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The Trauma and Attachment Report recently spoke with Susan Lucas, a sensorimotor psychotherapy Level II graduate. Q:  How would an individual who has experienced trauma benefit from sensorimotor psychotherapy? In Phase 3, body reading assesses any beliefs a client holds that interfere with daily functioning.  In Pat Ogden’s Trauma and the Body, an example is provided where a client’s cognitive distortion “I’m worthless, I must hide” is reflected in bodily tension such as the pulling in of the shoulders or a spinal curve (p.
An integrative model can be significant in its focus on a client’s symptoms through cognitions, emotions, and the underlying bodily communication that exists without words.
Cancer develops when normal cells in the body grow and reproduce uncontrollably because of “mistakes” in the DNA code. Editor’s note: Pending an FDA decision, 23andMe no longer offers new customers access to health reports referred to in this post. 23andMe and Genentech launched the InVite Study to understand how genes influence response to treatment for metastatic breast cancer. All 23andMe customers can participate in other scientific research through 23andMe’s research surveys.
What is (I believe) critically important is that you not be cuckholded by treatment predictive info [or think you want to be in that realm].
I love the work you guys are doing and am proud to be a customer of 23andMe, knowing that my support goes not only towards developing a great product for me personally but also towards medical advances that can help many worldwide.
Note that past blog posts may reflect versions of the product that may not be available currently.
This blog periodically lists news and interesting facts about Osteopathic Manipulative Treatment.Osteopathic manipulative treatment, or OMT, is hands-on care.
We previously reported that cloned embryos prepared with cumulus cell donor nuclei, without DMSO exposure during the procedure, exhibit altered culture medium preferences relative to normal and other control mouse embryos.
Our previous studies with cumulus cell cloned embryos prompted the hypothesis that the somatic cell genome may be expressed in the early cloned embryo and thereby alter its phenotype. The F1 myoblast cloned blastocysts obtained by culture in the F10:DMEM medium exhibited very robust, well-expanded morphologies (Fig. We previously found that cumulus cell cloned embryos favored culture media that contained a high concentration of glucose even as early as the one-cell stage.
Given the increased rate of glucose uptake in cloned embryos relative to control embryos, we wished to ascertain whether cloned embryos display altered glucose transporter expression, indicative of continued expression of donor cell type genes. Because glucose transporter type 4 (GLUT4) is expressed in muscle but not in preimplantation stage embryos, we examined the expression of this transporter in myoblast cloned embryos and controls.
All data for diploid cloned embryos are from myoblast cloned constructs except cumulus cloned constructs where indicated. This entry was posted in Somatic Cell and tagged Developmental Biology, early development, Embryo, Gene regulation. DNA (a copy of which is contained in each cell) contains finely tuned instructions for cell growth and production, but as cells copy and pass on this DNA they sometimes make mistakes. Customers who purchased prior to November 22, 2013 will still be able to see their health reports, but those who purchased after that time will not. Potential findings of this study may help to determine if a person’s genes could play a role in response to bevacizumab, also known as Avastin.
Chest pain is a common reason for patients to present to the osteopathic family physician's office. After correction of the genetic defect, the resulting embryonic stem cells are cultured and then induced to differentiate into stem germ cells. Clones made with these nuclei developed to the two-cell stage efficiently in WM but then exhibited a pronounced arrest in development to the four-cell stage (Table 2). Such an effect of the somatic cell genome could contribute to the overall poor success observed when culturing the cloned embryos made with F1 myoblasts in standard embryo culture media by shifting their culture medium preference toward a more somatic cell-like formulation.
Switching embryos to either KSOMaa or WM significantly reduced blastocyst formation in comparison to continuous culture in F10:DMEM (43% versus 18% and 25%, respectively). The preference of F1 myoblast cloned embryos for the F10: DMEM culture medium suggested that these embryos may also manifest an alteration in glucose requirement. Preimplantation stage mouse embryos express GLUT1 at all stages, and this transporter is also expressed in many somatic cell types. The myoblast cloned embryos at the late one-cell stage expressed significant quantities of GLUT4, well above the low level of background fluorescence observed in the parthenogenetic and fertilized control embryos (Figs. Laser therapy can be used any time a patient needs a non-invasive procedure for the control of pain, when conventional therapies have been ineffective, or when the acceleration of healing from injuries is desired.Is Laser Therapy Safe?A Laser therapy has been successfully used around the world for over 30+ years, with no reported long-term or irreversible side effects. These mistakes are technically called “mutations” and cause the DNA to be slightly different from the original.The mutations that make cells grow too much and thereby cause cancer arise in the course of a person’s lifetime (as opposed to being a change in the DNA that the person is born with) and are called “somatic” mutations. Those customers will have access to ancestry information as well as access to their uninterpreted raw data.
For a man with a functional ductal system and for whom the genetic defect resides within the germ cell, the genetically corrected stem germ cells could be injected into his seminiferous tubules to establish spermatogenesis.PowerPoint slides for teachingDownloading may take up to 30 seconds.
Similarly poor results were obtained with cloned embryos made with another established transgenic mouse myoblast line (data not shown). We therefore tested whether the somatic cell culture medium used to prepare growth medium for the F1 myoblasts could support improved cloned embryo development.
Switching parthenogenetic control embryos to WM but not KSOMaa had a slightly beneficial effect. To test whether these two types of cloned embryos differed from control embryos with regard to glucose uptake, we exposed embryos of each type to tritiated 2-deoxyglucose and then after extensive washing monitored uptake by scintillation counting.
We therefore examined the expression of GLUT1 in late one-cell stage cumulus and myoblast cloned embryos by immunofluorescence staining. Immunofluorescent staining for glucose transporters in myoblast clone embryos and controls.
Our Laser has been cleared by the FDA for the treatment of Carpal Tunnel Syndrome and other joint and muscle problems.
It is important to consider visceral etiologies, such as heart disease and upper gastrointestinal pathologies, but it is also important to diagnose and treat the musculoskeletal aspects of these patients (especially when visceral pathology has been ruled out). To test whether this twocell arrest was possibly related in any way to the two-cell arrest exhibited by some strains of fertilized embryos in some media, we tried different embryo culture medium formulations. Cloned embryos of either type exhibited a significant increase in glucose uptake at the late one-cell stage relative to control parthenogenetic embryos (Fig.
Cumulus cell cloned embryos exhibited a modest increase in GLUT1 expression relative to parthenogenetic control embryos (Fig. Diploid myoblast cloned embryos treated with a-amanitin showed greatly reduced signals for GLUT4 at the two-cell stage, indicating that the GLUT4 expression seen in untreated diploid cloned embryos was transcription dependent and not merely a result of protein or mRNA carryover from the donor cell.
Total fluorescence per embryo was expressed as a number ranging from 3 to 0 as judged by two observers blinded to the identity of the embryo.
A and C) Embryos stained with antibody to GLUT1 at the 2cell and blastocyst stages, respectively.
It has successfully treated chronic and acute pain, wounds, sports injuries, and more.How does laser light heal?Low-level lasers supply energy to the body in the form of non-thermal photons of light. Counterstrain is one form of osteopathic manipulative medicine (OMM) that lends itself well to this situation of acute pain in an adolescent. Cloned embryos constructed with nuclei from C2C12 myoblasts developed to blastocysts in this medium at a reduced rate as compared with cumulus cell cloned embryos (Table 1).
Tetraploid embryos expressed slightly elevated quantities of GLUT4 at the one-cell stage and two-cell stage, but this was less than that seen in the diploid cloned embryos (Figs. B and C) Bright-field and fluorescent DAPI stained image of a hatching myoblast cloned blastocyst.
B and D) Embryos stained with antibody to GLUT4 at the 2-cell and blastocyst stages, respectively.
Light is transmitted through the skin's layers (the dermis, epidermis and the subcutaneous tissue or tissue fat under the skin) at all wavelengths in the visible range; however, light waves in the near infrared ranges penetrate the deepest of all light waves in the visible spectrum. Also unlike cumulus cell cloned embryos, about half the C2C12 myoblast cloned embryos failed to progress to the two-cell stage. Interestingly, cumulus cell cloned embryos cultured initially in KSOM and then switched to KSOMaa formed blastocysts more efficiently under these conditions than when cultured continuously in KSOMaa and Table 2), similar to a previous study. The two-cell block was virtually eliminated, and over 40% of the cloned embryos developed to the blastocyst stage (Table 2). The cumulus cell cloned embryos also exhibited enhanced uptake of glucose relative to tetraploid control embryos and fertilized control embryos, and this pattern persisted in embryos immediately after cleavage.
Tetraploid embryos made with cumulus cell donor nuclei exhibited an intermediate level of staining. At least 10 embryos existed in each group, and each experiment was repeated at least two times. When low level laser light waves penetrate deeply into the skin, they optimize the immune responses of our blood. The underlying code for what the cancer “shows” to the rest of the body and how it will behave in the body is in part dependent on the DNA inside the cancer cells.


We’re interested in helping people explore their own DNA and what it can tell them about themselves.
Treatment with DMSO during oocyte activation, which previously improved cumulus cell cloned embryo development in CZB medium, failed to overcome this early block. Parthenogenetic control embryos developed efficiently to the blastocyst stage in all these media and Table 2). Thus, inner cell masses were, on average, a significant fraction of the total cells contained in a majority of the blastocysts.
The tetraploid one-cell stage embryos prepared with myoblast nuclei exhibited the same enhanced rate of glucose uptake as the diploid cloned embryos at the one-cell stage. Myoblast cloned embryos did not exhibit such an increase in GLUT 1 expression at the late one-cell stage or any later stage (Fig. Expression declined progressively in tetraploid embryos with development to the blastocyst stage. A) Data for GLUT1 staining in cumulus cell cloned embryos and controls at the one-cell stage.
Note: Blastocyst stage embryos have been compressed under coverslips to permit visualization of cell borders. And what’s becoming evident is that cancer is much more complicated than we used to think.Under each cancer umbrella there are actually many different rare diseases. However, we found that prolonging slightly the interval between hCG injection to induce superovulation and the oocyte activation step negatively affected the outcome, and DMSO treatment did have a positive effect in this situation. Glucose uptake was significantly elevated in myoblast cloned embryos relative to par-thenogenetic embryos and tetraploid embryos at the twocell stage, when embryo gene transcription has begun (Fig.
3B) but at the twocell stage exhibited enhanced plasma membrane localization of GLUT1, which normally does not occur until the eight-cell stage and which was not seen in either parthenogenetic or control embryos (Fig. Continued increased staining was seen in diploid myoblast cloned embryos at later stages for GLUT4, relative to parthenogenetic, tetraploid, and flushed fertilized embryos (Figs. B and C) Data for GLUT1 and GLUT4 staining, respectively, in myoblast cloned embryos and controls at the stages indicated.
It is a scientific fact that light transmitted to the blood in this way has a positive effect through-out the whole body, supplying vital oxygen and energy to every cell.A What to Expect During a Laser Therapy Treatment Sessiona€?For most people, laser therapy is quite passive.
Thus, the failure of the F1 myoblast cloned embryos to develop efficiently beyond the two-cell stage was a unique feature of these cloned embryos rather than a nonspecific effect of the culture system. Not surprisingly, parthenoge-netic embryos were unable to form blastocysts efficiently under these conditions. Statistically significant differences ascertained by t-test are indicated by different letters above bars.
Some patients have reported a slight tingling or tapping in a nerve or along a nerve pathway. By most accounts there are four established subtypes, defined based on how the cancer “looks”, both as you would view it under a microscope and on the molecular level.
These results also distinguish the established and easily cultivated C2C12 cell line from the F1 myoblasts with respect to effects of these donor nuclei on cloned embryo phenotype. Tetraploid embryos likewise did not form blastocysts efficiently in this medium but developed well in CZBG, indicating an effect of the oocyte-derived chromosomes on embryo phenotype.
In fact, two-cell stage myoblast cloned embryos displayed a rate of uptake that was nearly 6-fold greater than that of parthenogenetic embryos and nearly 3-fold greater than that of tetraploid embryos.
Cloned embryos treated with a-amanitin to inhibit transcription showed much reduced expression of GLUT1, indicating that the expression observed in untreated cloned embryos was transcription dependent (Fig.
Thus, diploid myoblast cloned embryos showed aberrant, high expression of GLUT4 throughout preimplantation development, distinguishing them from all three types of control embryos.
For instance, a “HER2+” cancer displays the “Human Epidermal Growth Factor Receptor 2” (HER2) molecule on its surface but doesn’t display the estrogen receptor (ER) or progesterone receptor (PR), molecules that catch certain hormones as they pass by. Thus, while the rate of glucose uptake in diploid cloned embryos remained elevated, the enhanced rate of glucose uptake seen in tetraploid embryos at the one-cell stage was reduced. Although enrichment of GLUT4 at the plasma membrane was not seen, such enhanced localization is often insulin dependent, and cycling of a fraction of the GLUT4 protein between cytoplasm and plasma membrane can nevertheless occur and contribute to glucose uptake.
D) Representative photographs show, from top to bottom, embryos assigned grades 0 through 3 of staining.
But for the most part, the treatment, which may last from 15 to 30 minutes, is not noticed at all.
Cancers that overexpress HER2 can be treated with specific drugs that target the HER2 molecule.
Translate the patient gently to the left, localizing side bending to the right at the fifth rib tenderpoint. The rate of glucose uptake was similar between cloned embryos and in vivo fertilized embryos (38 h post-hCG) (Fig. At the blastocyst stage, the localization of GLUT1 to the plasma membrane appeared to be reduced in myoblast cloned embryos in comparison to parthenogenetic and fertilized embryos (Fig.
Following (and even during) a laser therapy session, approximately 75-80% of patients being treated can notice an immediate improvement in their condition. But if a breast cancer is triple negative, meaning it doesn’t display any of these three receptors (HER, ER or PR), then drugs that target these molecules won’t be effective against the cancer.The DNA that someone is born with differs in various places from person to person (so-called “germline” variation) and can also impact the course of treatment. This will depend primarily on the type of condition and the length of time the condition has been present.
Most clinical trials performed today do not incorporate genetic testing into the design of the trial. It should be noted that parthenogenetic and tetraploid embryos are activated simultaneously and cultured in parallel with the cloned embryos, whereas the fertilized embryos may be slightly more advanced developmentally. When they discover that some trial participants react poorly while others are super responders, they look to data points such as age, other diseases the patient is suffering from or medications he or she is taking. Then flex the head forward, with some side bending to the right to relieve tension at the tenderpoint. These data indicate that during the two-cell stage, the rate of glucose uptake increases to a level similar to that in fertilized embryos more rapidly in myoblast cloned embryos than in parthenogenetic or tetraploid controls. Once again, the number of treatments depends upon the severity of the condition and its duration. The course of cancer depends on both the signature of the tumor, something that stems from you but takes on its own life, and you — the host — a necessary participant in the fight against the cancer. Usually rotation is needed toward the involved side, but occasionally it will be needed in the opposite direction.
There are some conditions that will never completely resolve but can be helped and maintained with laser therapy. Fine tune all planes of motion, including subtle rotation of the trunk.Reassess the tenderpoint.
Cells and tissues that are compromised have been shown to have a significantly higher response to LLLT irradiation than normal healthy structures.
Cell membranes, mitochondria and damaged neurological structures exhibit less than optimal metabolism and stasis conditions. Multiple studies have demonstrated that under these compromised conditions, the introduction of energy transfers response and the resultant enhancement of metabolic activity pronounced in biologically challenged cells, thus selectively targeting compromised cells, in reality, these cells exhibit a lowered reaction threshold to the effects of laser light and are more easily triggered to energy transfer responses. The result is that LLLT has a significant effect on damaged cells and tissues while normative biological constituents are appreciably less affected.1The cellular cascade effect a€” precipitated by the actions of enzymes and having a significant response in the presence of LLLT a€” has a significant impact on cellular and tissue function. Since a considerable number of the reactive proteins that respond to laser stimulation are enzymes, laser light effects are amplified in the stimulation of beneficial enzymes and depression of deleterious enzymes.A At the cellular level, cytochromes can be defined as electron or proton-transfer proteins that act as energy producers for human biological functions. Both of the cytochrome enzymes, Cytochrome c Oxydase and Nitric Oxide Synthase (NOS) have been found to be particularly reactive to laser photon stimulation. The particular affinity of these and other photo-reactive enzymes to accelerate their functions in the presence of LLLT provides critical increases in the molecule ATP and Nitric Oxide (NO) which enhances cellular activity & repairAlthough the various actions of LLLT in regards to inflammation, pain and healing have been separated categorically here for the purpose of process identification, their interactions are not so easily distinguished. In response to LLLT, the reduction in inflammation, pain and healing time all compliment each other and many of the processes are either simultaneous or overlapping.Acute Inflammation ReductionImmediately after an acute injury event, the body, in response to the disruption of the integrity of vascular, soft tissue, begins a series of biological responses. The first few degrees of movement should be very slow, and then the rest may be done more quickly.Reassess the tenderpoint with firm localized palpation.
A reduction in tenderness of at least a seventy percent indicates a therapeutic response.For physicians who want to learn more about counterstrain OMT, Laurence Jones' book, Jones Strain-Counterstrain (1995) is the definitive text and is easy to read. Injury responsive components such as Mast cells, Bradykinins and Prostaglandins are activated along with the vascular responses and cellular membrane reactions. All of these combined processes and events are represented by the symptoms of edema, inflammation, pain and functional debility.
LLLT can be effective in mediating both the symptoms and the underlying inflammatory process by the following actions:1. Stabilization of cellular membrane a€” Ca+ +, Na+ and K+ concentrations as well as the proton gradient over the mitochondria membrane are positively in This is accomplished in part by the production of beneficial Reactive Oxygen Species (ROS) wherein triplet oxygen molecules absorb laser light pro ducing singlet oxygen molecules. These ROS modulate intracellular Ca+ + concentrations and laser therapy improves Ca+ + uptake in the mitochondria.2,3,4A 2.
ATP production and synthesis are significantly enhanced, contributing to cel lular repair, reproduction and functional ability.


Laser stimulation of Cytochrome c Oxidase, a chromophore found on the mitochondria of cells, plays a major role in this rapid increase in production and synthesis of ATP.3A 3. Vasodilatation is stimulated via Histamine, Nitric Oxide (NO) and Serotonin increases, resulting in reduction of ischemia and improved perfusion.
Laser-mediated vasodilatation enhances the transport of nutrients and oxygen to the damaged cells and facilitates repair and removal of cellular debris.5,6A 4.
Beneficial acceleration of leukocytic activity results in enhanced removal of non-viable cellular and tissue components, allowing for a more rapid repair and regeneration process.A 5.
Increased Prostaglandin synthesis, particularly in conversion of the prostaglandins PGG2 and PGH2 periossides into prostaglandin PGI2. PGI2 (Prostacyclin), has a vasodilating and anti-inflammatory action with some attributes similar to Cox-I and Cox-II inhibitors.7A  6. In addition to increasing the number of lymphocytes, laser irradiation mediates the action of both lymphatic helper T-cells and suppressor T-cells in the inflammatory response.
Along with laser modification of beta cell activity, the entire lymphatic response is beneficially affected by LLLT.98.
Both blood capillaries and lymphatic capillaries have been clinically documented to undergo significant increase and regeneration in the presence of laser irradiation. The resulting improvement in circulation and perfusion enhances all repair and healing processes. Laser induced increases in NO and the growth factors a€” in particular cytokine INF-g a€” are contributory to this process.10,11A 9.
Areas of inflammation typically demonstrate temperature variations with the inflamed portion having an elevated temperature. Laser stimulated increases in cytokine SOD levels interact with other anti-inflammatory processes to accelerate the termination of the inflammatory process.
This rapid initiation of therapy in acute inflammation will assist in limiting the scope and duration of the inflammatory event and minimize the pain and severity associated with it.While the treatment regimen and course of therapy may be modified in chronic situations, the physiological responses and interactions remain consistent.
Chronic conditions may require longer treatment times.Pain ReductionThe unique pain reduction abilities of LLLT have been exten documented in numerous clinical studies and medical papers.
While there remains much to learn in re pain reduction characteristics, there is a wealth of knowledge currently available to demonstrate the effectiveness of laser therapy in this regard.Because the pain amelioration capabilities of LLLT are ac combination of local and systemic actions a€” utilizing enzymatic, chemical and physical interventions a€” the process is very complex. However, there is a preponderance of medical evidence that justifies a conclusion that effective pain reductions can be achieved via LLLT. The localized and systemic in-crease of this endogenous peptide after LLLT irradiation has been clinically reported in multiple studies with subsequent pain reductions.A  2. The pain blocking effect of LLLT can be pronounced, particularly in low velocity neural pathways, such as non-mylenated afferent axons from nociceptors. Laser irradiation suppresses the exci tation of these fibers in the afferent sensory pathway.13,14A  3.
As a neurotransmitter it is essential for normal nerve cell action potential in impulse transmission activity and, indirectly, the vasodilatation effect of NO can enhance nerve cell perfusion and oxygenation.A 4. Both compound muscle action potential (CMAP) values and nerve latency values have shown improvement with laser therapy.15A 5.
Several studies have documented the ability of LLLT to induce axonal sprouting and some nerve regeneration in damaged nerve tis sues.
Where pain sensation is being magnified due to nerve structure damage, cell regeneration and sprouting may assist in pain decrease.16,176.
Since Bradykinins elicit pain by stimulating nociceptive afferents in the skin and viscera, mitigation of elevated levels through LLLT can result in pain re Kininase II, and increase in NO are considered the contributors to this Bradykinin decrease.A 7.
By increasing the avail-able acetylcholine, LLLT help s in normalizing nerve signal trans-mission in the autonomic, somatic and sensory neural pathways.A 8. LLLT promotes normalization in Ca+ +, NA+ and K+ concentrations resulting in beneficial pain reduction results from these ion concentration shifts. Figure 2 presents a simplified representation of the effects of LLLT on pain improvement at the cellular level.Tissue HealingOne of the truly unique characteristics of LLLT is that it has the ability to actually promote and enhance healing, not just treat symptoms.
The irradiation by low-level laser light accelerates and enhances healing activities carried out by the body. LLLT can provide the following beneficial impacts in both open surface wounds and closed connective or soft tissue injuries as follows:1.
LLLT accelerates macrophage activity in phagocytosis, growth factor secretion and stimulation of collagen synthesis.A 3. The significant angiogenesis that occurs with laser therapy promotes revascularization with subsequent improvement in perfusion and oxygenation. The beneficial synthesis active factor ability of keratinocytes are enhanced by proliferation secondary to LLLT.20A 6.
Laser-stimulated acceleration of epithelial cell regeneration speeds up wound healing, minimizes scarring, and reduces infection opportunities.A 7. Two to five fold increases in growth-phase-specific DNA synthesis in normal fibroblasts, mus cells irradiated with IR light are reported.
Increases in vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF-2) secondary to IR light irradiation have also been reported.8. Laser-in duced increases in NO, ATP and other compounds that stimulate differentiation into mature cells.
Increased numbers of myofibroblasts, myofibrils, myotubes etc., as well as bone cell proliferation, have been clinically demonstrated with LLLT. Satellite cells, the precursor cells in the process of muscle regeneration, show significant increase in proliferation when irradiated with LLLT.21,22,239. Governmental agencies such as NASA are currently using tech medical conditions in space applications.
Olympic training facilities have just released state validate the growing acceptance in mainstream medicine for the medical efficacy of laser therapy as a viable, often superior therapeutic treatment modality.With over 200 clinical studies a€” many of which are double-blind, placebo-controlled a€” and in excess of 2000 published articles on LLLT, this innovative new technology has a well-documented research and application history. Having grown far beyond its distant Institutional Review Board (IRB) and experimental treatment status, LLLT is now being considered a therapy of choice for many difficult pain management challenges such as fibromyalgia and myofascial pain.
He has served as manager for several biomedical design and service facilities and participated as lead researcher for biomedical devices involved in emergency cardiac care, warmed intravenous fluid therapy and laser therapy.
Richard has participated in medical clinical trials for 15 years as a clinical trial analyst and contributing clinician.References1.
Analysis in vitro of the cellular proliferation of human gingival fibroblasts with low level laser. In vivo study on mast cells behavior following low-intensity visible and near infrared laser radiation. What is optimal dose, power density and timing for low level laser therapy in tendon injuries?
Abstract from the 7th International Congress of European Medical Laser Association, Dubrovnik, Croatia, June 2000.A 9. In vitro effects of low level laser irra diation at 660 nm on peripheral blood lymphocytes.
Department of Plastic and Reconstructive Surgery, Kyorin University School of Medicine, Tokyo, Japan.
Wound healing process: influence of LLLT on the proliferation of fi broblasts and on the lymphatic regeneration. Abstract from the 7th International Congress of European Medical Laser Association, Dubrovnik, Croatia, June 2000.12. Diode laser irradiation selectively diminishes slow component of axonal volleys to dor sal roots from the saphenous nerve. Laser therapy as a new modali ty in the treatment of incomplete peripheral nerve in-juries: Prospective Clinical Double-Blind Placebo-Controlled Randomized Study. Department of Neuro surgery, Rehabilitation and Physiotherapy, Tel Aviv Sourasky Medical Center, Israel. Abstract from the 7th International Congress of European Medical Laser Association, Dubrovnik, Croatia, June 2000.16.
Comparison of the low level laser therapy effects on cultured human gingival fibroblasts proliferation using different irradiance and same fluence. Enhancement of the blood growth promoting activity after exposure of volun teers to visible and infrared polarized light. Low energy laser irradiation pro-motes the survival and cell cycle entry of skeletal muscle satellite cells. The biological ef fects of laser therapy and other modalities on con nective tissue repair processes.
Low level laser therapy of soft tissue injuries upon sport activities and traffic acci dents: a multicenter, double-blind, placebo-controled clinical study on 132 patients.



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