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Cell division in eukaryotes takes place through mitosis or meiosis effective erectile dysfunction treatment generic 800 mg viagra vigour free shipping, processes that serve as the foundation for much of genetics erectile dysfunction medication canada purchase 800mg viagra vigour visa. These processes bring about the transmission of genetic information and are the basis of similarities and differences between parents and progeny erectile dysfunction premature ejaculation order viagra vigour 800mg with amex. A eukaryote has a compartmentalized cell structure with components bounded by intracellular membranes; eukaryotes are either unicellular or multicellular xatral erectile dysfunction discount viagra vigour 800 mg without a prescription. Research indicates that a division of life into two major groups, the prokaryotes and eukaryotes, is not so simple. Although similar in cell structure, prokaryotes include at least two fundamentally distinct types of bacteria: the eubacteria (true bacteria) and the archaea (ancient bacteria). Although eubacteria and archaea are similar in cell structure, some genetic processes in archaea (such as transcription) are more similar to those in eukaryotes, and the archaea are actually closer evolutionarily to eukaryotes than to eubacteria. Thus, from an evolutionary perspective, there are three major groups of organisms: eubacteria, archaea, and eukaryotes. In this book, the prokaryotic­eukaryotic distinction will be made frequently, but important eubacterial­archaeal differences also will be noted. In prokaryotic cells, the genetic material is in close contact with other components of the cell-a property that has important consequences for the way in which genes are controlled. Eukaryotic cells therefore require mechanisms that ensure that a copy of each chromosome is faithfully transmitted to each new cell. This generalization-a single, circular chromosome in prokaryotes and multiple, linear chromosomes in eukaryotes-is not always true. The close relationship between the genes of virus and host makes viruses useful for studying the genetics of host organisms. All cellular reproduction includes these three events, but the processes that lead to these events differ in prokaryotic and eukaryotic cells because of their structural differences. Viruses are neither prokaryotic nor eukaryotic, because they do not possess a cellular structure. Neither are viruses primitive forms of life: they can reproduce only within host cells, which means that they must have evolved after, rather than before, cells evolved. In addition, viruses are not an evolutionarily distinct group but are most 1 A virus consists of a protein coat. Prokaryotic Cell Reproduction When prokaryotic cells reproduce, the circular chromosome of the bacterium replicates and the cell divides in a process called binary fission (Figure 2. Replication usually begins at a specific place on the bacterial chromosome, called the origin of replication. In a process that is not fully understood, the origins of the two newly replicated chromosomes move away from each other and toward opposite ends of the cell. In at least some bacteria, proteins bind near the replication origins and anchor the new chromosomes to the plasma membrane at opposite ends of the cell. Finally, a new cell wall forms between the two chromosomes, producing two cells, each with an identical copy of the chromosome. At this rate, a single bacterial cell could produce a billion descendants in a mere 10 hours. The nucleus was once thought to be a fluid-filled bag in which the chromosomes floated, but we now know that the nucleus has a highly organized internal scaffolding called the nuclear matrix. Origin of replication Origin of replication the origins are anchored to opposite sides of the cell. The presence of two sets is a consequence of sexual reproduction: one set is inherited from the male parent and the other from the female parent. Each chromosome in one set has a corresponding chromosome in the other set, together constituting a homologous pair (Figure 2. The two chromosomes of a homologous pair are usually alike in structure and size, and each carries genetic information for the same set of hereditary characteristics. However, these two alleles need not be identical: one might encode brown hair and the other might encode blond hair. But not all eukaryotic cells are diploid: reproductive cells (such as eggs, sperm, and spores) and even nonreproductive cells of some organisms may contain a single set of chromosomes. Because eukaryotes possess multiple chromosomes, mechanisms exist to ensure that each new cell receives one copy of each chromosome. Most eukaryotic cells are diploid, and their two chromosome sets can be arranged in homologous pairs. Eukaryotic chromosomes Each eukaryotic species has a characteristic number of chromosomes per cell: potatoes have 48 chromosomes, fruit flies have 8, and humans have 46.

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Parents short short short short short long short long long long Progeny 4 short and 2 long 8 short 12 short 3 short and 1 long 2 long · Solution For this problem erectile dysfunction muse generic viagra vigour 800 mg with visa, it is useful to erectile dysfunction treatment in sri lanka generic viagra vigour 800mg online first gather as much information about the genotypes of the parents as possible on the basis of their phenotypes erectile dysfunction exercises dvd generic viagra vigour 800 mg visa. We can then look at the types of progeny produced to impotence quitting smoking purchase 800 mg viagra vigour overnight delivery provide the missing information. The 2 long-haired offspring Basic Principles of Heredity 65 must be homozygous (ss) because long hair is recessive and will appear in the phenotype only when both alleles for long hair are present. Because each parent contributes one of the two alleles found in the progeny, each parent must be carrying the s allele and must therefore be Ss. It is theoretically possible, although unlikely, that both parents are heterozygous (Ss Ss). Although no long-haired progeny are observed, it is possible that just by chance no long-haired rabbits would be produced among the 8 progeny of the cross. Let p equal the probability of a kitten being black and q equal the probability of a kitten being gray. The binomial is (p q)6, the expansion of which is: (p q)6 p6 6p5q 15p4q2 20p3q3 15p2q4 6p1q5 q6 (See the section on the Binomial Expansion and Probability for an explanation of how to expand the binomial. The probabilities of p and q are both 1/2; so the overall probability is 20(1/2)3 (1/2)3 20/64 5/16. The following genotypes are crossed: Aa Bb Cc Dd Aa Bb Cc Dd Give the proportion of the progeny of this cross having each of the following genotypes: (a) Aa Bb Cc Dd, (b) aa bb cc dd, (c) Aa Bb cc Dd. It is theoretically possible, although unlikely, that the parent is heterozygous and just by chance no long-haired progeny were produced. If this female has a litter of six kittens, what is the probability that three will be black and three will be gray? To find the probability of any combination of genotypes, simply multiply the probabilities of the different genotypes: a. In corn, purple kernels are dominant over yellow kernels, and full kernels are dominant over shrunken kernels. A corn plant having purple and full kernels is crossed with a plant having yellow and shrunken kernels, and the following progeny are obtained: purple, full purple, shrunken yellow, full yellow, shrunken 112 103 91 94 66 Chapter 3 What are the most likely genotypes of the parents and progeny? If the probability that the difference between observed and expected is due to chance is low, the progeny are not really in the predicted ratio and some other, significant factor must be responsible for the deviation. The observed and expected numbers are: Phenotype purple, full purple, shrunken yellow, full yellow, shrunken Observed 112 103 91 94 Expected 400 100 400 100 400 100 400 100 Purple yellow produces approximately 1/2 purple and 1/2 yellow. A 1: 1 ratio is usually caused by a cross between a heterozygote and a homozygote. Because purple is dominant, the purple parent must be heterozygous (Pp) and the yellow parent must be homozygous (pp). The purple progeny produced by this cross will be heterozygous (Pp) and the yellow progeny must be homozygous (pp). Full shrunken produces 1/2 full and 1/2 shrunken, or a 1: 1 ratio, and so these progeny phenotypes also are produced by a cross between a heterozygote (Ff) and a homozygote (ff); the full-kernel progeny will be heterozygous (Ff) and the shrunken-kernel progeny will be homozygous (ff). Now combine the two crosses and use the multiplication rule to obtain the overall genotypes and the proportions of each genotype: P Purple, full Pp Ff Yellow, shrunken pp ff /4 /4 1 /4 1 /4 1 1 To determine the probability that the difference between observed and expected is due to chance, we calculate a chisquare value with the formula 2 [(observed expected)2/ expected]: 2 = = = (112 - 100)2 (103 - 100)2 (91 - 100)2 (94 - 100)2 + + + 100 100 100 100 32 92 62 122 + + + 100 100 100 100 144 9 81 36 + + + 100 100 100 100 = 1. To obtain this probability, we first calculate the degrees of freedom, which F1 Pp Ff = 1 2 purple * 1 2 full = 1 4 purple, full for a goodness-of-fit chi-square test are n 1, where n equals 1 1 1 the number of expected phenotypic classes. In this case, there are Pp ff = 2 purple * 2 shrunken = 4 purple, shrunken four expected phenotypic classes; so the degrees of freedom 1 1 1 pp Ff = 2 yellow * 2 full = 4 yellow, full equal 4 1 3. We must now look up the chi-square value in a pp ff = 1 2 yellow * 1 2 shrunken = 1 4 yellow, shrunken chi-square table (see Table 3. We select the row corresponding to 3 degrees of freedom and look along this row to find our Our genetic explanation predicts that, from this cross, we should calculated chi-square value. The calculated chi-square value of see 1/4 purple, full-kernel progeny; 1/4 purple, shrunken-kernel 2. A total of 400 progeny were produced; so calculated chi-square value is therefore 0. These observed probability that the difference between what we observed and numbers do not fit the expected numbers exactly. Could the what we expected is due to chance, which in this case is high, difference between what we observe and what we expect be due and so chance is likely responsible for the deviation.

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Food frequency questionnaires are subject to erectile dysfunction generics discount 800mg viagra vigour overnight delivery the same difficulties impotence marriage buy discount viagra vigour 800 mg on line, and have the added problem that estimates of portion size are based on standard measures or impotence of proofreading poem buy viagra vigour 800 mg on-line, in the case of mailed questionnaires erectile dysfunction age range buy viagra vigour 800mg line, are made in the absence of visual aids such as food models or photographs. When respondents are asked to report their intake over a period of weeks they rely largely on generic knowledge of their diet and tend to report items that they are likely to have eaten or items that they routinely eat, rather than items that they specifically remember having eaten during the reference period. This tendency increases with the time interval between Measuring Food Intake 265 Table 10. Often, the purpose of the study also determines the level of precision that is required to meet the study objectives and therefore the sample size. These two considerations are the most important ones in determining the method to be used, because both the method and the size of the sample have implications for the human and financial resources needed for the study. Purpose of the study When dietary data are collected to describe the diet of a group for comparison with that of another group or groups, it is possible to use either a short-term method such as a 24 hour recall or record, or a longerterm method such as food records obtained over several days, a diet history, or a questionnaire about habitual intake. The final choice will depend on factors such as the importance of a representative study sample, the resources available, and the level of precision required. Usually, the most efficient approach is to measure the diet of as many individuals as possible for 1 day. However, if the purpose of the dietary study is to determine the proportion of individuals in the group who are at risk of dietary inadequacy or excess, relative to some standard of reference, then a single day of information on each individual is no longer adequate because it is necessary to have a reliable estimate of the distribution of habitual intake in the group. To determine the distribution of habitual food intake in a group, at least 2 days (preferably not consecutive) of information from each individual or a representative subsample of individuals from the group of interest are needed. If several days of intake are available they can be used to derive a mean intake for each individual and from this the distribution of average intakes for the group. Alternatively, statistical techniques can be used to adjust 1 day intake data, for the day-to-day variation that occurs in individuals, to provide a better estimate of the underlying distribution of habitual intake for the group than is given by the 1 day data (Dodd et al. While the use of appropriate statistical techniques can improve estimates of the proportion of individuals at risk of P:S ratio, ratio of polyunsaturated to saturated fatty acids in the diet. Oxford: Oxford University Press, 1991, with permission from Oxford University Press. Other reasons may include a desire to eat less in order to lose weight or to be seen to conform with dietary recommendations. If this is what happens in practice, then what is measured in short-term dietary records may be actual intake or desired intake, but not usual intake. Many studies have now demonstrated that there is a tendency, in most population subgroups, for shortterm dietary records to provide estimates of energy intake that are on average around 16% lower than would be expected on the basis of measured and/or estimated levels of energy expenditure. The fact that for some groups measurements of energy intake and energy expenditure agree quite closely indicates that it is possible to achieve recording without a concomitant change in diet when there is full cooperation from respondents, and highlights the importance of efforts to achieve such cooperation. When the purpose of the study is to assess the diet of specific individuals it is necessary to obtain dietary information over at least a week and preferably longer. This is best done by obtaining either multiple 24 hour recalls or 24 hour food records over an extended period. The minimum number of days needed to obtain an estimate of nutrient intake with a specified level of confidence differs for different nutrients. Information on energy intake, which tends to show less day-to-day variation than other nutrients, can be obtained over a shorter period (days) than information on a nutrient for which day-to-day intake is much more variable, such as vitamin A (weeks). Precision In studies of groups, precision is primarily a function of sample size, while in studies of individuals it is a function of the number of days of information available. Precision increases with sample size and with the number of days for which information is collected, but so does the cost of the study. Usually, what is required of the nutritionist is to be able to provide the statistician with an estimate of the level of difference that it is important to be able to detect (in nutritional, not statistical terms) and an estimate of the variance or standard deviation for the measurement(s) in question. For example, when looking for differences in energy intake between two groups, would a difference of 500 kJ or 1500 kJ be regarded as biologically significant? Since the variance of a dietary measurement depends not only on the real variation within or between respondents but also on the error of the measurement, the precision of a dietary estimate can be improved not only by increasing sample size but also by reducing measurement error. Resources It is inevitable that the resources available, both financial and human, also influence the choice of method. If the method or methods needed to answer the question are beyond the resources available it is better either to abandon the study or to redefine the question than to collect inadequate data. Repeatability Assessing the repeatability (also referred to as the reproducibility) of a laboratory method is relatively straightforward because, with care, it is possible to reproduce both what is measured and the conditions of measurement. Individuals do not eat exactly the same quantities or the same foods on different days or weeks.

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Since the introduction of vaccines against serogroup C meningococcus in these areas erectile dysfunction clinics purchase viagra vigour 800 mg with mastercard, it now contributes approximately 80% of total disease burden xyzal erectile dysfunction viagra vigour 800mg fast delivery, at least half of which occurs in children under the age of 2 years erectile dysfunction age young quality 800mg viagra vigour. Hajj visas will not be issued without proof of vaccination and a valid International Certificate of Vaccination or Prophylaxis; thus best erectile dysfunction pills side effects purchase 800 mg viagra vigour overnight delivery, all adults and children (>2 years) must have received a single dose of the quadrivalent A/C/Y/W-135 vaccine between 10 days and 3 years before the date of travel. Meningococcal infection is spread by droplet and direct contact, the incubation period being 2­7 days. Babies usually present with pyrexia, irritability, vomiting, limpness, pallor and cold extremities: older children with headache, drowsiness and limb pain. The petechial or purpuric rash, which does not blanch on pressure, is seldom an early feature. Infection is most common in children <4 years old, with a second small peak at 15­20 years. Prevention (chemoprophylaxis) is important in close contacts who should normally be given ciprofloxacin (q. Indications MenC conjugate vaccine: this vaccine, first introduced in 1999, is made from capsular polysaccharide that has been extracted from cultures of N. The polysaccharide is linked (conjugated) to a carrier protein to increase the immunogenicity. Hib/MenC conjugate vaccine: this vaccine is made from capsular polysaccharides of H. It boosts the responses to both Hib and MenC when given at 12­13 months of age to children who have received Hib and MenC conjugate vaccines. Although not yet licensed for children, it is recommended over the plain vaccine in children <5 years because data show a better and longer-lasting antibody response. Contraindications Immunisation should not be offered to any child who is acutely unwell or has had a severe, proven reaction to a previous injection. A booster is provided in the 12­13-month-old child by giving combined Hib/MenC conjugate vaccine, and a further dose of MenC vaccine during adolescence. In infants under 6 months, it can be given at 2, 3 and 4 months with a booster in the second year of life. A booster is again given during the second year of life as long as it is at least 2 months after the second dose. The MenC conjugate vaccine is available either as a lyophilised powder for reconstitution with a diluent (Menjugate Kit) or as a suspension in a syringe (NeisVac-C). After the lyophilised powder is reconstituted, the vaccine must be used within one hour. A third MenC vaccine, Meningitec, is not recommended in children under 12 months of age because it provides inadequate protection when administered as a single dose in infancy. The meningococcal groups A, C, W135 and Y conjugate vaccine is available in two forms as powder for reconstitution with a vial or syringe of diluent that delivers a 0. Prevention and control of meningococcal disease: recommendations for use of meningococcal vaccines in pediatric patients. One or two doses of quadrivalent meningococcal serogroups A, C, W-135 and Y tetanus toxoid conjugate vaccine is immunogenic in 9- to 12-month-old children. Effectiveness of antibiotics in preventing meningococcal disease after a case: systematic review. Cystinosis Cystinosis, first described by Aberhalden in 1903, is a rare autosomal recessive metabolic disorder. Three clinical types of this disorder are described based on the age at diagnosis and degree of cellular cystine deposition: infantile onset, adolescent onset and adult onset. Patients with infantile cystinosis (the most common and most severe) become symptomatic at 3­18 months of age with polyuria, followed by poor growth, photophobia and, if not diagnosed and treated, renal failure by age 6 years. Although most individuals are not diagnosed until after infancy, occasionally family history hastens postnatal diagnosis or allows prenatal diagnosis based on elevated cystine in amniocytes or chorionic villus samples. The renal tubular dysfunction leads to classic renal Fanconi syndrome with impaired reabsorption of glucose, phosphate, amino and organic acids and minerals. Renal phosphate losses lead to vitamin D-resistant rickets; chronic losses of sodium bicarbonate and potassium lead to chronic acidosis and hypokalaemia. With ongoing glomerular damage, there is a progressive renal impairment and an end-stage renal disease.


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