Citations

Showing 10 of 108015 citations.

Care of the Child with Diabetes
Schwenk, W Frederick, Schwenk, W Frederick

Mayo Clinic

Diabetes Care | December 11, 2014 | Volume: 10 | Issue: 4 | Pages: 528-528

10.2337/diacare.10.4.528b Get It

Webster's Medical Desk Dictionary
Gastineau, Clifford F.

Mayo Clinic

Diabetes Care | December 11, 2014 | Volume: 10 | Issue: 4 | Pages: 528-528

10.2337/diacare.10.4.528a Get It

Pancreatic Polypeptide as Marker for Autonomic Neuropathy: Reply
Service, F. John, Rizza, R. A., Go, V. L. W.

Mayo Clinic

Diabetes Care | December 11, 2014 | Volume: 10 | Issue: 2 | Pages: 253-253

10.2337/diacare.10.2.253a Get It

Measurements of Glucose Control
Service, F. John, O’Brien, Peter C. , Rizza, Robert A.

Mayo Clinic

Diabetes Care | December 11, 2014 | Volume: 10 | Issue: 2 | Pages: 225-237

10.2337/diacare.10.2.225 | PMID 3582083 Get It

Impotence in Male Diabetics
Sprague, Randall G.

Mayo Clinic

Diabetes | December 11, 2014 | Volume: 12 | Issue: 6 | Pages: 559-560

10.2337/diab.12.6.559 Get It

A Histopathologic Study of the Pancreas of Infants of Diabetic Mothers
D’Agostino, Anthony N., Bahn, Robert C.

Mayo Clinic

Diabetes | December 11, 2014 | Volume: 12 | Issue: 4 | Pages: 327-331

10.2337/diab.12.4.327 | PMID 14081845 Get It

Diagnosis and Treatment of Male Erectile Failure
Furlow, William L.

Mayo Clinic

Diabetes Care | December 11, 2014 | Volume: 2 | Issue: 1 | Pages: 18-25

10.2337/diacare.2.1.18 | PMID 510103 Get It

Idiopathic Hypoglycemosis In Children And Central Nervous System Damage
Burke, Edmund C.

Mayo Clinic

Diabetes | December 11, 2014 | Volume: 6 | Issue: 4 | Pages: 368-369

10.2337/diab.6.4.368 | PMID 13447769 Get It

Control of Diabetic Diarrhea with Antibiotic Therapy
Berge, Kenneth G., Sprague, Randall G., Green, Paul A

Mayo Clinic

Diabetes | December 11, 2014 | Volume: 17 | Issue: 6 | Pages: 385-387

10.2337/diab.17.6.385 | PMID 5652471 Get It

The ability of oral antibiotic treatment to control diabetic diarrhea was documented by a double-blind study involving a patient with this condition. When the patient was given Mysteclin-F, the diarrhea subsided promptly, only to recur when a placebo was substituted,. The erratic behavior of diabetic diarrhea is indicated, however, by the fact that a remission eventually occurred, and no further treatment was required. Although not all patients with diabetic diarrhea respond to antibiotic treatment, its trial merits consideration forthose patients who are refractory to the simpler forms of treatment.
Quantitative Aspects of Labile Diabetes
Molnar, George D., Gastineau, Clifford F., Rosevear, John W., Moxness, Karen E.

Mayo Clinic

Diabetes | December 11, 2014 | Volume: 14 | Issue: 5 | Pages: 279-288

10.2337/diab.14.5.279 | PMID 14280369 Get It

Eighteen diabetic patients representing a spectrum from hyperlabile to stable forms of this disease were investigated under metabolic ward conditions. Hyperlabile patients had the greatest daily and hourly variation in glycosuria and the most marked ketonuria. In our hyperlabile patients, multiple daily injections of short-acting insulin proved to be the only therapeutic measure that provided significant improvement in diabetic regulation when dietary and general health measures were already optimal. In more stable patients, longer acting insulin injected less frequently was found to be satisfactory therapy if careful adjustments to individual needs were made. Blood glucose and serum ketone-body and free fatty acid concentrations as well as qualitative estimates of glucose and ketone bodies in small samples of freshly voided urine were found to be suitable indicators of the immediate state of metabolic regulation. These parameters correlated with one another to a satisfactory degree, but they proved to be poorly correlated with measurements of urinary glucose and ketone bodies during periods of five to twenty-four hours. Quantitative analysis of individual blood samples or qualitative estimates of glucose or ketone bodies in freshly voided urine specimens proved to be unreliable indices of the patients' long-term metabolic compensation except in the most stable patients. Quantitations of urinary glucose and ketone bodiesin five, nine, and twenty-four-hour collections of urine, on the other hand, give satisfactory data to assess diabetic regulation, both as to accuracy of compensation and stability.