I. Sigmor. Pikeville College.
As Vata has a tendency to be present in excess in old age order 130mg malegra dxt erectile dysfunction treatment success rate, we expect this time of life to be associated with the corresponding symptoms of dry skin purchase malegra dxt 130 mg without a prescription erectile dysfunction drugs prostate cancer, arthritis (dry joints), constipation and sleep difficulties. The dementias and Parkinsonian disorders are also related to Vata derangement, expressed as improper movement and transport on the molecular and synaptic levels within the CNS, and on the grosser level as derangement in the movements of limbs and ambulation. The use of sound, aroma and changes in the environment of the individual are somewhat foreign to allopathic medicine, but are considered important parts of the therapeutic armamentarium of Vedic medicine, and are referenced in the Vedic literature. The use of sound is particularly important, and is based on the correspondence between the structure of the Vedic literature and human physiology. CORRESPONDENCE OF VEDA AND HUMAN PHYSIOLOGY An understanding of the expression of human physiology from the unified field is incomplete from a Vedic perspective without an appreciation of the role of the Vedic literature in this scheme. The relationship between the Veda and human physiology is analogous to the relationship between the full genomic sequence of DNA and the manifest organism on which it is based. The sequential unfolding of matter in general, and of human physiology in particular, from the level of the unified field, starts with the first syllable of Rk Veda. Nader, a neuroscientist and neurologist, brought to light the correspondence between the structure of the Vedas and human 1 anatomy and physiology, with particular reference to the nervous system. This 40 correspondence has been refined in great detail over the past 10 years, and has focused not as much on the meaning of individual words in Vedic texts as on their sound value and on the structure of the texts, including arrangements of syllables, words, intervening silences, verses, chapters and divisions. Evaluating the texts in this fashion has led to the discovery of a remarkable one-to-one correspondence between Vedic texts and functional and anatomic groupings within the nervous system. As an example, the Vedic text known as the Yoga Sutras, ascribed to the Vedic seer Patanjali, corresponds in theme, structure, number and grouping of verses (sutras) to the recognized groups of cortical association fibers. The first of the Vedas, Rk Veda, corresponds in its full complement of verses and structure to the set of all pairs of cranial and spinal nerves. Complementary therapies in neurology 184 Just as Vedic texts correspond in structure to different aspects of the nervous system, the sounds which comprise the Vedic texts also show this correspondence. This is the theoretical basis for the practical approaches of Vedic sound, Gandharva Veda and Maharishi Vedic Vibration Therapy (MVVT) as therapeutic modalities of MVM. The vibrational quality of Vedic sound, corresponding to a particular area in the nervous system, can have a localized therapeutic effect in that area. When one object vibrates, another in the vicinity with the same resonant frequency also vibrates. The notion of a therapeutic effect of sound, separate from any associated meaning, is not new. We understand that sound can affect the entire physiology on the basis of an initial sensory cortical activation with secondary activation more diffusely in the neocortex, and sequentially in the limbic system, hypothalamus and autonomic nervous system. This effect of sound can be independent of meaning, and be based on sound quality and sequence alone, as is evident for example in the subjective response and objective physiological response we may have to music of different types. The effect of MVVT on symptoms of chronic disease has been reported in a 41,42 preliminary form, and is encouraging. As more patients avail themselves of this technique, further data should be forthcoming. OTHER TECHNIQUES IN THE VEDIC APPROACH TO HEALTH The effect of environmental changes on health promotion and disease prevention is covered in part in the portion of the Vedic literature known as Stapathya Veda. Specific prescriptions are given concerning the orientation of homes and room arrangement within them. Principal among these is the prescription for the front door of a home to face east, with an unobstructed view of the rising sun. The physiological basis for such prescriptions may be rooted in the understanding that direction sensitive neurons have been identified in the thalamus. These procedures include an initial decrease in fat consumption followed by internal oleation, 37 often with a laxative effect, as well as external oleation. Preliminary research points to a decrease in circulating polyaromatic hydrocarbons, primarily stored in fat, as a result of 43 regular panchakarma therapy. VEDIC MEDICINE AND SPECIFIC NEUROLOGIC DISORDERS As discussed above, there is a positive effect of the TM technique, and Vedic herbal preparations including MAK, on cardiovascular and cerebrovascular disease, as noted by studies of the effect of these modalities on hypertension, angina, hypercholesterolemia Ayurvedic medicine 185 and carotid intima-media thickness, and in laboratory models of atherosclerosis and free radical scavenging. These data underscore the usefulness of these modalities as part of a cost-effective strategy for stroke prevention.
Neil buy malegra dxt 130mg without a prescription erectile dysfunction organic, MS CGC Orange discount 130 mg malegra dxt overnight delivery most effective erectile dysfunction pills, CA Obstetrix Medical Group of Texas Genetic Counselor Fort Worth, TX Long Island, NY Taria Greenberg, MHS Medical Writer Paul A. Nutting, MS CGC Houston, TX Medical Writer Senior Genetic Counselor San Diego, CA Phoenix Genetics Program David E. Greenberg, MD University of Arizona Medicine Resident Melissa Knopper Phoenix, AZ Baylor College of Medicine Medical Writer Houston, TX Chicago, IL Marianne F. Knutel, MS CGC Medical Writer Medical Student Genetic Counselor Farmington Hills, MI Baylor College of Medicine Chicago, IL Houston, TX Barbara Pettersen, MS CGC Karen Krajewski, MS CGC Genetic Counselor Farris Farid Gulli, MD Genetic Counselor Genetic Counseling of Central Plastic and Reconstructive Surgery Assistant Professor of Neurology Oregon Farmington Hills, MI Wayne State University Bend, OR Judy C. Hawkins, MS Detroit, MI Toni Pollin, MS CGC Genetic Counselor Sonya Kunkle Research Analyst The University of Texas Medical Medical Writer Division of Endocrinology, Branch Baltimore, MD Diabetes, and Nutrition Galveston, TX University of Maryland School of Renée Laux, MS David Helwig Medicine Certified Genetic Counselor Medical Writer Baltimore, MD Eastern Virginia Medical School London, ON, Canada Norfolk, VA Scott J. Lorson, PhD Division of Clinical and Metabolic Nottingham, England Assistant Professor Genetics Dept. Hunt, MS Arizona State University Toronto, ON, Canada Genetic Counselor Tempe, AZ University of New Mexico Health Robert Ramirez, BS Sciences Center Maureen Mahon, BSc MFS Medical Student Albuquerque, NM Medical Writer University of Medicine & Dentistry Calgary, AB of New Jersey Cindy Hunter, MS CGC Nicole Mallory, MS Stratford, NJ Genetic Counselor Medical Genetics Department Medical Student Julianne Remington Indiana University School of Wayne State University Medical Writer Medicine Detroit, MI Portland, OR Indianapolis, IN Ron C. Michaelis, PhD FACMG Jennifer Roggenbuck, MS CGC Kevin Hwang, MD Research Scientist Genetic Counselor Medical Writer Greenwood Genetic Center Hennepin County Medical Center Morristown, NJ Greenwood, SC Minneapolis, MN xvi GALE ENCYCLOPEDIA OF GENETIC DISORDERS Edward R. Rosick, DO MPH MS Genevieve Slomski, PhD Oren Traub, MD PhD University Physician/Clinical Medical Writer Resident Physician Assistant Professor New Britain, CT Dept. Solis, MS Hospitals Medical Writer Seattle, WA Judyth Sassoon, ARCS PhD Decatur, GA Amy Vance, MS CGC Medical Writer Genetic Counselor Dept. Biochemistry Genetic Counselor San Francisco, CA University of Bern University of Florida Bern, Switzerland Gainesville, FL Brian Veillette, BS Medical Writer Jason S. Assistant Director of Molecular Medical Writer Holland, OH Diagnostics Berkeley, CA SUNY Upstate Medical University Charles E. Sweet, MS CGC Laguna Hills, CA JC Self Research Center Cancer Genetic Counselor Jennifer F. Wilson, MS Greenwood Genetic Center James Cancer Hospital Science Writer Greenwood, SC Ohio State University Haddonfield, NJ Columbus, OH Philip J. Seaver, MD Catherine Tesla, MS CGC Research Fellow Clinical Geneticist Senior Associate, Faculty Dept. Zuck, PhD Health Educator/Medical Writer Medicine Medical Writer Wilmington, DE Atlanta, GA Boulder, CO GALE ENCYCLOPEDIA OF GENETIC DISORDERS xvii A 4p minus syndrome see Wolf-Hirschhorn Although the responsible gene has been identified, test- ing for gene mutations is available only in research labo- syndrome ratories. Aarskog syndrome is also called Faciogenital dysplasia, Faciogenitodigital syndrome, and Aarskog- 5p deletion syndrome see Cri du chat Scott syndrome. In most cases, the altered gene in syndrome affected males is inherited from a carrier mother. Since males have a single X chromosome, mutations in the 47,XXY syndrome see Klinefelter syndrome FGD1 gene produces full expression in males. Females who carry a mutation of the FGD1 gene on one of their two X chromosomes are usually unaffected, but may have subtle facial differences and less height than other females in the family. Female carriers have a 50/50 chance of transmitting IAarskog syndrome the altered gene to daughters and each son. They transmit their single X chromosome to all daughters who, there- Aarskog syndrome is an inherited disorder that fore, are carriers. Since males do not transmit their single causes a distinctive appearance of the face, skeleton, X chromosome to sons, all sons are unaffected. First described in a Norwegian family in 1970 by the pediatrician Dagfinn The gene affected in Aarskog FGD1 codes for a Aarskog, the disorder has been recognized worldwide in Rho/Rac guanine exchange factor. Because the responsible uct is complex and the details of its function are incom- gene is located on the X chromosome, Aarskog syn- pletely understood, it appears responsible for conveying drome is manifest almost exclusively in males. The messages within cells that influence their internal archi- prevalence is not known. However, the precise way in which mutations in FGD1 produce changes in facial appearance and in the skeletal Description and genital systems is not yet known. Aarskog syndrome is among the genetic disorders with distinctive patterns of physical findings and is con- Demographics fused with few others.
In response to a variety of stimuli purchase 130mg malegra dxt amex lipitor erectile dysfunction treatment, homeostatic functions are defensively altered through a series of complex feedback loops that monitor conditions in the peripheral tissues and make local and systemic adjustments as needed cheap malegra dxt 130mg without prescription erectile dysfunction injections cost. Their role and the role that somatic dysfunction specifically 30 124 plays in disturbing homeostasis through reflex and neuroendocrine-immune 146 responses to the inflammation, edema and nociceptive bio-chemical mediators have 22,70 been extensively documented. Osteopathic considerations in neurology 105 SUMMARY While seeking health, the osteopathic approach to patient care is also designed to arrive at a differential diagnosis that considers both structural and functional problems. It builds much of the distinctive aspects of its approach on biopsychosocial, anatomical and 147,148 pathophysiological models and attempts to modify any and all stimuli (stressors) felt significantly to drive neurological and neuroendocrine responses. This chapter has also introduced OMT as a treatment modality for specifically treating somatic dysfunction as well as for modifying underlying nociceptive, postural imbalance and allostatic mechanisms and reflexes between somatic and visceral systems. The integrated use of OMT is considered generally to assist in maintaining homeostasis while specifically addressing concomitant somatic dysfunction and reducing allostatic load. This latter perspective still separates OMT by osteopathic physicians in the USA from 149 MDs who practice manual medicine, but hopefully this chapter has demonstrated the value of continued dialog and research collaboration. For the neurologist, the implications of osteopathic diagnosis and treatment for enhancing differential diagnosis are significant. The evidence base surrounding the entity known as somatic dysfunction is still in development. Certainly removal of factors that modify or mimic a pathological neurological condition will aid in establishing more accurate diagnosis. Likewise, approaches designed to reduce pain and dysfunction and/or to diminish neuromusculoskeletal impediments to activities of daily living, balance, gait, or other movements should be conscientiously investigated for their potential to enhance the care of patients with various neurological diagnoses. Parallel and distinctive: the philosophic pathway for reform of osteopathic medical education. Spinal irritation: showing how near the medical profession came to the discovery of osteopathy. Kirksville, MO: Published by the author, 1908 Distributed, Indianapolis: American Academy of Osteopathy 8. Baltimore, MD: Lippincott, Williams & Wilkins, 2003:19–29 Complementary therapies in neurology 106 9. Kirksville, MO: Thomas Jefferson University Press, Northeast Missouri State University, 1992 10. Somatic dysfunction, osteopathic manipulative treatment, and the nervous system: a few facts, some theories, many questions. Baltimore, MD: Johns Hopkins University Press, 1982 Osteopathic considerations in neurology 107 36. Osteopathic Medicine: Past, Present, and Future: A Conference Sponsored by the Josiah Macy, Jr. Outline of Osteopathic Manipulative Procedures: The Kimberly Manual Millennium Edition. The Principles of Palpatory Diagnosis and Manipulative Technique, Newark, OH: American Academy of Osteopathy, 1992:146–52 41. Interexaminer reliability of osteopathic palpatory evaluation of the lumbar spine. Retention of interexaminer reliability in palpatory evaluation of the lumbar spine. In Spine: State of the Art Reviews Philadelphia, PA: Hanley & Belfus, 1995:463–90 55. Direct observations of the sensitization of articular afferents during experimental arthritis. Properties of peripherally induced persistent hindlimb flexion in rat: involvement of N-methyl-D-aspartate receptors and capsaicin-sensitive afferents. Long-lasting alterations of spinal reflexes: a potential basis for somatic dysfunction. Corticotropin-releasing factor, vasopressin, and prostaglandins mediate, and nitric oxide restrains, the hypothalamic-pituitary-adrenal response to acute local inflammation in the rat. The role of the sacroiliac joints in coupling between spine, pelvis, legs and arms. Baltimore, MD: Lippincott, Williams & Wilkins, 2003:762–83 Osteopathic considerations in neurology 109 80. The relationship of the double crush to carpal tunnel syndrome (an analysis of 1000 cases of carpal tunnel syndrome).
Thioridazine is a low-potency piperidine phe- (A) Imipramine nothiazine agent with signiﬁcant afﬁnity for 1- (B) Chlorpromazine adrenergic and muscarinic receptors discount malegra dxt 130 mg with mastercard erectile dysfunction caused by performance anxiety, having a high (C) Clozapine potential for sedation as a side effect purchase 130 mg malegra dxt mastercard erectile dysfunction killing me. Haloperidol is (D) Fluoxetine a high-potency butyrophenone with its primary ac- (E) Thiothixene tion at the D2 dopaminergic receptor, so it produces 4. Which clinical condition poses the greatest concern a signiﬁcant incidence of extrapyramidal toxicity to a patient on antipsychotic therapy? Clozapine is a low-potency atyp- (A) Epilepsy ical antipsychotic that binds primarily to D4, (B) Nausea associated with motion sickness 5-HT2, and 1 receptors and possesses very little ex- (C) Manic phase of bipolar disorder trapyramidal toxicity but signiﬁcant sedative and (D) Hallucinogen-induced psychosis autonomic side effects. James began haloperidol therapy for schizo- convulsant; neither possesses signiﬁcant antipsy- phrenia and within several weeks developed chotic properties. This question concerns the most important ex- choses were well controlled, he was switched to an- trapyramidal reaction to long-term antipsychotic other agent, thioridazine, which proved to be as ef- administration—tardive dyskinesia—and its gener- fective as haloperidol in managing his primary ally accepted basis. Although some tolerance to the condition and did not result in the undesirable sedative effects of antipsychotics can occur, there is symptoms. However, a decrease in that of haloperidol, it also has much greater an- dopamine synthesis has not been linked with tar- timuscarinic activity. On the contrary, lower dopamine sate for dopamine receptor blockade in the nigro- tone would more resemble a parkinsonian state, striatal tract, so that extrapyramidal function is whereas in tardive dyskinesia, antidopaminergic more appropriately maintained. Thioridazine has drugs tend to suppress the dyskinetic symptoms, greater 1-adrenergic blocking activity than and dopaminergic agonists worsen the condition. The neuroleptic malignant syndrome is an infre- There is no evidence that the antipsychotics lead to quent extrapyramidal reaction with a relatively high loss of striatal cholinergic neurons. It may result from that occurs most commonly after long-term admin- too-rapid block of dopaminergic receptors in indi- istration of high-potency butyrophenone, thioxan- viduals who are highly sensitive to the extrapyrami- thene, or phenothiazine. Chlorpromazine is a low-potency phe- sists of control of fever, use of muscle relaxants, and nothiazine agent with moderate potential to cause administration of the dopamine agonist bromocrip- extrapyramidal signs. Clozapine is well known to tine, which is likely to worsen the psychotic symp- have the lowest potential for producing tardive toms. The question concerns actions of antipsychotic SUPPLEMENTAL READING agents that may have untoward consequences when Ananth J, Burgoyne KS, Gadasalli R, and Aquino S. Antipsychotic drugs and have antiemetic properties but generally are more neuroplasticity: Insights into the treatment and neu- potent than is necessary to treat motion sickness. A clinical review of cognitive Haloperidol has high afﬁnity for D2-dopaminergic therapy for schizophrenia. Newer atyp- The drug has no direct action on GABAergic neu- ical antipsychotic medication in comparison to rons and does not act presynaptically to affect clozapine: A systematic review of randomized trials. Anderson is a 29-year-old single woman ANSWER: Clozapine would be the next best choice in Mwho was diagnosed with schizophrenia more the treatment of this patient. She started with haloperidol and has been reported to salvage as many as 50% of then after several months switched to thiothixene. While her extrapyramidal signs with these agents Clozapine does not have the status of a ﬁrst-line were not unacceptable, the frequency of her acute agent because of its undesirable side effects. De psychotic episodes marked by paranoid delusions novo seizures occur in 2 to 5% of treated patients, was not substantially diminished. The signiﬁcance was also given a trial of thioridazine with a similar of agranulocytosis is not the incidence (1–2%) but clinical response to those of the earlier agents. As antipsychotic agent would be the most appropriate a result, weekly blood counts are mandatory for pa- next choice for this patient? Patients should also be concerns with the use of this drug, and what precau- alert for sudden onset of any fever or chills. Other tions should be taken during therapy with this atypical antipsychotics, such as risperidone and agent? Dewey DRUG LIST GENERIC NAME PAGE GENERIC NAME PAGE Alfentanil 408 Marijuana 416 Amobarbital 411 MDA 418 Amphetamine 410 MDMA 418 Buprenorphine 408 Mescaline 417 Butorphanol 408 Methadone 408 Caffeine 410 Methamphetamine 410 Chlordiazepoxide 411 Methylphenidate 410 Cocaine 410 Midazolam 411 Diazepam 411 Morphine 409 Disulﬁram 415 Nicotine 411 Ethanol 412 Pentobarbital 411 Fentanyl 408 Phencyclidine 417 Flurazepam 411 Phenmetrazine 410 Heroin 409 Psilocybin 417 Lorazepam 411 Secobarbital 411 LSD 417 The phrases substance abuse and drug abuse are of- the excessive self-administration of any substance for ten applied to the use of an illegal or illicit chemical nonmedical purposes. However, these terms abuse is the production of hazardous or harmful ef- may be applied when a legally obtainable medication fects to the individual and/or to society. Inappropriate use, or abuse, is menting behavior and sometimes an inappropriate at- 406 35 Contemporary Drug Abuse 407 tempt at self-medication to treat a real or perceived Chronic use of a drug over a long period sometimes disease state. It is also clear that drug abuse is a func- produces a state of tolerance that may be classiﬁed as tion of the pharmacology of each drug.
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