Results 1 to 10 of about 193 (66)

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

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   +22 more sources

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

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

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   +2 more sources

Distrofia muscular congénita merosina positiva, anormalidades da substância branca e displasia cortical occipital posterior bilateral.

open access: yesActa Médica Portuguesa, 2003
Congenital muscular dystrophy (CMD) is one of the most frequent dystrophies of childhood, which is commonly characterized by neonatal muscle impairment with or without clinical evidence of central nervous system involvement.
Valentina T Ribeiro   +5 more
doaj   +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

Distrofia muscular congênita merosina negativa: um relato de caso

open access: yesActa Fisiátrica, 2022
A Distrofia muscular laminin subunit alpha 2 (DM LAMA2) é caracterizada pela deficiência da proteína da cadeia laminina α2, apresentando sintomas distróficos que progridem na infância. Objetivo: Apresentar dados da avaliação fisioterapêutica de uma criança com DM LAMA2 em acompanhamento ambulatorial. Métodos: Pesquisou-se em prontuário dados referentes
Maria Caroline Heinz   +3 more
openaire   +1 more source

Efeitos do treinamento muscular inspiratório na performance muscular inspiratória de um paciente com distrofia muscular congênita com deficiência de merosina: um relato de caso

open access: yesResearch, Society and Development, 2021
A distrofia muscular congênita com deficiência da merosina (MDC1A) é caracterizada por um comprometimento da fibra muscular pela deficiência parcial ou completa da laminina α2 (merosina) uma proteína extracelular responsável pela manutenção da estrutura celular.
Iara Tainá Cordeiro de Souza   +4 more
openaire   +2 more sources

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

Home - About - Disclaimer - Privacy