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1
Gender and Animals in History: Yearbook of Women’s History 42
Gender and Animals in History: Yearbook of Women’s History 42
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Gender and Animals in History: Yearbook of Women’s History 42

Sandra Swart Sarah Carmichael; Claudia Hacke; Ernestine Hoegen; Kirsten Kamphuis; Marleen Reichgelt; Larissa Schulte Nordholt; Iris van der Zande

Amsterdam University Press 2024

Acesso online

2
Atlas de anatomia
Atlas de anatomia
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Atlas de anatomia

Anne M Gilroy; Brian R MacPherson; Lawrence M Ross

Rio de Janeiro Guanabara Koogan 2008

Localização: EEFE - Esc. Educação Física e Esporte    (796.021 A-2 ) e outros locais(Acessar)

3
Prometheus atlas de anatomia anatomia geral e aparelho locomotor
Prometheus atlas de anatomia anatomia geral e aparelho locomotor
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Prometheus atlas de anatomia anatomia geral e aparelho locomotor

Michael Schünke 1950- Erik Schulte; Udo Schumacher; Jürgen Rude; Markus Voll; Karl Wesker; Adilson Dias Salles; Cláudia Lúcia Caetano de Araujo; Marcelo Sampaio Narciso; Telma Lúcia de Azevedo Hennemann; Walter Martin Roland Oelemann

Rio de Janeiro Guanabara Koogan 2006

Localização: FM - Fac. Medicina    (QS17 S149pro 2006 ex.7 ) e outros locais(Acessar)

4
GBA-associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study
GBA-associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study
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GBA-associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study

Brockmann, Kathrin ; Srulijes, Karin ; Pflederer, Sylvia ; Hauser, Ann-Kathrin ; Schulte, Claudia ; Maetzler, Walter ; Gasser, Thomas ; Berg, Daniela

Movement disorders, 2015-03, Vol.30 (3), p.407-411 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
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Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

van Rooij, Jeroen ; Uitterlinden, André G ; Kraaij, Robert ; Heutink, Peter ; Nalls, Mike A ; Plagnol, Vincent ; Sharma, Manu ; Saad, Mohamad ; Simón-Sánchez, Javier ; Schulte, Claudia ; Lesage, Suzanne ; Arepalli, Sampath ; Barker, Roger ; Ben, Yoav ; Berendse, Henk W ; Berg, Daniela ; Bhatia, Kailash ; de Bie, Rob M A ; Bloem, Bas ; Bochdanovits, Zoltan ; Bonin, Michael ; Bras, Jose M ; Brockmann, Kathrin ; Brooks, Janet ; Burn, David J ; Majounie, Elisa ; Charlesworth, Gavin ; Lungu, Codrin ; Chen, Honglei ; Chong, Sean ; Clarke, Carl E ; Mark Cooper, J ; Corvol, Jean Christophe ; Counsell, Carl ; Damier, Philippe ; Dartigues, Jean-François ; Deloukas, Panos ; Dexter, David T ; van Dijk, Karin D ; Durif, Frank ; Dürr, Alexandra ; Evans, Jonathan R ; Foltynie, Thomas ; Gardner, Michelle ; Raphael Gibbs, J ; Gray, Emma ; Guerreiro, Rita ; Harris, Clare ; van Hilten, Jacobus J ; Hofman, Albert ; Hollenbeck, Albert ; Holton, Janice ; Hu, Michele ; Huang, Xuemei ; Wurster, Isabel ; Hudson, Gavin ; Hunt, Sarah E ; Lees, Andrew ; Lichtner, Peter ; Lopez, Grisel ; Lorenz, Delia ; McNeill, Alisdair ; Moorby, Catriona ; Moore, Matthew ; Morris, Huw R ; Morrison, Karen E ; Pearson, Justin ; Perlmutter, Joel S ; Pétursson, Hjörvar ; Pollak, Pierre ; Riess, Olaf ; Rivadeneira, Fernando ; Ryten, Mina ; Schapira, Anthony ; Scheffer, Hans ; Shaw, Karen ; Shoulson, Ira ; Shulman, Joshua ; Sidransky, Ellen ; Smith, Colin ; Spencer, Chris C A ; Stefánsson, Hreinn ; Bettella, Francesco ; Stockton, Joanna D ; Strange, Amy ; Talbot, Kevin ; Tanner, Carlie M ; Tashakkori-Ghanbaria, Avazeh ; Trabzuni, Daniah ; Uitterlinden, André G ; Walker, Robert ; van de Warrenburg, Bart ; Wickremaratchi, Mirdhu ; Williams, Nigel ; Williams-Gray, Caroline H ; Winder-Rhodes, Sophie ; Martinez, Maria ; Wood, Nicholas W ; Brice, Alexis ; Gasser, Thomas

Brain (London, England : 1878), 2017-12, Vol.140 (12), p.3191-3203 [Periódico revisado por pares]

Oxford University Press

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6
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
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Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

Kia, Demis A ; Zhang, David ; Guelfi, Sebastian ; Manzoni, Claudia ; Hubbard, Leon ; Reynolds, Regina H ; Botía, Juan ; Ryten, Mina ; Ferrari, Raffaele ; Lewis, Patrick A ; Williams, Nigel ; Trabzuni, Daniah ; Hardy, John ; Wood, Nicholas W

Archives of neurology (Chicago), 2021-04, Vol.78 (4), p.464-472 [Periódico revisado por pares]

United States: American Medical Association

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7
Alterations in Blood Monocyte Functions in Parkinson's Disease
Alterations in Blood Monocyte Functions in Parkinson's Disease
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Alterations in Blood Monocyte Functions in Parkinson's Disease

Nissen, Sara Konstantin ; Shrivastava, Kalpana ; Schulte, Claudia ; Otzen, Daniel Erik ; Goldeck, David ; Berg, Daniela ; Møller, Holger Jon ; Maetzler, Walter ; Romero‐Ramos, Marina

Movement disorders, 2019-11, Vol.34 (11), p.1711-1721 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Post-COVID-19-associated morbidity in children, adolescents, and adults: A matched cohort study including more than 157,000 individuals with COVID-19 in Germany
Post-COVID-19-associated morbidity in children, adolescents, and adults: A matched cohort study including more than 157,000 individuals with COVID-19 in Germany
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Post-COVID-19-associated morbidity in children, adolescents, and adults: A matched cohort study including more than 157,000 individuals with COVID-19 in Germany

Roessler, Martin ; Tesch, Falko ; Batram, Manuel ; Jacob, Josephine ; Loser, Friedrich ; Weidinger, Oliver ; Wende, Danny ; Vivirito, Annika ; Toepfner, Nicole ; Ehm, Franz ; Seifert, Martin ; Nagel, Oliver ; König, Christina ; Jucknewitz, Roland ; Armann, Jakob Peter ; Berner, Reinhard ; Treskova-Schwarzbach, Marina ; Hertle, Dagmar ; Scholz, Stefan ; Stern, Stefan ; Ballesteros, Pedro ; Baßler, Stefan ; Bertele, Barbara ; Repschläger, Uwe ; Richter, Nico ; Riederer, Cordula ; Sobik, Franziska ; Schramm, Anja ; Schulte, Claudia ; Wieler, Lothar ; Walker, Jochen ; Scheidt-Nave, Christa ; Schmitt, Jochen Persson, Lars Åke

PLoS medicine, 2022-11, Vol.19 (11), p.e1004122 [Periódico revisado por pares]

United States: Public Library of Science

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9
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease
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A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease

Liu, Hui ; Koros, Christos ; Strohäker, Timo ; Schulte, Claudia ; Bozi, Maria ; Varvaresos, Stefanos ; Ibáñez de Opakua, Alain ; Simitsi, Athina Maria ; Bougea, Anastasia ; Voumvourakis, Konstantinos ; Maniati, Matina ; Papageorgiou, Sokratis G. ; Hauser, Ann‐Kathrin ; Becker, Stefan ; Zweckstetter, Markus ; Stefanis, Leonidas ; Gasser, Thomas

Movement disorders, 2021-07, Vol.36 (7), p.1624-1633 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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10
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Mok, Kin Y, FRCP ; Sheerin, Una, MRCP ; Simón-Sánchez, Javier, PhD ; Salaka, Afnan, PhD ; Chester, Lucy, MPharm ; Escott-Price, Valentina, PhD ; Mantripragada, Kiran, PhD ; Doherty, Karen M, MD ; Noyce, Alastair J, MRCP ; Mencacci, Niccolo E, MD ; Lubbe, Steven J, PhD ; Williams-Gray, Caroline H, PhD ; Barker, Roger A, Prof ; van Dijk, Karin D, MD ; Berendse, Henk W, Prof ; Heutink, Peter, Prof ; Corvol, Jean-Christophe, Prof ; Cormier, Florence, MD ; Lesage, Suzanne, PhD ; Brice, Alexis, Prof ; Brockmann, Kathrin, MD ; Schulte, Claudia, PhD ; Gasser, Thomas, Prof ; Foltynie, Thomas, PhD ; Limousin, Patricia, Prof ; Morrison, Karen E, Prof ; Clarke, Carl E, Prof ; Sawcer, Stephen, Prof ; Warner, Tom T, Prof ; Lees, Andrew J, Prof ; Morris, Huw R, Prof ; Nalls, Mike A, PhD ; Singleton, Andrew B, PhD ; Hardy, John, Prof ; Abramov, Andrey Y, Prof ; Plagnol, Vincent, PhD ; Williams, Nigel M, Dr ; Wood, Nicholas W, Prof

Lancet neurology, 2016-05, Vol.15 (6), p.585-596 [Periódico revisado por pares]

England: Elsevier Ltd

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Deste Autor:

  1. Schumacher, U
  2. Salles, A
  3. Wesker, K
  4. Kamphuis, K
  5. Voll, M

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Humans
  4. Female
  5. Neurosciences & Neurology

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

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