Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elena De Amicis"'
Publikováno v:
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
Spinal muscular atrophy (SMA) is a severe neuromuscular disease affecting children, due to mutation/deletion of survival motor neuron 1 (SMN1) gene. The lack of functional protein SMN determines motor neuron (MN) degeneration and skeletal muscle atro
Externí odkaz:
https://doaj.org/article/bbba8f6e51404cb6b0df6e4954d4f06e
Increasing Agrin Function Antagonizes Muscle Atrophy and Motor Impairment in Spinal Muscular Atrophy
Autor:
Marina Boido, Elena De Amicis, Valeria Valsecchi, Marco Trevisan, Ugo Ala, Markus A. Ruegg, Stefan Hettwer, Alessandro Vercelli
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 12 (2018)
Spinal muscular atrophy (SMA) is a pediatric genetic disease, characterized by motor neuron (MN) death, leading to progressive muscle weakness, respiratory failure, and, in the most severe cases, to death. Abnormalities at the neuromuscular junction
Externí odkaz:
https://doaj.org/article/d2735a6d2bf2470b865b9ab8fa12ae0d
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128560 (2015)
Spinal muscular atrophy (SMA) is a severe neuromuscular disease, the most common in infancy, and the third one among young people under 18 years. The major pathological landmark of SMA is a selective degeneration of lower motor neurons, resulting in
Externí odkaz:
https://doaj.org/article/663355e339d443a5a2176223996afbcb
Autor:
Paolo d'Errico, Marina Boido, Antonio Piras, Valeria Valsecchi, Elena De Amicis, Denise Locatelli, Silvia Capra, Francesco Vagni, Alessandro Vercelli, Giorgio Battaglia
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the most common inherited cause of infant mortality. Even though the SMA phenotype is traditionally considered as related to spinal motor neuron loss, it
Externí odkaz:
https://doaj.org/article/faebacf483944dcd9bb330b83995b183
Publikováno v:
European Journal of Histochemistry. 65
Spinal muscular atrophy (SMA) is a severe neuromuscular disease affecting children, due to mutation/deletion of survival motor neuron 1 (SMN1) gene. The lack of functional protein SMN determines motor neuron (MN) degeneration and skeletal muscle atro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cee2b88463a0b65a2922fe170646d22
https://doi.org/10.4081/ejh.2021.3294
https://doi.org/10.4081/ejh.2021.3294
Publikováno v:
European Journal of Histochemistry : EJH
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
Spinal muscular atrophy (SMA) is a severe neuromuscular disease affecting children, due to mutation/deletion of survival motor neuron 1 (SMN1) gene. The lack of functional protein SMN determines motor neuron (MN) degeneration and skeletal muscle atro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7c49b90a6e23943f4228d91a467ba29d
http://europepmc.org/articles/PMC8586821
http://europepmc.org/articles/PMC8586821
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128560 (2015)
PLoS ONE
PLoS ONE
Spinal muscular atrophy (SMA) is a severe neuromuscular disease, the most common in infancy, and the third one among young people under 18 years. The major pathological landmark of SMA is a selective degeneration of lower motor neurons, resulting in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03c85dfa6f627a5bea75bc79641be5f7
http://hdl.handle.net/2318/1530170
http://hdl.handle.net/2318/1530170
Autor:
Giorgio Battaglia, Marina Boido, Antonio Piras, Francesco Vagni, Denise Locatelli, Paolo d'Errico, Elena De Amicis, Valeria Valsecchi, Silvia Capra, Alessandro Vercelli
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the most common inherited cause of infant mortality. Even though the SMA phenotype is traditionally considered as related to spinal motor neuron loss, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43634f90887817a7b63affdfb9f1ad70
http://europepmc.org/articles/PMC3855775
http://europepmc.org/articles/PMC3855775