Hypovitaminosis D3, Leukopenia, and Human Serotonin Transporter Polymorphism in Anorexia Nervosa and Bulimia Nervosa

Autor: Anna Tasegian, Francesco Curcio, Laura Dalla Ragione, Francesca Rossetti, Samuela Cataldi, Michela Codini, Francesco Saverio Ambesi-Impiombato, Tommaso Beccari, Elisabetta Albi

Publikováno v: Mediators of Inflammation, Vol 2016 (2016)

Vitamin D3 has been described to have different extraskeletal roles by acting as parahormone in obesity, diabetes, cancer, cognitive impairment, and dementia and to have important regulatory functions in innate immunity. There are no studies showing

Externí odkaz: https://doaj.org/article/7903dcdf82b74eaf91960bd5406b7d2f

Cerebrospinal fluid β-glucocerebrosidase activity is reduced in parkinson's disease patients

Autor: Paolo Calabresi, Nicola Tambasco, Silvia Paciotti, Davide Chiasserini, Lucilla Parnetti, Bruno Bembi, Tommaso Beccari, Stefania Zampieri, Anna Tasegian, Andrea Dardis, Paolo Eusebi

Publikováno v: Movement Disorders. 32:1423-1431

Background Reduced β-glucocerebrosidase activity was observed in postmortem brains of both GBA1 mutation carrier and noncarrier Parkinson's disease patients, suggesting that lower β-glucocerebrosidase activity is a key feature in the pathogenesis o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::35b23241a4d1a394c5afb8109b3dde3e
https://doi.org/10.1002/mds.27136

5-HT2AR and BDNF gene variants in eating disorders susceptibility

Autor: Michela Codini, Marica Franzago, M. Rachele Ceccarini, Elisabetta Albi, F. Filomena Patria, Carmela Conte, Anna Tasegian, Matteo Bertelli, Liborio Stuppia, Tommaso Beccari, Laura Dalla Ragione

Publikováno v: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric GeneticsREFERENCES. 183(3)

Evidence from family and twin studies points to a genetic contribution to the etiology of eating disorders (EDs), confirmed by the association of several single nucleotide polymorphisms (SNPs) with this group of disorders. Previous reports have sugge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c377b13b0270ef2639740792157a96b3
https://pubmed.ncbi.nlm.nih.gov/31746551

Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson’s Disease and Dementia with Lewy Bodies

Autor: Angela Ingrassia, Paolo Eusebi, Tommaso Beccari, Gonzalo Duran-Pacheco, Wilma D.J. van de Berg, Tim Moors, Guido J. Breedveld, Vincenzo Bonifati, Thomas Kremer, Marialuisa Quadri, Anna Tasegian, Paolo Calabresi, Silvia Paciotti, Davide Chiasserini, Lucilla Parnetti

Publikováno v: Moors, T E, Paciotti, S, Ingrassia, A, Quadri, M, Breedveld, G, Tasegian, A, Chiasserini, D, Eusebi, P, Duran-Pacheco, G, Kremer, T, Calabresi, P, Bonifati, V, Parnetti, L, Beccari, T & van de Berg, W D J 2019, ' Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson’s Disease and Dementia with Lewy Bodies ', Molecular Neurobiology, vol. 56, no. 2, pp. 1344-1355 . https://doi.org/10.1007/s12035-018-1090-0
Molecular Neurobiology
Molecular Neurobiology, 56(2), 1344-1355. Humana Press

Mutations in the GBA gene, encoding the lysosomal hydrolase glucocerebrosidase (GCase), are the most common known genetic risk factor for Parkinson’s disease (PD) and dementia with Lewy bodies (DLB). The present study aims to gain more insight into

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bdb58fd2052a751ff081aee2c586103
http://hdl.handle.net/11391/1436133

Cerebrospinal fluid β-glucocerebrosidase activity is reduced in parkinson's disease patients

Autor: Lucilla, Parnetti, Silvia, Paciotti, Paolo, Eusebi, Andrea, Dardis, Stefania, Zampieri, Davide, Chiasserini, Anna, Tasegian, Nicola, Tambasco, Bruno, Bembi, Paolo, Calabresi, Tommaso, Beccari

Publikováno v: Movement disorders : official journal of the Movement Disorder Society. 32(10)

Reduced β-glucocerebrosidase activity was observed in postmortem brains of both GBA1 mutation carrier and noncarrier Parkinson's disease patients, suggesting that lower β-glucocerebrosidase activity is a key feature in the pathogenesis of PD. The o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a9cd3400432d193fceb729b40d928c84
https://pubmed.ncbi.nlm.nih.gov/29068500