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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

Hudson, Gavin ; Nalls, Mike ; Evans, Jonathan R ; Breen, David P ; Winder-Rhodes, Sophie ; Morrison, Karen E ; Morris, Huw R ; Williams-Gray, Caroline H ; Barker, Roger A ; Singleton, Andrew B ; Hardy, John ; Wood, Nicholas E ; Burn, David J ; Chinnery, Patrick F

Neurology, 2013-05, Vol.80 (22), p.2042-2048 [Periódico revisado por pares]

Hagerstown, MD: American Academy of Neurology

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2
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Spencer, Chris C A ; Plagnol, Vincent ; Strange, Amy ; Gardner, Michelle ; Paisan-Ruiz, Coro ; Band, Gavin ; Barker, Roger A ; Bellenguez, Celine ; Bhatia, Kailash ; Blackburn, Hannah ; Blackwell, Jennie M ; Bramon, Elvira ; Brown, Martin A ; Brown, Matthew A ; Burn, David ; Casas, Juan-Pablo ; Chinnery, Patrick F ; Clarke, Carl E ; Corvin, Aiden ; Craddock, Nicholas ; Deloukas, Panos ; Edkins, Sarah ; Evans, Jonathan ; Freeman, Colin ; Gray, Emma ; Hardy, John ; Hudson, Gavin ; Hunt, Sarah ; Jankowski, Janusz ; Langford, Cordelia ; Lees, Andrew J ; Markus, Hugh S ; Mathew, Christopher G ; McCarthy, Mark I ; Morrison, Karen E ; Palmer, Colin N A ; Pearson, Justin P ; Peltonen, Leena ; Pirinen, Matti ; Plomin, Robert ; Potter, Simon ; Rautanen, Anna ; Sawcer, Stephen J ; Su, Zhan ; Trembath, Richard C ; Viswanathan, Ananth C ; Williams, Nigel W ; Morris, Huw R ; Donnelly, Peter ; Wood, Nicholas W

Human molecular genetics, 2011-01, Vol.20 (2), p.345-353 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Nalls, Michael A ; Plagnol, Vincent ; Hernandez, Dena G ; Sharma, Manu ; Sheerin, Una-Marie ; Saad, Mohamad ; Simón-Sánchez, J ; Schulte, Claudia ; Lesage, Suzanne ; Sveinbjörnsdóttir, Sigurlaug ; Stefánsson, Kári ; Martinez, Maria ; Hardy, John ; Heutink, Peter ; Brice, Alexis ; Gasser, Thomas ; Singleton, Andrew B ; Wood, Nicholas W

The Lancet (British edition), 2011-02, Vol.377 (9766), p.641-649 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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4
Effects of Hydroxychloroquine on Immune Activation and Disease Progression Among HIV-Infected Patients Not Receiving Antiretroviral Therapy: A Randomized Controlled Trial
Effects of Hydroxychloroquine on Immune Activation and Disease Progression Among HIV-Infected Patients Not Receiving Antiretroviral Therapy: A Randomized Controlled Trial
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Effects of Hydroxychloroquine on Immune Activation and Disease Progression Among HIV-Infected Patients Not Receiving Antiretroviral Therapy: A Randomized Controlled Trial

Paton, Nicholas I ; Goodall, Ruth L ; Dunn, David T ; Franzen, Samuel ; Collaco-Moraes, Yolanda ; Gazzard, Brian G ; Williams, Ian G ; Fisher, Martin J ; Winston, Alan ; Fox, Julie ; Orkin, Chloe ; Herieka, Elbushra A ; Ainsworth, Jonathan G ; Post, Frank A ; Wansbrough-Jones, Mark ; Kelleher, Peter ; Hydroxychloroquine Trial Team, for the

JAMA : the journal of the American Medical Association, 2012-07, Vol.308 (4), p.353-361 [Periódico revisado por pares]

Chicago, IL: American Medical Association

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5
Prognostic and Therapeutic Impact of Argininosuccinate Synthetase 1 Control in Bladder Cancer as Monitored Longitudinally by PET Imaging
Prognostic and Therapeutic Impact of Argininosuccinate Synthetase 1 Control in Bladder Cancer as Monitored Longitudinally by PET Imaging
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Prognostic and Therapeutic Impact of Argininosuccinate Synthetase 1 Control in Bladder Cancer as Monitored Longitudinally by PET Imaging

ALLEN, Michael D ; PHUONG LUONG ; LATTANZIO, Laura ; CHMIELEWSKA-KASSASSIR, Malgorzata ; TOMLINSON, Ian ; ROYLANCE, Rebecca ; WHITAKER, Hayley C ; WARREN, Anne Y ; NEAL, David ; FREZZA, Christian ; BELTRAN, Luis ; JONES, Louise J ; HUDSON, Chantelle ; CHELALA, Claude ; WU, Bor-Wen ; BOMALASKI, John S ; JACKSON, Robert C ; LU, Yong-Jie ; CROOK, Tim ; LEMOINE, Nicholas R ; MATHER, Stephen ; FOSTER, Julie ; SOSABOWSKI, Jane ; LEYTON, Julius ; AVRIL, Norbert ; LI, Chien-Feng ; SZLOSAREK, Peter W ; DELAGE, Barbara ; GHAZALY, Essam ; CUTTS, Rosalind ; MING YUAN ; SYED, Nelofer ; LO NIGRO, Cristiana

Cancer research (Chicago, Ill.), 2014-02, Vol.74 (3), p.896-907 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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6
Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior
Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior
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Sequence variants at CHRNB3 - CHRNA6 and CYP2A6 affect smoking behavior

Perola, Markus ; McCarthy, Mark I ; Keskitalo, Kaisu ; Pergadia, Michele L ; Salomaa, Veikko ; Stefansson, Hreinn ; Kovacs, Peter ; Aben, Katja K ; Peltonen, Leena ; Giegling, Ina ; Lezcano, Victoria ; Mueller, Thomas ; Thorsteinsdottir, Unnur ; Geller, Frank ; Hartikainen, Anna-Liisa ; Rujescu, Dan ; Franklin, Wilbur A ; Ashraf, Haseem ; Stefansson, Kari ; Walter, Stefan ; van Duijn, Cornelia M ; Mayordomo, Jose I ; Willemsen, Gonneke ; Kiemeney, Lambertus A ; Pedersen, Jesper Holst ; Huei-Yi, Shen ; Tyrfingsson, Thorarinn ; Stumvoll, Michael ; Jones, Gregory T ; Uitterlinden, André G ; Allen, Maxine ; Dieplinger, Benjamin ; Krestyaninova, Maria ; Amin, Najaf ; van Rij, Andre M ; Gulcher, Jeffrey R ; Valdes, Ana M ; Mangino, Massimo ; Heath, Andrew C ; Döring, Angela ; Gieger, Christian ; Gudjonsdottir, Iris H ; Hofman, Albert ; Jonsson, Steinn ; Kaprio, Jaakko ; Mägi, Reedik ; Dirksen, Asger ; Nelis, Mari ; Thompson, John R ; Hottenga, Jouke Jan ; Garcia-Prats, Maria D ; Metspalu, Andres ; Hall, Alistair S ; Oostra, Ben A ; Matthiasson, Stefan E ; Prokopenko, Inga ; Dahmen, Norbert ; Madden, Pamela A F ; Wolf, Holly ; Steves, Claire ; Nitz, Barbara ; Kettunen, Johannes ; Martin, Nicholas G ; Spector, Tim D ; Thorgeirsson, Thorgeir E ; Haltmayer, Meinhard ; Ripatti, Samuli ; Gudbjartsson, Daniel F ; Esko, Tõnu ; Rafnar, Thorunn ; Soranzo, Nicole ; Vink, Jacqueline M ; De Diego, Veronica ; Laitinen, Jaana ; Järvelin, Marjo-Riitta ; Wichmann, H-Erich ; Pouta, Anneli ; Penninx, Brenda W ; Boomsma, Dorret I ; Surakka, Ida ; Rawal, Rajesh ; Aulchenko, Yurii S ; Sulem, Patrick ; Gretarsdottir, Solveig ; Oskarsson, Hogni ; Isohanni, Matti ; Tönjes, Anke ; Saez, Berta ; Lindholt, Jes S ; Tiemeier, Henning ; Samani, Nilesh J ; den Heijer, Martin ; Vogelzangs, Nicole ; Montgomery, Grant W

Nature Genetics, 2010-05, Vol.42 (5), p.448-453 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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7
A systematic review of physicians' survival predictions in terminally ill cancer patients
A systematic review of physicians' survival predictions in terminally ill cancer patients
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A systematic review of physicians' survival predictions in terminally ill cancer patients

Glare, Paul ; Virik, Kiran ; Jones, Mark ; Hudson, Malcolm ; Eychmuller, Steffen ; Simes, John ; Christakis, Nicholas

BMJ, 2003-07, Vol.327 (7408), p.195-198 [Periódico revisado por pares]

London: British Medical Journal Publishing Group

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8
Candidate genes for the hypoxic tumor phenotype
Candidate genes for the hypoxic tumor phenotype
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Candidate genes for the hypoxic tumor phenotype

KOONG, A. C ; DENKO, N. C ; GIACCIA, A. J ; HUDSON, K. M ; SCHINDLER, C ; SWIERSZ, L ; KOCH, C ; EVANS, S ; IBRAHIM, H ; LE, Q. T ; TERRIS, D. J

Cancer research (Chicago, Ill.), 2000-02, Vol.60 (4), p.883-887 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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9
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

KELLER, Margaux F ; SAAD, Mohamad ; SCHULTE, Claudia ; MOSKVINA, Valentina ; DURR, Alexandra ; HOLMANS, Peter ; KILARSKI, Laura L ; GUERREIRO, Rita ; HERNANDEZ, Dena G ; BRICE, Alexis ; YLIKOTILA, Pauli ; STEFANSSON, Hreinn ; BRAS, Jose ; MAJAMAA, Kari ; MORRIS, Huw R ; WILLIAMS, Nigel ; GASSER, Thomas ; HEUTINK, Peter ; WOOD, Nicholas W ; HARDY, John ; MARTINEZ, Maria ; SINGLETON, Andrew B ; NALLS, Michael A ; BETTELLA, Francesco ; NICOLAOU, Nayia ; SIMON-SANCHEZ, Javier ; MITTAG, Florian ; BÜCHEL, Finja ; SHARMA, Manu ; RAPHAEL GIBBS, J

Human molecular genetics, 2012-11, Vol.21 (22), p.4996-5009 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Distribution of ABO Blood Group Antibody Titers in Pediatric Patients Awaiting Renal Transplantation: Implications for Organ Allocation Policy
Distribution of ABO Blood Group Antibody Titers in Pediatric Patients Awaiting Renal Transplantation: Implications for Organ Allocation Policy
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Distribution of ABO Blood Group Antibody Titers in Pediatric Patients Awaiting Renal Transplantation: Implications for Organ Allocation Policy

BARNETT, A. Nicholas R ; HUDSON, Alex ; HADJIANASTASSIOU, Vassilis G ; MARKS, Stephen D ; REID, Christopher J. D ; MAGGS, Tim P ; VAUGHAN, Robert ; MAMODE, Nizam

Transplantation, 2012-08, Vol.94 (4), p.362-368 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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