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MAO deficiency

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Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. - PubMed - NCBI

Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. - PubMed - NCBI

Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans.  - PubMed - NCBI

Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. - PubMed - NCBI

Haloperidol inhibition of monoamine oxidase in vivo and in vitro.  - PubMed - NCBI

Haloperidol inhibition of monoamine oxidase in vivo and in vitro. - PubMed - NCBI

MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.

MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.

Cataplexy and monoamine oxidase deficiency in Norrie disease.  - PubMed - NCBI

Cataplexy and monoamine oxidase deficiency in Norrie disease. - PubMed - NCBI

ADHD and Disruptive Behavior scores - associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescents.  - PubMed - NCBI

ADHD and Disruptive Behavior scores - associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescents. - PubMed - NCBI

Monoamine oxidases A and B gene polymorphisms in migraine patients.  - PubMed - NCBI

Monoamine oxidases A and B gene polymorphisms in migraine patients. - PubMed - NCBI

Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.  - PubMed - NCBI

Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements. - PubMed - NCBI

Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.  - PubMed - NCBI

Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy. - PubMed - NCBI

ical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.  Collins FA1, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Author information Abstract Norrie disease is a rare X-linked recessive disorder characterized by blindness from infancy. The gene for Norrie disease has been localized to Xp11.3…

ical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes. Collins FA1, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Author information Abstract Norrie disease is a rare X-linked recessive disorder characterized by blindness from infancy. The gene for Norrie disease has been localized to Xp11.3…

www.jneurosci.org content jneuro 32 25 8574.full.pdf

www.jneurosci.org content jneuro 32 25 8574.full.pdf

BEHAVIORAL OUTCOMES OF MONOAMINE OXIDASE DEFICIENCY: PRECLINICAL AND CLINICAL EVIDENCE

BEHAVIORAL OUTCOMES OF MONOAMINE OXIDASE DEFICIENCY: PRECLINICAL AND CLINICAL EVIDENCE


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