Results 1 to 10 of about 59 (59)

Conditioned serum in vitro treatment of chondrocyte pellets and osteoarthritic explants

open access: yesEquine Veterinary Journal, Volume 55, Issue 2, Page 325-335, March 2023., 2023
Abstract Background Autologous conditioned serum (ACS) is used to treat osteoarthritis in horses, although its effects are not fully investigated. Objectives To investigate the effects of equine serum and conditioned serum on chondrocytes stimulated with interleukin (IL)‐1β and cartilage explants with mild osteoarthritis.
Maria Löfgren   +8 more
wiley   +1 more source

Ullrich congenital muscular dystrophy and bethlem myopathy: clinical and genetic heterogeneity Distrofia muscular congênita com hiperextensibilidade articular distal (Ullrich) e miopatia de Bethlem: heterogeneidade clínica e genética

open access: yesArquivos de Neuro-Psiquiatria, 2005
Ullrich congenital muscular dystrophy (UCMD), due to mutations in the collagen VI genes, is an autosomal recessive form of CMD, commonly associated with distal joints hyperlaxity and severe course.
Umbertina Conti Reed   +6 more
doaj   +1 more source

Colágeno na cartilagem osteoartrótica

open access: yesRevista Brasileira de Reumatologia, 2003
A cartilagem articular é um tecido altamente especializado, composto por células, os condrócitos, e um conjunto de macromoléculas, como o colágeno e os proteoglicanos.
Ana Paula P. Velosa   +2 more
doaj   +1 more source

64. Ingeniería tisular cardíaca. Beneficio de la asociación de una matriz extracelular a la inyección intramiocárdica de células madre en la miocardiopatía isquémica

open access: yesCirugía Cardiovascular, 2010
Evaluar la asociación de una matriz extracelular impregnada de células e inyección intramiocárdica de células madre en pacientes con cardiopatía isquémica. Métodos: El estudio incluye 45 pacientes con cardiopatía isquémica, cicatriz post-IAM, fracción de
J. Herreros, J. Barba
doaj   +1 more source

Análise da expressão do colágeno VI na distrofia muscular congênita Analysis of the expression of collagen VI in congenital muscular dystrophy

open access: yesArquivos de Neuro-Psiquiatria, 2005
A distrofia muscular congênita (DMC) compõe um grupo de miopatias caracterizadas por hipotonia e fraqueza muscular notadas já no primeiro ano de vida.
Regina Toni Loureiro de Freitas   +3 more
doaj   +1 more source

Distrofia muscular congênita de Ullrich moderadamente progressiva

open access: yesJornal de Pediatria, 2012
OBJETIVOS: Descrever características clínicas e genéticas da distrofia muscular congênita de Ullrich (DMCU), e relatar o caso de um paciente diagnosticado com DMCU após uma exaustiva investigação, que incluiu análise imuno-histoquímica e genômica do ...
Gerson Carakushansky   +2 more
doaj   +1 more source

Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives Distrofia muscular congênita. Parte II: revisão da patogênese e perspectivas terapêuticas

open access: yesArquivos de Neuro-Psiquiatria, 2009
The congenital muscular dystrophies (CMDs) are a group of genetically and clinically heterogeneous hereditary myopathies with preferentially autosomal recessive inheritance, that are characterized by congenital hypotonia, delayed motor development and ...
Umbertina Conti Reed
doaj   +1 more source

Biological Principles and Physiology of Bone Regeneration under the Schneiderian Membrane after Sinus Lift Surgery: A Radiological Study in 14 Patients Treated with the Transcrestal Hydrodynamic Ultrasonic Cavitational Sinus Lift (Intralift)

open access: yesInternational Journal of Dentistry, Volume 2012, Issue 1, 2012., 2012
Introduction. Sinus lift procedures are a commonly accepted method of bone augmentation in the lateral maxilla with clinically good results. Nevertheless the role of the Schneiderian membrane in the bone‐reformation process is discussed controversially.
A. Troedhan   +3 more
wiley   +1 more source

Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects Distrofia muscular congênita. Parte I: revisão dos aspectos fenotípicos e diagnósticos

open access: yesArquivos de Neuro-Psiquiatria, 2009
The congenital muscular dystrophies (CMDs) are a group of genetically and clinically heterogeneous hereditary myopathies with preferentially autosomal recessive inheritance, that are characterized by congenital hypotonia, delayed motor development and ...
Umbertina Conti Reed
doaj   +1 more source

Distrofias musculares congénitas

open access: yesRevista Médica Clínica Las Condes, 2018
Resumen: Las distrofias musculares congénitas (DMC) son enfermedades musculares hereditarias muy heterogéneas. Su diagnóstico se basa en criterios histológicos (signos distróficos en músculo) y clínicos (de inicio neonatal o durante la infancia precoz ...
Susana Quijano-Roy, MD, PhD   +1 more
doaj   +1 more source

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