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CRITERIA Approved only for members with seizure disorder, post-herpetic neuralgia and other indications supported by well-documented, published clinical studies. Allegra: Requires documentation that member has experienced treatment failure of or intolerance to OTC loratadine. Clarinex, Zyrtec D: Requires documentation of treatment failure with OTC loratadine and Allegra D. Requires documentation that member has experienced failure of or intolerance to at least two formulary SSRIs, including Prozac g ; and Paxil g ; . Approved for members who have had a recent myocardial infarction MI ; or stroke, or have established peripheral arterial disease, or are at increased risk of having a future ischemic event. Members must have documented aspirin allergy or intolerance, or experienced treatment failure with aspirin. Approved if member requires concomitant use with a fibrate Lopid g ; or T4icor g or if treatment failure or intolerance to formulary alternatives Mevacor g ; , Lipitor, Zocor ; . Prevacid: Requires documentation that member has experienced failure of or intolerance to Prilosec OTCTM or Prilosec g ; . Aciphex, Protonix, Prevacid Naprapak, Prevacid Solutab, Zegerid: Requires treatment failure with Prilosec OTC omeprazole and Prevacid. Nexium: Requires treatment failure with Prilosec OTC Prilosec g ; and Prevacid must have tried high dose ; . Approved only for members with narcolepsy and for other indications supported by well-documented, published clinical studies. Requires prior treatment with at least two months of successful continuous, daily Prozac g ; and documentation that continued use of daily Prozac g ; would adversely affect the member's mental health. Requires approval by BCN's Care Management team. For members age 30: requires diagnosis of acne or related disorder.
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Difference in survival time was found between FIV-infected and healthy cats. Prevalence of FeLV has constantly decreased in the last years, and today, prevalence of infection with FIV and FeLV is similar. Comparable risk factors for both infections have been determined. Cats at risk and cats with typical laboratory abnormalities should be tested, and prevalence and risk factors should be taken into consideration before vaccination against FeLV or FIV infection, for instance, tricor zocor.
TriCore Reference Laboratories is making good progress transitioning to the SurePathTM liquid methodology for Pap testing. As part of our ongoing effort to improve the quality of patient care, the change stems from TriCore's own exhaustive evaluation of existing FDA-approved technologies, backed by published research and discussions with other laboratories across the United States and Canada. Several questions about SurePathTM have come up during recent visits with clients to introduce the new system. Here are the answers to those questions: Using FDA-cleared test kits, TriCore will continue to perform testing for Human Papillomavirus HPV ; and Chlamydia trachomatis and Neisseria gonorrhoeae on the same samples you submit for Pap testing. We have completed in-house validation studies on the use of SurePathTM collection vials with these tests. There is no difference in price between ordering these tests as addons to SurePathTM Pap testing where the additional tests are performed on the SurePathTM specimen ; and ordering them on specimens submitted in separate devices. Specimens accidentally collected in non-SurePathTM vials will be processed and tested by TriCore. There is no need to collect a second patient specimen. As always, we will continue to accept conventional Pap smears for testing. Research-study specimens still can be submitted in nonSurePathTM vials. While this is a significant process change for all of us, we do not anticipate any impact on results turnaround times, and will strive to continue providing results within five working days from receipt of specimen. As an extra benefit, the move to SurePathTM will position TriCore to implement automated screening in conjunction with manual screening for all Pap smears liquid-based as well as conventional ; later this year, offer l an additional level of scrutiny for every patient sample. TriCore is excited to offer SurePath'sTM many benefits to you and your patien Please contact me at 505-938-8922 800-245-3296 if you have questio about the program.
Ported by our measurements of respiration rate which showed that total respiration in the P. tricornutum cultures decreased dramatically during the first day in darkness see below ; . In the Phaeodactylum tricornutum culture inoculated with bacteria in Experiment A, we found a decrease of 36 % of the POC over the course of the experiment, a loss of 21 % more POC than in the absence of bacteria. The concentration of DOC in this culture vessel did not increase Fig. 2B ; . Therefore, bacteria may have accounted for a loss of organic carbon totalling 36 % of the initial POC concentration P. tricornutum respiration was negligible ; . Since 40 % of the organic carbon removed by bacteria was DOC released by P. tricornutum compare Fig. 2A with 2B ; , a loss of 21 % of the initial POC may have been due to bacterial decomposition of POC in living diatoms. However, we believe that aggregation of bacteria and diatoms and their attachment to the walls of the culture vessel, rather than the decomposition of living diatoms, may explain most of the additional loss of POC which was observed in this culture vessel. Wall growth in the presence of the mixed bacterial assemblage in the P. tricornutum cultures of Experiment A may have reduced the POC concentration observed in the siphon-collected samples, resulting in a n overestimation of the potential importance of bacteria in POC loss. This hypothesis is supported by the observation that living phytoplankton are not readily susceptible to bacterial attack Droop & Elson 1966 ; , and by the fact that the loss of POC in the P. tricornutum culture inoculated with a pure culture of Pseudornonas halodurans was only 9 % of the POC initially present in this culture Fig. 1B ; .Aggregation and wall growth were much more apparent in Experiment A compared to Experiment B, and were presumably due to bacterial processes carried out by the mixed bacterial assemblage but not by P. halodurans Biddanda 1985 and flavoxate.
Based on the available evidence, SJW appears to be Likely Safe and Likely Effective see Chart 2 ; . Therefore, SJW could be considered for use in patients who have mild to moderate major depression; however, SJW does not appear to offer a significant advantage over conventional SSRI antidepressants. SJW also has the disadvantage of potentially causing numerous interactions with drugs. Since herbal products are not required to follow standardized, good manufacturing practices, it is very possible that SJW products may not always contain what is stated on the label. As a result, patients could end up using products with too little or too much active ingredient. In this respect, conventional antidepressants offer the advantage of providing a consistently manufactured, high-quality product. Although there is enough evidence to consider recommending SJW for some patients, due to potential disadvantages of using SJW, conventional antidepressants should generally be preferred.
Discount prescription drug generic for tricor - drug interactions usually drug interactions occur when the effect of a particular drug is altered when it is taken with another drug or with food and urispas.
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The drug may provoke diarrhoea, although it provides some protection against the bacterial causes of traveller's diarrhoea and flunarizine.
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Cyclic tricorrelation replacing in 10 ; all cyclic moments by their estimation of the form 22 ; . 22 ; , because the cyclostationary signal There is no diculty in computing A similar form is obtained for the moment-based and fluvoxamine.
Competitors will eventually and inevitably overtake any company that stops improving and innovating. Ultimately, the only way to sustain a competitive advantage is to upgrade it. So why are certain companies based in certain regions capable of consistent innovation? The answer lies in four broad attributes, because tricor muscle.
17 with complete enhancemt, 11 with girth enhancement ; The avarage gain in length was 3 cm remarkable in flaccidity ; . The gain in girth was 30% of the original remarkable in erection and flaccidity ; . The overall complications rate was 9.4 %. Two patients had a prolonged wound oozing, 6 owund dehiscence, 1 partial migration of the dorsal implat to the foreskin, 2 phimosis and 1 flatening of the shaft. Conclusion: Elseweifi techniques for enhancement phalloplasty provide permanent excellent results with a low complication`s rate and low costs in comparison the other techniques. Patient's response to coronary heart disease preventive intervention in better access to it: The first results Gertsen M. "Cardiology" Research and Practice Center, Republic of Belarus Objective: The aim of the investigation was to study the response of patients to preventive intervention at the newly organized Prevention Centre for Cardiovascular Diseases. Method: 38 males and 54 females aged 17-62 years underwent detailed examination for cardiovascular system functional state. Each patient was offered to fill in the symptom status questionnaire the first item of which was as follows: "Why did you decide to see the doctor?" All the patients with major risk factors RF ; for coronary heart disease CHD ; were offered to undertake the course of CHD prevention program. Results: Most of the patients especially men failed to specify personally meaningful purposes for their visit to the centre's physician. Major RF were detected in more than 80% of patients. Among them, 22% of men and 30% of women undertook CHD prevention program fully or partially. Conclusions: The majority of patients particularly of men were probably not enough open to discussing their issues and motivations regarding the health personally important to them. That is why they were not motivated enough to perceive lifestyle modification program as relevant to their personal needs. Attempts to understand patients personal needs more fully will help the physician to implement the setting of purposes for preventive intervention proceeding not only from the patients absolute coronary risk but also taking into greater consideration their current personal motivations which will eventually contribute to advanced CHD prevention and luvox.
Anglicanistic Australian College of Theology accredited by the State of New South Wales ; . Thus, Queensland lost the State of Origin also in matters of accreditation! To me, the basic issue was and still is the choice between fallible accreditation of the Church by higher critics such as the Queensland and New South Wales Statist Accreditation Departments -- or infallible accreditation of the Christian Church by her Highest Critic, the Lord Jesus Christ. So, with a heavy heart, on 2nd November 1998 I then writtenly resigned my Professorship at the Seminary -- effective when I would at retirement age turn 65 in December 1999. Here is that letter of mine to the General Assembly of the Presbyterian Church of Queensland: -"Dear brethren, I wish to thank the Queensland Presbyterian Church State Assembly for the privilege of teaching many years at our Theological Hall. Ever since my 1980 Queensland State Assembly appointment to its Faculty of Theology, effective January 1981, I have been the full-time Lecturer in: Systematic Theology; Christian Ethics; Comparative Religions; Christian Variations; History of Doctrine; Westminster Confession of Faith; and, for many years, also Philosophy & Apologetics. "After the departure of Rev. John Campbell, I assumed also the extra duty of CaldwellMorrow Lecturer in Church History, and hence then needed to relinquish the teaching of Philosophy & Apologetics to Rev. Graham Nicholson ; . Since then, assisted by Revs. Kim Dale & Lesleigh Hall, I have also taught Mediaeval and Reformational and Calvinistic and Modern Church History. "Provision will now need to be made for appointing timeously at least one full-time Lecturer or its part-time equivalents ; , effective 1st January 2000, to co-ordinate and to teach the above-mentioned subjects. I would suggest such person s ; be appointed to the Faculty, and certainly a new Faculty Secretary shall be needed. For respectfully, I need to draw the Committee s attention to the following facts: a ; that Lord willing, I hope to attain the age of sixty-five in December 1999; b ; that Rule 7.8 of our Queensland Code declares: A Professor retires from his office when he reaches the age of sixty-five years, unless invited by the State Assembly to continue therein etc.; c ; that I accordingly expect to retire at the end of the year 1999. Yours faithfully in Christ s service, Rev. Professor Dr. ; Nigel Lee. "cc.: General Assembly of the P.C.Q., C O Clerk of the P.C.Q; Queensland Presbyterian Theological College Faculty, C O Secretary; Queensland Presbyterian Theological College Principal." During the next months, the Committee on Training for the Ministry in my absence from its deliberations ; considered three options. The first was to "continue Dr. Lee s appointment annually for a further four years" -- an option unacceptable to me. The second option was to "continue Dr. Lee s appointment until 2001." The third option was "to call for applications for the new Professor to start 1 2001 -- and, if Dr. Lee is willing and funds permitting, ask Dr. Lee to be a Part-Time Lecturer in 2001." I supported the second option which would enable the Seminary to advertize for and finalize the successor to my Professorship effective January 2001 ; . Too, I supported also the first but not the second part of the third option above -- indicating I would not be prepared to lecture on after the end of the year 2000. So the Queensland State Assembly resolved to record its "sincere appreciation and thanks for the work of.the Rev. Prof. Dr. F.N. Lee" and to "continue.the Appointment of Dr. Lee as Professor of Systematic Theology and CaldwellMorrow Lecturer in Church History for the year 2000 under the same conditions and terms as - 99, for example, tricor generic name.
Or co-administration with sinomenine hydrochloride to the rats n 6, each group ; , the pharmacokinetic parameters of paeoniflorin are presented in Table 4. Computation of pharmacokinetic parameters using PK solutions 2.0 software summitpk ; showed that many parameters i.e. tmax , Cmax , AUC, t1 2 , CL and Vd ; were dramatically altered by co-administration of paeoniflorin plus sinome and folic.
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Assessment of the vestibulo-ocular reflex is useful in confirming a peripheral origin of vertigo. It is also useful in determining which labyrinth is abnormal. The vestibulo-ocular reflex can be assessed by performing the head-impulse or head-thrust test. This test involves asking the patient to fixate on the examiner's nose. The examiner then rapidly rotates the patient's head to either side after excluding any significant neck problem ; . A 1020 movement is usually sufficient. In healthy people the eyes remain fixed on the examiner's nose regardless of the head position. In a patient with a labyrinthine lesion, the eyes will move with the head when turned to the side of the lesion and then after a short delay the visual system will trigger a quick corrective eye movement back to the examiner's nose. This quick corrective eye movement is the abnormality sought when undertaking the test. The test will also be abnormal when the head is thrusted to either side in a patient with bilateral peripheral vestibular disease, for example gentamicin vestibulotoxicity. The head-impulse test is also useful in the differential diagnosis of cerebellar infarcts and vestibular neuritis. The test is positive in vestibular neuritis, but negative with a cerebellar infarct and fosinopril.
Collection All scholastic records should be filed in a central location accessible to professional personnel within the school or within the central office. The principal of the school and or his designee s ; or the designated official for record management shall be responsible for the collection of data, record maintenance and security, access to records, dissemination of information from records, and content of the scholastic record s ; . The principal shall provide for the periodic evaluation of the records by professional personnel and the removal of data no longer pertinent. This must be accomplished the last year the student is in the elementary school, the first year the student is in the middle high school, and the end of grade 12 but may be done more frequently at the discretion of the principal. The principal, with the assistance of appropriate staff members, shall establish and use necessary procedures for implementing all regulations relative to student records and to ensure the protection of confidentiality. This collection and transfer of records shall be accomplished annually under appropriate security safeguards and in a timely and efficient manner. All persons collecting or using personally identifiable information in scholastic records shall receive training or instruction regarding the state's policies and procedures for management of scholastic records. Destruction Destruction of records of personally identifiable information collected, maintained or used may take place when records are no longer needed to provide educational services to the student. A. Personally identified information on a handicapped student may be retained permanently unless the parent s ; or eligible student request that it be destroyed. It must be destroyed at request of parent s ; or eligible student, however, a.
In the English speaking countries there are mini-UDRPs for Canada " " ; , Australia ".au" ; and the U.K. " " ; . They are modeled on but differ from the UDRP in significant ways. In fact, the auDRP contains an express warning: 1.4 Please Note: Some parts of the auDRP are substantively different from the UDRP. Prospective complainants should not assume that principles derived from UDRP decisions will be applicable to auDRP disputes. The administrator for the " " country code, for example, offers an appeal procedure and its Dispute Resolution Service Policy defines "abusive registration" as a domain name that "has been used in a manner which took unfair advantage of or was unfairly detrimental to the Complainant's Rights." Under the auDRP, Complainant is required to establish either bad faith registration or bad faith use. The auDRP Policy reads at 4 a ; iii ; : " your domain name has been registered or subsequently used in bad faith." The comments below are limited to the policy and rules implemented by the Canadian Internet Registration Authority "CIRA" ; under the Cira Dispute Resolution Policy "CDRP" ; . For the other Policies, go to Dispute Resolution Policies. In common with the UDRP, a CIRA complainant must prove that it has the right to invoke the CDRP, but after that the provisions deviate. The CDRP has less room for construction than the UDRP in that it defines terms that the UDRP leaves for its Panels. For example, the CDRP defines "rights", "confusingly similar", "use" and "used." Paragraphs 3.3, 3.4 and 3.5 of the CDRP ; , whereas ICANN Panels have defined these terms through the process of construction and geodon and tricor, for example, tric0r medicine.
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Table 6. Treatment-Emergent * Adverse Events in AZILECT 1 mg-Treated Monotherapy Patients.
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Bentz, J., S. Nir, and J. Wilschut. 1983. Mass action kinetics of vesicle aggregation and fusion. Colloids Surf. 6: 333363. Borst, P., and R. O. Elferink. 2002. Mammalian ABC transporters in health and disease. Annu. Rev. Biochem. 71: 537592. Butor, C., and J. Davoust. 1992. Apical to basolateral surface area ratio and polarity of MDCK cells grown on different supports. Exp. Cell Res. 203: 115127. Chan, H. S., and K. A. Dill. 1998. Protein folding in the landscape perspective: Chevron plots and non-Arrhenius kinetics. Proteins. 30: 233. Chang, G. 2003. Structure of MsbA from Vibrio cholera: a multidrug resistance ABC transporter homolog in a closed conformation. J. Mol. Biol. 330: 419430. Chang, G., and C. B. Roth. 2001. Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette ABC ; transporters. Science. 293: 17931800. Chen, Z., and R. P. Rand. 1997. The influence of cholesterol on phospholipid membrane curvature and bending elasticity. Biophys. J. 73: 267276. Demant, E. J., M. Sehested, and P. B. Jensen. 1990. A model for computer simulation of P-glycoprotein and transmembrane delta pH-mediated anthracycline transport in multidrug-resistant tumor cells. Biochim. Biophys. Acta. 1055: 117125. Doppenschmitt, S., H. Spahn-Langguth, C. G. Regardh, and P. Langguth. 1999. Role of P-glycoprotein-mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein. J. Pharm. Sci. 88: 10671072. Evers, R., M. Kool, A. J. Smith, L. van Deemter, M. de Haas, and P. Borst. 2000. Inhibitory effect of the reversal agents V-104, GF120918 and Pluronic L61 on MDR1 Pgp-, MRP1- and MRP2-mediated transport. Br. J. Cancer. 83: 366374. Gaede, H. C., and K. Gawrisch. 2003. Lateral diffusion rates of lipid, water, and a hydrophobic drug in a multilamellar liposome. Biophys. J. 85: 17341740. Goh, L. B., K. J. Spears, D. Yao, A. Ayrton, P. Morgan, W. C. Roland, and T. Friedberg. 2002. Endogenous drug transporters in in vitro and in vivo models for the prediction of drug disposition in man. Biochem. Pharmacol. 64: 15691578. Gottesmann, M. M. 2002. Mechanisms of cancer drug resistance. Annu. Rev. Med. 53: 615627. Gottesmann, M. M., and I. Pastan. 1993. Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu. Rev. Biochem. 62: 385427. Hill, W. G., and M. L. Zeidel. 2000. Reconstituting the barrier properties of a water-tight epithelial membrane by design of leaflet-specific liposomes. J. Biol. Chem. 275: 3017630185.
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| History of TricorTricor fenofibrate ; also reduces serum uric acid levels in hyperuricemic and normal individuals by increasing the urinary excretion of uric acid.
The drug was pulled from the market september 29, 2004 after a clinical trial confirmed long-standing concerns that the drug raises the risk of heart attack and stroke for people who use the drug more than 18 months.
Many of the issues identified for people with mental disorders also apply to persons with addictions and concurrent mental health and substance use problems. However there are some unique factors relative to housing in the field of addictions. Often housing options like supportive recovery or even crisis shelters require abstinence in order to accept clients. This requirement does not parallel the mental health system, since supported housing does not require that clients be free of the symptoms of their mental disorder. The result is that many addicted persons fail to qualify for entry into these facilities, and remain on the streets or in environments that are not conducive to addressing their substance use problems. This situation suggests the potential viability of wet or damp housing options [that is, dry would be substance-use-free] that provide a safe environment for stabilization to clients who are unable to maintain abstinence. The need for transitional housing has frequently been recognized within the addictions service system, and is provided through emergency shelters and supportive recovery facilities.These solutions however are short-term. This creates challenges since people coming out of treatment or supportive recovery may be left with no place to live, a situation which can put their recovery in jeopardy. Stable housing also gives people an environment in which they are better able to deal with their substance use problems. A Vancouver study found that a group of homeless or formerly homeless people were almost all involved with drugs or alcohol, and that they were more likely to address their addiction if they were housed. When people are secure and happy in their living environment, their chances of maintaining their mental health increase dramatically, for instance, what is tricor.
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Cities are cankerous sores on the healthy republican body, consuming her vitality and virtue. For Jefferson, the expansion of cities, and the rising influence of progress perverts the self and leads to the degeneration of society: `I think our governments will remain virtuous for many centuries; as long as they are chiefly agricultural; and this will be as long as there shall be vacant lands in any part of America. When they get piled upon one another in large cities, as in Europe, they will become corrupt as in Europe'.33 Within the principles of republicanism is this deeply rooted fear of the inevitability of history repeating itself, which manifests in the narrative of the invaded pastoral and in the Gothic metaphors of disease, degeneracy, and corruption.
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Patients often use the word "flu" when describing a "common cold". However, subtle differences in symptoms between the two conditions should allow differentiation. It is helpful to remember that the "flu season" tends to be between December and March, whereas the "common cold" can strike at any time. The onset of influenza is sudden and the typical symptoms are shivering, chills, malaise, and marked aching of the limbs, insomnia, a nonproductive cough and loss of appetite. Flu is therefore normally debilitating and a person with flu is much more likely to send a third party to the pharmacy for medication than present in person.
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In consideration of a Health Impairment, again the team looks for evidence of a qualifying handicapping condition, such as an attentional disorder. While a firm diagnosis of such is not contained in [the Student's] file, we are satisfied that parents could produce such documentation if needed. Once a qualifying condition is identified, the team looks at the impact of this disability on the student to make a determination if specially designed instruction is needed, or if accommodations provided in general education are sufficient to meet the student's educational needs. In this case, it appears that [the Student] has developed a number of compensatory strategies over time to help her deal with her attention deficit, which was not diagnosed until this year. Her ability to keep on top of her assignments and to maintain the grades that she earns suggests that she does not require specially designed instruction because of an attention deficit at this time.
1. Koiwai O, Aono S, Adachi Y, et al. Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait. Hum Mol Genet 1996; 5 ; : 645-7. 2. Sampietro M, Iolascon A. Molecular pathology of CriglerNajjar type I and II and Gilbert's syndromes. Haematologica 1999; 84 2 ; : 150-7. 3. Berk PD, Noyer CM. The familial unconjugated hyperbilirubinemias. Semin Liver Dis 1994; 14: 356-85. Arias IM, Gartner LM, Cohen M, et al. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity. J Med 1969; 47 3 ; : 395-409. 5. Kraemer D, Scheurlen M. Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus. Med Klin 2002; 97 9 ; : 528-32. 6. Poddar B, Bharti B, Goraya J, Parmar VR. Kernicterus in a child with Crigler-Najjar syndrome type II. Trop Gastroenterol 2002; 23 1 ; : 33-4. 7. Ito T, Katagiri C, Ikeno S, et al. Phenobarbital following phototherapy for Crigler-Najjar syndrome type II with good fetal outcome: a case report. J Obstet Gynaecol Res 2001; 27 1 ; : 33-5. 8. Younossi ZM, Foroozan P. Treatment of Crigler-Najjar type II with small-dose phenobarbital. Dig Dis Sci 1995; 40 3 ; : 575. 9. Schwegler U, May B, Muller KM. Crigler-Najjar syndrome type II in a 17-year-old girl. Z Gastroenterol 1993; 31 Suppl 2 ; : 83-4. 10. Jakobson A, Gustafsson R. Crigler-Najjar type II syndrome does not normally demand long-term care. Lakartidningen 1986; 3 46 ; : 3921-2. 11. Jansen PL. Diagnosis and management of Crigler-Najjar syndrome. Eur J Pediatr 1999; 158 Suppl 2 ; : S89-94. 12. Watanabe A, Wakabayashi H, Kuwabara Y, et al. Liver bilirubin UDP-glucuronosyltransferase activity in chronic nonhemolytic unconjugated hyperbilirubinemia of adults. Res Exp Med Berl ; 1998; 197 6 ; : 329-36. 13. Seppen J, Bosma PJ, Goldhoorn BG, et al. Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine J Clin Invest 1994; 94 6 ; : 2385-91. 14. Gunn CH. Hereditary acholuric jaundice in a new mutant strain of rats. J Hered 1938; 29: 137-9. Sinaasappel M, Jansen PL. The differential diagnosis of Crigler-Najjar disease, types 1 and 2, by bile pigment analysis. Gastroenterology 1991; 100 3 ; : 783-9. 16. Takahashi M, Ilan Y, Chowdhury NR, et al. Long term correction of deficiency in Gunn rats by administration of a recombinant adenovirus during the neonatal period. J Biol Chem 1996; 271 43 ; : 26536-42. 17. Jones PH. Hyperlipoproteinemias. In: Rakel RE, ed. Conn's Current Therapy 2000. Philadelphia: W.B. Saunders Company, 2000; 578-84. 18. Hoivik DJ, Qualls CW Jr, Mirabile RC, et al. Fibrates induce hepatic peroxisome and mitochondrial proliferation without overt evidence of cellular proliferation and oxidative stress in cynomolgus monkeys. Carcinogenesis 2004; 25 9 ; : 1757-69.
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