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P0387 DERMATITIS HERPETIFORMIS: DATA ON INCIDENCE AND OUTCOME FROM A LARGE SERIES OF PATIENTS

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (Supplement 1), p.S203

2004

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P0387 DERMATITIS HERPETIFORMIS: DATA ON INCIDENCE AND OUTCOME FROM A LARGE SERIES OF PATIENTS

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (S1), p.S203-S203

2004

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137. CF related diabetes in adult patients

Netherlands journal of medicine, 1999-06, Vol.54, p.S59

PIZZAMIGLIO, G

1999

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Viral delivery of a peptide-based immunomodulator enhances T cell priming during vaccination

Frontiers in pharmacology, 2022-12, Vol.13, p.1029636-1029636

2022

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"Seeing Law in Terms of Music": A Short Essay on Affinities between Music and Law

Cahiers de droit (Québec), 2017-03, Vol.58 (1-2), p.67

Arban, Erika

2017

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Subsidiarity in European and Canadian law: a comparison

Canadian public administration, 2013-06, Vol.56 (2), p.219-234

Arban, Erika

2013

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6-(3,4-Dichlorophenyl)-1-[(Methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: A New Potent and Selective Triple Reuptake Inhibitor

Journal of medicinal chemistry, 2010-07, Vol.53 (13), p.4989-5001

2010

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Transient forebrain over-expression of CRF induces plasma corticosterone and mild behavioural changes in adult conditional CRF transgenic mice

Pharmacology, biochemistry and behavior, 2009-07, Vol.93 (1), p.17-24

2009

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1-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes and 6-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes: A New Series of Potent and Selective Triple Reuptake Inhibitors

Journal of medicinal chemistry, 2010-03, Vol.53 (6), p.2534-2551

2010

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Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: Novel, potent, and selective series of Vasopressin1b receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (17), p.5044-5049

2010

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Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (21), p.3863-3866

2003

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Potent antihyperalgesic activity without tolerance produced by glycine site antagonist of N-methyl-D-aspartate receptor GV196771A

The Journal of pharmacology and experimental therapeutics, 1999-07, Vol.290 (1), p.158

1999

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Characterisation of the selective 5-HT1B receptor antagonist SB-616234-A (1-[6-(cis-3,5-dimethylpiperazin-1-yl)-2,3-dihydro-5-methoxyindol-1-yl]-1-[2'-methyl-4'-(5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methanone hydrochloride): in vivo neurochemical and behavioural evidence of anxiolytic/antidepressant activity

Neuropharmacology, 2006-06, Vol.50 (8), p.975-983

2006

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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (16), p.3713-3716

2005

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Characterisation of the selective 5-HT sub(1B) receptor antagonist SB-616234-A (1-[6-(cis-3,5-dimethylpiperazin-1-yl)-2,3-dihydro-5-methoxy indol-1-yl]-1-[2'-methyl-4'- (5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methanone hydrochloride): In vivo neurochemical and behavioural evidence of anxiolytic/antidepressant activity

Neuropharmacology, 2006-06, Vol.50 (8), p.975-983

2006

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Characterisation of the selective 5-HT 1B receptor antagonist SB-616234-A (1-[6-(cis-3,5-dimethylpiperazin-1-yl)-2,3-dihydro-5-methoxyindol-1-yl]-1-[2′-methyl-4′-(5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methanone hydrochloride): In vivo neurochemical and behavioural evidence of anxiolytic/antidepressant activity

Neuropharmacology, 2006, Vol.50 (8), p.975-983

2006

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Substituted tetraazaacenaphthylenes as potent CRF 1 receptor antagonists for the treatment of depression and anxiety

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (16), p.3713-3716

2005

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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety: G-protein-coupled receptors in drug discovery

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (16), p.3713-3716

2005

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Dostoïevski et Napoléon

Europe, 1969-04, Vol.47 (480), p.184

ARBAN, Dominique

1969

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Le livre qu'il n'a pas écrit

Europe, 1956-11, Vol.34 (131), p.64

ARBAN, Dominique

1956

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Le Double» de Dostoïevski

Femmes Diplômées, 1965, Vol.55 (1), p.102-105

Arban, Dominique

1965

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UN DEMI-SIÈCLE DE PARIS

Hommes et mondes, 1950-01, Vol.11 (42), p.97-100

ARBAN, DOMINIQUE

1950

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VINGT-CINQ ANS DE PARIS

Hommes et mondes, 1949-06, Vol.9 (35), p.353-357

ARBAN, DOMINIQUE

1949

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Circulation Research Editors’ Yearly Report: 1999–2000

Circulation research, 2000-08, Vol.87 (4), p.261-263

2000

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Dysgerminoma

The Journal of the Kentucky Medical Association, 1961-04, Vol.59, p.370

1961

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P0387 DERMATITIS HERPETIFORMIS: DATA ON INCIDENCE AND OUTCOME FROM A LARGE SERIES OF PATIENTS

P0387 DERMATITIS HERPETIFORMIS: DATA ON INCIDENCE AND OUTCOME FROM A LARGE SERIES OF PATIENTS

137. CF related diabetes in adult patients

Viral delivery of a peptide-based immunomodulator enhances T cell priming during vaccination

"Seeing Law in Terms of Music": A Short Essay on Affinities between Music and Law

Subsidiarity in European and Canadian law: a comparison

6-(3,4-Dichlorophenyl)-1-[(Methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: A New Potent and Selective Triple Reuptake Inhibitor

Transient forebrain over-expression of CRF induces plasma corticosterone and mild behavioural changes in adult conditional CRF transgenic mice

1-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes and 6-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes: A New Series of Potent and Selective Triple Reuptake Inhibitors

Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: Novel, potent, and selective series of Vasopressin1b receptor antagonists

Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor

Potent antihyperalgesic activity without tolerance produced by glycine site antagonist of N-methyl-D-aspartate receptor GV196771A

Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety

Substituted tetraazaacenaphthylenes as potent CRF 1 receptor antagonists for the treatment of depression and anxiety

Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety: G-protein-coupled receptors in drug discovery

Dostoïevski et Napoléon

Le livre qu'il n'a pas écrit

Le Double» de Dostoïevski

UN DEMI-SIÈCLE DE PARIS

VINGT-CINQ ANS DE PARIS

Circulation Research Editors’ Yearly Report: 1999–2000

Dysgerminoma

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