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1

Ramanathan, C., and G. J. Smelt. "Desensitisation." BMJ 302, no. 6778 (1991): 726–27. http://dx.doi.org/10.1136/bmj.302.6778.726-c.

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2

Xu, Lei, and Haocheng Zhou. "An Automated Data Desensitisation System Based on the Middle Platform." Security and Communication Networks 2022 (September 21, 2022): 1–8. http://dx.doi.org/10.1155/2022/6888441.

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Built on top of a big data platform, the Middle Platform develops data through abstraction, sharing, and reuse capabilities to provide data products and data services for upper-level business development. While fully analysing and mining the intrinsic value of data, privacy and sensitive information in the data must also be protected, so the Middle Platform needs a data desensitisation system to ensure the safe and open use of data. In order to solve the problems of high usage costs, low efficiency, and lack of standardised results of desensitisation that exist in conventional data desensitisa
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3

Aye, Sofyan, Sutarto Wijono, and Arianti Ina Restiani Hunga. "Pola Kecemasan Perempuan Penyintas Kekerasan Dalam Pacaran: Kajian Perspektif Behavioral." PSIKOLOGI KONSELING 19, no. 2 (2021): 1136. http://dx.doi.org/10.24114/konseling.v19i2.30474.

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Tujuan review ini adalah untuk mendeskripsikan perspektif behavioral teknik desensitisasi sistematis, dan bagaimana terapi ini dapat menjadi terapi yang tepat untuk memulihkan kecemasan penyintas yang mengalami kekerasan dalam berpacaran. Metode pengumpulan data bersumber dari jurnal elektronik dan buku yang relevan dengan kajian. Pertama, dibahas mengenai kasus kekerasan dalam berpacaran di Indonesia. Selanjutnya, dibahas mengenai teknik desensitisasi sistematis, dan hasil-hasil penelitian sebelumnya mengenai teknik desensitisasi sistematis. Berdasarkan kajian ini, teknik desensitisasi sistem
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4

Blaszczynski, Alex, and Lia Nower. "Imaginal Desensitisation." Journal of Clinical Activities, Assignments & Handouts in Psychotherapy Practice 2, no. 4 (2003): 1–14. http://dx.doi.org/10.1300/j182v02n04_01.

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5

Pottle, A., and M. Barbir. "Statin desensitisation." Atherosclerosis Supplements 28 (September 2017): e11. http://dx.doi.org/10.1016/j.atherosclerosissup.2017.08.020.

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6

Eiser, N. "Desensitisation today." BMJ 300, no. 6737 (1990): 1412–13. http://dx.doi.org/10.1136/bmj.300.6737.1412.

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7

Ganderton, M. A. "Desensitisation today." BMJ 301, no. 6746 (1990): 293. http://dx.doi.org/10.1136/bmj.301.6746.293-a.

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8

Yamamoto, Akihito, Seiryu Kamoi, Shigeru Matsuda, Rieko Kawase, Kazuho Nakanishi, and Shunji Suzuki. "Efficacy and Adverse Events of Carboplatin Desensitisation Therapy for Gynaecological Cancer: A Retrospective Study." Medicines 9, no. 4 (2022): 26. http://dx.doi.org/10.3390/medicines9040026.

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Background: Carboplatin, the key drug used in treating gynaecological cancer, has an approximately 12–16% risk of hypersensitivity reactions. We aimed to investigate the efficacy and adverse effects of carboplatin desensitisation therapy for gynaecological cancer. Methods: The desensitisation protocol was standardised as a four-step, 4-h, carboplatin administration in the hospital. A retrospective medical record review was conducted on 15 patients who underwent carboplatin desensitisation for gynaecological malignancies at our hospital. Patients’ data were analysed to evaluate the treatment su
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9

&NA;. "Cotrimoxazole desensitisation successful." Inpharma Weekly &NA;, no. 1089 (1997): 21. http://dx.doi.org/10.2165/00128413-199710890-00048.

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10

&NA;. "Cotrimoxazole desensitisation successful." Reactions Weekly &NA;, no. 653 (1997): 4. http://dx.doi.org/10.2165/00128415-199706530-00008.

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11

Kelsey, S. M., G. R. Struthers, T. Beswick, and D. R. Blake. "Desensitisation to allopurinol." Annals of the Rheumatic Diseases 46, no. 1 (1987): 84. http://dx.doi.org/10.1136/ard.46.1.84.

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12

Ridley, M. G., and J. A. Mathews. "Desensitisation to allopurinol." Annals of the Rheumatic Diseases 46, no. 11 (1987): 875. http://dx.doi.org/10.1136/ard.46.11.875-a.

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13

Vaughan, K., M. Wiese, R. Gold, and N. Tarrier. "Eye-Movement Desensitisation." British Journal of Psychiatry 164, no. 4 (1994): 533–41. http://dx.doi.org/10.1192/bjp.164.4.533.

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A novel approach is described for the treatment of post-traumatic stress disorder (PTSD). Eye-movement desensitisation (EMD) requires the patient to generate images of the trauma in the mind and define physiological and emotional arousal states. While concentrating on these states, lateral multisaccardic eye movements are induced. Ten consecutive cases are reported who presented with symptoms originating from a range of traumas. The effectiveness of EMD in reducing symptoms outlined by DSM–III–R is described. An independent rater indicated that eight of the ten cases showed considerable improv
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14

Hamilton, Carlene A., та John L. Reid. "α1-Adrenoceptor desensitisation". European Journal of Pharmacology 152, № 1-2 (1988): 179–83. http://dx.doi.org/10.1016/0014-2999(88)90853-9.

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15

Tejasri, B. Prudhvi, R Arunachalam, Kumaresan, and S. Kiruthika. "DESENSITISATION THERAPY IN POST STROKE PAIN SYNDROME: A CASE STUDY." International Journal of Physiotherapy and Research 5, no. 6 (2017): 2541–44. http://dx.doi.org/10.16965/ijpr.2017.245.

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16

Rakhit, S., R. Murdoch, and S. M. Wilson. "Persistent desensitisation of the beta 2 adrenoceptors expressed by cultured equine sweat gland epithelial cells." Journal of Experimental Biology 201, no. 2 (1998): 259–66. http://dx.doi.org/10.1242/jeb.201.2.259.

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Adrenaline, forskolin and ATP all evoked accumulation of cyclic AMP in equine sweat gland epithelial cells, although the response to adrenaline was more transient than that to forskolin and ATP. Cells preincubated in adrenaline (10 micromol l-1, 32 min) showed essentially complete, homologous desensitisation, and this phenomenon reversed slowly (half-time 6.3+/-0.9 h). After 10 min of recovery from preincubation in adrenaline, isobutylmethylxanthine (IBMX, 5 mmol l-1) had no effect upon the desensitisation and the cells showed no loss of sensitivity to ATP and forskolin. After 10 h, however, t
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17

Blaszczynski, Alex, Juliette Drobny, and Zachary Steel. "Home-Based Imaginal Desensitisation in Pathological Gambling: Short-Term Outcomes." Behaviour Change 22, no. 1 (2005): 13–21. http://dx.doi.org/10.1375/bech.22.1.13.66782.

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AbstractRandomised controlled outcome studies have demonstrated the efficacy of imaginal desensitisation in inpatient settings. The purpose of this study was to evaluate the effects of a prerecorded audiocassette version of the imaginal desensitisation procedure that was designed for home-based use in reducing gambling urges and behaviours on a sample of diagnosed pathological gamblers who sought treatment at a university teaching hospital at 2-month follow-up. Pretreatment to 2-month follow-up repeated measures revealed a significant reduction in visual analogue scale ratings of urge, preoccu
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18

&NA;. "Success with homeopathic desensitisation." Reactions Weekly &NA;, no. 548 (1995): 2. http://dx.doi.org/10.2165/00128415-199505480-00001.

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19

&NA;. "Successful desensitisation to zidovudine." Inpharma Weekly &NA;, no. 880 (1993): 20–21. http://dx.doi.org/10.2165/00128413-199308800-00051.

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20

&NA;. "Cotrimoxazole desensitisation was successful." Reactions Weekly &NA;, no. 511 (1994): 2. http://dx.doi.org/10.2165/00128415-199405110-00002.

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21

Rodrigues, J., D. Malheiro, C. Botelho, M. C. Cruz, and M. G. Castel-Branco. "Successful desensitisation to Anastrozole." Allergologia et Immunopathologia 37, no. 1 (2009): 50–51. http://dx.doi.org/10.1016/s0301-0546(09)70253-8.

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22

Lanzara, Richard G. "Pharmaceutical Desensitisation Or Fade." Emerging Therapeutic Targets 1, no. 1 (1997): 271–73. http://dx.doi.org/10.1517/14728222.1.1.271.

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23

Villanueva Bueno, C., LL Poyatos Ruiz, V. Santana Pareja, E. Montecatine Alonso, MI Sierra Torres, and MD Santos Rubio. "PP-035 Albumin desensitisation." European Journal of Hospital Pharmacy 22, Suppl 1 (2015): A130.2—A130. http://dx.doi.org/10.1136/ejhpharm-2015-000639.315.

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24

Snape, S. E., R. G. Finch, and P. Venkatesan. "Aciclovir desensitisation and rechallenge." Case Reports 2011, mar01 1 (2011): bcr1020103392. http://dx.doi.org/10.1136/bcr.10.2010.3392.

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25

Unavailable, Name. "Case Series on Applications of EMDR to OCD." Advances in Social Sciences Research Journal 8, no. 3 (2021): 306–18. http://dx.doi.org/10.14738/assrj.83.9880.

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This paper is an attempt to draw a parallel between the exposure and response prevention (ERP) procedures in CBT (cognitive behaviour therapy) and the desensitisation procedures in EMDR (eye movement desensitisation processing). This paper also suggests an alternative targeting sequence that follows from the standard EMDR protocol to draw upon the strengths and application of ERP procedures in the treatment of OCD (obsessive compulsive disorder).
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26

Patriarca, G., A. Buonomo, C. Roncallo, et al. "Oral Desensitisation in Cow Milk Allergy: Immunological Findings." International Journal of Immunopathology and Pharmacology 15, no. 1 (2002): 53–58. http://dx.doi.org/10.1177/039463200201500107.

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In the literature there are several reports dealing with the possibility of a desensitising treatment in food allergy, but there are very few studies concerning the immunological mechanisms of or al desensitisation. We studied the immunological modifications in four children who underwent oral desensitisation with cow milk. Four children with cow milk allergy underwent oral desensitisation according to a standardized protocol. Total IgE, eosinophilic cationic protein in serum, and specific IgE and IgG4 to α-lactalbumin, to β-lactoglobulin and to casein were determined at the beginning of the t
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27

McArdle, CA, J. Franklin, L. Green, and JN Hislop. "Signalling, cycling and desensitisation of gonadotrophin-releasing hormone receptors." Journal of Endocrinology 173, no. 1 (2002): 1–11. http://dx.doi.org/10.1677/joe.0.1730001.

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Sustained stimulation of G-protein-coupled receptors (GPCRs) typically causes receptor desensitisation, which is mediated by phosphorylation, often within the C-terminal tail of the receptor. The consequent binding of beta-arrestin not only prevents the receptor from activating its G protein (causing desensitisation), but can also target it for internalisation via clathrin-coated vesicles and can mediate signalling to proteins regulating endocytosis and mitogen-activated protein kinase (MAPK) cascades. GnRH acts via phospholipase C (PLC)-coupled GPCRs on pituitary gonadotrophs to stimulate a C
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28

Schaff, Mathieu, Nicolas Receveur, Catherine Bourdon та ін. "β-arrestin-1 participates in thrombosis and regulates integrin αIIbβ3 signalling without affecting P2Y receptors desensitisation and function". Thrombosis and Haemostasis 107, № 04 (2012): 735–48. http://dx.doi.org/10.1160/th11-06-0430.

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Summaryβ-arrestin-1 (β-arr1) and β-arrestin-2 (β-arr2) are cytosolic proteins well-known to participate in G protein-coupled receptor desensitisation and signalling. We used genetically-inactivated mice to evaluate the role of β-arr1 or β-arr2 in platelet function, P2Y receptor desensitisation, haemostasis and thrombosis. Platelet aggregation, soluble fibrinogen binding and P-selectin exposure induced by various agonists were near normal in β-arr1−/− and β-arr2−/− platelets. In addition, deficiency in β-arr1 or β-arr2 was not critical for P2Y receptors desensitisation. A functional redundancy
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29

Lapner, K. N., C. J. Montpetit, and S. F. Perry. "Desensitisation of chromaffin cell nicotinic receptors does not impede catecholamine secretion during acute hypoxia in rainbow trout (Oncorhynchus mykiss)." Journal of Experimental Biology 203, no. 10 (2000): 1589–97. http://dx.doi.org/10.1242/jeb.203.10.1589.

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Experiments were performed on adult rainbow trout (Oncorhynchus mykiss) in vivo using chronically cannulated fish and in situ using a perfused posterior cardinal vein preparation (i) to characterise the desensitisation of chromaffin cell nicotinic receptors and (ii) to assess the ability of fish to secrete catecholamines during acute hypoxia with or without functional nicotinic receptors. Intra-arterial injection of nicotine (6.0×10(−)(7)mol kg(−)(1)) caused a rapid increase in plasma adrenaline and noradrenaline levels; the magnitude of this response was unaffected by an injection of nicotine
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30

Kitchiner, Neil J., Neil Roberts, and Jonathan I. Bisson. "Eye movement desensitisation reprocessing (EMDR)." Mental Health Practice 9, no. 7 (2006): 40–44. http://dx.doi.org/10.7748/mhp2006.04.9.7.40.c1908.

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31

Watts, D., and J. Bird. "Oxcarbazepine sensitivity treated by desensitisation." Journal of Neurology, Neurosurgery & Psychiatry 54, no. 4 (1991): 376. http://dx.doi.org/10.1136/jnnp.54.4.376.

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32

Vischer, T. L., and W. Van Eden. "Oral desensitisation in rheumatoid arthritis." Annals of the Rheumatic Diseases 53, no. 11 (1994): 708–10. http://dx.doi.org/10.1136/ard.53.11.708.

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33

Bell, EvanT, MichaelL Tapper, and AlanA Pollock. "SULPHADIAZINE DESENSITISATION IN AIDS PATIENTS." Lancet 325, no. 8421 (1985): 163. http://dx.doi.org/10.1016/s0140-6736(85)91930-0.

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34

MacCulloch, M. J. "Eye movement desensitisation and reprocessing." Advances in Psychiatric Treatment 5, no. 2 (1999): 120–25. http://dx.doi.org/10.1192/apt.5.2.120.

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Eye movement desensitisation and reprocessing (EMDR) was described by Shapiro (1989a,b) as a new method for treating post-traumatic stress disorder (PTSD). In May 1987, while walking in the park, Shapiro noticed that her own disturbing thoughts changed then disappeared “without any conscious effort” (Shapiro, 1995) when they had been temporally paired with diagonal upward to and fro eye movements. Over the next six months Shapiro worked with approximately 70 people to develop a procedure based on the temporal pairing of distressing images and thoughts with various eye movements. Shapiro began
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35

Sangrador-Pelluz, C., M. Martinez-García, MD Pérez-Serrano-Lainosa, R. Olivares-Pallerols, JP Navarro-Ferrando, and E. Soler-Company. "DGI-019 Cisplatin Desensitisation Protocol." European Journal of Hospital Pharmacy 20, Suppl 1 (2013): A102.1—A102. http://dx.doi.org/10.1136/ejhpharm-2013-000276.285.

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36

Shadur, Bella, Toby Nicholas Trahair, Tracey O'Brien, Susan Jane Russell, and John Bernard Ziegler. "Desensitisation to liposomal amphotericin B." Journal of Allergy and Clinical Immunology: In Practice 5, no. 1 (2017): 181–83. http://dx.doi.org/10.1016/j.jaip.2016.08.006.

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37

Page, Andrew C., and Rocco D. Crino. "Eye-Movement Desensitisation: A Simple Treatment for Post-Traumatic Stress Disorder?" Australian & New Zealand Journal of Psychiatry 27, no. 2 (1993): 288–93. http://dx.doi.org/10.1080/00048679309075779.

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Eye-movement desensitisation has been identified in a number of case studies to be an effective treatment for post-traumatic stress disorder (PTSD). A further case study reporting success is presented. The treatment appears rapid and may represent a potentially cost-effective treatment for PTSD. However, no treatment study to date has conformed to the ideal methodology of a double-blind placebo controlled trial and therefore its efficacy remains to be demonstrated. A minimal but stringent set of criteria for identification of treatment efficacy are outlined. The implications of eye-movement de
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38

Başoğlu, Burhan, Mustafa Önder Şekeroğlu, and Emrah Altun. "Relationship between burnout level and socio-democraphic variables of teachers: Ayaş, Güdül, Beypazarı, Nallıhan of sample." Journal of Human Sciences 13, no. 1 (2016): 2007. http://dx.doi.org/10.14687/ijhs.v13i1.3763.

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In this study, Maslach Burnout Inventory was used to determine the relationship between 533 teachers’ level of burnout; who work in Ayaş, Güdül, Beypazarı and Nallıhan provinces in the northern of Ankara in different positions and their socio-demographic variables. According to obtained data results; number of children, staff position and felt wealth level in desensitisation dimension and gender, education level and staff position in personal success dimension were determined as significant. It was concluded that marital status, duration of experience in job and staff position in management we
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39

Sari, Siska Permata, and Yeni Karneli. "Penggunaan Desensitisasi untuk Mengurangi Phobia." Lentera Negeri 1, no. 2 (2020): 40–42. http://dx.doi.org/10.29210/99760.

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Phobia adalah rasa ketakutan kuat (berlebihan) terhadap suatu benda, situasi atau kejadian, yang ditandai dengan keinginan untuk menjauhi sesuatu yang ditakuti itu. Jika sudah parah bisa sangat mengganggu aktifitas seseorang. Seperti seseorang akan sesak nafas, deg-degan, keringat dingin, gemetaran, bahkan sampai tidak bisa menggerakkan badannya. Dengan menggunakan teknik desensitisasi agar bisa mengurangi tingkat ketakutan seseorang terhadap phobianya atau rasa takutnya terhadap suatu hal. Teknik ini dapat membuat penderita merasakan relaksasi/ketenangan sehingga ketakutan nya akan berkurang
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40

Jeanneton, O., M. Delvaux, Y. Langlois, et al. "Correlation of desensitisation of platelet activating factor (PAF) receptors with intensity of inflammation and intestinal PAF content during experimental ileitis in guinea pig." Gut 43, no. 3 (1998): 356–64. http://dx.doi.org/10.1136/gut.43.3.356.

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Aim—To determine the kinetics of platelet activating factor (PAF) and prostaglandin E2 (PGE2) receptor desensitisation during intestinal inflammation induced by trinitrobenzenesulphonic acid (TNB) instillation and to study the relation between receptor regulation, inflammatory lesions, and PAF content of the gut wall.Methods—Receptor desensitisation was assessed on isolated smooth muscle cells from the circular layer. PAF content of the intestinal wall was determined by thin layer chromatography and radioimmunoassay.Results—After an acute inflammatory phase on day 1, subacute changes appeared
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41

Prasasti, Suci, and Donosuko. "TEKNIK DESENSITISASI DALAM MANAJEMEN STRESS (Kepanikan Sosial Masa Pandemi)." PROFICIO 2, no. 02 (2021): 74–78. http://dx.doi.org/10.36728/jpf.v2i02.1549.

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ABSTRAK
 Dampak kebijakan untuk menekan laju kasus Covid ternyata menimbulkan kepanikan secara ekonomi karena adanya pembatasan melintasi suatu wilayah dan membuka usaha agar tidak terjadi kerumunan yang besar. Masyarakat mengalami kecemasan fisik dan psikis. Tujuannya memberikan solusi kepada ibu – ibu khususnya di desa Sepat Kecamatan Masaran tentang teknik Desensitisasi untuk mengurangi kecemasan atau ketakutan dalam menghadapi masa pandemi. Metode yang digunakan adalah metode ceramah, latihan, simulasi dan diskusi. Hasil pemberian teknik desensitisasi adalah menunjukkan perkembangan m
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42

Malapert, M., H. Guizouarn, B. Fievet, et al. "Regulation of Na+/H+ antiporter in trout red blood cells." Journal of Experimental Biology 200, no. 2 (1997): 353–60. http://dx.doi.org/10.1242/jeb.200.2.353.

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The trout red blood cell Na+/H+ antiporter (beta NHE) plays two interesting properties: it is the only NHE own to be activated by cyclic AMP, and the activation process is followed by a desensitisation of the transport system itself. Cloning and expression of beta NHE have provided inificant information about Na+/H+ activation, in particular that activation by cyclic AMP is directly dependent upon the presence of two protein kinase A consensus sites in the cytoplasmic tail of the antiporter. Expression of beta NHE in fibroblasts demonstrates that the protein kinase A (PKA) and protein kinase C
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43

&NA;. "Aspirin desensitisation cost effective for AERD." Reactions Weekly &NA;, no. 1192 (2008): 3. http://dx.doi.org/10.2165/00128415-200811920-00005.

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44

&NA;. "Cotrimoxazole desensitisation has high success rate." Reactions Weekly &NA;, no. 602 (1996): 3. http://dx.doi.org/10.2165/00128415-199606020-00005.

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45

&NA;. "Aspirin desensitisation cost effective for AERD." Inpharma Weekly &NA;, no. 1627 (2008): 5. http://dx.doi.org/10.2165/00128413-200816270-00009.

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46

&NA;. "Allopurinol desensitisation protocol: safe and effective." Reactions Weekly &NA;, no. 843 (2001): 5. http://dx.doi.org/10.2165/00128415-200108430-00010.

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47

&NA;. "Sulfadiazine desensitisation not recommended in AIDS." Reactions Weekly &NA;, no. 377 (1991): 1. http://dx.doi.org/10.2165/00128415-199103770-00001.

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48

&NA;. "Desensitisation to PCP prophylaxis in AIDS." Inpharma Weekly &NA;, no. 913 (1993): 21. http://dx.doi.org/10.2165/00128413-199309130-00050.

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49

Durham, Stephen R. "Allergen immunotherapy (desensitisation) for allergic diseases." Clinical Medicine 6, no. 4 (2006): 348–51. http://dx.doi.org/10.7861/clinmedicine.6-4-348.

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50

&NA;. "Desensitisation to PCP prophylaxis in AIDS." Reactions Weekly &NA;, no. 477 (1993): 2. http://dx.doi.org/10.2165/00128415-199304770-00004.

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