Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Elena Radi"'
Autor:
Patrizia Formichi, Lucilla Parnetti, Elena Radi, Gabriele Cevenini, Maria Teresa Dotti, Antonio Federico
Publikováno v:
International Journal of Alzheimer's Disease, Vol 2010 (2010)
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is considered a model of pure vascular dementia (VD) because it occurs in young adults unlikely to have concomitant age and Alzheimer's Disease-(AD-)
Externí odkaz:
https://doaj.org/article/66edc1bec76445c99cdfca6d70e5ba4d
Publikováno v:
Journal of Alzheimer's Disease. 42:S125-S152
Neurodegenerative disorders affect almost 30 million individuals leading to disability and death. These disorders are characterized by pathological changes in disease-specific areas of the brain and degeneration of distinct neuron subsets. Despite th
Autor:
Carla Battisti, Benedetta Rossi, Patrizia Formichi, Raffaella Guazzo, Ermelinda Tarquini, Elena Radi, Maria Margherita De Santi, Sergio Tripodi, Antonio Federico
Publikováno v:
Journal of cellular physiology. 233(1)
Niemann-Pick type C disease (NPC) is a disorder characterized by abnormal intracellular accumulation of unesterified cholesterol and glycolipids. Two distinct disease-causing genes have been isolated, NPC1 and NPC2. The NPC1 protein is involved in th
Autor:
Elena Radi, Gian Nicola Gallus, Elena Cardaioli, Paola Da Pozzo, Antonio Federico, Patrizia Formichi
Publikováno v:
Journal of the Neurological Sciences. 322:254-262
Mitochondria are involved in ATP supply to cells through oxidative phosphorylation (OXPHOS), synthesis of key molecules and response to oxidative stress, as well as in apoptosis. They contain many redox enzymes and naturally occurring inefficiencies
Autor:
Maria Teresa Dotti, Chiara Branca, Antonio Federico, Elena Radi, Paola Da Pozzo, Patrizia Formichi, Luisa Bracci, Carla Battisti, Fabio Giannini, Jlenia Brunetti
Publikováno v:
Journal of the neurological sciences. 368
Background POLG-related disorders are a group of heterogeneous diseases characterized by an overlapping clinical presentations and associated with mutations in the POLG gene. POLG codes for the catalytic subunit of mitochondrial polymerase gamma (POL
Autor:
Patrizia Formichi, Lorenzo Leoncini, Giuseppe Di Maio, Elena Radi, Antonio Federico, Anna Onnis, Silvia Bianchi, Ermelinda Tarquini
Publikováno v:
Journal of Cellular Physiology. 227:1771-1775
Notch3 is a single pass transmembrane protein belonging to the Notch receptor family. Notch proteins are involved in a very conserved signaling system (Notch signaling) with a broad spectrum of functions, from cell proliferation and differentiation t
Publikováno v:
Journal of the Neurological Sciences. 308:49-56
Alagille syndrome (AGS) is an autosomal dominant disorder characterized by cholestasis, cardiac, skeletal and ocular abnormalities. Increasing importance is being given to vascular and central nervous system impairment. AGS is in most cases caused by
Autor:
Carla Battisti, Anna Laura Pasqui, Elena Radi, Pietro Enea Lazzerini, Patrizia Formichi, Franco Laghi-Pasini, Anna Di Stefano, Antonio Federico, G. Pompella, Alessandra Leonini
Publikováno v:
Journal of Cellular Physiology. 212:737-743
Globoid cell leukodystrophy or Krabbe disease (KD), is a hereditary disorder caused by galactosylceramidase deficiency. Progressive accumulation of psychosine is considered to be the critical pathogenetic mechanism of cell death in the Krabbe brain.
Autor:
Antonio Federico, Eleonora Giorgi, Elena Radi, Patrizia Formichi, Carla Battisti, Jlenia Brunetti, Maria Teresa Dotti, Luisa Bracci, Alessandra Rufa, Gian Nicola Gallus, Rossella Franceschini
Autosomal dominant optic atrophy (ADOA) is a hereditary optic neuropathy characterized by bilateral symmetrical visual loss, decrease in retinal ganglion cells and a loss of myelin within the optic nerve. ADOA is associated to mutations in Optic atro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13923f31f29c1676fe99575c40f42e89
http://hdl.handle.net/11365/976816
http://hdl.handle.net/11365/976816
Autor:
Antonio Federico, Giuseppe Di Maio, Elena Radi, Dafin F. Muresanu, Patrizia Formichi, Carla Battisti
Publikováno v:
Journal of Cellular and Molecular Medicine
Cerebrolysin is the only drug available for clinical use containing active fragments of some important neurotrophic factors obtained from purified porcine brain proteins, which has long been used for the treatment of dementia and stroke sequels. Cere