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However hypertension jnc 8 guidelines pdf purchase 80mg verapamil with mastercard, it is important to see your doctor if you have any unusual symptoms, or symptoms that don`t go away so that you can be examined and treated appropriately. A haematologist specialises in the care of people with diseases of the blood, bone marrow and immune system. These include lack of energy, persistent tiredness and fatigue, weakness, dizziness or feeling unusually short of breath when physically active. Increased bleeding or bruising A very low platelet count can cause bruising for no apparent reason, or excessive or prolonged bleeding following minor cuts or injury. Some people notice frequent or severe nose bleeds or bleeding gums and some women may have unusually heavy menstrual periods. Red or purple flat pinhead sized purple spots may appear on the skin, especially on the legs. This involves taking a sample of your blood, usually from a vein in your hand or arm, and sending it to the laboratory for examination under the microscope. Most will also have a high white cell count with large numbers of abnormal leukaemic blast cells (lymphoblasts) in the circulating blood the presence of leukaemic cells in the bloodstream suggests that you have leukaemia. A small percentage of patients may not have lymphoblasts detected in their blood at diagnosis. In all cases, the diagnosis will need to be confirmed by examining the cells in your bone marrow. Your full blood count will be checked regularly both during and after treatment to see how well your disease is responding. These may present as minor skin infections, slow healing of minor cuts and grazes, a sore throat, sore mouth, coughing, urinary tract infections (frequent passing of urine with a sensation of burning) and often fevers. Bone pain Pain in the bones and joints is common and results from the marrow being crowded with leukaemic cells. Bone marrow examination A bone marrow examination (or biopsy) involves taking a sample of bone marrow, usually from the back of the iliac crest (hip bone) and sending it to the laboratory for examination under the microscope. Under normal circumstances the bone marrow contains a small proportion of normal or healthy blast cells, usually less than 5 per cent. The bone marrow examination may be done in the hospital or outpatient clinic under local anaesthesia or, in selected cases, under sedation. A mild pain-killer is given beforehand and the skin is numbed using a local anaesthetic; this is given as an injection under the skin. The injection takes a minute or two, and you should feel only a mild stinging sensation. After allowing time for the local anaesthetic to work, a long thin needle is inserted through the skin and outer layer of bone into the bone marrow cavity. If a sedative is used you might feel a bit drowsy afterwards, and it is advised you take a family member or friend along who can take you home. There may be some mild bruising or discomfort, which usually is managed effectively by paracetamol. These tests provide more information about the exact type of disease, the likely course of the disease and the best way to treat it. Standard cytogenetic tests involve examining the chromosomes under the microscope. An example of this is the Philadelphia (Ph) chromosome, found in some leukaemic cells. Tyrosine kinase continually signals the bone marrow to make too many abnormal blood cells. Its frequency increases with age and is as high as 50 per cent in people over the age of 50 years. In suitable patients, an allogeneic (donor) stem cell transplant may be considered at an earlier stage. These tests are capable of measuring minute traces of leftover (residual) leukaemic cells not normally visible under the microscope. The presence of left over disease gives the doctor some indication of the likelihood of future relapse (return of the original disease). Using this highly sensitive technology, subtle changes in your disease can be detected earlier and where necessary treated earlier. This test is done on a machine called a flow cytometer and the test is often called flow cytometry. Specific patterns of antigens on leukaemia cells can be used to follow the leukaemia and check how well it is responding.

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Community participation is essential in order to blood pressure chart xls verapamil 80 mg with mastercard maximize the effect of control strategies, including case detection, vector control and control of animal reservoirs. It was found that the cost­effectiveness depends more on the cost of treatment than on that of testing. A strategy based on the rK39 rapid test or the direct agglutination test is more efficient than one based on bone-marrow or lymph node aspiration, as the sensitivity of a test is paramount in this fatal disease. These calculations do not include other direct or indirect costs and may differ widely from country to country. Coadministration of miltefosine with paromomycin for 10 days or a combination of single-dose liposomal amphotericin B with paromomycin were competitive in terms of cost­ effectiveness with short-course monotherapy on the Indian subcontient (depending on the drug costs). Ultra-short regimens, such as single-dose liposomal amphotericin B, are therefore the most advantageous. Drug prices are, however, rapidly changing, and policy-makers need updated cost information to make informed decisions on the best treatment options. Although the cost of cutaneous leishmaniasis treatment is usually lower than that for visceral leishmaniasis (see Annex 6), formal data on the costs of diagnosis and treatment of cutaneous leishmaniasis or New World visceral leishmaniasis are not available. Vector and reservoir control No information is available on the cost­effectiveness of measures for vector and reservoir control. In the context of weak health systems in many Leishmania-endemic countries, a number of factors contribute to lack of access to medicines. National treatment protocols often do not reflect the latest developments, and few or no medicines for leishmaniasis are included in national essential drug lists. Medicines for which preferential prices have been negotiated in lowand middle-income countries are not always registered by the companies where they are needed, as there is no profitable market. Medical practitioners in these countries experience great difficulty in obtaining the small quantities of medicines needed ad hoc. Problems with quality, low production capacity and lack of an adequate forecast of needs (resulting in long lead times for drug orders) regularly cause stock ruptures in endemic countries. There are no central buffer stocks that can be accessed in such cases, and there is no platform for indicating drug needs; therefore, the quantities needed globally cannot be estimated and drug production cannot be appropriately planned. Overall monitoring of access to leishmanial medicines should be strengthened, with pricing, registration and global needs taken into account. Moreover, the regulation of drug policies and quality assurance should be strengthened at all levels. The use of counterfeit medicines (toxic batches of antimonials, fake miltefosine) has led to several avoidable deaths in the past. The supply of diagnostics for visceral leishmaniasis is marked by similar problems, as the market is relatively small and not profitable. During the past 10 years, several new drugs have been developed for leishmaniasis, due to increased collaboration between international organizations, foundations, private pharmaceutical companies, governments and universities. Distribution of Old World leishmaniasis by country or territory, 2009 Country or territory Species Clinical form Proven or suspected Proven or Phlebotomus vector suspected animal reservoir P. Distribution of New World leishmaniasis by country or territory, 2009 Country or territory Leishmania spp. Clinical form Proven or suspected Proven or Lutzomyia vector suspected animal reservoir L. Published figures indicate an estimated incidence of 2 million new cases per year (0. Visceral leishmaniasis causes an estimated over 50 000 deaths annually, a rate surpassed among parasitic diseases only by malaria, and 2 357 000 disability-adjusted life years lost, placing leishmaniasis ninth in a global analysis of infectious diseases. Making accurate estimates is extremely challenging, however, because (as for other neglected tropical diseases) empirical data 104 on leishmaniasis incidence are sparse. In Brazil, India, Nepal and the Sudan, the estimated prevalence has so far remained below 10% but is expected to rise, as long as there continues to be little access to antiretroviral treatment. The characteristic geographical clustering of leishmaniasis cases, especially when the transmission is anthroponotic, complicates estimation of disease burden, because the incidence figures for a small area cannot be extrapolated confidently to a much larger area. Passive surveillance data from health facilities are generally the most comprehensive source available for estimating country-level disease burden; however, the extent of underreporting in most leishmaniasis-endemic countries is known to be substantial, ranging from two- to 40-fold in targeted studies. These findings imply that different, largely undetermined correction factors should be applied for each setting. The results of a village-based study in India suggested that as many as 20% of visceral leishmaniasis patients, disproportionately poor and female, died before their disease was recognized. The leishmaniases are widely dispersed, with transmission to humans on five continents, but the human disease burden is concentrated mainly in a few major foci.

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In contrast hypertension nursing intervention order verapamil 120 mg otc, moderate to heavy pressure applied to a Trigger Point causes the pain to initially increase, but then as the muscle relaxes the pain will fade. If there is no decrease in pain after one minute, stop the pressure-this is probably not a Trigger Point! After applying pressure to Trigger Points, the relaxed muscle should be stretched. If the muscles are not returned to normal length, there is a greater likelihood the Trigger Points will reoccur. The Pressure Pointer is the best tool available for self-applied Trigger Point therapy! Trigger Points result in muscles which have been traumatized by accidents, sports, occupational stress, and overuse. The Trigger Point restricts motion of the muscles and decreases circulation, depriving the muscle of nutrients and oxygen and resulting in a collection of metabolic waste that cannot be properly filtered away. Pain is now being caused by mechanical (pressure) and chemical (waste product) stimulation. Pain signals in the body that come from several sources are known to merge into a single nerve at the spine before continuing on to the brain. As these signals merge, it becomes possible for mistaken impressions as to the true source of the pain to occur. Additionally, Trigger Points create shortened muscles which often compress nearby nerves. The Brachial Plexus is a network of nerves originating in the neck, and supplying the neck, upper back, shoulders, arms, forearms, and hands. This explains why many Trigger Points found in the neck and upper back can lead to pain and dysfunction throughout the upper body. Stretching or contracting muscles affected by Trigger Points can cause intense pain, and the body responds by trying to protect itself-a phenomenon called "splinting" or "guarding. What was originally decreased movement based on trying to avoid pain ultimately results in the incapacity of the muscle to move correctly. Treating myofascial trigger points yourself addresses the source of that kind of common pain and is not just a way of temporarily relieving it. When pressure is applied to the Trigger Point, the chemical/pressure cycle is interrupted, which helps to stop the contraction and the pain in the muscle. Additionally, the muscle is heated and kneaded during treatment, which helps to increase circulation and to remove the metabolic waste products. Another effect is that muscle fibers become lengthened and stretched which decreases the pressure component of the pain cycle. Finally, adding a stimulus (pressure) to the trigger point overrides the pain signals being transmitted, much like a train track which can be switched. The advantage of the Pressure Pointer is that while applying the pressure to the Trigger Points, the muscles involved are able to be fully relaxed during treatment, allowing deeper penetration. It is important to understand that Trigger Points are not the same as acupressure points. For treatment to be effective, the specific Trigger Point, or contracted portion of the muscle, must be contacted. Self treatment of Trigger Points is one of the best and most effective ways to achieve long lasting pain relief. For Trigger Point therapy to be effective, you must use moderate to heavy pressure. Using these tools requires arm and hand strength, which is often difficult if these are already painful areas. The Pressure Pointer relies on leg power to provide the firm pressure needed without tiring sore and painful upper body muscles. Another advantage during treatment is that the target muscles are free to be taken through ranges of motion or to perform specific stretches while applying pressure at the same time. Finally, the Pressure Pointer provides a Foot Pressure allows the comprehensive target muscles to relax, and treatment manual that keeps you from getting tired the Pressure Pointer teaches you about your during treatment.

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This aspect is the result of a highly frequent enzymatic decomposition arteria sacralis order 120mg verapamil visa, reduced membrane permeation at the level of the intestine and, more relevant, the reduced solubility in water. Cyclodextrin Complexes Another way of increasing drug solubility to assist oral absorption is using cyclodextrins. Cyclodextrins are hydrophilic cyclic oligosaccharides which possess a hydrophilic extrinsic space and a central lipophilic concavity employed as promoters of drug absorption upon delivery. Through a sequence of tests, it has been proved that meglumine antimoniate complexed with cyclodextrin yielded an improved oral bioavailability [138]. The production of an AmB-loaded oil-in-water (O/W) microemulsion showed ability to increase drug dissolution by 1000-fold with a reduction in toxic effects on cells [143]. Also, another test performed with a self-emulsifying formulation of AmB with mono- and diglycerides plus vitamin E (stabilizer) proved to be stable in the intestinal fluid with the AmB concentration remaining constant for 6 hours and with improved oral bioavailability [144]. Pathogens 2019, 8, 119 21 of 33 Mixed micelles with amphiphilic compounds are able to reproduce the physiological systems where the lipids from the food are transformed into mixed micelles constituted by bile salts [145]. AmB-loaded micelles composed of phospholipids and bile acids improved the absorption of the drug in a prototype of intestinal loop perfusion in rats, although not tested in the healthy animal [146]. Nanocochleats are cigar-shaped nanostructures consisting of negatively charged lipid bilayers, attached to a divalent cation, usually calcium. Increase in Resistance Time Another alternative that aims to promote the oral bioavailability of drugs is the increase in the drug residence time at the absorption site. Chitosan is an interesting polysaccharide, combining bio-adhesion with absorption-enhancing characteristics. Chitosan is a natural polysaccharide composed of glucosamine and N-acetylglucosamine which is obtained from chitin of crustaceans. This compound may further function as an absorption promoter through the intestinal epithelium, due to its capacity to strengthen the diffusion of mucoadhesive systems. Intracellular bacterial infections caused by protozoa present physical barriers that hinder the arrival of significant portions of the drug to the target site. In turn, phosphatidylcholine and stearylamine tested alone did not reveal any activity against parasites, Pathogens 2019, 8, 119 22 of 33 reinforcing the idea that the association of both in a liposome is of extreme relevance for antiparasitic activity [158,159]. The same authors also demonstrated the in vitro activity of allopurinol-loaded polyethylcyanoacrylate nanospheres against Trypanossoma cruzi epimastigotes, with a response twice as effective in comparison with the free drug. However, to be validated, the studies require in vivo confirmation of the nanospheres efficacy [164]. The formulation led to the cure of trypanosomiasis with a dose-dependent activity. Regardless of the few advances achieved through these studies, they are expected to contribute to original approaches as they are still very inconclusive and require further research. Nanometric-scale formulations prepared with products derived from medicinal plants and their leishmanicidal activity are reported below, with liposomes, niosomes, and nanoparticles as the main addressed systems. A considerable effectiveness of flavonoids against Trypanossoma and Leishmania species has been described by means of an assay using quercetin. Nanoparticles loaded with andrografolide, a diterpenoid extracted from the Andrographis paniculata, displayed strong leishmanicidal activity [168]. In fact, nanoparticles with smaller than 200 nm have been linked to increased phagocytosis by macrophages infected with Leishmania [169,170]. The liposomal and niosomal preparations of this molecule decreased the parasite incidence in the spleen by 69 and 90%, respectively, while the free drug in the same amount obtained an outcome of 39% [172]. However, the harmine action mechanism against Leishmania is poorly elucidated, thus requiring further study [174]. This process was described for the first time in the 1970s and, since then, it is being used to describe cancer and degenerative disorders. Their life cycle development requires several stages, which entail various hosts until they infect humans and proliferate. The infectious forms do not divide while the non-infectious forms have an undefined track. Both in vitro (using distinct harsh conditions as AmB or H2 O2) and in vivo (using L.

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The Committee was divided into subgroups hypertension pregnancy verapamil 240 mg free shipping, each was assigned a specific section, and preliminary drafts were developed. The outline and the drafts were reviewed, and evidence-based recommendations were discussed and finalized by consensus. These were reviewed in detail, and members with perceived conflicts abstained from the discussion of specific questions related to their conflicts of interest. The revised document incorporated the comments and input from all Committee members. Document Structure Patients: Most people in this situation would want the recommended course of action and only a small proportion would not Clinicians: Most patients should receive the recommended course of action Policy makers: the recommendation can be adopted as a policy in most situations d d Weak recommendation. Each Committee member was asked to assess the identified literature relevant to his/her section, and decide about inclusion of individual articles. Searching the literature before 1993 was not done systematically since the discovery of nitric oxide in asthma was first reported in 1993. The literature search was limited to all relevant studies including randomized controlled trials, cohort studies, case-control studies, and cross-sectional studies published in the English language. Sections that did not yield specific recommendations were written after a thorough review of the available literature in a narrative review format. Asthma is a clinical diagnosis and there is no single diagnostic test for the disease. The background pathology of asthma is often but not always due to eosinophilic airway inflammation. There are several inflammatory phenotypes in asthma most commonly described as eosinophilic, neutrophilic, mixed, and paucigranulocytic (32). For each question, the Committee graded the quality of the evidence available (high, moderate, low, or very low), and made a recommendation for or against. Consensus on the recommendations was reached among all the members of the Committee. The strength of a recommendation has important implications for patients, clinicians, and policy makers (30). American Thoracic Society Documents 605 decide which therapies to select or stop (33­35). In the largest study to date (n ј 566), the correlation was of a similar order (0. These limited correlations reflect the fact that whereas sputum eosinophilia is always abnormal, exhaled nitric oxide is present even in health with its distribution skewed to the right. It is also necessary to bear in mind that negative and positive predictive values are limited in their generalizablity, given that they depend on the prevalence of the condition in the tested population. Again, these outcomes may differ somewhat depending on the target population: for the most part these data are derived from patients with mild to moderate asthma. The diagnosis of asthma is well defined, and the background pathology is often but not always due to eosinophilic airway inflammation. Similarly, in patients who have already been treated with inhaled steroids, the test may be falsely negative. This information is much more clinically relevant because it enables the clinician to bypass an empiric "trial of steroids" or unnecessary long-term corticosteroid treatment. The data used to prepare this composite figure were obtained from Shaw and colleagues (51) and Olin and colleagues (73) after consultation with the authors. It is important to choose the appropriate cut point in relation to the clinical setting and question. It is unlikely that reference values derived from a "normal" population will be as helpful as cut points in patients with airways disease or respiratory symptoms. Even when individuals with atopy or diagnosed asthma are excluded, the upper limit of "normal" ranges from 27 to 57 ppb depending on sex (69). This overlaps with the range of values obtained in populations with asthma in relation to sputum eosinophilia (see Figure 1). There are important differences between these studies with regard to the size of the examined population, as well as the range of statistical variables that have been included or excluded, limiting their value (76, 77, 80­83). The importance of current smoking and atopic status is generally agreed upon (28), but there are inconsistencies between the studies regarding which other factors ought to be accounted for when deriving and applying reference values (Table 1).

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In the middle of one of these very intense conversations heart attack mp3 generic verapamil 240mg fast delivery, she exclaimed "Wow, he did it! Griffin and I developed was that the health department should stop collecting stool specimens from asymptomatic convalescing school children, teachers, and day care staff. We felt that these groups, even though recently infected, would be very unlikely to transmit Shigella if they had formed stools and could be relied on to wash their hands after going to the toilet. We also recommended against the practice of testing asymptomatic contacts of persons with shigellosis. We reasoned that the decreased burden of specimen collection, ensuring exclusions from work or school, and following up on multiple stool culture results would permit the public health professionals to focus on handwashing in key locations where people congregated and would permit a proactive rather than reactive approach. Because we could not be certain that preschool aged children could be expected to wash their hands reliably, we recommended that asymptomatic convalescing preschool aged children be excluded from group child care until two stool cultures were negative for Shigella. This recommendation was a policy change from the practice of excluding children from child care facilities only during the time that they had diarrhea. On June 10th, the day after we provided our recommendations, the Commissioner of Health created a Shigella Task Force consisting of health department staff from the clinic, the laboratory, the field service section, the school health section and the environmental health division. The commissioner called a meeting with key leaders in each of these areas and presented our recommendations. I believe the commissioner created the task force to empower the leaders to take responsibility for controlling the outbreak. The leaders decided to implement a community-wide handwashing campaign with monitoring of handwashing at sites controlled by community services considered to be at high risk of transmission. The task force initiated onsite handwashing promotion at day care centers, summer schools, summer camps, and free lunch sites. The handwashing promotion included problem solving at each site to ensure that appropriate handwashing could be accomplished everyday. In the 3 to 4 days after the creation of the task force, I accompanied public health professionals on several of their site visits to child care facilities, elementary schools, summer camps, and free lunch sites. At each of these sites, I observed the direct advice and problem solving of the public health professionals and recorded and photographed key areas of concern regarding handwashing. For example, we observed and recorded children lining up for free lunches without handwashing and a paucity of handwashing facilities available at summer camps. At child care centers, we observed sinks that were too high for the children to reach to wash their hands. At schools, we observed that no soap was available in some of the bathrooms; this was a safety issue because children would squirt soap on the floor and then slip on the soap. I planned to return to each of these sites in a few weeks to observe changes in the accessibility of soap and water and handwashing practices. After creating the task force, assistance in handwashing promotion was sought from the community at large. Poundstone held a press conference and sought cooperation from the media, the Parks and Recreation Office, the Community Services Agency, and the school board. A local television station aired a video several evenings each week that emphasized the prevention of shigellosis through handwashing and taught proper handwashing technique. The Community Services Agency and the Parks and Recreation provided liquid soap and water to all free lunch sites and summer camps. The school board ensured that all summer students viewed a video on shigellosis and handwashing and that all students would be monitored in handwashing on arrival to school, after using the toilet, and before eating lunch or snacks. Child care facilities and elementary summer schools were directed to keep track of illnesses from school or day care and to advise those with diarrhea to seek rapid diagnosis and treatment at the health department clinic. The health department set up a special diarrhea clinic so that persons with diarrhea would not need to wait for an appointment to get tested and treated. This was a conference that I funded on my own, to present a paper from work I had done during my internal medicine residency. As can be imagined, I had a very enjoyable week, both at the conference and traveling in Italy with my boyfriend (now husband) Mark. Mark lived in California while I was in Atlanta, and we very much appreciated any time that we could spend together. My departure from Lexington permitted the health department and greater community to implement the handwashing campaign unencumbered by meetings with me.

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With rapid developments in communications technology blood pressure visual chart buy generic verapamil 80mg online, the ways in which such recordings are able to be made are likely to become ever more varied. These recordings have included conversations between the ultrasound practitioner and the patient. It can then prove very difficult to have these removed, especially if there is no statement of policy placed in waiting rooms or otherwise publicly available. Departments should have a clear policy on this issue following a risk assessment that takes account of the following: i) ii) the views of members of the professional workforce both as a group and individually should clearly be taken into account. Possible medico-legal complications arising if, for example, an abnormality is recorded that is not reported or acted upon. Conversations between the ultrasound practitioner and the patient and anyone accompanying them may also be recorded. The employer must be aware of any local arrangements if it is decided to allow this as they may impact on its risk strategy and insurance arrangements. It can be a great distraction and can increase stress levels for the ultrasound practitioner at a time when they require very high levels of concentration. It has the potential to extend the time of the examination or treatment which may be contrary to published safety guidelines and advice. Providers should take into consideration the possible existence of local policies allowing, for example, the recording of a birth. Many employing authorities do try to facilitate this type of request within the Directorates that have responsibility for maternity services. Providers should consider consulting with any relevant patient liaison groups that the employing authority may have and ensure the final agreed policy is publically available. Removal of material from social media that has included the ultrasound practitioner without their consent may be difficult, particularly so if no prior notice of policy has been made available. Providers might also wish to consider how staff should respond to situations where filming begins or continues without permission and contrary to the agreed policy. Some ultrasound practitioners set up private or other forms of company, work as franchisors or franchisees or as a sole trader. There are therefore a wide ranges of ways in which independent ultrasound practitioners can work. These Guidelines cannot provide specific advice although the following information may be of help. Ultrasound practitioners practicing independently in the devolved countries are advised to contact the equivalent organisations in their own countries for advice about any legal requirements that may apply. Many contracts of employment with Trusts and Health Boards and independent companies require disclosure of independent work and activities that may have a bearing on the work of the employer and even if not stated may be implied or judged to be so once operational. Independent practitioners are advised to seek advice, for example from their employer or seek independent legal advice. Ultrasound practitioners should be entirely clear on when they are working independently (self-employed) and when they are working as an employee. This should be made clear in any written contracts but some are very poorly written and constructed and this is not always apparent. Ultrasound practitioners working independently must be aware of, and follow the requirements and conditions of, their professional indemnity insurer. Many professional indemnity policies will apply only to the individual practitioner and not to companies. The safety of patients is paramount and ultrasound practitioners must have documented evidence of their competencies, continuing professional development and reflective practice and show evidence of audit of all aspects of the service(s) they provide. Governance arrangements should include protocols and procedures for image acquisition, storage and retention (See section 2. Providers are advised to make their own enquiries with clinical commissioning groups they hold contracts with as the rules are complex. They include diagnostic procedures such as biopsy, fine needle aspiration, hystero-salpingo contrast sonography (HyCoSy), drainage of body cavities and therapeutic procedures such as joint injections. Like all ultrasound examinations the sonographer must be trained, competent and authorised to undertake them.

References:

  • http://soynewuses.org/wp-content/uploads/52724_1_SoyProductsGuide-2015_LR.pdf
  • http://www.awcc.state.ar.us/opinions/alj/2012/mo/MCCUIEN_KIMBERLY_G005312_G108212_20120510.pdf
  • https://teachpsych.org/resources/Documents/otrp/syllabi/TD14sleepanddreams.pdf
  • https://rasopathiesnet.org/wp-content/uploads/2014/01/265_Noonan_Guidelines.pdf
  • https://www.thepharmajournal.com/archives/2012/vol1issue5/PartA/2.2.pdf