Results 191 to 200 of about 91,225 (237)
Some of the next articles are maybe not open access.
The Journal of Pediatrics, 1969
Abstract Significant abnormality of nitroblue tetrazolium (N.B.T.) oxidation, and of bacterial killing, in the fathers of patients with chronic granulomatous disease suggests a pattern of sex-modified autosomal recessive inheritance. The data suggest that the defect may be much commoner than is at present recognised.
JackC. Bass, StellaB. Kontras
+10 more sources
Abstract Significant abnormality of nitroblue tetrazolium (N.B.T.) oxidation, and of bacterial killing, in the fathers of patients with chronic granulomatous disease suggests a pattern of sex-modified autosomal recessive inheritance. The data suggest that the defect may be much commoner than is at present recognised.
JackC. Bass, StellaB. Kontras
+10 more sources
Pediatric and Developmental Pathology, 2003
CLINICAL SUMMARY A 3-year-old African-American boy presented with limping due to a thigh mass of recent appearance. The lesion was initially painless and nonmobile, without erythema or swelling. There was no fever or other constitutional symptom. Four days before admission, a second tumor appeared on the left parietal region.
Rebecca E. Rosenberg +4 more
openaire +6 more sources
CLINICAL SUMMARY A 3-year-old African-American boy presented with limping due to a thigh mass of recent appearance. The lesion was initially painless and nonmobile, without erythema or swelling. There was no fever or other constitutional symptom. Four days before admission, a second tumor appeared on the left parietal region.
Rebecca E. Rosenberg +4 more
openaire +6 more sources
Pediatric Radiology, 1981
The report describes a ten year old boy with a form of chronic granulomatous disease characterised by hepatic and tibial granulomatous, hilar and broncopulmonar inflammatory processes, and an absolute defect in PMN-mediated ADCC.
F. Bassani +3 more
openaire +3 more sources
The report describes a ten year old boy with a form of chronic granulomatous disease characterised by hepatic and tibial granulomatous, hilar and broncopulmonar inflammatory processes, and an absolute defect in PMN-mediated ADCC.
F. Bassani +3 more
openaire +3 more sources
Pediatric Clinics of North America, 1977
Since 1971, significant deviations from the classic pattern of chronic granulomatous disease have been recognized, and the disease appears to be more common that it did formerly. Knowledge of the basic underlying molecular defect has been broadened, and some new concepts of diagnosis and management have been formed. This report summarizes new knowledge
Richard B. Johnston, Simon L. Newman
openaire +3 more sources
Since 1971, significant deviations from the classic pattern of chronic granulomatous disease have been recognized, and the disease appears to be more common that it did formerly. Knowledge of the basic underlying molecular defect has been broadened, and some new concepts of diagnosis and management have been formed. This report summarizes new knowledge
Richard B. Johnston, Simon L. Newman
openaire +3 more sources
Annual Review of Medicine, 1992
Chronic granulomatous disease (CGD) encompasses a group of rare inherited disorders characterized by defects in a phagocyte-specific NADPH-oxidase complex that forms the superoxide radical during the respiratory burst. In this chapter, the protein components and cellular biochemistry of the oxidase are reviewed in light of recent genetic and ...
M C, Dinauer, S H, Orkin
openaire +4 more sources
Chronic granulomatous disease (CGD) encompasses a group of rare inherited disorders characterized by defects in a phagocyte-specific NADPH-oxidase complex that forms the superoxide radical during the respiratory burst. In this chapter, the protein components and cellular biochemistry of the oxidase are reviewed in light of recent genetic and ...
M C, Dinauer, S H, Orkin
openaire +4 more sources