System, method, and applications of using the fundamental code unit and brain language
The present invention relates to a non-invasive system with diagnostic and treatment capacities that use a unified code that is intrinsic to physiological brain function. In an embodiment of the present invention, an approach to the treatment of disorders that supplements existing diagnostic and treatment methods with robust quantitative data analysis are presented. This is achieved by a unification of cognitive and neural phenomena known as the Fundamental Code Unit (FCU), representing identifiable patterns of brain activity at the submolecular, molecular, and cellular levels (intra-brain communications), as well as their manifestations in thought and language (inter-brain communications).
1. A method for affecting living tissue comprising:
receiving input from living tissue through at least one read modality;
determining at least one identifiable pattern of tissue activity at a submolecular, molecular, or cellular level based on the received input, the identifiable pattern of tissue activity indicating a defective tissue function;
computing at least one signal to effect alterations to the living tissue so as to correct the defective tissue function based on the determined pattern; and
delivering the at least one signal to the living tissue through at least one write modality.
2. The method of claim 1 wherein the at least one read modality comprises:
neurotransmitter level and chirality measurement, linguistic analysis, functional magnetic resonance imaging, electroencephalography, deep brain stimulation, audiovisual stimulation, or motion tracking/gait analysis.
3. The method of claim 1 wherein the at least one write modality comprises:
protein transduction, electrochemical methods of signaling, neurotransmitter level and chirality regulation, linguistic analysis, transcranial magnetic stimulation, deep brain stimulation, ultrasound signaling, audiovisual stimulation, photonic pathways inside and outside the brain, proton pathways inside and outside the brain.
4. The method of claim 3 wherein the use of photonic pathways inside and outside the brain provides broad regulatory power over neuroplasticity.
5. The method of claim 3 wherein the use of photonic pathways inside and outside the brain provides broad regulatory power over memory function.
6. The method of claim 3 wherein the use of proton pathways inside and outside the brain provides broad regulatory power over neuroplasticity.
7. The method of claim 3 wherein the use of proton pathways inside and outside the brain provides broad regulatory power over memory function.
8. The method of claim 1 wherein the at least one signal is computed using a structural mathematical system.
9. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises ATP and ADP-mediated signaling through neuronal and glial receptors.
10. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises events related to autofluorescence.
11. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises a neuropsin-mediated unary-coded photonic signaling scheme.
12. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises a neuropsin-mediated unary-coded multi-photonic signaling scheme.
13. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises stimulating or decelerating growth of specific cells throughout a body using Deep Cell Stimulation (DCeS).
14. The method of claim 1 wherein the method is used for diagnosis and treatment of neurodegenerative disorders including at least one of Alzheimer's Disease, Parkinson's Disease, and Huntington's Disease, or for diagnosis and treatment of other disorders.
15. The method of claim 1 wherein the method is used for Pain Detection and Pain Management.
16. The method of claim 1 , wherein the living tissue is neural tissue.
17. The method of claim 1 wherein the at least one read modality or the at least one write modality comprises at least two of: ATP and ADP- mediated signaling through neuronal and glial receptors, events related to autofluorescence, a neuropsin-mediated unary-coded photonic signaling scheme, and a neurospin-mediated unary-coded multi-photonic signaling scheme.