Results 11 to 20 of about 118,522 (245)

Neoplasias cerebrais primárias associadas a malformações vasculares estudo anatomopatológico de dois casos [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 1990
A associação de malformações vasculares intracerebrais com neoplasias cerebrais primárias é rara. Mais comumente encontrados são os aneurismas arteriais intracranianos com neoplasias primárias. Relatamos dois casos de malformações vasculares associadas a
João Norberto Stavale   +3 more
doaj   +4 more sources

K-ras and p53 mutations in colonic lavage fluid of patients with colorectal neoplasias [PDF]

open access: yes, 2001
Background: The adenoma-carcinoma sequence has its molecular basis in several gene mutations of which K-ras and p53 are of paramount importance. The aims of this study were to evaluate whether these genetic alterations can be detected in colonic lavage ...
Folwaczny, Christian   +3 more
core   +1 more source

Occurrence of gastric cancer and carcinoids in atrophic gastritis during prospective long-term follow up [PDF]

open access: yes, 2015
Objective. Atrophic gastritis (AG) is a risk condition for gastric cancer and type I gastric carcinoids. Recent studies assessing the overall risk of gastric cancer and carcinoids in AG at long-term follow up are lacking.
Annibale, Bruno   +6 more
core   +2 more sources

Neutrophil gelatinase-associated lipocalin (NGAL) predicts response to neoadjuvant chemotherapy and clinical outcome in primary human breast cancer [PDF]

open access: yes, 2012
In our previous work we showed that NGAL, a protein involved in the regulation of proliferation and differentiation, is overexpressed in human breast cancer (BC) and predicts poor prognosis.
Arnold, Norbert   +18 more
core   +6 more sources

Studies on the clinical significance of nonesterified and total cholesterol in urine [PDF]

open access: yes, 1981
Gas-liquid chromatographic determinations of nonesterified and total urinary cholesterol were performed in 137 normals, 264 patients with various internal diseases without evidence of neoplasias or diseases of the kidney or urinary tract, 497 patients ...
A. Pickel   +35 more
core   +2 more sources

Linfomas não Hodgkin

open access: yesRevista Brasileira de Cancerologia, 2023
Nos dias 2 e 3 de dezembro de 1977, foram desenvolvidos em Brasília-DF, os Trabalhos do Seminário de Atualização em Oncologia Pediátrica sobre Linfomas Não-Hodgkin, sob o patrocínio da Divisão Nacional de Câncer.
Comissão Nacional de Neoplasias da Infância
doaj  

Neoplasias endócrinas múltiplas.

open access: yesActa Médica Portuguesa, 2007
The knowledge of genetics has increased in recent years and has led to important changes in management of hereditary diseases. Multiple endocrine neoplasia is characterized by the occurrence of benign or malign tumours involving two or more endocrine ...
Joana Guimarães
doaj   +1 more source

Hallazgos incidentales en cirugía abdominal: masas y sarcomas retroperitoneales

open access: yesRevista Colombiana de Cirugía, 2022
Introducción. El retroperitoneo es una estructura que se extiende desde el diafragma hasta la pelvis, está delimitado adelante por el peritoneo parietal, atrás y a los lados por la fascia transversalis y se divide en 9 compartimientos.
Rodrigo Burgos-Sánchez   +6 more
doaj   +1 more source

Molecular analysis of appendiceal mucinous cystadenoma and rectal adenocarcinoma in a patient with urothelial carcinoma: a case report [PDF]

open access: yes, 2013
Introduction: In this report, we present the case of a patient affected by appendiceal cystadenoma, a colorectal adenocarcinoma, and a concomitant bladder carcinoma, as well as the results of the molecular study of the most relevant mutational pathways ...
Colombino, Maria   +6 more
core   +1 more source

TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis [PDF]

open access: yes, 2015
Truncating mutations in the tumor suppressor gene adenomatous polyposis coli (APC) are the initiating step in the vast majority of sporadic colorectal cancers, and they underlie familial adenomatous polyposis (FAP) syndromes.
Creytens, David   +8 more
core   +3 more sources

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