Results 1 to 10 of about 4,831 (106)

Clinical Efficacy and Safety of Percutaneous Spinal Endoscopy versus Traditional Open Surgery for Lumbar Disc Herniation: Systematic Review and Meta-Analysis.

J Healthc Eng, 2022
Objective. Systematic analysis of the incidence of percutaneous spinal endoscopic technique and traditional open surgery for lumbar disc herniation. Methods. A randomized controlled trial (RCT) and cohort study on complications related to traditional open surgery was searched on the MEDLINE, Cochrane Library, PubMed, Web of Science, Chinese journal ...
Xu X, Chen C, Tang Y, Wang F, Wang Y.
europepmc   +2 more sources

Los mastocitos perivasculares y la expresión de VEGF, laminina-332 y MMP-9 en neoplasias colorrectales humanas

Revista de Gastroenterología de México, 2023
Resumen: Introducción y objetivos: El cáncer colorrectal (CCR) es uno de los más prevalentes en el mundo y contribuye significativamente a las muertes relacionadas con el cáncer. La mayoría de los casos surgen de pólipos adenomatosos.
L. Meloti-Fiorio, I. Silva-Sinara-Alves, F. Rohor-de-Souza, W. Grassi-Bautz, F. Silva-Souza-Ribeiro, L. Pinto-Nogueira-da-Gama, L. Nogueira-da-Gama-de-Souza   +6 more
doaj   +1 more source

Efecto del veneno de bothrops diporus sobre la expresión de laminina 5 en biopsias de pie equino

Revista de Investigaciones Veterinarias del Perú, 2018
El objetivo del presente trabajo fue estudiar la expresión de laminina 5 en cortes de biopsias de pie equino precultivados con veneno de serpiente Bothrops diporus por histopatología e inmunohistoquímica contra controles no tratados. Las membranas basales de las láminas de las biopsias, así como las de las arteriolas y venas interlamelares evidenciaron
Teibler, Pamela, Aguirre, María, Todaro, Juan, Stoyanoff, Tania, Núñez, Sandra, Maruñak, Silvana   +5 more
openaire   +6 more sources

Genética Molecular das Epidermólises Bolhosas Molecular Genetics of Epidermolysis Bullosa

Anais Brasileiros de Dermatologia, 2002
O estudo das alterações moleculares das epidermólises bolhosas tem contribuído para que se compreenda melhor essas enfermidades. Na epidermólise bolhosa simples a maioria dos casos está associada com alteração nas citoqueratinas basais 5 (gen KRT5) e 14 (
Hiram Larangeira de Almeida Jr
doaj   +1 more source

Histopathological and immunohistochemical differentiation of epithelial alterations in vocal nodule comparing to polyps and to laryngeal edema [PDF]

, 2004
AIM: To evaluate by histological and immunohistochemical methods the epithelial lesions in vocal nodule and correlate with polyp, laryngeal edema and vocal folds without macroscopic lesions. STUDY DESIGN: Chart review.
G. Neto, João, Neves, Beatrice M. J., Pontes, Paulo   +2 more
core   +5 more sources

Effect of Agaricus blazei Murill on the Pulmonary Tissue of Animals with Streptozotocin‐Induced Diabetes

Journal of Diabetes Research, Volume 2010, Issue 1, 2010., 2010
The present study was designed to evaluate the oxidative stress as well as the therapeutic effect of Agaricus blazei Muril (A. Blazei) in rats with streptozotocin‐induced diabetes. We used 25 Wistar rats, and DM was induced by injecting streptozotocin (70 mg/Kg i.p.). Agaricus blazei Muril was administered daily starting 40 days after disease onset. A.
Fábio Cangeri Di Naso, Rodrigo Noronha de Mello, Sílvia Bona, Alexandre Simões Dias, Marilene Porawski, Alexandre de Barros Falcão Ferraz, Marc François Richter, Norma Possa Marroni, Subrata K. Chakrabarti   +8 more
wiley   +1 more source

Extracellular matrix in hematopoiesis and hematologic malignancies [PDF]

, 2008
The extracellular matrix (ECM) is a complex structure composed of collagens, proteoglycans, glycosaminoglycans and adhesive glycoproteins. Interactions between the cells and the ECM are crucial to determine cell behavior, such as growth, death ...
Dreyfuss, Juliana Luporini, Oliveira, José Salvador Rodrigues de   +1 more
core   +3 more sources

Molecular bases of diabetic nephropathy [PDF]

, 2007
The determinant of the diabetic nephropathy is hyperglycemia, but hypertension and other genetic factors are also involved. Glomerulus is the focus of the injury, where mesangial cell proliferation and extracellular matrix occur because of the increase ...
Amemiya S, Amiri F, Anderson S, Andrade MC, Araujo M, Ardaillou R, Ayo SH, Banes AK, Banes-Berceli AK, Beatriz D’Agord Schaan, Beswick RA, Brownlee M, Brune B, Bruno RM, Burns KD, Burns KD, Camargo de Andrade MC, Castellot JJ, Jr., Cattell V, Chang PC, Chin TY, Claudia J. Lagranha, Conti FG, Danesh FR, Derubertis FR, Doi T, Dulce Elena Casarini, Erwin PA, Feliers D, Fleming I, Fogo AB, Fried LF, Fulton D, Gould GW, Haas CS, Haralson MA, Harris MB, Henry DN, Hirata K, Hovind P, Hua H, Huang TH, Hubchak SC, Isono M, Kang SW, Kannel WB, Kashtan CE, Kato H, Katso R, Kennefick TM, Khamaisi M, Kim YS, Kimmelsteil P, King H, Komers R, Kroetz DL, Kroetz DL, Lagranha C, Lee HS, Leehey DJ, Li Y, Lin S, Lovett DH, Mai M, Malerbi DA, Maria Claudia Irigoyen, Matsusaka T, Mene P, Mervaala EM, Michell BJ, Mohaupt M, Moncada S, Mukherjee AB, Nagy L, Nasrallah R, Nath AK, Noh H, Nose A, Obara K, Okado T, Padival AK, Parameswaran N, Parving HH, Patricia Fiorino, Peppa M, Quinto BM, Reddy MA, Righetti AE, Rodriguez-Pena AB, Rossing P, Routh RE, Ruiz-Ortega M, Santos RA, Schaan BD, Schaan BD, Schnaper HW, Seikaly MG, Seshiah PN, Simonson MS, Singh AK, Singh R, Singh R, Striker GE, Studer RK, Sun L, Tsuchiya T, Uchiyama-Tanaka Y, Veelken R, Vestri S, Vidotti DB, Wang X, Way KJ, Wilmer WA, Wolf G, Wolf G, Xu D, Yamamoto S, Yang CW, Zangar RC, Zhang J, Zintzaras E, Ziyadeh FN, Zou AP   +122 more
core   +3 more sources

Bullous keratopathy: etiopathogenesis and treatment [PDF]

, 2008
Bullous keratopathy is characterized by corneal stromal edema with epithelial or subepithelial bullae due to cell loss and endothelial decompensation.
Campos, Mauro Silveira de Queiroz, Farias, Charles Costa de, Gomes, José Álvaro Pereira, Gonçalves, Eliana Domingues, Paris, Fabiana dos Santos   +4 more
core   +2 more sources

Motor function evaluation in merosin-deficient congenital muscular dystrophy children [PDF]

, 2005
Congenital muscular dystrophy (CMD) is a heterogeneous group of disorders characterized by early onset of hypotonia and weakness. Almost 50% of the cases are caused by primary deficiency of a protein named merosin (MD), and present a homogenous phenotype
Beteta, Javier Toledano, Fernandes, Antônio Carlos, Luz, Fernanda H. Gianini, Oliveira, Acary Souza Bulle, Rocco, Fernanda M., Rossato, Alexsander Junquera, Zanoteli, Edmar   +6 more
core   +3 more sources