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Seafarers working on Wadan trawlers are less likely to be vulnerable to HIV infection than seafarers working in Walat trawlers because of the different operating styles of each boat-type. Wadan trawlers can catch more fish and so the concession fee is higher than for Walat. Consequently, Wadan must make more trips to cover their costs and this allows seafarers fewer days in port. Frequent trips allow crew members more time to meet with their families and to become aware of HIV messages. Moreover, they are paid a little pocket money for each trip ashore and bonuses and salaries are only paid out at the end of the fishing trip. Seafarers thus earn a lump sum and are able to save it. Their self-esteem improves accordingly and they are able to sustain their ambitions. Wadan crew must be skilled in fishing and net-repair so captains and foremen tend to respect them accordingly. There are approximately 35-40 sailors per Wadan and most originate from the same place in Myanmar. This contributes to social cohesion and adherence to accepted social norms
Neut D, Van Horn JR, Van Kooten TG, Van der Mei HC, Busscher HJ. Detection of biomaterial-associated infections in orthopaedic joint implants. Clin Orthop 2003; 413: 261-8.
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REFERENCES Absar, S. S. 2001. "Problems Surroundings Wages: the Ready Made Garment Sector in Bangladesh." Labour and Management in Development Journal 2: 2-17. Asian Development Bank ADB ; . 2001a. Key Indicators 2001: Growth and Change in Asia and the Pacific. Asian Development Bank: Manila 2001b. "Women in Bangladesh". Asian Development Bank: Manila. Afsar, R. 2000. Rural Urban Migration in Bangladesh. Causes, Consequences and Challenges. Dhaka: University Press Limited 2003. "Internal Migration and the Development Nexus, the Case of Bangladesh." Paper presented at the Regional Conference on Migration, Development and Pro-poor Policy Choices, Dhaka, June 22-24. Ahmed, A., F. Naher, and J.Garrett. 2003. Crime and Violence in Dinajpur. Evidence from a SHAHAR Survey. Final report submitted to CARE-Bangladesh. Ahmed, I. unknown ; "Violence, Mastanocracy and Chronic Poverty." mimeo. ; University of Dhaka Department of International Relations: Dhaka. Ahmed, S. and Z. Sattar. 2004. "Trade Liberalization, Growth and Poverty Reduction: The Case of Bangladesh." World Bank Report IDP-190. Washington, D.C. Amin, S. et al. 1997. "Transition to Adulthood of Female Workers: Some Evidence from Bangladesh." Population Council Policy Research Division Working Paper 102. New York. Amin, S. et al. 2003. "Does Microcredit Reach the Poor and Vulnerable? Evidence from Northern Bangladesh." Journal of Development Economics 70 1 ; : 59-82. Amin, S. et al. 2004. "Poverty and Other Determinants of Child Labor in Bangladesh." Southern Economic Journal 70 4 ; : 876-892. Arndt, C. et al. 2002. "Opportunities and Challenges in Agriculture and Garments: A General Equilibrium Analysis of the Bangladesh Economy." International Food Policy Research Institute IFPRI ; Discussion Paper 107, Bangladesh and the World Trade Organization WTO ; Project. Washington, D.C. Barkat, A. and S Akhter.1999. "Human Deprivation in the Urban Slums and Squatter Settlements in Bangladesh: A Rapid Survey." mimeo. ; Dhaka.
Dear Friends, We have experienced a dramatic increase in the international travel during decades. However, during the last years new problems associated with travel have emerged.Terrorism and international spread of an entirely new epidemic of fatal lower respiratory tract infection, SARS, have challenged the travel industry and travel medicine as never before. During this meeting we will discuss these new frontiers in travel medicine but also more traditional issues such as new vaccines in the pipeline, repellents, the elderly, new travel destinations and pre-travel medicine. We will continue the successful tradition of previous meetings and include both practical and theoretical aspects of travel medicine in our agenda. Most welcome to wonderful Stockholm in May of 2004! The 4th Scandinavian Forum for Travel Medicine 2004 will take place in centre of Stockholm, Sweden, between May 911, 2004 at Stockholm City Conference Centre, Folkets Hus.
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Harada-Ito procedure for excyclotropia consists of advancement and lateralization of the superior oblique tendon. The anterior portion of superior oblique is transposed anteriorly and temporally. This procedure increases the intorsion effect of the superior oblique by 915 degrees. It has found favor with many ophthalmologists. However, there is a limitation, it can not be performed in patients who have undergone superior oblique tenotomy or if there is congenital aplasia of the muscle. The effect of this operation is generally seen to decrease with time. 2 ; For excyclotropia in primary position as well as in depression: Temporal transposition of superior rectus tendon and nasal transposition33-34 of the inferior rectus tendon. These procedures add the action of torsion to the vertical action of the vertical recti. The superior rectus insertion shifted temporally will add an action of intorsion to the elevation action of the muscle. Similarly, the insertion of inferior rectus shifted nasally will add an intorsion to the muscle's depression action figure 3 ; . The amount of correction obtained by these procedures is 8-10 degrees of excyclotropia. 3 ; For excyclotropia in depression only: The temporal transposition of the insertion of the inferior rectus 33 will usually look after the excyclotropia and mirapex
Family of Richardson, Prospect House, Dundalk, Co. Louth 10 Sept 1912 Richardson settlement Counsel's opinion 27 Nov. 1880 Lease for 31 years by Thomas M. Richardson, Prospect House to James G.S. Campbell, Crinsetown, Co. Louth of Richardstown Crinstown. Rent: 125 p.a. Sketch map included 18 April 1891 Agreement between Thomas M. Richardstown, Prospect House and Maxwell J. Boyle, Tullyvin House, Co. Cavan re. fishing on river Dee, Richardstown, Co. Louth. Consideration: 5 24 Sept 1908 Copy probate of the will of Nicholastown, Kilcock, Co. Kildare. P.R. Will dated 16 Oct. 1906 Codicil dated 2 Aug. 1908 John Murray.
20 The largest single section in this chapter discusses the temporal implicatures of the non pastreferring aspects 21739 ; . It is important to remember that this section is directed towards pragmatics, not semantics; i.e., it does not suggest that the tense forms convey time in and of themselves, but rather that the way they are used in various contexts is suited to the range of temporal reference illustrated below. Semantics or code is restricted to aspect but the contextual considerations of pragmatics may result in temporal implicature. Omnitemporal.An omnitemporal proposition is "one that says that something has been, is and always will be so" 217, citing Lyons ; . Often this has been called the gnomic use; Porter uses omnitemporalinstead because it "is more precise as a linguistic category" and because gnomic "seems to imply a value-structure" in addition to the atemporal reference 218 ; . Probably the most common explanation of the gnomic aorist posits a specific past action behind the tense reference e.g., BDF 333; MHT 1: 135 ; . This explanation and several others as well ; is judged inadequate by Porter and inconsistent with his thesis that there is no temporal reference in the Greek verb. If aspect is the only category, then it is not difficult to see the aorist tense form used to describe events that are omnitemporal in nature.12 Illustrative examples of the omnitemporal aorist include the following. John 15: 6a, 8, eja; n mhv ti" mevnh ejn ejmoiv, ejblhvqh e[xw wJ" to; klh'ma kai; ejxhravnqh. ejn touvtw ejdoxavsqh oJ pathvr mou If anyone does not remain in me, he is cast out as a branch and burned. in this my father is glorified ; . Although eja; n. mevnh is best classed as timeless, the underlined forms seem "to establish a general rule of nature. with the aorist depicting the event as complete" 222 ; . Likewise in Rom. 3: 23, pavnte" ga; r h marton kai; uJsterou'ntai th'" dovxh" tou' qeou' for all sin and fall short of God's glory ; . Though this could refer to Adam's sin or the sin of all in Adam ; , more likely the pavnte" and the parallel aorist and present forms indicate an omnitemporal reference. A classic example is found in 1 Peter 1: 2425, pa'sa sa; rx wJ" covrto" kai; pa'sa dovxa aujth'" wJ" a[nqo" covrtou: ejxhravnqh oJ covrto" kai; to; a[nqo" ejxevpesen: to; de; rJh'ma kurivou mevnei eij" to; n aijw'na all flesh is as grass, and all of its glory is as the flower of the field; the grass withers and the flower falls, but the word of the Lord abides forever ; . See also Eph. 5: 29; 1 Tim. 6: 7; and Jas. 1: 11 and mitomycin.
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Freedom Three is the freedom to help build your community by publishing an improved version of the software. People used to say to me, "If the software's free, then nobody will get paid to work on it, so why should anybody work on it?" Well, of course, they were confusing the two meanings of free, so their reasoning was based on a misunderstanding. But, in any case, that was their theory. Today, we can compare that theory with empirical fact, and we find that hundreds of people are being paid to write free software, and over 100, 000 are doing it as volunteers. We get lots of people working on free software, for various different motives. When I first released GNU Emacsthe first piece of the GNU system that people actually wanted to useand when it started having users, after a while, I got a message saying, "I think I saw a bug in the source code, and here's a fix." And I got another message, "Here's code to add a new feature." And another bug fix. And another new feature. And another, and another, and another, until they were pouring in on me fast that just making use of all this help I was getting was a big job. Microsoft doesn't have this problem. [audience laughs] Eventually, people noted this phenomenon. In the 1980's a lot of us thought that maybe free software wouldn't be as good as the non-free software, because we wouldn't have as much money to pay people. And of course people like me, who value freedom and community, said, "Well, we'll use the free software anyway." It's worth making a little sacrifice in some mere technical convenience to have freedom. But what people began to note, around 1990, was that our software was actually better. It was more powerful, and more reliable, than the proprietary alternatives. In the early '90's, somebody found a way to do a scientific measurement of reliability of software. Here's what he did. He took several sets of comparable programs that did the same jobsthe exact same jobsin different systems. Because there were certain basic Unix-like utilities. And the jobs that they did were more.
The following insurance carriers and payers currently use Emergis to adjudicate drug claims for their clients. In the following chart, the preceding numbers represent the insurance carriers' or payers' identification number, also commonly referred to as the carrier identification or the carrier number. 11 16 17 Great West Life Sun Life Financial BCE Group of Companies Reliable Standard Life Chamber of Commerce Equitable Life DA Townley Gingras 37 40 44 WSBC-BC Global Johnston Group WSIB PBAS La Capitale L'Excellence eSampling and mitotane.
PCIneo plasmid. Using this approach, a 237-bp fragment would be amplified by RT-PCR of transfected COS-1 cell total RNA when no exonic sequences were present within the genomic fragment being scanned. If exonic sequences were present, however, a longer DNA fragment would be amplified, corresponding to an mRNA in which exons were spliced into the pCIneo-derived transcript Fig. 3 ; . Exonic sequences were trapped from within a large 9-kbp HindIII restriction fragment that included exon 1 of mouse Has2 plus 6 kbp of the first intron. Exonic sequences were not trapped from within intron 2 nor from the region immediately upstream of Has2 exon 1 Fig. 3 and data not shown ; . Sequence analyses indicated that 4 exons had been trapped and that two RNA species had been trapped, corresponding to the short and long splice variants similar to those seen for human HASNT. Significantly, the alternate splice site was located in an identical position in human and mouse. Two of the four trapped exons shared complementary sequence to exon 1 of mouse Has2 Fig. 3 ; . The total antisense sequence amounted to 266 nucleotides for L-Hasnt and 181 for S-Hasnt. Sequence analyses revealed that all of the putative mouse Hasnt exons were flanked by consensus splice acceptor and donor sequences. Scanning of sequences located within the proximal promoter region for mouse Has2 resulted in the identification of consensus poly A ; signals encoded on the opposite antisense ; strand of the mouse Has2 locus in a location equivalent to those poly A ; signals that were identified for the human HASNT gene. EST data base searches identified one putative transcript GenBankTM accession number BY724531 ; that included one of the antisense exons for mouse Hasnt, in addition to what appears to be a sequence split into two additional exons that are derived from a region 92110 kbp further downstream with respect to our Hasnt exons, i.e. located 5 of the mouse Has2 gene. Thus, it is formally possible that Hasnt exons in the mouse are part of a transcript in which exons are distributed over a much greater distance than that observed for human HASNT. Overall, our data suggest that the mouse Hasnt gene is made up of at least 6 exons; the first exon would not have been trapped using our exon-trapping approach, which relies upon the presence of flanking splice donor and acceptor sequences. A short ORF was predicted in the mouse Hasnt cDNA sequence, but the predicted polypeptide shared no significant sequence identity to any known gene product nor to the short polypeptide predicted from within the human HASNT sequence. The possible functionality of this predicted polypeptide is considered questionable. Expression of HASNT in U2-OS Cells and Human Tissues-- The expression of HASNT in U2-OS cells and in different tissues was examined by RT-PCR. The HASNT RT-PCR amplified a 264-bp fragment, which represented the expected size of the HASNT RT-PCR amplicon Fig. 4 ; . It should be stressed that only HASNT cDNAs and not HAS2 cDNAs ; would be amplified using this approach. First, we used a gene-specific reverse primer corresponding to the HASNT sequence during the first strand synthesis. Second, the primers were designed to flank an intron of HASN T, such that a fragment of the expected size would only be amplified from first strand cDNA generated off a correctly spliced HASNT mRNA. The identity of this RT-PCR fragment was confirmed as HASNT by automated DNA sequencing. Northern analyses of 30 g U2-OS cell total RNA using the HASNT probe showed a HASNT-positive fragment of 6 kbp data not shown ; . In addition, Northern analyses identified a transcript of 6.6 kbp in skeletal muscle and 2.0 kbp in liver. This would suggest that the 1.6-kbp sequence that we have derived may be part of a larger transcript in most human cells and tissues. We examined the tissue expression pattern by RT-PCR and automated DNA sequenc.
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DISCUSSION To our knowledge, augmented by a MEDLINE search of the years 1966 2001 using the key words "preeclampsia, " "epidural analgesia, " and "clinical trials, " the trial reported herein is the first randomized comparison of epidural and intravenous opioid analgesia in a selected population of women with severe preeclampsia. Lucas et al10 reported a randomized trial of 738 women with pregnancy-induced hypertension who received epidural analgesia with bupivacaine versus intravenous meperidine. Although there was no difference in the cesarean delivery rate, the majority of their population did not have severe hypertensive disease. Similar to our findings, these investigators noted significantly greater requirements for ephedrine in women with severe preeclampsia who received epidural analgesia and reported no attributable adverse effects. Wallace et al evaluated the administration of epidural analgesia in women with severe preeclampsia who underwent cesarean delivery, and reported that clinically significant hypotension requiring intravenous ephedrine occurred in 30% of women who received epidural analgesia.11 A retrospective study of 200 women with pregnancyassociated hypertension demonstrated significantly higher rates of ominous fetal heart rate tracings in the hypertensive cohort as compared with a cohort of 2023 normotensive gravidas.4 This effect was more pronounced in the hypertensive group who received epidural analgesia. Compared with normotensive women with epidural analgesia, women with hypertension and epidural analgesia had a three-fold increased risk of ominous fetal heart rate tracings. In the cohort that did not receive epidural analgesia, there was a two-fold increased risk between the hypertensive and normotensive women. In the current study, epidural analgesia appeared to be a safe method of pain relief with low rates of maternal hypotension and maternal morbidities; however, our sample size was not large enough to confirm the relative safety of these two methods with regard to uncommon complications. The apparent safety of epidural analgesia in our population is likely a function of both our intrapartum management of women with severe preeclampsia as well as our standardized protocol for administration of epidural analgesia. In agreement with previous studies, 12 epidural analgesia provided superior pain relief and had the additional advantage of facilitating surgical anesthesia in women who underwent a cesarean delivery.13 All three of the observed neonatal deaths occurred in infants born to women who received epidural analgesia; however, these infants were all extremely preterm 24, 26, and 28 weeks' gestation ; , and death occurred remote and modafinil.
Recebido do Received from ; Department of Anesthesia, Mount Sinai Hospital, University of Toronto, Ontario, Canada 1. Clinical and Research Fellow in Obstetric Anesthesia, Mount Sinai Hospital 2. Associate Professor of Anesthesia and Obstetrics and Gynecology, University of Toronto; Director, Obstetric Anesthesia, Mount Sinai Hospital 3. Assistant Professor, Department of Anesthesia, University of Toronto; Staff Anesthesiologist, Mount Sinai Hospital Apresentado Submitted ; em 18 de fevereiro de 2004 Aceito Accepted ; para publicao em 16 de agosto de 2004 Endereo para correspondncia Correspondence to ; Mrinalini Balki, M.D. Department of Anesthesia, Mount Sinai Hospital 600 University Avenue, Room 1514 Toronto, Ontario, M5G 1X5 E-mail: mrinalbalki yahoo Sociedade Brasileira de Anestesiologia, 2004.
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Other xanthine derivatives Aminophyline Choline theophylline Diprophylline Caffeine, etc. CNS stimulants Ephedrine hydrochloride Ephedra herb, etc. Sympathetic nervous system stimulants -stimulants ; Isoprenaline hydrochloride Clenbuterol hydrochloride Tulobuterol hydrochloride Terbutaline sulphate Procaterol hydrochloride, etc. Adverse reactions due to -stimulants such as hypokalemia or cardiovascular symptoms tachycardia, arrhythmia, etc. ; may be potentiated. Caution should be exercised with respect to adverse reactions. In the event of abnormal findings, appropriate measures such as discontinuation of the medication or reduction in dosage, should be taken. Adverse reactions such as arrhythmia, etc. may be potentiated. Also, continuous coadministration with halothane may cause an increase in the blood theophylline concentration. Caution should be exercised with respect to adverse reactions. In the event of abnormal findings, appropriate measures such as discontinuation of the medication or reduction in dosage, should be taken. Convulsions may occur. Caution should be exercised with respect to convulsions. In the event of abnormal findings, appropriate measures such as the administration of an anticonvulsant, should be taken. Symptoms of theophylline toxicity may occur. [See "Overdosage" section.] Caution should be exercised with respect to adverse reactions. In the event of abnormal findings, appropriate measures such as discontinuation of the medication or reduction in dosage, should be taken and modicon.
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Phenytoin Dilantin ; Capsule, extended release: 30 mg, 100 mg Capsule, immediate release: 100 mg Injection: 50 mg mL Suspension, oral: 125 mg 5 mL Tablet, chewable: 50 mg Physostigmine Antilirium ; Injection: 1 mg mL Phytonadione Vitamin K1, Mephyton, Konakion ; Injection, aqueous colloidal: 2 mg mL, 10 mg mL Injection, aqueous IM only ; : 2 mg mL, 10 mg mL Tablet: 5 mg Pilocarpine Isopto Carpine ; Solution, ophthalmic, as hydrochloride: 1%, 2%, 4% Pimecrolimus Elidel ; Cream: 1% Pneumococcal Vaccine, Polyvalent Pneumovax ; Injection, single dose Podophyllum Resin Liquid, topical: 25% in benzoin Poliovirus Vaccine, Inactivated IPOL ; Injection, single dose Polycarbophil Fibercon, Fiber-Lax ; Tablet: 500 mg, 600 mg, 625 mg, 650 mg Polyethylene Glycol MiraLax ; Powder for oral solution Polymyxin B Bacitracin Polysporin ; Ointment, ophthalmic: Polymyxin B 10, 000 units Bacitracin 500 units Ointment, topical: Polymyxin B 10, 000 units Bacitracin 500 units Powder, topical: Polymyxin B 10, 000 units Bacitracin 500 units Polymyxin B Neomycin Neosporin ; Cream: Polymyxin B 10, 000 units Neomycin 3.5 mg Polymyxin B Trimethoprim Polytrim ; Solution, ophthalmic: Polymyxin B 10, 000 units Trimethoprim 1 mg mL and molindone.
The as as male rats 1213 wk of age ; were deeply anesthetized with ether and perfused through the heart with 3% glutaraldehyde in 10 mM Hepes saline pH 7.3 ; . The perfusion-fixed testes were cut into small pieces 1 mm3 ; and fixed for another 2 h. After fixation with osmium tetroxide, the specimens were processed for conventional electron microscopy. Ultrathin sections about 80 nm ; stained with uranyl acetate and lead citrate and miralax.
Such repairs, alterations or modifications arises from the particular manner in which Lessee uses the Premises, and repairs, alterations or modifications to the Premises as a result of any laws, orders and regulations of the federal, state and municipal governments or any of their departments affecting the Premises which are required of all owners and tenants generally, and do not arise from the particular manner in which an owner or tenant uses its premises, shall be undertaken by and at the sole cost and expense of Lessor and same may be included in Operating Costs pursuant to Article 23 of this Lease. Lessor shall, subject to the same being included in Operating Costs except as expressly excluded in the immediately preceding sentence. ; , make all necessary repairs to the Premises, Common Facilities and to the assigned parking areas, if any, except where the repair has been made necessary by misuse or neglect by Lessee or Lessee's agents, servants, visitors or licensees, in which event Lessor shall nevertheless make the repair but Lessee shall pay to Lessor, as Additional Rent, immediately upon demand, the costs therefor. All improvements made by Lessee to the Premises, which are so attached to the Premises, shall become the property of Lessor upon installation. Not later than the last day of the Term, Lessee shall, at Lessee's expense, remove all Lessee's personal property and those improvements made by Lessee which have not become the property of Lessor, including trade fixtures, cabinetwork, movable paneling, partitions and the like; repair all injury done by or in connection with the installation or removal of said property and improvements; and surrender the Premises in as good condition as they were at the beginning of the Term, reasonable wear and damage by fire, the elements, casualty or other cause not due to the misuse or neglect by Lessee, Lessee's agents, servants, visitors or licensees excepted and excluding maintenance and repairs required to be undertaken by Lessor. All other property of Lessee remaining on the Premises after the last day of the Term of this Lease shall be conclusively deemed abandoned and may be removed by Lessor, and Lessee shall reimburse Lessor for the cost of such removal. Lessor may have any such property stored at Lessee's risk and expense. ENVIRONMENTAL b ; COMPLIANCE WITH ENVIRONMENTAL LAWS. Lessee shall, at Lessee's own expense, promptly comply with each and every federal, state, county and municipal environmental law, ordinance, rule, regulation, order, directive and requirement, now or hereafter existing "Environmental Laws" ; , applicable to the Premises, Lessee, Lessee's operations at the Premises, or all of them, except if there is any violation of Environmental Laws with regard to the Premises existing at the date of this Lease, Lessor shall comply therewith at its sole cost and expense, which cost and expense shall not be included in Operating Costs. c ; ISRA COMPLIANCE. Lessee shall, at Lessee's own expense, comply with the Industrial Site Recovery Act, N.J.S.A. 13: 1K-6 et seq., the regulations promulgated thereunder and any amending and successor legislation and regulations "ISRA" ; , if and to the extent the need for such compliance is triggered by Lessee having become an Industrial Establishment as defined in ISRA ; with respect to its use of the Premises. d ; INFORMATION TO LESSOR. At no expense to Lessor, Lessee shall promptly provide all information and sign all documents requested by Lessor with respect to compliance with Environmental Laws. e ; LESSOR AUDIT. Lessee shall permit Lessor and its representatives access to the Premises, from time to time, to conduct an environmental assessment, investigation and sampling, all at Lessor's own expense. If such assessment, investigation and sampling reveal a violation of this provision, the cost shall be borne by Lessee. f ; LESSEE REMEDIATION. Should any assessment, investigation or sampling reveal the existence of any spill, discharge or placement of Contaminants in, on, under, or about, or migrating from or onto the Premises, the Building or the Office Building Area, as a result of the action or omission of Lessee or a "Lessee Representative", then, in addition to being in default under this Lease and Lessor having all rights available to Lessor under this Lease and by law by reason of such default, Lessee shall, at Lessee's own expense, in accordance with Environmental Laws, undertake all action required by Lessor and any governmental authority, including, without 4 and moxifloxacin.
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Of monoglycerides, diglycerides, triglycerides and free fatty acids in biological samples. Gun. Chem. 17, 145 1971 ; . 2. Folch, J., Less, M., and Sloane Stanley, G. A., A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Ghem. 226, 497 1957 ; . 3. Carr, J. J., and Drekter, I. J., Simplified rapid technique for the extraction and determination of serum cholesterol without saponification. Glin. Chem. 2, 353 1956 ; . 4. Abell, L. L., Levy, B. B., Brodie, B. D., and Kendall, F. E., Simplified method for the estimation of total cholesterol in serum and demonstration of its specificity. J. Biol. Chem. 195, 357 1952 ; . 5. Anderson, J. T., Keys, A., Fidanza, F.
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