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1
Cognitive performance is associated with glomerular filtration rate in patients with chronic kidney disease: results from the CKD-REIN cohort
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Cognitive performance is associated with glomerular filtration rate in patients with chronic kidney disease: results from the CKD-REIN cohort

Pépin, Marion ; Levassort, Hélène ; Boucquemont, Julie ; Lambert, Oriane ; Alencar de Pinho, Natalia ; Turinici, Monica ; Helmer, Catherine ; Metzger, Marie ; Cheddani, Lynda ; Frimat, Luc ; Combe, Christian ; Fouque, Denis ; Laville, Maurice ; Ayav, Carole ; Liabeuf, Sophie ; Jacquelinet, Christian ; Teillet, Laurent ; Stengel, Bénédicte ; Massy, Ziad A ; Pinho, Natalia Alencar de ; Ayav, Carole ; Combe, Christian ; Fouque, Denis ; Frimat, Luc ; Jacquelinet, Christian ; Laville, Maurice ; Liabeuf, Sophie ; Massy, Ziad A ; Pascal, Christophe ; Robinson, Bruce M ; Pecoits-Filho, Roberto ; Stengel, Bénédicte ; Lange, Céline ; Metzger, Marie ; Speyer, Elodie ; Hannedouche, T. ; Moulin, B. ; Klein, A. ; Combe, C. ; Bourdenx, J.P. ; Keller, A. ; Delclaux, C. ; Vendrely, B. ; Deroure, B. ; Lacraz, A. ; Lobbedez, T. ; Landru, I. ; Massy, Z. ; Lang, P. ; Belenfant, X. ; Thervet, E. ; Urena, P. ; Delahousse, M. ; Vela, C. ; Essig, M. ; Clément, D. ; Sekhri, H. ; Smati, M. ; Jamali, M. ; Hacq, B. ; Panescu, V. ; Bellou, M. ; Kamar, N ; Noël, C. ; Glowacki, F. ; Maisonneuve, N. ; Azar, R. ; Hoffmann, M. ; Hourmant, M. ; Testa, A. ; Besnier, D. ; Choukroun, G. ; Lambrey, G. ; Burtey, S. ; Lebrun, G. ; Magnant, E. ; Laville, M. ; Fouque, D. ; Chazot, C. ; Zaoui, P. ; Kuentz, F.

Journal of neurology, neurosurgery and psychiatry, 2023-06, Vol.94 (6), p.457-466 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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2
E01Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease
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E01Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease

Brauner, H ; Metzger, S ; Riess, O ; Nguyen, H P

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A19-bh-A20 [Periódico revisado por pares]

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3
M12 A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells
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M12 A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

Walter, C. ; Metzger, S. ; Weiss, A. ; Riess, O. ; Phuc Nguyen, H.

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A98-A98 [Periódico revisado por pares]

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4
M12A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells
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M12A769662 Leads to AMPK Activation, Induces Autophagy and has Beneficial Effects IN HD Cells

Walter, C ; Metzger, S ; Weiss, A ; Riess, O ; Phuc Nguyen, H

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A98-A98 [Periódico revisado por pares]

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5
E01 Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease
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E01 Analysis of mitochondrial genes as potential genetic modifiers of the age-at-onset in Huntington disease

Brauner, H ; Metzger, S ; Riess, O ; Nguyen, HP

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A19-A20 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
E04Autophagy-related gene Atg7 is a genetic modifier of AAO specific in the Italian population
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E04Autophagy-related gene Atg7 is a genetic modifier of AAO specific in the Italian population

Futter, C ; Metzger, S ; Saukko, M ; Tong, L ; Riess, O ; Nguyen, H P

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A20-bk-A20 [Periódico revisado por pares]

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7
E04 Autophagy-related gene Atg7 is a genetic modifier of AAO specific in the Italian population
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E04 Autophagy-related gene Atg7 is a genetic modifier of AAO specific in the Italian population

Futter, C ; Metzger, S ; Saukko, M ; Tong, L ; Riess, O ; Nguyen, HP

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A20-A20 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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8
C07 Localisation of sequence variations in PGC-1[alpha] influence their modifying effect in Huntington's disease
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C07 Localisation of sequence variations in PGC-1[alpha] influence their modifying effect in Huntington's disease

Metzger, S ; Van Che, H ; Deyle, C ; Riess, O ; Nguyen, H P

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81, p.A18 [Periódico revisado por pares]

London: BMJ Publishing Group LTD

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9
C07 Localisation of sequence variations in PGC-1α influence their modifying effect in Huntington's disease
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C07 Localisation of sequence variations in PGC-1α influence their modifying effect in Huntington's disease

Metzger, S ; Van Che, H ; Deyle, C ; Riess, O ; Nguyen, H P

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (Suppl 1), p.A18-A18 [Periódico revisado por pares]

BMJ Publishing Group Ltd

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10
C10 Duo as a potential genetic modifier of Huntington's disease
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C10 Duo as a potential genetic modifier of Huntington's disease

Tsai, Y-C ; Soehn, A S ; Metzger, S ; Nguyen, H P

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (Suppl 1), p.A19-A19 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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