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Refinado por: assunto: Middle Aged remover
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1
Infliximab safety profile and long‐term applicability in inflammatory bowel disease: 9‐year experience in clinical practice
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Artigo
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Infliximab safety profile and long‐term applicability in inflammatory bowel disease: 9‐year experience in clinical practice

ZABANA, Y. ; DOMÈNECH, E. ; MAÑOSA, M. ; GARCIA‐PLANELLA, E. ; BERNAL, I. ; CABRÉ, E. ; GASSULL, M. A.

Alimentary pharmacology & therapeutics, 2010-03, Vol.31 (5), p.553-560 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Clinical evolution of luminal and perianal Crohn's disease after inducing remission with infliximab: how long should patients be treated?
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Clinical evolution of luminal and perianal Crohn's disease after inducing remission with infliximab: how long should patients be treated?

DOMÈNECH, E. ; HINOJOSA, J. ; NOS, P. ; GARCIA‐PLANELLA, E. ; CABRÉ, E. ; BERNAL, I. ; GASSULL, M. A.

Alimentary pharmacology & therapeutics, 2005-12, Vol.22 (11‐12), p.1107-1113 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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3
Azathioprine without oral ciclosporin in the long‐term maintenance of remission induced by intravenous ciclosporin in severe, steroid‐refractory ulcerative colitis
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Azathioprine without oral ciclosporin in the long‐term maintenance of remission induced by intravenous ciclosporin in severe, steroid‐refractory ulcerative colitis

Domènech, E. ; Garcia‐Planella, E. ; Bernal, I. ; Rosinach, M. ; Cabré, E. ; Fluvià, L. ; Boix, J. ; Gassull, M. A.

Alimentary pharmacology & therapeutics, 2002-12, Vol.16 (12), p.2061-2065 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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4
Genetic analysis of CHCHD2 in a southern Spanish population
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Artigo
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Genetic analysis of CHCHD2 in a southern Spanish population

Tejera-Parrado, C ; Jesús, S ; Huertas-Fernández, I ; Bernal-Bernal, I ; Bonilla-Toribio, M ; Córdoba-Tevar, I ; Abreu-Rodríguez, I ; Carrillo, F ; Bernal-Escudero, M ; Vargas-González, L ; Carballo, M ; Gómez-Garre, P ; Mir, P

Neurobiology of aging, 2017-02, Vol.50, p.169.e1-169.e2 [Periódico revisado por pares]

United States: Elsevier Inc

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5
A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3
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A Gene for Hypotrichosis Simplex of the Scalp Maps to Chromosome 6p21.3

Betz, Regina C. ; Lee, Young-Ae ; Bygum, Anette ; Brandrup, Flemming ; Bernal, Ana I. ; Toribio, Jaime ; Alvarez, J. Ignacio ; Kukuk, Guido M. ; Ibsen, Hans Henning W. ; Rasmussen, Hanne B. ; Wienker, Thomas F. ; Reis, André ; Propping, Peter ; Kruse, Roland ; Cichon, Sven ; Nöthen, Markus M.

American journal of human genetics, 2000-06, Vol.66 (6), p.1979-1983 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Lack of efficacy of mefloquine in the treatment of New World cutaneous leishmaniasis in Colombia
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Artigo
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Lack of efficacy of mefloquine in the treatment of New World cutaneous leishmaniasis in Colombia

Hendrickx, EP ; Agudelo, SP ; Munoz, DL ; Puerta, JA ; Velez Bernal, ID

The American journal of tropical medicine and hygiene, 1998-12, Vol.59 (6), p.889-892 [Periódico revisado por pares]

Lawrence, KS: ASTMH

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7
Progressive nodular histiocytosis accompanied by systemic disorders
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Artigo
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Progressive nodular histiocytosis accompanied by systemic disorders

GONZALEZ RIUZ, A ; BERNAL RUIZ, A. I ; ARAGONESES FRAILE, H ; PERAL MARTINEZ, I ; GARCIA MUNOZ, M

British journal of dermatology (1951), 2000-09, Vol.143 (3), p.628-631 [Periódico revisado por pares]

London: Blackwell

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8
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

Ahmed, Sarah ; Jesús, Silvia ; Méndez‐del‐Barrio, Carlota ; Vargas‐González, Laura ; Tartari, Juan Pablo ; Mondragon, Elisabet ; Vinagre‐Aragon, Ana ; Dols‐Icardo, Oriol ; Pascual‐Sedano, Berta ; Ezquerra, Mario ; Cámara, Ana ; Compta, Yaroslau ; Fernández, Manel ; Sierra, María ; Menéndez‐González, Manuel ; García‐Ruiz, Pedro ; Vela‐Desojo, Lydia ; Barrero, Francisco Javier ; Mínguez‐Castellanos, Adolfo ; Cerdan, Debora ; Gomez Heredia, Maria Jose ; Feliz, Cici ; Lopez‐Sendon, Jose Luis ; Martínez Torres, Irene ; Kim, Jonggeol Jeffrey ; Botia, Juan A. ; Morrison, Karen E. ; Morris, Huw ; Edsall, Connor ; Vives, Francisco ; Duran, Raquel ; Hoenicka, Janet ; Alvarez, Victoria ; Marti, Maria José ; Singleton, Andrew ; Noyce, Alastair J ; Holmans, Peter ; Trabzuni, Daniah ; Bras, Jose ; Wood, Nicholas W ; Guerreiro, Rita ; Guelfi, Sebastian ; Chelban, Viorica ; Foltynie, Thomas ; Morrison, Karen E. ; Brockmann, Kathrin ; Gasser, Thomas ; Cookson, Mark R ; Blauwendraat, Cornelis ; Craig, David W. ; Faghri, Faraz ; Gibbs, J Raphael ; Shulman, Joshua M. ; Leonard, Hampton L. ; Nalls, Mike A. ; Robak, Laurie ; Lubbe, Steven ; Mencacci, Niccolo E. ; Alcalay, Roy N. ; Krohn, Lynne ; Aguilar, Miquel ; Alvarez, Ignacio ; Yarza, Jesús Alberto Bergareche ; Blazquez, Marta ; Botía, Juan A. ; Boungiorno, María Teresa ; Buiza-Rueda, Dolores ; Clarimón, Jordi ; Casa, Beatríz ; Diez-Fairen, Monica ; Dols-Icardo, Oriol ; Duarte, Jacinto ; Fernández, Manel ; Heredia, Maria Jose Gomez ; Hoenicka, Janet ; Infante, Jon ; Jesús, Silvia ; Jimenez-Escrig, Adriano ; Arregui, Adolfo López de Munain ; Marín, Juan ; Mata, Marina ; Mínguez, Adolfo ; Mir, Pablo ; Pascual-Sedano, Berta ; Pastor, Pau ; Errazquin, Francisco Perez ; Ruiz-Martínez, Javier ; Rodriguez, Antonio Sanchez ; Sierra, María ; Suarez-Sanmartin, Esther ; Tolosa, Eduard ; Valldeoriola, Francesc ; Vargas-González, Laura ; Zimprich, Alexander ; Taba, Pille ; Dalgard, Clifton L. ; Adeleye, Adelani ; Soltis, Anthony R. ; Bacikova, Dagmar ; Wilkerson, Matthew D.

Movement disorders, 2019-12, Vol.34 (12), p.1851-1863 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
Identification of sixteen novel candidate genes for late onset Parkinson's disease
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Identification of sixteen novel candidate genes for late onset Parkinson's disease

Gialluisi, Alessandro ; Reccia, Mafalda Giovanna ; Modugno, Nicola ; Nutile, Teresa ; Lombardi, Alessia ; Di Giovannantonio, Luca Giovanni ; Pietracupa, Sara ; Ruggiero, Daniela ; Scala, Simona ; Gambardella, Stefano ; Iacoviello, Licia ; Gianfrancesco, Fernando ; Acampora, Dario ; D'Esposito, Maurizio ; Simeone, Antonio ; Ciullo, Marina ; Esposito, Teresa

Molecular neurodegeneration, 2021-06, Vol.16 (1), p.35-35, Article 35 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease
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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease

Leonard, Hampton ; Blauwendraat, Cornelis ; Krohn, Lynne ; Faghri, Faraz ; Iwaki, Hirotaka ; Ferguson, Glen ; Day-Williams, Aaron G ; Stone, David J ; Singleton, Andrew B ; Nalls, Mike A ; Gan-Or, Ziv

Journal of medical genetics, 2020-05, Vol.57 (5), p.331-338 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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