Torthaí cuardaigh - Jan Haavik
- 1 - 20 toradh as 89 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Mutations in human monoamine-related neurotransmitter pathway genes de réir Jan Haavik, Nenad Blau, Beat Thöny
Foilsithe / Cruthaithe 2008Revisão -
2
Set-Shifting in Adults with ADHD de réir Helene Barone Halleland, Jan Haavik, Astri J. Lundervold
Foilsithe / Cruthaithe 2012Artigo -
3
Tyrosine and tryptophan hydroxylases as therapeutic targets in human disease de réir Kai Waløen, Rune Kleppe, Aurora Martı́nez, Jan Haavik
Foilsithe / Cruthaithe 2016Revisão -
4
The 14-3-3 proteins in regulation of cellular metabolism de réir Rune Kleppe, Aurora Martı́nez, Stein Ove Døskeland, Jan Haavik
Foilsithe / Cruthaithe 2011Revisão -
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Resonance Raman studies on the blue-green-colored bovine adrenal tyrosine 3-monooxygenase (tyrosine hydroxylase). Evidence that the feedback inhibitors adrenaline and noradrenaline... de réir Kristoffer Andersson, DavidD. Cox, L. Que, Torgeir Flatmark, Jan Haavik
Foilsithe / Cruthaithe 1988Artigo -
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Functional Studies of Tyrosine Hydroxylase Missense Variants Reveal Distinct Patterns of Molecular Defects in <scp>Dopa</scp> ‐Responsive Dystonia de réir Agnete Fossbakk, Rune Kleppe, Per M. Knappskog, Aurora Martı́nez, Jan Haavik
Foilsithe / Cruthaithe 2014Artigo -
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Regulation of recombinant human tyrosine hydroxylase isozymes by catecholamine binding and phosphorylation de réir Bjørg Almås, B. Le Bourdellès, Torgeir Flatmark, Jacques Mallet, Jan Haavik
Foilsithe / Cruthaithe 1992Artigo -
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Validity and accuracy of the Adult Attention‐Deficit/Hyperactivity Disorder (ADHD) Self‐Report Scale (ASRS) and the Wender Utah Rating Scale (WURS) symptom checklists in discrimina... de réir Erlend J. Brevik, Astri J. Lundervold, Jan Haavik, Maj‐Britt Posserud
Foilsithe / Cruthaithe 2020Artigo -
11
Potassium channels in behavioral brain disorders. Molecular mechanisms and therapeutic potential: A narrative review de réir Kazi Asraful Alam, Pernille Svalastoga, Aurora Martı́nez, Jeffrey Glennon, Jan Haavik
Foilsithe / Cruthaithe 2023Revisão -
12
Risk factors of suicidal spectrum behaviors in adults and adolescents with attention-deficit / hyperactivity disorder – a systematic review de réir Amalie Austgulen, Nanna Karen Gilberg Skram, Jan Haavik, Astri J. Lundervold
Foilsithe / Cruthaithe 2023Revisão -
13
The dopamine hypothesis for ADHD: An evaluation of evidence accumulated from human studies and animal models de réir Hayley J. MacDonald, Rune Kleppe, Peter D. Szigetvari, Jan Haavik
Foilsithe / Cruthaithe 2024Revisão -
14
Structure/Function Relationships in Human Phenylalanine Hydroxylase de réir Per M. Knappskog, Torgeir Flatmark, Johanna M. Aarden, Jan Haavik, Aurora Martı́nez
Foilsithe / Cruthaithe 1996Artigo -
15
Adult attention deficit hyperactivity disorder is associated with asthma de réir Ole Bernt Fasmer, Anne Halmøy, Tomas Eagan, Ketil J. Øedegaard, Jan Haavik
Foilsithe / Cruthaithe 2011Artigo -
16
Conformational Properties and Stability of Tyrosine Hydroxylase Studied by Infrared Spectroscopy de réir Aurora Martı́nez, Jan Haavik, Torgeir Flatmark, José Luis R. Arrondo, Arturo Muga
Foilsithe / Cruthaithe 1996Artigo -
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Adult ADHD and Comorbid Somatic Disease: A Systematic Literature Review de réir Johanne Telnes Instanes, Kari Klungsøyr, Anne Halmøy, Ole Bernt Fasmer, Jan Haavik
Foilsithe / Cruthaithe 2016Revisão -
19
Associations between attention-deficit/hyperactivity disorder and autoimmune diseases are modified by sex: a population-based cross-sectional study de réir Tor‐Arne Hegvik, Johanne Telnes Instanes, Jan Haavik, Kari Klungsøyr, Anders Engeland
Foilsithe / Cruthaithe 2017Artigo -
20
Male to female ratios in autism spectrum disorders by age, intellectual disability and attention‐deficit/hyperactivity disorder de réir Maj‐Britt Posserud, Berit Skretting Solberg, Anders Engeland, Jan Haavik, Kari Klungsøyr
Foilsithe / Cruthaithe 2021Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Psychology
Biology
Psychiatry
Genetics
Attention deficit hyperactivity disorder
Gene
Clinical psychology
Genotype
Internal medicine
Neuroscience
Single-nucleotide polymorphism
Environmental health
Population
Genome-wide association study
Biochemistry
Attention deficit
Developmental psychology
Cognition
Computer science
Genetic architecture
Genetic association
Autism
Comorbidity
Computational biology
Genome
Phenotype
Chemistry
Disease
Endocrinology