Glibenclamide


Evidence and i agree it would be good to do some studies on life-span and general health of kratom users-or some animal studies on lifespan of those given kratom how do you get a dog to chew a quid of leaf. She is currently taking oral antidiabetic agents namely metformin, a biguanide, and glibenclamide, a sulphonylurea.

I feel the difference the next day if i forget to take glibenclamide.

Improves patient outcomes. Thus the committee advises against routine measurement in the primary prevention population. The potential benefit of therapies may be substantial and should be considered an important area of future research. Regarding cutpoints to utilize for identifying high risk patients, the committee suggests the 80th percentile of the control reference population. Note that it is well known the reference intervals for BNP and particularly NT-proBNP show a dependence on age and gender. As with any biomarker, analytical specifications for BNP and NT-proBNP must be driven by a balance between physiology and clinical utilization. A recent report aimed at improving the quality of immunochemical measurements of BNP and NTproBNP was recently published by the IFCC Committee on Standardization of Markers of Cardiac Damage 26 ; . The recommendations proposed were intended for use by manufacturers of commercial assays, by clinical laboratories using those assays, by clinical trial groups and research investigators, as well as by regulatory agencies such as the United States Food and Drug Administration 26 ; . This document was developed by experts who reviewed and abstracted the scientific literature pertaining to the needed quality specifications for BNP and NT-proBNP assays. These evidence-based recommendations encourage manufacturers of BNP and NT-proBNP diagnostics to include information in their package inserts that includes assay design, preanalytical performance characteristics, analytical performance characteristics, and clinical performance. In addition, regulatory agencies are encouraged to adopt a minimal and uniform set of criteria to help guide manufacturers seeking clearance for new and, or improved assays. Knowledge in the context of the natriuretic is evolving rapidly. Utilization of BNP and NT-proBNP measurements is complicated by preanalytical issues such as natural biological variability, age, and gender differences, analytical issues such as specimen stability and assay performance, as well as post analytical issues such as result reporting and recognizing that different diseases and patient populations must utilize the test differently. Communication, cooperation and education, both initially and continuous learning, are vital components for appropriate utility of BNP and NTproBNP measurements in patient care, for instance, glimepiride glibenclamide.

Print this article forward this article register for free email updates metformin glibenclamide glucovance ; for type 2 diabetes mellitus met-for-min, gli-ben-cla-mide ; this document has been updated since its original release. I use chemotherapy up front in patients with life-threatening or very bulky HER2-positive disease. In these patients, chemotherapy selection depends on their adjuvant treatment. Traditionally we'll start with a taxane and trastuzumab. For patients in visceral crisis or with bulky disease, I've been adding weekly carboplatin. Although Nick Robert's randomized trial evaluated an every threeweek schedule, we see a fair amount of thrombocytopenia with that treatment schedule, so we've been using weekly carboplatin, paclitaxel or docetaxel, and trastuzumab. As soon as the patients have a good response, we discontinue the chemotherapy and continue with every three-week trastuzumab alone. I also use capecitabine with trastuzumab, and it's been very effective. Patients with HER2-overexpressing disease are often very receptive to capecitabine. So it's important to use that drug as part of the treatment approach for these patients and glucovance. Table 6. Drugs used on the Pediatric clinic in year 1996. and percentage of humanitarian assistance. During the study period, treatment regimen was changed in 2 patients. A 42 year old male patient treated with metformin, 250 mg bd had no improvement in glycaemic status for 2 months and could not tolerate higher doses of the drug due to gastric problems. He was prescribed glibenclamide 2.5 mg bd with which glycaemic control improved. A 30 year old female did not show glycaemic response with pioglitazone and when changed to glimepiride after a month, showed significant reduction in blood glucose. As shown in Table 2, baseline FPG, 2h plasma glucose 2h PG ; and HbA1c values were the lowest in the control group, due to the selection criteria. Between the other three groups no significant difference was observed in these parameters. Significant improvement in glycaemic parameters were observed in all groups. Mean cholesterol values decreased significantly in groups 3 and 4. LDL cholesterol showed a significant reduction only with pioglitazone 135 35 to 112 23 mg dl, p 0.001 ; . Glimepiride and pioglitazone reduced the mean TG values. HDL cholesterol showed an improvement with metformin and pioglitazone, though statistical significance was seen with pioglitazone only. Improvement in HbA1c, FPG, 2h PG are shown in Table 3. Patients on diet therapy showed the least improvement while the difference between the other groups was not statistically significant. HbA1c of 7.5% was seen in 73.3%, 50%, 52.4% and 87% of subjects in groups 1 to 4, in respective order. FPG showed improvement in 57% of patients treated with metformin while the other two groups showed improvement in significantly higher percentages. Table 4 shows the hormonal profile in the study groups and inderal. Figure 1. Dose-response relations relating coronary conductance and plasma adenosine concentration under baseline conditions and after glibenclamide GB ; , 0.3 mg kg, and an additional 0.7 mg kg. L liter.
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Knombre works with established businesses and start-ups in need of unique, url-able names and identities with strategic meaning and lasting appeal and itraconazole. One in 10 teenagers self-harms, according to the largest ever study of self-harm among 1516-year-olds, led by Professor Keith Hawton of Oxford's Centre for Suicide Research. The research took place in 41 schools across Oxfordshire, Northamptonshire and Birmingham in 2000 and 2001, and surveyed 6, 000 teenagers. Pupils were asked to complete a questionnaire which explored issues surrounding self-harm and suicidal thoughts, together with other factors such as depression, anxiety, impulsiveness and self-esteem. The findings are published in a book called By Their Own Young Hand Jessica Kingsley Publishers ; , which also includes a review of the international literature on adolescent self-harm. Additionally, the book provides advice for teachers, social workers, mental health professionals, and others likely to come into contact with those who self-harm or are at risking of self-harming. The survey found that 11 per cent of girls had self-harmed in the last year, and three per cent of boys. Thirteen per cent of the self-harming incidents resulted in a hospital visit. Motives given for self-harming included wanting relief from a terrible state of mind, wanting to punish oneself, and wanting to die. The majority of those who said they self-harmed said that it was an impulsive act rather than something they had thought about for a long time. For both sexes, deliberate selfharm was correlated with consumption of cigarettes, alcohol and drug use. Self-harm was more common in pupils who had been bullied and was very common in those who had been physically or sexually abused. Awareness of selfharm by peers or family members was also important. Professor Hawton said: `Deliberate self-harm is one of the most important health issues in adolescents. While the behaviour will for many individuals be a temporary phenomenon, we now know that self-harm in adolescence often foretells mental health problems and further self-harm in young adulthood. Preventive initiatives, which are discussed in the book, are therefore crucial.'. Analysis conducted by the Guild shows that females still predominate once figures have been adjusted to allow for total male female population numbers in various age cohorts. Table 2.9 lists the number of Item 900 services per 100, 000 people by gender and age cohort and kamagra.
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Fig effects of glibenclamide in anesthetized dogs on the time courses of map, ci, svr, and lvsw, expressed as the difference d ; between the value recorded at the indicated time point and the value recorded at 60 min.

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859-866 8 ; publisher: blackwell publishing previous article next article view table of contents key: - free content - new content - subscribed content - free trial content abstract: aims  this study compared the effects of 52 weeks' treatment with pioglitazone, a thiazolidinedione that reduces insulin resistance, and glibenclamide, on insulin sensitivity, glycaemic control, and lipids in patients with type 2 diabetes and ketoconazole.

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138. Gray D, Moskos M, Keller T. Utah youth suicide study new findings. Washington, DC, American Association of Suicidology. Proceedings of the 36th Annual Meeting of the American Association of Suicidology. 2003. 139. Food and Drug Administration. Class Suicidality Labeling Language for Antidepressants. Available at : fda.gov cder drug antidepressants PI template . 2005. 140. DeRubeis RJ, Hollon SD, Amsterdam JD, et al. Cognitive therapy vs medications in the treatment of moderate to severe depression. Arch Gen Psychiatry. 2005; 62: 409-416, for example, dissolution.

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22, 23 in two studies, mean postprandial glucose excursions difference between 2 hour-postprandial glucose and fpg ; were reduced slightly more than with metformin or glibenclamide monotherapy 3 7 mmol l and 4 9 mmol l, respectively and lamisil. EDUCATIONAL OBJECTIVE: At the conclusion of this presentation, the participants should be able to discuss the presentations and outcomes of children with subperiosteal orbital abscesses secondary to acute sinusitis. Participants should be able to explain differences in the presentations of patients managed medically compared to patients treated surgically. Participants should be able to discuss our criteria for which children with medial orbital abscesses may be managed medically. OBJECTIVES: To evaluate the presentations and outcomes of pediatric orbital abscesses secondary to acute sinusitis treated both medically and surgically. STUDY DESIGN: Retrospective review of children admitted with orbital abscesses secondary to acute sinusitis from January, 1995 to July, 2002. METHODS: Records of 43 patients were reviewed. RESULTS: Thirty-eight abscesses were medially located and 5 were superiorly located. Children with superior orbital abscesses were older mean 12.4 years ; than patients with medial orbital abscesses mean 6.5 years, p 0.01 ; . 18 patients resolved their infection with medical management only and 25 patients underwent surgical drainage. Abscess drainage was performed endoscopically in 18 and externally in 7 patients. Purulence was identified in 22 of surgical patients. Compared to 22 patients with drained purulence, the 18 patients with abscesses managed medically had significant differences p 0.05 ; for: chemosis in 2 18 11.1% ; vs. 14 22 63.6% ; , proptosis in 10 18 55.6% ; vs. 20 22 90.9% ; , elevated intraocular pressure in 0 18 0% ; vs. 11 22 50% ; , severe restriction of extraocular movements in 1 18 5.6% ; vs. 12 22 54.5% ; , and vision loss of 20 40 worse in 1 18 5.6% ; vs. 7 22 31.8% ; . Significant differences were found for the means for age 6.1 vs 9.0 years ; , abscess height 0.8 vs. 1.6 cm. ; , abscess width 0.3 vs. 1.4 cm ; , abscess length 1.1 vs 1.8 cm ; , and length of stay 4.3 vs. 6.1 days ; . Persistent morbidities occurred in no patients managed medically and in 2 25 8% ; managed surgically. CONCLUSIONS: Children with small medial orbital abscesses secondary to acute sinusitis may be managed medically with favorable outcomes. 9: 30 TRIOLOGICAL SOCIETY THESIS PRESENTATION Aerodynamics of the Human Larynx During Vocal Fold Vibration Randall L. Plant, MD MS * , Anchorage, AK, for example, what is glibenclamide. Directed by the guy who directed the awesome City of God. This one's about a guy whose wife is brutally murdered. He goes a journey across Africa and Europe to find the truth behind the murder and uncovers a vast conspiracy. The last time I uncovered a vast conspircay my hand was cut off. Oh yeah, and pharmaceuticals are evil. Matthew Broderick plays Ferris Bueller, who is an expert at escaping school. He fools his parents and outwits his obsessive principal, and then steals his friend's father's convertible. Then he dies- er shit, I made that up. But yeah, awesome 80's movie that is fun and very watchable with soy sauce. So Disney shut down its old 2D animation studios, and from now on they're planning on only dealing in 3D animation. Chicken Little is their first attempt. And no, this isn't from Pixar, the people who gave you Toy Story and The Incredibles; this is Disney's own inept attempt. Still, if you want to see a mediocre animated movie, you should enjoy this. Asian horror is where it's at lately. The Ring, Dark Water, and The Grudge are just some of the Hollywood imports from Japan. This film is a collection of 3 short horror films from across Asia, and they're pretty damn extreme. Extremely bloody, or disturbing, or freaky; I'm not sure, but they are extreme. Are you extreme enough the take it? Just watch your extremities. What the hell I talking about? and lansoprazole.

Do not drive, operate dangerous machinery, or participate in any hazardous activity that requires full mental alertness until you are sure the medication is not affecting you in this way.

Figure 3. Effects of glibenclamide 20 M ; on stimulation of [Ca2 ]i in isolated human adipocyte. Glibenclamise was added at time designated by the arrow. [Ca2 ]i measurement as described in Materials and Methods and levofloxacin. Four weeks later his dosage of glibenclamide was increased to 5 mg thrice a day for more effective control of diabetes. The present study was carried out solely on cells exhibiting the characteristics of the dopamine-containing neurons of ventral midbrain reviewed in Lacey, 1993 ; . Establishing this was important for the interpretation of the present findings in the context of previous work by others, and also on the functional significance of the results. It has been reported that anoxia either had no effect on dopamine neurons recorded intracellularly in brain slices Murphy and Greenfield, 1992 ; , or caused a hyperpolarization that was ghbenclamide insensitive Mercuri et al., 1994 ; . Our observations suggest that under conditions such as anoxia, where intracellular ATP levels are likely to fall, sulfonylurea-sensitive potassium channels would be expected to be activated. Indeed, anoxia has been shown to activate sulfonylurea-sensitive potassium channels in acutely dissociated rat dopamine neurons Jiang et al., 1994 ; . However, as these observations, as well as our own, were made on rats aged 9-20 d, it is conceivable that developmental changes, or some other events during experimental anoxia in adult brain slice preparations, may serve to obscure the consequence of the increased conductance through K-ATPs. The high-affinity `H-glibenclamide binding site in substantia nigra appeared insensitive to 6-hydroxydopamine lesions, which reduced considerably the numbers of dopamine neurons Hicks et al., 1994 ; . As indicated above, reconciliation of this with our demonstration of the effectiveness of gibenclamide may be that the high-affinity ?H-glibenclamide binding site is distinct from and lexapro and glibenclamide. In Sections 6.2 and 6.4 we discussed some reasons for not including price in our model. Looking at the data of the rhinitis category we find three more arguments. Firstly, there are no generic drugs within this category see Section 6.2 ; . Secondly, we observe small differences in price positioning among the drugs. This seems to indicate that if there are no big differences in the price of competing drugs, factors other than price, such as advertising, are used by firms to compete. Price does not seem to be a key factor in this category to influence the switching from one branded drug to another. Thirdly, multicollinearity problems appeared when we included both price and the other marketing instruments in the model. Although we focus on the rhinitis category, an especially interesting category given the large number of introductions 14 out of 16 drugs ; in the period 19932000, we also calibrate the model on another two categories: and asthma. These two categories together with rhinitis belong to the "Top-10 market" of prescription drugs in the US in 2000; i.e. the 10 major categories of prescription drugs that have the prescription drugs with the largest amount of sales among those with annual sales of 25$ million or more in the US in 2000. Although and asthma categories have a lower proportion of new drugs than rhinitis 9 out of 20 drugs and 11 out of 26 drugs, respectively ; , they are also appropriate for calibration of our model for three reasons. First, these two categories use the same promotional instruments as rhinitis: detailing, medical journal advertising, physician meetings and also directto-consumer advertising. Second, it is interesting to analyze the results for other categories with similar and different characteristics to rhinitis. This is the case for and asthma. The asthma category resembles the rhinitis category in terms of symptoms and seasonal patterns, whereas the is completely different. Third, in contrast to the rhinitis category, the category and the asthma category contain both branded drugs and generic drugs. Table 6.5 shows code identification number of the drug ; , name, kind of drug branded or generic drug ; and introduction month for each drug within each category.

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24 26 safety issues metformin glibfnclamide fixed-dose combination tablets can cause gastro-intestinal adverse effects, hypoglycaemia and weight gain and loratadine.

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2 By `government departments', we mean those bodies or agencies within national governments that are responsible for particular areas of government functioning. Our intent is to generalize for types of government department and not to refer to specific national agencies, although there are obviously important national distinctions in the constitution and function of such bodies. Similarly, we believe that the international scope of medical and pharmaceutical research and the transnational nature of many of the major pharmaceutical companies make broad generalizations about attitudes towards pharmacogenomics appropriate for our discussion of rhetoric and hype. 3 The use of tradenames is for product identification purposes only and does not imply endorsement.

DRUG REGULATION ISSUES AND DRUG POLICY The opposition to moving marijuana to a less restrictive category schedule II ; is largely based on the fears that its illicit recreational use, already documented to be very high in the United States, would increase even further. Whether right or wrong, the recreational use of marijuana, the unquantified addictive potential of the smoked botanical product, and its perceived potential as an initiation into the use of "hard" drugs obfuscate the scientific and medical issues. "The driving force for the adoption of medical marijuana laws is the broad legalization of marijuana; it goes beyond reclassifying marijuana, " noted Eric Voth, MD, clinical associate professor of medicine at the University of Kansas in Kansas City and chair of the Institute on Global Drug Policy. Voth emphasized that "We should not have medicine by popular vote but by the tried-and-true FDA drug-development process." Certainly, there is a wide division between persons fighting the war on drugs and those who espouse antiregulatory principles. The latter includes groups that charge that a government conspiracy is suppressing data that unequivocally demonstrate marijuana's therapeutic efficacy. Whether the grass-roots efforts to petition the DEA to reschedule marijuana as a schedule II substance are wholly antiregulatory is debatable. In the middle of the U.S. drug policy and drug regulation tug-of-war are many scientists and physicians who agree that the classic pathway for drug development needs to be followed but also acknowledge that it may be nearly impossible to fulfill the FDA's require. A number of medications are available for osteoporosis prevention and treatment. While these medications do allow bone to rebuild itself to some degree, they are not a "cure" for osteoporosis. Other bone protective measures must be continued, such as adequate calcium and vitamin D intake, appropriate exercise, smoking cessation, and fall prevention.
Measurement of KATP channel current using voltage-clamp or patch-clamp techniques is impossible during muscle contraction because of possible damage to the cell membrane by microelectrodes. We therefore measured 86Rb efflux before, during, and after fatigue to estimate the activity of KATP channels. 86Rb is qualitatively a satisfactory marker for K movements through several K channels, including the KATP channel 9 ; . Solutions, muscle stimulation, and the fatigue protocol were all as described for force measurements. The muscle chamber was a methyl acrylate cuvette in which muscles were attached vertically at one end to a hook and the other to a Grass FT03 force transducer. Tetanic forces were recorded on a Grass Polygraph Model 7D ; . Muscles were immersed throughout the experiment in 1.7 ml of solution constantly bubbled with 95% O2-5% CO2 and maintained at 37C. Muscles were loaded with 86Rb 48 Ci ml ; for 60 min with a change of fresh solution after 30 min ; . 86Rb loading was followed by an initial 40-min washout in a series of three cuvettes 15, and 10 min ; containing 1.7 ml of nonradioactive saline solution preliminary washout experiments showed that a constant 86Rb efflux was reached after 40 min, results not shown ; . Glibenclam8de or pinacidil were added during the initial washout so muscles would be exposed to either drug 30 min before fatigue as described above for the experiments on force measurements. Basal 86Rb efflux was measured before fatigue by changing the cuvette three times every 5 min. During the 3-min fatigue period and the first 3 min of recovery, cuvettes were changed every minute. The last two cuvettes were used to measure 86Rb efflux between the 3rd and 5th and between the 5th and 10th minutes of recovery. From each cuvette, 1.0 ml of incubation fluid was added to 10.0 ml of biodegradable counting scintillant CBS; Amersham ; for radioactive counting. The 86Rb content remaining in muscles was determined by homogenizing muscles in 2 ml perchloric acid. The resulting solution was centrifuged at 10, 000 g for 10 min, and 1.0 ml of the supernatant was added to the counting scintillant. 86Rb counting was done using a WinSpectral liquid scintillation counter model 1414; Wallac Instruments ; . Quenching was corrected by counting 1 Ci of 86Rb in 1.0 ml of physiological solution and another 1 Ci in 1.0 ml of 6% perchloric acid. ATP and PCr Measurements Solutions, fatigue protocol, muscle stimulation, and experimental chamber were all as described for 86Rb efflux measurements. All muscles were first allowed to equilibrate 30 min in the absence control ; or presence of glibenclamide or pinacidil. Muscles were then freeze-clamped in liquid nitrogen immediately after the 30-min equilibrium or after the 3-min fatigue period. All muscles were stored at 80C until analyzed. The extraction of ATP and PCr was as described by Passoneau and Lowry 35 ; , with some modifications. Briefly, muscles were freeze-dried overnight with a freeze drier model Freezemobile 6; Virtis ; . Tendons were then removed and muscle tissues broken in small pieces under a microscope. A weighed amount of dried muscle tissue 0.82.0 mg. I was just wondering if the medication you were talking about may be better seeing my mom gave me some composene supp and glucovance.

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Frosch called on lawmakers to change the rules to force drug companies to provide more information about the medications they advertise.

If she just had some hot flashes, that doesn't mean you keep her on the drug for 15 years.
Drugs that can effectively treat the mother without adversely affecting the fetus. Placental passage of a drug is a function of multiple factors such as protein binding, lipid solubility and ionization constant pKa ; , but fetal exposure to drugs also depends on maternal pharmacokinetics including the volume of distribution, the rate of metabolism and excretion by the placenta, the pH difference between maternal and fetal fluids, and the effect of haemodynamic changes in the mother during pregnancy Table 1 ; . Ideally, one may wish to identify drugs that will not cross the placental barrier. However, with the exception of drugs with large molecular weights, such as heparin or insulin, most drugs appear to cross the placenta and are associated with varying degrees of fetal exposure. Recently we have been witnessing a pharmacological breakthrough: glibenclamide Glyburide ; , a drug used to treat gestational diabetes, does not appear to demonstrate significant maternal to fetal transfer. In vitro, studies by Elliott et al. [13] have demonstrated negligible levels of glibenclamide in the fetal compartment even when maternal concentrations were 8 times greater than therapeutic concentrations. Glibenclamide's poor maternal to fetal transfer may be due to its high protein binding 99.8% ; , its short elimination half-life 6 h ; and importantly the role of specific placental transporters such as P-glycoprotein P-gP ; , multidrug resistance protein 1 MRP1 ; , multidrug resistance protein 2 MRP2 ; or multidrug resistance protein 3 MRP3 ; [24, 25]. Indeed, in a recent placental perfusion study, we have documented that glibenclamide is transferred from the fetal to the maternal circulation against its concentration gradient. This may be the first generation of drugs on the journey.

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Jacobs, D. B., and Jung, C. Y. 1985 ; Sulfonylurea potentiates insulin-induced recruitment of glucose transport carrier in rat adipocytes. J. Biol. Chem. 260, 25932596 Martz, A., Jo, I., and Jung, C. Y. 1998 ; Sulfonylurea binding to adipocyte membrane and potentiation of insulin stimulated hexose transport. J. Biol. Chem. 264, 1367213678 Rajan, A. S., Zhao, L. T., Barbara, K. B., John, P. C., Samuel, W. C., and Aubrey, E. B. 1994 ; Do adipocytes contain high affinity sulfonylurea receptor? Endocrinology 134, 15811588 Maloff, B. L., and Lockwood, D. H. 1981 ; In vitro effects of a sulfonylurea on insulin action in adipocytes. J. Clin. Invest. 68, 8590 Muller, G., and Geisen, K. 1996 ; Characterization of the molecular mode of action of the sulfonylurea, glimepiride at adipocytes. Horm. Metab. Res. 28, 469 487 Muller, G., Wied, S., Wetekam, E-M., Crecelius, A., Unkelbach, A., and Punter, J. 1994 ; Stimulation of glucose utilization in 3T3L1 adipocytes and rat diaphragm in vitro by the sulfonylureas, glimepiride and glibenclamide, is correlated with modulations of the cAMP regulatory cascade. Biochem. Pharmacol. 48, 985996 Inagaki, N., Gonoi, T., Clement, J. P., Namba, N., Inazawa, J., Gonzalez, G., Bryan, L. A., Seino, S., and Bryan, J. 1996 ; Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor. Science 270, 11671170 Chagnon, Y. C., Perusse, L., and Boochard, C. 1998 ; The human obesity gene map: the 1997 update. Obesity Res. 6, 76 92 Hani, E. H., Clement, K., Velho, G., Vionnet, N., Hager, J., Philippi, A., Dida, L., Inove, H., Permott, M. A., Basdevant, A., North, M., Demenais, F., Guy-Grand, M., and Frogvel, P. 1997 ; Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians. Diabetes. 46, 688 694 Received for publication February 23, 1999. Revised for publication March 23, 1999.
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