Concepedia

Brief Report: Treatment of Chronic Inflammatory Bowel Disease in Glycogen Storage Disease Type Ib with Colony-Stimulating Factors

Thomas F. Roe, Thomas D. Coates, Danièl Thomas, John H. Miller, Vicente Gilsanz

New England Journal of Medicine · 1992 · 118 citations · 21 references

DOI

Concepts

Abstract

GLYCOGEN storage disease Type Ib is a rare hereditary metabolic disorder characterized by growth failure, hepatomegaly, hypoglycemia, lactic acidosis, and neutrophil deficiency.1 , 2 Except for the...

References

21

Biological Defense Mechanisms. THE PRODUCTION BY LEUKOCYTES OF SUPEROXIDE, A POTENTIAL BACTERICIDAL AGENT

Bernard Babior, Ruby S. Kipnes, John T. Curnutte · Journal of Clinical Investigation · 1973 · 2.9K citations · Full text

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Gastrointestinal Manifestations of Chronic Granulomatous Disease

Marvin E. Ament, Hans D. Ochs · New England Journal of Medicine · 1973 · 186 citations

, , +15

Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.

Aksel Lange, William J. Arion, Arthur L. Beaudet · Journal of Biological Chemistry · 1980 · 171 citations · Full text

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Neutropenia and impaired neutrophil migration in type IB glycogen storage disease

Arthur L. Beaudet, Donald C. Anderson, Virginia V. Michels et al. · The Journal of Pediatrics · 1980 · 151 citations

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A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system

Kuniaki Narisawa, Yutaka Igarashi, Hiromi Otomo et al. · Biochemical and Biophysical Research Communications · 1978 · 144 citations

, , +16