A deletion polymorphism in the human alpha-2-macroglobulin (A2M) gene.

par Matthijs, G, Marynen, P
Publié 1991

Individual differences in dopamine efflux in nucleus accumbens shell and core during instrumental learning

par Cheng, Jingjun, Feenstra, Matthijs G.P.
Publié 2006

Desensitization to cytoplasmic Ca2+ and Ca2+ sensitivities of guinea-pig ileum and rabbit pulmonary artery smooth muscle.

par Himpens, B, Matthijs, G, Somlyo, A P
Publié 1989

Carbohydrate deficient glycoprotein (CDG) syndrome type I.

par Jaeken, J, Matthijs, G, Barone, R, Carchon, H
Publié 1997

Noradrenergic Action in Prefrontal Cortex in the Late Stage of Memory Consolidation

par Tronel, Sophie, Feenstra, Matthijs G.P., Sara, Susan J.
Publié 2004

Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families

par Becker, K, Beales, P., Calver, D, Matthijs, G, Mohammed, S
Publié 2002

The Potential of Cannabidiol as a Treatment for Psychosis and Addiction: Who Benefits Most? A Systematic Review

par Batalla, Albert, Janssen, Hella, Gangadin, Shiral S., Bossong, Matthijs G.
Publié dans J Clin Med (2019)

The Impact of Cannabidiol on Human Brain Function: A Systematic Review

par Batalla, Albert, Bos, Julian, Postma, Amber, Bossong, Matthijs G.
Publié dans Front Pharmacol (2021)

Factors Moderating the Association between Cannabis Use and Psychosis Risk: A Systematic Review

par Sanne J. van der Steur, Albert Batalla, Matthijs G. Bossong
Publié 2020-02-01

Triplication of distal chromosome 10q

par Devriendt, K., Matthijs, G., Holvoet, M., Schoenmakers, E., Fryns, J.
Publié 1999

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome

par Vogels, A, Matthijs, G, Legius, E, Devriendt, K, Fryns, J
Publié 2003

Factors Moderating the Association between Cannabis Use and Psychosis Risk: A Systematic Review

par van der Steur, Sanne J., Batalla, Albert, Bossong, Matthijs G.
Publié dans Brain Sci (2020)

Noradrenaline and Dopamine Efflux in the Prefrontal Cortex in Relation to Appetitive Classical Conditioning

par Mingote, Susana, de Bruin, Jan P. C., Feenstra, Matthijs G. P.
Publié dans J Neurosci (2004)

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A.

par Matthijs, G, Schollen, E, Van Schaftingen, E, Cassiman, J J, Jaeken, J
Publié 1998

Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event

par Vermeesch, J, Thoelen, R, Salden, I, Raes, M, Matthijs, G, Fryns, J
Publié 2003

Mosaicism for duplication 12q (12q13→12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant

par Vermeesch, J, Syrrou, M, Salden, I, Dhondt, F, Matthijs, G, Fryns, J
Publié 2002

Human Striatal Response to Reward Anticipation Linked to Hippocampal Glutamate Levels

par Bossong, Matthijs G, Wilson, Robin, Appiah-Kusi, Elizabeth, McGuire, Philip, Bhattacharyya, Sagnik
Publié dans Int J Neuropsychopharmacol (2018)

Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes.

par Pirard, M, Achouri, Y, Collet, J F, Schollen, E, Matthijs, G, Van Schaftingen, E
Publié 1999

Increased recurrence risk in congenital disorders of glycosylation type Ia (CDG-Ia) due to a transmission ratio distortion

par Schollen, E, Kjaergaard, S, Martinsson, T, Vuillaumier-Barro..., S, Dunoe, M, Keldermans, L, Seta, N, Matthijs, G
Publié 2004

Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1

par DE RAVEL, T J L, MATTHIJS, G, HOLVOET, M, WOUTERS, C, LEGIUS, E, FRYNS, J
Publié 2000