Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Estela M. Bruxel"'
Autor:
Estela M. Bruxel, Amanda M. doCanto, Danielle C. F. Bruno, Jaqueline C. Geraldis, Iscia Lopes‐Cendes
Publikováno v:
Epilepsia Open, Vol 7, Iss S1, Pp S94-S120 (2022)
Abstract Mesial temporal lobe epilepsy (MTLE) is the most common type of focal epilepsy in adults, and hippocampal sclerosis (HS) is a frequent histopathological feature in patients with MTLE. Pharmacoresistance is present in at least one‐third of
Externí odkaz:
https://doaj.org/article/adb60feb56b54acc842acc7e829ebdb4
Autor:
Mariana R. Botton, Patrícia P. Viola, Mariana R. Meireles, Estela M. Bruxel, Priccila Zuchinali, Eliane Bandinelli, Luis E. Rohde, Tiago L. L. Leiria, Joyce Y. Y. Salamoni, Arthur P. Garbin, Mara H. Hutz
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 1 suppl 2 (2020)
Abstract Warfarin is an oral anticoagulant prescribed to prevent and treat thromboembolic disorders. It has a narrow therapeutic window and must have its effect controlled. Prothrombin test, expressed in INR value, is used for dose management. Time i
Externí odkaz:
https://doaj.org/article/43d2e924621442f08f60b901d791fc29
Autor:
Claudia V Maurer-Morelli, Jaira F de Vasconcellos, Estela M Bruxel, Cristiane S Rocha, Amanda M do Canto, Helder Tedeschi, Clarissa L Yasuda, Fernando Cendes, Iscia Lopes-Cendes
Publikováno v:
Exp Biol Med (Maywood)
Most patients with pharmacoresistant mesial temporal lobe epilepsy (MTLE) have hippocampal sclerosis on the postoperative histopathological examination. Although most patients with MTLE do not refer to a family history of the disease, familial forms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ef7b38d36106c672bab5e09c030832
https://doi.org/10.1177/15353702221126666
https://doi.org/10.1177/15353702221126666
Autor:
Jaqueline C Geraldis, Estela M. Bruxel, Danielle do Carmo Ferreira Bruno, Alexandre B Godoi, Mariana Martin, Amanda Morato do Canto, Iscia Lopes-Cendes
Publikováno v:
Seizure. 90:34-50
Mesial temporal lobe epilepsy (MTLE) is one of the most common types of focal epilepsy in the adult population. MTLE is frequently associated with a specific histopathological lesion in the medial temporal structures, namely hippocampal sclerosis (HS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa4b051ac094794588f73d8cd753de8
https://doi.org/10.1016/j.seizure.2021.03.002
https://doi.org/10.1016/j.seizure.2021.03.002
Autor:
Marieke Klein, Claiton H.D. Bau, Paula Rovira, Thomas P. Quinn, Barbara Franke, Carlos Renato Moreira-Maia, Nina Roth Mota, Djenifer B. Kappel, Mauricio Arcos-Burgos, Cristina Sánchez-Mora, Eugenio H. Grevet, Luis Augusto Rohde, Mara H. Hutz, M. Ribasés, Glaucia Chiyoko Akutagava-Martins, Estela M. Bruxel
Publikováno v:
Molecular Psychiatry, 26, 6, pp. 2277-2285
Molecular Psychiatry, 26, 2277-2285
Molecular Psychiatry, 26, 2277-2285
Contains fulltext : 237889.pdf (Publisher’s version ) (Open Access) The gene encoding adhesion G protein-coupled receptor L3 (ADGRL3, also referred to as latrophilin 3 or LPHN3) has been associated with ADHD susceptibility in independent ADHD sampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7886d7a4514b720bb4b47d38b2f4f51
https://doi.org/10.1038/s41380-020-0673-0
https://doi.org/10.1038/s41380-020-0673-0
Autor:
Iscia Lopes-Cendes, Amanda Morato do Canto, Danielle do Carmo Ferreira Bruno, Jaqueline C Geraldis, Estela M. Bruxel
Publikováno v:
Epilepsia open. 7
Mesial temporal lobe epilepsy (MTLE) is the most common type of focal epilepsy in adults, and hippocampal sclerosis (HS) is a frequent histopathological feature in patients with MTLE. Pharmacoresistance is present in at least one third of patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::388785a691b97831961d724fd6d98ceb
https://pubmed.ncbi.nlm.nih.gov/34486831
https://pubmed.ncbi.nlm.nih.gov/34486831
GAD1gene polymorphisms are associated with hyperactivity in Attention-Deficit/Hyperactivity Disorder
Autor:
Angélica Salatino-Oliveira, Marcelo Schmitz, Cristian Patrick Zeni, Mara H. Hutz, Rodrigo Chazan, Guilherme V. Polanczyk, Glaucia Chiyoko Akutagava-Martins, Estela M. Bruxel, Luis Augusto Rohde, Julia P. Genro
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 171:1099-1104
Attention-Deficit/Hyperactivity Disorder (ADHD) is one of the most common neurodevelopmental disorders of childhood. Recent studies suggest a role for γ-aminobutyric acid (GABA) on ADHD hyperactive/impulsive symptoms due to behavioral disinhibition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::438293314bb086a8adbe44df88c3828e
https://doi.org/10.1002/ajmg.b.32489
https://doi.org/10.1002/ajmg.b.32489
Autor:
Cristian Patrick Zeni, Flávia Wagner, Estela M. Bruxel, Christian Kieling, Mara H. Hutz, Guilherme V. Polanczyk, Glaucia Chiyoko Akutagava-Martins, Angélica Salatino-Oliveira, Luis Augusto Rohde, Julia P. Genro
Publikováno v:
European Archives of Psychiatry and Clinical Neuroscience. 266:359-366
Diverse efforts have been done to improve the etiologic understanding of mental disorders, such as attention-deficit/hyperactivity disorder (ADHD). It becomes clear that research in mental disorders needs to move beyond descriptive syndromes. Several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c380b277008f2bcab94d8597f269d187
https://doi.org/10.1007/s00406-015-0626-9
https://doi.org/10.1007/s00406-015-0626-9
Autor:
Cristian Patrick Zeni, Mara H. Hutz, Estela M. Bruxel, Angélica Salatino-Oliveira, Luiz Rohde, Marcelo Schmitz, Guilherme V. Polanczyk, Rodrigo Chazan, Mauricio Arcos-Burgos, Glaucia Chiyoko Akutagava-Martins, Julia P. Genro, Luciana Tovo-Rodrigues
Publikováno v:
Genes, Brain and Behavior. 14:419-427
Latrophilin 3 (LPHN3) is a brain-specific member of the G-protein coupled receptor family associated to both attention-deficit/hyperactivity disorder (ADHD) genetic susceptibility and methylphenidate (MPH) pharmacogenetics. Interactions of LPHN3 vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb41ee9c93db3f67567bd19a3abf5746
https://doi.org/10.1111/gbb.12224
https://doi.org/10.1111/gbb.12224
Autor:
Luis Augusto Rohde, Estela M. Bruxel, Angélica Salatino-Oliveira, Verônica Contini, Christian Kieling, Mara H. Hutz, Glaucia Chiyoko Akutagava-Martins
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 165:263-282
Attention-deficit/hyperactivity disorder (ADHD) is a complex and heterogeneous disorder, affecting individuals across the life cycle. Although its etiology is not yet completely understood, genetics plays a substantial role. Pharmacological treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f27bc5a73e177caaec452f46fe10c6cc
https://doi.org/10.1002/ajmg.b.32240
https://doi.org/10.1002/ajmg.b.32240