Applying the International Classification of Functioning, Disability and Health (ICF) to measure childhood disability
…, J Hollenweger, A Martinuzzi - Disability and …, 2003 - Taylor & Francis
The International Classification of Functioning, Disability and Health-ICF addresses the
broad need for a common language and classification of functioning and disability. A parallel …
broad need for a common language and classification of functioning and disability. A parallel …
[HTML][HTML] 20 Years of ICF—International Classification of Functioning, Disability and Health: uses and applications around the world
…, N Kostanjsek, A Fornari, A Raggi, A Martinuzzi… - International journal of …, 2022 - mdpi.com
The International Classification of Functioning Disability and Health (ICF) was approved in
2001 and, since then, several studies reported the increased interest about its use in different …
2001 and, since then, several studies reported the increased interest about its use in different …
[HTML][HTML] The impacts of higher education institutions on sustainable development: A review and conceptualization
…, R Lozano, D Reider, A Martinuzzi - International Journal of …, 2019 - emerald.com
Purpose This paper aims to conceptualize impacts of higher education institutions (HEIs) on
sustainable development (SD), complementing previous literature reviews by broadening …
sustainable development (SD), complementing previous literature reviews by broadening …
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream …
A Chomyn, A Martinuzzi, M Yoneda… - Proceedings of the …, 1992 - National Acad Sciences
The pathogenetic mechanism of the mitochondrial tRNA(LeuUUR) gene mutation responsible
for the MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like …
for the MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like …
MELAS: clinical features, biochemistry, and molecular genetics
…, MA Donati, C Garcia, A Martinuzzi… - Annals of Neurology …, 1992 - Wiley Online Library
We studied 23 patients with clinically defined mitochondrial encephalomyopathy, lactic
acidosis, and stroke‐like episodes (MELAS), 25 oligosymptomatic or asymptomatic maternal …
acidosis, and stroke‐like episodes (MELAS), 25 oligosymptomatic or asymptomatic maternal …
Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin
…, JE Faust, M Micaroni, A Egorova, A Martinuzzi… - Nature, 2009 - nature.com
Establishment and maintenance of proper architecture is essential for endoplasmic reticulum
(ER) function. Homotypic membrane fusion is required for ER biogenesis and maintenance…
(ER) function. Homotypic membrane fusion is required for ER biogenesis and maintenance…
Bellagio STAMP: Principles for sustainability assessment and measurement
L Pintér, P Hardi, A Martinuzzi… - Routledge handbook of …, 2018 - taylorfrancis.com
Revisiting the way society defines and measures progress has been identified as one of the
key levers in tackling the root causes of unsustainable development. The recent economic …
key levers in tackling the root causes of unsustainable development. The recent economic …
Corporations, stakeholders and sustainable development I: a theoretical exploration of business–society relations
R Steurer, ME Langer, A Konrad, A Martinuzzi - Journal of business ethics, 2005 - Springer
Sustainable development (SD) – that is, “Development that meets the needs of current
generations without compromising the ability of future generations to meet their needs and …
generations without compromising the ability of future generations to meet their needs and …
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy
…, FN Ross-Cisneros, L Caparrotta, A Martinuzzi… - Brain, 2011 - academic.oup.com
Leber’s hereditary optic neuropathy, the most frequent mitochondrial disease due to
mitochondrial DNA point mutations in complex I, is characterized by the selective degeneration of …
mitochondrial DNA point mutations in complex I, is characterized by the selective degeneration of …
Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage
…, V Carelli, A Martinuzzi… - Proceedings of the …, 2005 - National Acad Sciences
Dysfunction of mitochondrial complex I is a feature of human neurodegenerative diseases
such as Leber hereditary optic neuropathy and Parkinson's disease. This mitochondrial defect …
such as Leber hereditary optic neuropathy and Parkinson's disease. This mitochondrial defect …