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Your search keyword '"Tyrosine 3-Monooxygenase deficiency"' showing total 93 results

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93 results on '"Tyrosine 3-Monooxygenase deficiency"'

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1. Nigrostriatal tract defects in mice with aromatic l-amino acid decarboxylase deficiency.

2. Co-transplantation of autologous T reg cells in a cell therapy for Parkinson's disease.

3. Histopathological Analysis of Tumor Microenvironment and Angiogenesis in Pheochromocytoma.

4. Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?

5. Tyrosine hydroxylase is crucial for pupal pigmentation in Zeugodacus tau (Walker) (Diptera: Tephritidae).

6. CRISPR/Cas9-mediated Tyrosine hydroxylase knockout resulting in larval lethality in Agrotis ipsilon.

7. A follow-up on desiderosmia (olfactory craving), a novel symptom associated with iron deficiency anemia.

8. Effects of Selective Deletion of Tyrosine Hydroxylase from Kisspeptin Cells on Puberty and Reproduction in Male and Female Mice.

9. Parkinson's disease without nigral degeneration: a pathological correlate of scans without evidence of dopaminergic deficit (SWEDD)?

10. Non-motor symptoms in genetically defined dystonia: Homogenous groups require systematic assessment.

11. Relative contributions of severe dopaminergic neuron ablation and dopamine depletion to cognitive impairment.

12. Cerebrospinal fluid synaptic proteins as useful biomarkers in tyrosine hydroxylase deficiency.

13. [Tyrosine hydroxylase deficiency: a case of autosomal recessive dopa-responsive dystonia].

14. Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease.

15. Contributions of signaling by dopamine neurons in dorsal striatum to cognitive behaviors corresponding to those observed in Parkinson's disease.

16. Role of convergent activation of glutamatergic and dopaminergic systems in the nucleus accumbens in the development of methamphetamine psychosis and dependence.

17. In vivo catecholaminergic metabolism in the medial prefrontal cortex of ENU2 mice: an investigation of the cortical dopamine deficit in phenylketonuria.

18. Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.

19. Retinal dopamine mediates multiple dimensions of light-adapted vision.

20. A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy.

21. Sall3 correlates with the expression of TH in mouse olfactory bulb.

22. Tyrosine hydroxylase deficiency in Taiwanese infants.

23. Novel mutations in the tyrosine hydroxylase gene in the first Czech patient with tyrosine hydroxylase deficiency.

24. Dopamine transporter loss in 6-OHDA Parkinson's model is unmet by parallel reduction in dopamine uptake.

25. Contributions of striatal dopamine signaling to the modulation of cognitive flexibility.

26. Hereditary progressive dystonia with marked diurnal fluctuation.

27. Requirement of dopamine signaling in the amygdala and striatum for learning and maintenance of a conditioned avoidance response.

28. Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency.

29. A novel compound heterozygous tyrosine hydroxylase mutation (p.R441P) with complex phenotype.

30. Dystonia-plus syndromes.

31. Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.

32. Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.

33. Pontine norepinephrine defects in Mecp2-null mice involve deficient expression of dopamine beta-hydroxylase but not a loss of catecholaminergic neurons.

34. Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

35. Neuroimaging findings in children with paediatric neurotransmitter diseases.

36. Tyrosine hydroxylase deficiency with severe clinical course.

37. Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse.

38. Differential involvement of striosome and matrix dopamine systems in a transgenic model of dopa-responsive dystonia.

39. [Pharmacological treatment of Rett syndrome improves breathing and survival in a mouse model].

40. Tyrosine hydroxylase deficiency presenting with a biphasic clinical course.

41. Inherited disorders affecting dopamine and serotonin: critical neurotransmitters derived from aromatic amino acids.

42. Viral restoration of dopamine signaling to the dorsal striatum restores instrumental conditioning to dopamine-deficient mice.

43. Beta1-adrenergic receptors maintain fetal heart rate and survival.

44. Molecular genetics of tyrosine 3-monooxygenase and inherited diseases.

45. Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.

46. Dopamine is not required for the hyperlocomotor response to NMDA receptor antagonists.

47. Analysis of the human locus coeruleus in perinatal and infant sudden unexplained deaths. Possible role of the cigarette smoking in the development of this nucleus.

48. Dysregulation of striatal dopamine signaling by amphetamine inhibits feeding by hungry mice.

49. Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency.

50. A role for dopamine in feeding responses produced by orexigenic agents.

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