Some salivary factors in insulin-dependent diabetics

References

• Bánóczy J, Albrecht M, Rigó O, Ember G, Ritlop B. Salivary secretion rate, pH, lactobacilli and yeast counts in diabetic women. Acta Diabetol Lat 1987; 24: 223–8
   PubMedGoogle Scholar
• Harrison R, Bowen W H. Flow rate and organic constituents of whole saliva in insulin-dependent diabetic children and adolescents. Pediatr Dent 1987; 9: 287–91
   PubMedGoogle Scholar
• Connor S, Iranpour B, Mills J. Alteration in parotid salivary flow in diabetes mellitus. Oral Surg 1970; 30: 55–9
   PubMedGoogle Scholar
• Kjellman O. Secretion rate and buffering action of whole mixed saliva in subjects with insulin-treated diabetes mellitus. Odontol Rev 1970; 21: 159–68
   PubMedGoogle Scholar
• Marder M Z, Abelson D C, Mandel I D. Salivary alterations in diabetes mellitus. J Periodontol 1975; 46: 567–9
   PubMedGoogle Scholar
• Sharon A, Ben-Aryed H, Itzhak B, Yoram K, Szar-Gel R, Gutman D. Salivary composition in diabetic patients. J Oral Med 1985; 40: 23–26
   PubMedGoogle Scholar
• Tenovuo J, Alanen P, Larjava H, Viikari J, Lehtonen O-P. Oral health of patients with insulin-dependent diabetes mellitus. Scand J Dent Res 1986; 94: 338–46
   PubMedGoogle Scholar
• Faulconbridge A R, Bradshaw W CL, Jenkins P A, Baum J D. The dental status of a group of diabetic children. Br Dent J 1981; 151: 253–5
   PubMed Web of Science ®Google Scholar
• Englander H R, Jeffay A I, Fuller J B, Chauncey H H. Glucose concentrations in blood plasma and parotid saliva of individuals with and without diabetes mellitus. J Dent Res 1963; 42: 1246
   PubMedGoogle Scholar
• Campbell M JA. Glucose in the saliva of the non-diabetic and the diabetic patient. Arch Oral Biol 1965; 10: 197–205
   PubMedGoogle Scholar
• Mehrotra K K, Chawla T N. Quantitative estimation of salivary glucose. J Indian Dent Assoc 1968; 40: 243–8
   Google Scholar
• Kjellman O. The presence of glucose in gingival exudate and resting saliva of subjects with insulin-treated diabetes mellitus. Swed Dent J 1970; 63: 11–9
   Google Scholar
• Knight L, Fletcher J. Growth of Candida albicans in saliva: stimulation by glucose associated with antibiotics, corticosteroids and diabetes mellitus. J Infect Dis 1971; 123: 371–7
   PubMed Web of Science ®Google Scholar
• Tenovuo J, Lehtonen O-P, Viikari J, Larjava H, Vilja P, Tuohimaa P. Immunoglobulins and innate antimicrobial factors in whole saliva of patients with insulin-independent diabetes mellitus. J Dent Res 1986; 65: 62–6
   PubMed Web of Science ®Google Scholar
• Cawson R A. Thrush in adult out-patients. Dental Pract 1965; 15: 361–4
   Google Scholar
• Burman L R, Bartels H A, Bailey R. Oral moniliasis in a diabetic patient. J Oral Med 1966; 21: 177–9
   PubMedGoogle Scholar
• Johnston R D, Chick E W, Johnston N S, Jarvis M A. Asymptomatic quantitative increase of Candida albicans in the oral cavity: predisposing conditions. South Med J 1967; 60: 1244–7
   PubMed Web of Science ®Google Scholar
• Winner H I. The transition from commensalism to parasitism. Br J Dermatol 1969; 81(suppl 1)62–8
   Google Scholar
• Pindborg J J. Atlas of diseases of the oral mucosa, 3rd ed. Munksgaard, Copenhagen 1980; 54: 118–200
   Google Scholar
• Dreizen S. Oral Candidiasis. Am J Med 1984; 30: 28–33
   Google Scholar
• Davidson D, Leibel B S, Berris B. Asymptomatic parotid gland enlargement in diabetes mellitus. Ann Intern Med 1969; 70: 31–6
   PubMed Web of Science ®Google Scholar
• Rao K S, Rao Y K. Parotid biopsies in young diabetics. J Indian Med Assoc 1979; 72: 77–9
   PubMedGoogle Scholar
• Russotto S B. Asymptomatic parotid gland enlargement in diabetes mellitus. Oral Surg 1981; 52: 594–8
   PubMedGoogle Scholar
• Murrah V A, Crosson J T, Sauk J J. Parotid gland basement membrane variation in diabetes mellitus. J Oral Pathol 1985; 14: 236–46
   PubMedGoogle Scholar
• Hugoson A, Thorstensson H, Falk H. Periodontal conditions in insulin-dependent diabetics. J Clin Periodontol 1989; 16: 311–9
   PubMedGoogle Scholar
• Möller Å, Jr. Microbiological examination of root canals and periapical tissues of human teeth. Methodological studies. Thesis, Odont Tidskr. 1966; 5–6, [spec iss]
   Google Scholar
• Ericsson Y. Clinical investigations of the salivary buffering action. Acta Odontol Scand 1959; 17: 131–65
   Google Scholar
• Falk H, Hugoson A, Thorstensson H. Number of teeth, prevalence of caries and periapical lesions in insulin-dependent diabetics. Scand J Dent Res 1989; 97: 198–206
   PubMedGoogle Scholar
• Thorstensson H, Falk H, Hugoson A. Dental care habits and knowledge of oral health in insulin-dependent diabetics. Scand J Dent Res 1989; 97: 207–15
   PubMedGoogle Scholar
• Mandel I D. Sialochemistry in diseases and clinical situations affecting salivary glands. CRC Crit Rev Clin Lab Sci 1980; 12: 321–66
   Web of Science ®Google Scholar
• Nilsson S, Kuylenstierna J, Andersson O P, Sjöstrand Å, Tisell A. Omfattande hypertonimedicinering hos diabetiker. Lakartidningen 1985; 82: 1048–51
   PubMedGoogle Scholar
• Parvinen T, Parvinen I, Larmas M. Stimulated salivary flow rate, pH and lactobacillus and yeast concentrations in medicated persons. Scand J Dent Res 1984; 92: 524–32
   PubMedGoogle Scholar
• Saifer A, Gerstenfeld S. The photometric micro-determination of blood glucose with glucose oxidase. J Lab Clin Med 1958; 51: 448–60
   PubMed Web of Science ®Google Scholar
• Raabo E, Terkildsen T C. On the enzymatic determination of blood glucose. Scand J Clin Lab Invest 1960; 12: 402–7
   PubMed Web of Science ®Google Scholar
• Washko M E, Rice E W. Determination of glucose by an improved enzymatic procedure. Clin Chem 1961; 7: 542–5
   PubMed Web of Science ®Google Scholar
• Levin K, Linde S. Bestämning av glykos i blod, liquor och urin med ett nytt glykosexidasreagens. Lakartidningen 1962; 59: 3016–26
   Google Scholar
• Ficara A J, Levin M P, Grower N F, Kramer G D. A comparison of the glucose and protein content of gingival fluid from diabetics and non-diabetics. J Periodont Res 1975; 10: 171–5
   PubMed Web of Science ®Google Scholar