Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna Maria Pia Griguoli"'
Autor:
Marianna Storto, Anna Maria Pia Griguoli, Stefania Zampatti, Roberta Fantozzi, Francesco Fornai, Stefano Gambardella, Carmelo D'Alessio, Simona Scala, Larisa Ryskalin, Rosa Campopiano, Veronica Albano, Rosangela Ferese, Laura Scorzolini, Emiliano Giardina
Publikováno v:
Acta virologica. 61:273-279
In the last few years, polymerase chain reaction analysis is frequently required to improve the detection of pathogen infections in central nervous system as a potential cause of neurological disorders and neuropsychiatric symptoms. The goal of this
Autor:
Anna Maria Pia Griguoli, Giovanni Capelli, Ferdinando Squitieri, Barbara D’Alessio, Antonio Porcellini
Publikováno v:
Clinical Genetics. 89:367-370
Huntington disease (HD) prevalence shows geographic variability and has been recently updated by taking into account the mutation diagnostic test. In Italy, the last epidemiological estimation was reported well before the HTT gene discovery and the a
Autor:
Marianna Storto, Giuseppe Novelli, Francesca Biagioni, Rosangela Ferese, Carla L. Busceti, Stefano Gambardella, Fiona Limanaqi, Anna Maria Pia Griguoli, Francesco Fornai, Rosa Campopiano
Publikováno v:
Frontiers in Cellular Neuroscience
The functional anatomy of the reticular formation (RF) encompasses a constellation of brain regions which are reciprocally connected to sub-serve a variety of functions. Recent evidence indicates that neuronal degeneration within one of these regions
Autor:
Carmelo D'Alessio, Emiliano Giardina, Anderson Gaglione, Francesco Fornai, Mattia Falconi, Giuseppe Novelli, Federico Iacovelli, Simona Scala, Stefano Gambardella, Rosangela Ferese, Stefania Zampatti, Rosa Campopiano, Veronica Albano, Anna Maria Pia Griguoli, Marianna Storto
Myotonia congenita belongs to the group of non-dystrophic myotonia caused by mutations in _CLCN_1gene, and can be inherited either in autosomal dominant (Thomsen disease) or recessive (Becker disease) forms. Here we describe a 46-year-old male patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36852d039a741ce83ce87dceeff83a61
https://hdl.handle.net/11576/2665354
https://hdl.handle.net/11576/2665354
Autor:
Simona Scala, Rosangela Ferese, Veronica Albano, Rosa Campopiano, Francesco Fornai, Giuseppe Barrano, Anna Maria Pia Griguoli, Stefania Zampatti, Emiliano Giardina, Giuseppe Novelli, Stefano Gambardella
X-linked hydrocephalus (XLH) is a genetic disorder leading to a syndrome characterized by mental retardation, bilateral adducted thumbs, and spasticity of upper and lower limbs. In most cases, X-linked mutation leads to a defective activity of the ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b37a3c40b2aced44be35ffc5eed4c43
https://hdl.handle.net/11576/2664948
https://hdl.handle.net/11576/2664948