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1

Dalton, J. "Sulphadimidine residues." Veterinary Record 123, no. 3 (1988): 86–87. http://dx.doi.org/10.1136/vr.123.3.86.

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2

Woodward, K. N. "Carcinogenicity of Sulphadimidine." Human & Experimental Toxicology 11, no. 1 (1992): 60–61. http://dx.doi.org/10.1177/096032719201100111.

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3

Agbo, Joseph, Alhaji Saganuwan Saganuwan, and Patrick Azubuike. "Tissue distribution of sulphadimidine sodium in non-starved and starved grower turkeys (meleagris gallopavo)." International Journal of Pharmacology and Toxicology 4, no. 2 (2016): 154. http://dx.doi.org/10.14419/ijpt.v4i2.6513.

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Background: The use of veterinary drugs in food-producing animals has potential to generate residues in edible tissues and posses health hazard to consumers especially when the withdrawal period is not observed.Objectives: The study was conducted to determine the tissue residue and withdrawal period of sulphadimidine in non-starved and starved grower turkeys following a single intramuscular administration.Methods: Forty two turkeys of both sexes and 12 weeks old weighing 1.57±0.2 kg were divided into two groups of twenty one each. One group was administered a single intramuscular dose of sulph
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4

Sorrenti, M., G. P. Bettinetti, and A. Negri. "Thermoanalytical characterization of pseudopolymorphs of sulphadimidine and sulphadimidine–trimethoprim molecular complexes." Thermochimica Acta 321, no. 1-2 (1998): 67–72. http://dx.doi.org/10.1016/s0040-6031(98)00441-9.

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5

Lawrence, K. "Electrostatic properties of sulphadimidine." Veterinary Record 123, no. 5 (1988): 139. http://dx.doi.org/10.1136/vr.123.5.139-b.

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6

Rampen, FH, HL Van der Meer, and LM Stolk. "Acetylation phenotype and skin complexion." Acta Dermato-Venereologica 66, no. 4 (1986): 334–36. http://dx.doi.org/10.2340/0001555566334336.

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The relationship of acetylation phenotype to skin complexion was studied in 155 healthy Caucasians. Individuals received 500 mg sulphadimidine at 11.00 p.m.; urine was collected eight hours later. The percentage of acetylated sulphadimidine in urine was measured with high performance liquid chromatography. There was a slight but insignificant preponderance of slow acetylators in the dark skin types. It is concluded that slow acetylation phenotype is not correlated with light skin complexion. Therefore, it is unlikely that acetylation of xenobiotic carcinogens plays a dominant role in melanoma
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7

Smit, Laurentius A., N. Haagsma, and A. Ruiter. "Stability of sulphadimidine during raw fermented sausage preparation: reaction of sulphadimidine with nitrite." Zeitschrift f�r Lebensmitteluntersuchung und -Forschung A 206, no. 2 (1998): 94–98. http://dx.doi.org/10.1007/s002170050221.

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8

Geertsma, M. F., J. F. M. Nouws, J. L. Grondel, M. M. L. Aerts, T. B. Vree, and C. A. Kan. "Residues of sulphadimidine and its metabolites in eggs following oral sulphadimidine medication of hens." Veterinary Quarterly 9, no. 1 (1987): 67–75. http://dx.doi.org/10.1080/01652176.1987.9694077.

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9

Agbo, Joseph Odeh, Patrick Azubuike Onyeyili, Alhaji Saganuwan Saganuwan, and Joel Aondohulugh Bosha. "Effect of age on the pharmacokinetics of sulphadimidine in West African Dwarf (WAD) goats following a single intramuscular administration." GSC Biological and Pharmaceutical Sciences 9, no. 2 (2019): 044–49. https://doi.org/10.5281/zenodo.4283253.

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Due to the low cost and effectiveness of sulphadimidine against a wide variety of animal diseases, it is still being widely used in veterinary medicine. The present study was carried out to determine the effect of age on the pharmacokinetics of sulphadimidine in West African Dwarf (WAD) goats following intramuscular route of administration. Eight (8) WAD goats separated into two groups of four animals consisting of two males and two female goats each were used. Sulphadimdine sodium was administered at a dose of 100 mg/kg body weight. The goats in group one (3 months of age) and goats in group
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10

McCaughey, W., C. Elliott, and S. Crooks. "Sulphadimidine in drinking troughs at bacon factories." Veterinary Record 128, no. 6 (1991): 125–26. http://dx.doi.org/10.1136/vr.128.6.125.

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11

Smit, Laurentius A., Nel Haagsma, and A. Ruiter. "Binding of sulphadimidine to glucose in sausage." European Food Research and Technology 209, no. 3-4 (1999): 201–4. http://dx.doi.org/10.1007/s002170050480.

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12

Jones, D. K., M. Hakim, J. Wallwork, T. W. Higenbottam, and D. J. White. "Serious interaction between cyclosporin A and sulphadimidine." BMJ 292, no. 6522 (1986): 728–29. http://dx.doi.org/10.1136/bmj.292.6522.728.

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13

Ali, B. H., and A. A. Bashir. "Polymorphic Acetylation of Sulphadimidine in Healthy Northern Sudanese." Annals of Saudi Medicine 11, no. 4 (1991): 483–84. http://dx.doi.org/10.5144/0256-4947.1991.483.

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14

YOUNAN, W., J. F. M. NOUWS, A. M. HOMEID, T. B. VREE, and M. DEGENt. "Pharmacokinetics and metabolism of sulphadimidine in the camel." Journal of Veterinary Pharmacology and Therapeutics 12, no. 3 (1989): 327–29. http://dx.doi.org/10.1111/j.1365-2885.1989.tb00679.x.

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15

Crooks, S. R. H., W. J. Mccaughey, C. T. Elliott, J. D. Mcevoy, and S. A. Hewitt. "The production of pig tissue sulphadimidine reference material." Food Additives and Contaminants 13, no. 2 (1996): 211–19. http://dx.doi.org/10.1080/02652039609374399.

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16

Hombhanje, Francis. "Possible Optimization of Sulphadimidine Dosage for Acetylator Phenotyping." Japanese Journal of Pharmacology 56, no. 4 (1991): 531–34. http://dx.doi.org/10.1016/s0021-5198(19)39846-4.

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17

Hombhanje, Francis. "Possible Optimization of Sulphadimidine Dosage for Acetylator Phenotyping." Japanese Journal of Pharmacology 56, no. 4 (1991): 531–34. http://dx.doi.org/10.1254/jjp.56.531.

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18

Dalgaard-Mikkelsen, Svend, and Emil Poulsen. "Renal Excretion of Sulphathiazole and Sulphadimidine in Pigs." Acta Pharmacologica et Toxicologica 12, no. 2 (2009): 233–39. http://dx.doi.org/10.1111/j.1600-0773.1956.tb01382.x.

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19

Smit, Laurentius A., Laurentius A. P. Hoogenboom, Marcel C. J. Berghmans, and Nel Haagsma. "Stability of sulphadimidine during raw fermented sausage preparation." Zeitschrift f�r Lebensmittel-Untersuchung und -Forschung 198, no. 6 (1994): 480–85. http://dx.doi.org/10.1007/bf01192844.

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20

Hosny, E. A., A. Kassem, and H. H. El-shattawy. "Availability of Anhydrous Ampicillin and Sulphadimidine from Their Suspensions." Drug Development and Industrial Pharmacy 14, no. 6 (1988): 779–89. http://dx.doi.org/10.3109/03639048809151900.

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21

Jain, S. K., J. S. Punia, and B. D. Garg. "Pharmacokinetics and Urinary Excretion of Sulphadimidine in Buffalo Calves." Journal of Veterinary Medicine Series A 47, no. 8 (2000): 501–5. http://dx.doi.org/10.1046/j.1439-0442.2000.00311.x.

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22

Gouda, Moustafa A., Hatem E. Gafer, and Mohamed Gouda. "Synthesis and anti-hypertensive activity of novel sulphadimidine derivatives." Medicinal Chemistry Research 21, no. 11 (2011): 3902–6. http://dx.doi.org/10.1007/s00044-011-9935-3.

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23

Kmošťák, Svatomír, and Miroslav Dvořák. "Capillary gas chromatographic determination of sulphadimidine in pork tissues." Journal of Chromatography A 503 (January 1990): 260–65. http://dx.doi.org/10.1016/s0021-9673(01)81508-9.

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24

Bozkurt, A., N. E. Basci, S. Kalan, M. Tuncer, and S. O. Kayaalp. "N-acetylation phenotyping with sulphadimidine in a Turkish population." European Journal of Clinical Pharmacology 38, no. 1 (1990): 53–56. http://dx.doi.org/10.1007/bf00314803.

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25

Rais, Rubina, Kanwar Kumar Malhi, Samita Giri, et al. "Morphological, Physio-biochemical Properties and Antibiogram of the Clostridium chauvoei." International Journal of Medicine and Biomedical Sciences 1, no. 3 (2016): 1–5. http://dx.doi.org/10.55530/ijmbiosnepal.v1i3.17.

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Clostridium chauvoei is one of the deadly micro-organism that causes disease in cattle and sheep. We tested Clostridium chauvoei on different culture media, physio-biochemical agents and antibiotics. The best grwoth of organism was observed on blood and nutrient agar at pH 7.2-7.5, and temperature in between 37-40ºC. No effect of centrifugation was observed. Fourteen different antibiotics were tested against the Clostridium chauvoei. Highly effective antibiotics were chloramphenicol, tetracycline, baquiloprim/sulphadimidine, erythromycin, gentamicin, compound sulphonamides.
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26

Meher, MM, M. Afrin, Z. Hassan, and J. Alam. "Epidemiological investigation of peste des petits ruminants virus infection in goat with therapeutic managementat at Bera upazila of Pabna in Bangladesh." Progressive Agriculture 28, no. 2 (2017): 114–19. http://dx.doi.org/10.3329/pa.v28i2.33472.

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Peste des petits ruminants (PPR), a fatal viral disease of goats causes high mortality and large economic losses, and is considered as one of the major constrains of goat farming worldwide.This study was undertaken to determine the prevalence, alteration of vital signs and effective therapeutics of PPR affected goats inBeraupzilla ofPabna district, Bangladeshduring the period of November 2014 to April 2015. A total number of 465 diseased goats were clinically examined of which 253 (54.41%) were found to be affected with PPR. The highest prevalence (72.27%) was found in Black Bengal goats where
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27

Vree, T. B., Monika L. Vree, and J. F. M. Nouws. "Acetylation and Hydroxylation of Sulphadimidine in the Snail Cepaea hortensis." Journal of Veterinary Medicine Series A 33, no. 1-10 (1986): 633–36. http://dx.doi.org/10.1111/j.1439-0442.1986.tb00574.x.

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28

JO, Agbo, Ajibawi DO, Nwankwo HC, and Gberindyer FA. "Tylosin can alter the disposition kinetics of Sulphadimidine in goats." International Journal of Veterinary Sciences and Animal Husbandry 9, no. 6 (2024): 428–31. https://doi.org/10.22271/veterinary.2024.v9.i6g.1909.

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29

Davies, A. M., and N. M. Mackenzie. "Pharmacokinetics of baquiloprim and sulphadimidine in pigs after intramuscular administration." Research in Veterinary Science 57, no. 1 (1994): 69–74. http://dx.doi.org/10.1016/0034-5288(94)90084-1.

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30

Ali, B. H., and H. A. El Shekh. "Pharmacokinetics of antipyrine and sulphadimidine in camels, sheep and goats." European Journal of Pharmacology 183, no. 5 (1990): 1846. http://dx.doi.org/10.1016/0014-2999(90)92174-h.

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31

Grondel, J. L., J. F. M. Nouws, and O. L. M. Haenen. "Fish and antibiotics: Pharmacokinetics of sulphadimidine in carp (Cyprinus carpio)." Veterinary Immunology and Immunopathology 12, no. 1-4 (1986): 281–86. http://dx.doi.org/10.1016/0165-2427(86)90131-5.

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32

Ahmad, B., and J. W. Powell. "N1-Glucosides as urinary metabolites of sulphadimidine, sulphamerazine and sulphamethoxazole." European Journal of Drug Metabolism and Pharmacokinetics 13, no. 3 (1988): 177–83. http://dx.doi.org/10.1007/bf03189937.

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33

Pontiroli, A. E., A. De Pasqua, L. Bonisolli, and G. Pozza. "Ageing and acetylator phenotype as determined by administration of sulphadimidine." European Journal of Clinical Pharmacology 28, no. 4 (1985): 485–86. http://dx.doi.org/10.1007/bf00544374.

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34

El-Ashram, Saeed, Shawky M. Aboelhadid, Asmaa A. Kamel, Lilian N. Mahrous, and Khatib H. Abdelwahab. "Diversity of Parasitic Diarrhea Associated with Buxtonella Sulcata in Cattle and Buffalo Calves with Control of Buxtonellosis." Animals 9, no. 5 (2019): 259. http://dx.doi.org/10.3390/ani9050259.

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The association between parasite isolates, including Buxtonella sulcata, in suckling and post-weaning calves and diarrhea was studied with the aim to control diarrhea caused by B. sulcata. A total of 1100 diarrheic fecal samples were collected from 609 suckling calves and 491 post-weaning calves with diarrhea. Salt floatation and modified Ziehl–Neelsen techniques were applied for the microscopic examination of the presence or absence of parasite eggs and oocysts/cysts. The microscopic findings revealed that 20.36% of the calves had parasitic diarrhea, with a prevalence rate of 19.54% in suckli
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35

Fais, Theofanis, Nektarios Giadinis, Elias Papadopoulos, et al. "Effect of Toxoplasma gondii on Ram Sperm Quality after Experimental Infection." Pathogens 9, no. 12 (2020): 1004. http://dx.doi.org/10.3390/pathogens9121004.

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The aim of this study was to investigate the effect of experimental Toxoplasma gondii infection on ram sperm quality. Five months old, pre-pubertal, rams were divided into four groups (n = 8 per group). Group A was the control group; the remaining animals received per os (p.o.) 5000 oocysts per ram. Group B did not receive treatment post-infection (p.i.). Group C received sulphadimidine (intermuscular injection (i.m.) 33 mg/kg for eight days; every 48 h) two months p.i. and Group D received the same drug twice (24 h p.i. and two months later). Blood samples were collected every 15 days to dete
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36

., M. H. Al-Nazawi, and A. M. Homeida . "Residues of Sulphadimidine and its Metabolite N4-acetyl in Camel Milk." International Journal of Pharmacology 1, no. 3 (2005): 249–51. http://dx.doi.org/10.3923/ijp.2005.249.251.

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37

Gouda, Moustafa Ahmed, Hadeer Fakhr Eldien, Margret Mansour Girges, and Moged Ahmed Berghot. "Synthesis and antioxidant evaluation of some new sulphadimidine incorporating thiophene moiety." European Journal of Chemistry 5, no. 4 (2014): 595–600. http://dx.doi.org/10.5155/eurjchem.5.4.595-600.1106.

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38

ELSHEIKH, H. A., B. H. ALI, A. M. HOMEIDA, T. HASSAN, and H. J. HAPKE. "Pharmacokinetics of antipyrine and sulphadimidine (sulfamethazine) in camels, sheep and goats." Journal of Veterinary Pharmacology and Therapeutics 14, no. 3 (1991): 269–75. http://dx.doi.org/10.1111/j.1365-2885.1991.tb00837.x.

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39

Conway, Brain. "Determination of sulphadimidine in animal feeds by high-performance liquid chromatography." Analyst 113, no. 9 (1988): 1397. http://dx.doi.org/10.1039/an9881301397.

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40

McCaughey, W. J., C. T. Elliott, and S. R. H. Crooks. "Determination of sulphadimidine in animal feedstuffs by an enzyme‐linked immunoassay." Food Additives and Contaminants 7, no. 2 (1990): 259–64. http://dx.doi.org/10.1080/02652039009373890.

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41

Kshirsagar, N. A., Y. S. Saraf, M. R. Takle, et al. "Effect of iron deficiency anaemia and its treatment on sulphadimidine absorption." European Journal of Clinical Pharmacology 33, no. 3 (1987): 323–25. http://dx.doi.org/10.1007/bf00637571.

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42

ĈELEDA, L., Z. URBANOVÁ, I. PAVLÁSEK, et al. "The effect of intermittent treatment with sulphadimidine on coccidiosis in preruminant calves." Journal of Veterinary Pharmacology and Therapeutics 8, no. 2 (1985): 174–80. http://dx.doi.org/10.1111/j.1365-2885.1985.tb00941.x.

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43

Soliman, Sobhi A., Saied Belal, and Mona Bediar. "Non-Aqueous Titrimetric Determination of Sulphadimidine Sodium and Sulphadiazine Sodium in Injections." Analytical Letters 18, no. 20 (1985): 2497–505. http://dx.doi.org/10.1080/00032718508064482.

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44

Etuk, E. U., A. M. Umarudeen ., P. A. Onyeyili ., and A. T. Elsa . "Tissue Residues and Elimination of Sulphadimidine in Non-Starved and Starved Rabbits." Journal of Medical Sciences 6, no. 5 (2006): 862–65. http://dx.doi.org/10.3923/jms.2006.862.865.

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45

Elliott, C., W. McCaughey, S. Crooks, and J. McEvoy. "Effects of short term exposure of unmedicated pigs to sulphadimidine contaminated housing." Veterinary Record 134, no. 17 (1994): 450–51. http://dx.doi.org/10.1136/vr.134.17.450.

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46

Svensson, C. "Prevention of Eimeria alabamensis coccidiosis by a long-acting baquiloprim/sulphadimidine bolus." Veterinary Parasitology 74, no. 2-4 (1998): 143–52. http://dx.doi.org/10.1016/s0304-4017(97)00154-4.

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47

Nkya, W. M. M. M., D. G. Shija, and A. P. G. Mayala. "Schistosoma haematobium: effect of non-schistosomicidal drugs (tetracycline and sulphadimidine) on schoolchildren." Transactions of the Royal Society of Tropical Medicine and Hygiene 80, no. 1 (1986): 25–28. http://dx.doi.org/10.1016/0035-9203(86)90187-2.

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48

Zysset, Th, and E. Peretti. "Effect of concomitant isoniazid administration on determination of acetylator phenotype by sulphadimidine." European Journal of Clinical Pharmacology 30, no. 4 (1986): 463–66. http://dx.doi.org/10.1007/bf00607961.

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49

Šimůnek, J., Eva Hegerová, Jaroslava Klimešová, and Radka Zavadilová. "Effect of Sulphadimidine on the Toxicity of Phenobarbital in Cockerels of Different Ages." Acta Veterinaria Brno 54, no. 3-4 (1985): 183–87. http://dx.doi.org/10.2754/avb198554030183.

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50

Hall, Sten. "Evaluation of the Sulphadimidine Acetylator Phenotyping Test in Patients with Reduced Renal Function." Acta Medica Scandinavica 209, no. 1-6 (2009): 505–7. http://dx.doi.org/10.1111/j.0954-6820.1981.tb11636.x.

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