss 1315, p 1315 (2021)
Diagnostics; Volume 11; Issue 8; Pages: 1315
Melanoma is a melanocytic tumor that is responsible for the most skin cancer-related deaths. By contrast, seborrheic keratosis (SK) is a very common benign lesion with a clinical picture that may resemble melanoma. We used a multispectral imaging dev
Autor:
Peter Igaz, Michaela Luconi, Judit Doczi, Attila Patócs, Judit Pápay, Christos Chinopoulos, Zoltán Hujber, Letizia Canu, Lilla Krokker, Anna Sebestyén, Henriett Butz, Balázs Sarkadi, Gábor Barna, Ildikó Krencz, Sara Zakarias, Otto Darvasi, Meszaros Katalin
Publikováno v:
Endocrine Abstracts.
Autor:
Katalin Mészáros, Judit Pápay, Otto Darvasi, Ildikó Krencz, Henriett Butz, Anna Sebestyén, Balázs Sarkadi, Sara Zakarias, Attila Patócs, Lilla Krokker, Peter Igaz, Michaela Luconi, Christos Chinopoulos, Zoltán Hujber, Judit Doczi, Gábor Barna, Letizia Canu
Publikováno v:
Cancers
Cancers, Vol 12, Iss 3, p 599 (2020)
Volume 12
Issue 3
Cancers, Vol 12, Iss 3, p 599 (2020)
Volume 12
Issue 3
Pheochromocytoma/paragangliomas (Pheo/PGL) are rare endocrine cancers with strong genetic background. Mutations in the SDHB subunit of succinate dehydrogenase (SDH) predispose patients to malignant disease with limited therapeutic options and poor pr
Autor:
Peter Igaz, Ildikó Krencz, Attila Patocs, Christos Chinopoulos, Katalin Borka, Anna Sebestyen, Balázs Sarkadi, Sara Zakarias, Zoltán Hujber, Judit Pápay, Gabor Barja, Katalin Mészáros, Miklos Toth, Kinga Németh
Publikováno v:
Endocrine Abstracts.
Autor:
Luca Fésűs, Norbert Wikonkál, Tamas Aranyi, Alexey Lihachev, Pálma Anker, Dóra Plázár, Sara Zakarias, András Bánvölgyi, Norbert Kiss, Márta Medvecz, Marta Lange, Szabolcs Bozsányi, Ilze Lihacova, K. Farkas
Publikováno v:
Diagnostics, Vol 11, Iss 260, p 260 (2021)
Diagnostics
Volume 11
Issue 2
Diagnostics
Volume 11
Issue 2
Pseudoxanthoma elasticum (PXE) is a rare multisystemic autosomal recessive connective tissue disease. In most cases, skin manifestations of PXE are the first to develop, followed later by severe ocular and cardiovascular complications. In our present
Autor:
Peter Igaz, Attila Patócs, Miklós Tóth, Balázs Sarkadi, Sara Zakarias, Henriett Butz, István Likó, Vince Kornél Grolmusz, Nikolette Szücs
Publikováno v:
Endocrine Abstracts.
Autor:
Szabolcs Bozsányi, Klára Farkas, András Bánvölgyi, Kende Lőrincz, Luca Fésűs, Pálma Anker, Sára Zakariás, Antal Jobbágy, Ilze Lihacova, Alexey Lihachev, Marta Lange, Dmitrijs Bliznuks, Márta Medvecz, Norbert Kiss, Norbert M. Wikonkál
Publikováno v:
Diagnostics, Vol 11, Iss 8, p 1315 (2021)
Melanoma is a melanocytic tumor that is responsible for the most skin cancer-related deaths. By contrast, seborrheic keratosis (SK) is a very common benign lesion with a clinical picture that may resemble melanoma. We used a multispectral imaging dev
Externí odkaz:
https://doaj.org/article/fc2553d1f38e47ee85af3d7d93c532ac
Autor:
Pálma Anker, Norbert Kiss, István Kocsis, Éva Czemmel, Krisztina Becker, Sára Zakariás, Dóra Plázár, Klára Farkas, Balázs Mayer, Nikoletta Nagy, Márta Széll, Nándor Ács, Zsuzsanna Szalai, Márta Medvecz
Publikováno v:
Life, Vol 11, Iss 7, p 624 (2021)
Collodion baby is a congenital, transient phenotype encountered in approximately 70–90% of autosomal recessive congenital ichthyosis and is an important entity of neonatal erythroderma. The clinical outcome after this severe condition is variable.
Externí odkaz:
https://doaj.org/article/bcc1326cb5a44ea7b20651ae08bfd1f6
Autor:
Klára Farkas, Szabolcs Bozsányi, Dóra Plázár, András Bánvölgyi, Luca Fésűs, Pálma Anker, Sára Zakariás, Ilze Lihacova, Alexey Lihachev, Marta Lange, Tamás Arányi, Norbert M. Wikonkál, Márta Medvecz, Norbert Kiss
Publikováno v:
Diagnostics, Vol 11, Iss 2, p 260 (2021)
Pseudoxanthoma elasticum (PXE) is a rare multisystemic autosomal recessive connective tissue disease. In most cases, skin manifestations of PXE are the first to develop, followed later by severe ocular and cardiovascular complications. In our present
Externí odkaz:
https://doaj.org/article/20b54f3e80814531918f4b997ecf607f