Results 1 to 10 of about 40 (29)

GIS analysis of land cover changes on the territory of the Prokuplje Municipality. [PDF]

open access: yesScientificWorldJournal, 2014
The monitoring of the territory of Prokuplje Municipality was done based on 1 : 25,000 topographic maps in three different time periods (1969, 1974, and 1984) and land cover map in 2012. Analogous topographic maps done in 1969, 1974, and 1984 were used, while in 2012 the land cover map obtained by using CORINE‐like approach was used.
Valjarević A   +4 more
europepmc   +2 more sources

MicroRNA Profiling in Patients with Upper Tract Urothelial Carcinoma Associated with Balkan Endemic Nephropathy. [PDF]

open access: yesBiomed Res Int, 2016
Balkan endemic nephropathy (BEN) is a disease that affects people that live in the alluvial plains along the tributaries of the Danube River in the Balkan region. BEN is a chronic tubulointerstitial disease with a slow progression to terminal renal failure and has strong association with upper tract urothelial carcinoma (UTUC).
Popovska-Jankovic K   +9 more
europepmc   +2 more sources

Agricultural advisors' role in the use of ICTs as a tool for a more sustainable Serbian agriculture [PDF]

open access: yesEkonomika Poljoprivrede (1979), 2021
The aim of this paper was to show the role and importance of agricultural advisers in the development and implementation of information and communication technologies (ICTs) in a path to the more sustainable agriculture, and achieving the SDG2 Zero ...
Radović Vesela   +3 more
doaj   +1 more source

Teachers’ competencies for Media Education [PDF]

open access: yesIn Medias Res, 2020
In the modern age, competencies for media education have become an integral feature of a successful teacher. Nevertheless, the topic of media literacy of teachers in our area has not yet been thoroughly researched.
Jelena Maksimović   +2 more
doaj   +1 more source

Avaliação da função motora em crianças com distrofia muscular congênita com deficiência da merosina Motor function evaluation in merosin-deficient congenital muscular dystrophy children

open access: yesArquivos de Neuro-Psiquiatria, 2005
A distrofia muscular congênita (DMC) compõe um grupo de miopatias caracterizadas por hipotonia e fraqueza muscular notadas até o primeiro ano de vida. Em torno de 40% a 50% dos casos são decorrentes de deficiência primária da proteína merosina (DM), os ...
Fernanda M. Rocco   +6 more
doaj   +1 more source

Distrofia muscular congênita e deficiência de merosina Congenital muscular dystrophy and merosin deficiency

open access: yesArquivos de Neuro-Psiquiatria, 1997
Uma proporção variável de pacientes com distrofia muscular congênita (DMC) da forma clássica ou ocidental apresenta deficiência da cadeia α2 da merosina, uma proteína da matriz extracelular.
Lineu Cesar Werneck   +2 more
doaj   +1 more source

Merosin-positive congenital muscular dystrophy: neuroimaging findings Distrofia muscular congênita merosina-positiva: achados de neuroimagem

open access: yesArquivos de Neuro-Psiquiatria, 2007
Congenital muscle dystrophy (CMD) is a heterogeneous group of autosomal recessive myopathies. It is known that CMD may affect the central nervous system (CNS).
André Palma da Cunha Matta   +1 more
doaj   +1 more source

Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases Complexo distrofina-glicoproteínas associadas na distrofia muscular congênita: análise imuno-histoquímica em 59 casos

open access: yesArquivos de Neuro-Psiquiatria, 2005
The congenital muscular dystrophies (CMD) are heterogeneous muscular diseases with early and dystrophic pattern on muscle biopsy. Many different subtypes have been genetically identified and most phenotypes not yet identified belong to the merosin ...
Lucio Gobbo Ferreira   +6 more
doaj   +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

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

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