skip to main content
Idioma:
Primo Advanced Search
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search prefilters
Busca Simples
Resultados 1 2 3 4 5 next page
Mostrar Somente
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Comparison between Electrocardiographic and Earlobe Pulse Photoplethysmographic Detection for Evaluating Heart Rate Variability in Healthy Subjects in Short- and Long-Term Recordings
Comparison between Electrocardiographic and Earlobe Pulse Photoplethysmographic Detection for Evaluating Heart Rate Variability in Healthy Subjects in Short- and Long-Term Recordings
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparison between Electrocardiographic and Earlobe Pulse Photoplethysmographic Detection for Evaluating Heart Rate Variability in Healthy Subjects in Short- and Long-Term Recordings

Vescio, Basilio ; Salsone, Maria ; Gambardella, Antonio ; Quattrone, Aldo

Sensors (Basel, Switzerland), 2018-03, Vol.18 (3), p.844 [Periódico revisado por pares]

Switzerland: MDPI AG

Texto completo disponível

Citações Citado por
2
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Johnson, Janel O ; Pioro, Erik P ; Boehringer, Ashley ; Chia, Ruth ; Feit, Howard ; Renton, Alan E ; Pliner, Hannah A ; Abramzon, Yevgeniya ; Marangi, Giuseppe ; Winborn, Brett J ; Gibbs, J Raphael ; Nalls, Michael A ; Morgan, Sarah ; Shoai, Maryam ; Hardy, John ; Pittman, Alan ; Orrell, Richard W ; Malaspina, Andrea ; Sidle, Katie C ; Fratta, Pietro ; Harms, Matthew B ; Baloh, Robert H ; Pestronk, Alan ; Weihl, Conrad C ; Rogaeva, Ekaterina ; Zinman, Lorne ; Drory, Vivian E ; Borghero, Giuseppe ; Mora, Gabriele ; Calvo, Andrea ; Rothstein, Jeffrey D ; Drepper, Carsten ; Sendtner, Michael ; Singleton, Andrew B ; Taylor, J Paul ; Cookson, Mark R ; Restagno, Gabriella ; Sabatelli, Mario ; Bowser, Robert ; Chiò, Adriano ; Traynor, Bryan J

Nature neuroscience, 2014-05, Vol.17 (5), p.664-666 [Periódico revisado por pares]

United States: Nature Publishing Group

Texto completo disponível

Citações Citado por
3
Clinical spectrum of SCN1A mutations
Clinical spectrum of SCN1A mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical spectrum of SCN1A mutations

Gambardella, Antonio ; Marini, Carla

Epilepsia (Copenhagen), 2009-05, Vol.50 (s5), p.20-23 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

Texto completo disponível

Citações Citado por
4
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Majounie, Elisa, PhD ; Renton, Alan E, PhD ; Mok, Kin, MSc ; Dopper, Elise GP ; Waite, Adrian, PhD ; Rollinson, Sara, PhD ; Chiò, Adriano, MD ; Restagno, Gabriella, MD ; Nicolaou, Nayia, MSc ; Simon-Sanchez, Javier, PhD ; van Swieten, John C, Prof ; Abramzon, Yevgeniya ; Johnson, Janel O, PhD ; Sendtner, Michael, Prof ; Pamphlett, Roger, MD ; Orrell, Richard W, MD ; Mead, Simon, MD ; Sidle, Katie C, MD ; Houlden, Henry, Prof ; Rohrer, Jonathan D, MD ; Morrison, Karen E, Prof ; Pall, Hardev, MD ; Talbot, Kevin, Prof ; Ansorge, Olaf, MD ; Hernandez, Dena G, MSc ; Arepalli, Sampath, MS ; Sabatelli, Mario, MD ; Mora, Gabriele, MD ; Corbo, Massimo, MD ; Giannini, Fabio, MD ; Calvo, Andrea, MD ; Englund, Elisabet, MD ; Borghero, Giuseppe, MD ; Floris, Gian Luca, MD ; Remes, Anne M, Prof ; Laaksovirta, Hannu, MD ; McCluskey, Leo, MD ; Trojanowski, John Q, Prof ; Van Deerlin, Vivianna M, MD ; Schellenberg, Gerard D, Prof ; Nalls, Michael A, PhD ; Drory, Vivian E, MD ; Lu, Chin-Song, Prof ; Yeh, Tu-Hsueh, MD ; Ishiura, Hiroyuki, MD ; Takahashi, Yuji, MD ; Tsuji, Shoji, Prof ; Le Ber, Isabelle, MD ; Brice, Alexis, Prof ; Drepper, Carsten, PhD ; Williams, Nigel, PhD ; Kirby, Janine, PhD ; Shaw, Pamela, Prof ; Hardy, John, Prof ; Tienari, Pentti J, MD ; Heutink, Peter, Prof ; Morris, Huw R, MD ; Pickering-Brown, Stuart, Prof ; Traynor, Bryan J, Dr

Lancet neurology, 2012-04, Vol.11 (4), p.323-330 [Periódico revisado por pares]

England: Elsevier Ltd

Texto completo disponível

Citações Citado por
5
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity
Material Type:
Artigo 		Adicionar ao Meu Espaço

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity

Fruscione, Floriana ; Valente, Pierluigi ; Sterlini, Bruno ; Romei, Alessandra ; Baldassari, Simona ; Fadda, Manuela ; Prestigio, Cosimo ; Giansante, Giorgia ; Sartorelli, Jacopo ; Rossi, Pia ; Rubio, Alicia ; Gambardella, Antonio ; Nieus, Thierry ; Broccoli, Vania ; Fassio, Anna ; Baldelli, Pietro ; Corradi, Anna ; Zara, Federico ; Benfenati, Fabio

Brain (London, England : 1878), 2018-04, Vol.141 (4), p.1000-1016 [Periódico revisado por pares]

England: Oxford University Press

Texto completo disponível

Citações Citado por
6
Uric acid and late-onset Alzheimer’s disease: results from the ReGAl 2.0 project
Uric acid and late-onset Alzheimer’s disease: results from the ReGAl 2.0 project
Material Type:
Artigo 		Adicionar ao Meu Espaço

Uric acid and late-onset Alzheimer’s disease: results from the ReGAl 2.0 project

Boccardi, Virginia ; Carino, Silvia ; Marinelli, Elisa ; Lapenna, Maria ; Caironi, Giulia ; Bianco, Anna Rita ; Cecchetti, Roberta ; Ruggiero, Carmelinda ; Mecocci, Patrizia

Aging clinical and experimental research, 2021-02, Vol.33 (2), p.361-366 [Periódico revisado por pares]

Cham: Springer International Publishing

Texto completo disponível

Citações Citado por
7
Personality disorders in individuals with functional seizures: a systematic review
Personality disorders in individuals with functional seizures: a systematic review
Material Type:
Artigo 		Adicionar ao Meu Espaço

Personality disorders in individuals with functional seizures: a systematic review

Sammarra, Ilaria ; Martino, Iolanda ; Marino, Laura ; Fortunato, Francesco ; Gambardella, Antonio

Frontiers in psychiatry, 2024-08, Vol.15 [Periódico revisado por pares]

Frontiers Media S.A

Texto completo disponível

Citações Citado por
8
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients

Licchetta, Laura ; Pippucci, Tommaso ; Baldassari, Sara ; Minardi, Raffaella ; Provini, Federica ; Mostacci, Barbara ; Plazzi, Giuseppe ; Tinuper, Paolo ; Bisulli, Francesca ; Bianchi, Amedeo ; Striano, Pasquale ; Gambardella, Antonio ; Giordano, Lucio ; Santucci, Margherita ; Meletti, Stefano ; Crichiutti, Giovanni ; Marini, Carla ; Vignoli, Aglaia ; Dilena, Roberto ; Briatore, Eleonora

Seizure (London, England), 2020-01, Vol.74, p.60-64 [Periódico revisado por pares]

England: Elsevier Ltd

Texto completo disponível

Citações Citado por
9
Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy
Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy

Cava, Claudia ; Manna, Ida ; Gambardella, Antonio ; Bertoli, Gloria ; Castiglioni, Isabella

Molecular therapy. Nucleic acids, 2018-12, Vol.13, p.275-290 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
10
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia

Procopio, Radha ; Fortunato, Francesco ; Gagliardi, Monica ; Talarico, Mariagrazia ; Sammarra, Ilaria ; Sarubbi, Maria Chiara ; Malanga, Donatella ; Annesi, Grazia ; Gambardella, Antonio

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5505 [Periódico revisado por pares]

Switzerland: MDPI AG

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (450)
  2. Revistas revisadas por pares (430)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (460)
  2. Reports  (20)
  3. Book Chapters  (7)
  4. Conjunto de Dados  (2)
  5. Anais de Congresso  (1)
  6. Livros  (1)
  7. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1997  (29)
  2. 1997Até2002  (58)
  3. 2003Até2008  (53)
  4. 2009Até2015  (140)
  5. Após 2015  (213)
  6. Mais opções open sub menu

Idioma 

  1. Japonês  (48)
  2. Francês  (2)
  3. Serbian  (1)
  4. Espanhol  (1)
  5. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.