Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Karla Lais Pegas"'
Autor:
Karla Lais Pegas, Roberta Rohde, Clotilde Druck Garcia, Viviane de Barros Bittencourt, Elizete Keitel, Jose Antonio Tesser Poloni, Eduardo Cambruzzi
Publikováno v:
Brazilian Journal of Nephrology, Vol 36, Iss 1, Pp 93-95 (2014)
Lipoprotein glomerulopathy (LPG) is a rare autosomal recessive glomerulopathy associated with the deposition of lipoprotein thrombi in the capillary lumina due to apoE gene mutations. Abnormal plasma lipoprotein profile and marked increase in serum a
Externí odkaz:
https://doaj.org/article/468a5bb3f4c740ff80b531a2b2abb8be
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 41, Iss 1, Pp 76-78 (2008)
Caso de criptococose por Cryptococcus deficiente de cápsula, no qual cultivo do espécime clínico e pesquisa do antígeno capsular no líquor e soro foram negativos. As técnicas histopatológicas foram: Hematoxilina-eosina, Grocott, Mucicarmim de
Externí odkaz:
https://doaj.org/article/591acdaad03e4811b87e059e7fa54b24
Autor:
Alceu Migliavaca, Karla Lais Pegas, Guilherme Geib, Walter Escouto Machado, José Miguel Dora, Ana Luiza Maia, Jose Ricardo Guimaraes
Publikováno v:
The Endocrinologist. 20:112-114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc16e0b4c41b0c4a350c47c59c2b9249
https://doi.org/10.1097/ten.0b013e3181dffed2
https://doi.org/10.1097/ten.0b013e3181dffed2
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical. 41(1)
A case of cryptococcosis due to capsule-deficient Cryptococcus is presented, in which culturing of the clinical specimen and tests for capsular antigen in cerebrospinal fluid and serum were negative. The histopathological techniques evaluated were he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0423bb3ddac20b05bbf6996bf0b6222f
https://pubmed.ncbi.nlm.nih.gov/18368276
https://pubmed.ncbi.nlm.nih.gov/18368276
Autor:
Eduardo Cambruzzi, Júlia Rispoli dos Santos, Karla Lais Pêgas, William Mazzuco Nesi, William Pegoraro Kus, Felipe Lourezon Schiavo, Samir Cezimbra dos Santos
Publikováno v:
Brazilian Neurosurgery, Vol 39, Iss 03, Pp 222-227 (2020)
Introduction Angiosarcoma (AG) is a malignant mesenchymal neoplasm that predominantly affects the soft tissues and, to variable degrees, expresses the morphological and functional characteristics of the endothelium. The incidence of sarcomas of the c
Externí odkaz:
https://doaj.org/article/3a88b2b41c614e0fadf5e8550a4bfef4
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 86, Iss , Pp 14-16 (2020)
Externí odkaz:
https://doaj.org/article/e228e3e63ba549939907ee2996d40dc8
Autor:
Eduardo Cambruzzi, Karla Lais Pêgas, Gabriella Bezerra Cortês Nascimento, José Nathan Andrade Muller da Silva, Natália Brandelli Zandoná, William Pegoraro Kus, Felipe Lourezon Schiavo, Samir Cezimbra dos Santos
Publikováno v:
Brazilian Neurosurgery, Vol 40, Iss 02, Pp e195-e199 (2021)
Neuroparacoccidiodimycosis (NPDM) is an uncommon granulomatous disease, which more frequently affects immunocompromised male patients over 30 years of age in the course of chronic lung disease. Paracoccidioides brasiliensis (PB) is an endemic fungus
Externí odkaz:
https://doaj.org/article/067777c9e47e4228b451d16655597a0f
Autor:
Karla Lais Pêgas
Publikováno v:
Jornal Brasileiro de Patologia e Medicina Laboratorial, Vol 54, Iss 6, Pp 412-418 (2018)
ABSTRACT Despite the advances in knowledge of the neoplasm behavior, the exact understanding of the biological processes that involve the malignant tumors is not yet fully elucidated. Mechanisms such as subversion of phagocytosis, cytokines and chemo
Externí odkaz:
https://doaj.org/article/fb98dd3a063d4238b87635ded0c03bd1
Autor:
Eduardo Cambruzzi, Karla Lais Pêgas, Gabriella Bezerra Cortês Nascimento, José Nathan Andrade Muller da Silva, Natália Brandelli Zandoná, Mateus Scarabelot Medeiros
Publikováno v:
Interdisciplinary Neurosurgery, Vol 23, Iss , Pp 100913- (2021)
Purpose: Central nervous system embryonal tumors, not otherwise specified (ETNOS), comprise a group of rare, poorly differentiated embryonal neoplasms of neuroectodermal origin (WHO grade IV) that lack the specific histopathological features and mole
Externí odkaz:
https://doaj.org/article/679eb2159fcf44a081723d88c74996f1
Publikováno v:
Brazilian Journal of Nephrology, Vol 38, Iss 2, Pp 260-264 (2016)
Resumo A Doença relacionada a IgG4 (IgG4RD) é um processo inflamatório recente de etiologia supostamente autoimune, que se caracteriza por níveis séricos elevados de IgG4, um denso infiltrado mononuclear rico em plasmócitos IgG4 positivos e fib
Externí odkaz:
https://doaj.org/article/f8ebd9193cb246e4ab55bec0ad88c50a