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S Piomelli

Showing results (71-80 of 108) with videos related to

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The Journal of Investigative Dermatology|November 5, 1997
Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase geneX Wang, S Piomelli, M Peacocke, et al.
The Journal of Clinical Investigation|August 1, 1973
Disparate enzyme activity in erythocytes and leukocytes. A variant of hypoxanthine phosphoribosyl-transferase deficiency with an unstable enzymeJ Dancis, L C Yip, R P Cox, et al.
Biochimica Et Biophysica Acta|June 9, 1995
Systematic screening for RNA with skipped exons--splicing mutations of the ferrochelatase geneX Wang, M Poh-Fitzpatrick, T Chen, et al.
Stroke|December 1, 1988
Transcranial Doppler measurements of the middle cerebral artery. Effect of hematocritL M Brass, S G Pavlakis, D DeVivo, et al.
The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine|November 1, 1971
Roentgenographic manifestations of pyruvate kinase deficiency hemolytic anemiaM H Becker, N B Genieser, S Piomelli, et al.
Archives of Dermatology|August 1, 1974
Rapid quantitative assay for erythrocyte porphyrinsM B Poh-Fitzpatrick, S Piomelli, P Young, et al.
Pediatric Radiology|November 1, 1995
Deferoxamine-induced platyspondyly in hypertransfused thalassemic patientsT L Levin, S Sheth, W E Berdon, et al.
Blood|April 1, 1980
The molecular mechanism of the inherited phosphofructokinase deficiency associated with hemolysis and myopathyS Vora, L Corash, W K Engel, et al.
Pediatric Radiology|February 7, 1998
Pulmonary embolism developing in patients with sickle cell disease on hypertransfusion and IV deferoxamine chelation therapyS Sheth, C Ruzal-Shapiro, A Hurlet-Jensen, et al.
Photodermatology, Photoimmunology & Photomedicine|February 1, 1995
Human protoporphyria: genetic heterogeneity at the ferrochelatase locusL T Ostasiewicz, J L Huang, X Wang, et al.
Pageof 11

Showing results (71-80 of 108) with videos related to

Sort By:
Pageof 11
The Journal of Investigative Dermatology|November 5, 1997
Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase geneX Wang, S Piomelli, M Peacocke, et al.
The Journal of Clinical Investigation|August 1, 1973
Disparate enzyme activity in erythocytes and leukocytes. A variant of hypoxanthine phosphoribosyl-transferase deficiency with an unstable enzymeJ Dancis, L C Yip, R P Cox, et al.
Biochimica Et Biophysica Acta|June 9, 1995
Systematic screening for RNA with skipped exons--splicing mutations of the ferrochelatase geneX Wang, M Poh-Fitzpatrick, T Chen, et al.
Stroke|December 1, 1988
Transcranial Doppler measurements of the middle cerebral artery. Effect of hematocritL M Brass, S G Pavlakis, D DeVivo, et al.
The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine|November 1, 1971
Roentgenographic manifestations of pyruvate kinase deficiency hemolytic anemiaM H Becker, N B Genieser, S Piomelli, et al.
Archives of Dermatology|August 1, 1974
Rapid quantitative assay for erythrocyte porphyrinsM B Poh-Fitzpatrick, S Piomelli, P Young, et al.
Pediatric Radiology|November 1, 1995
Deferoxamine-induced platyspondyly in hypertransfused thalassemic patientsT L Levin, S Sheth, W E Berdon, et al.
Blood|April 1, 1980
The molecular mechanism of the inherited phosphofructokinase deficiency associated with hemolysis and myopathyS Vora, L Corash, W K Engel, et al.
Pediatric Radiology|February 7, 1998
Pulmonary embolism developing in patients with sickle cell disease on hypertransfusion and IV deferoxamine chelation therapyS Sheth, C Ruzal-Shapiro, A Hurlet-Jensen, et al.
Photodermatology, Photoimmunology & Photomedicine|February 1, 1995
Human protoporphyria: genetic heterogeneity at the ferrochelatase locusL T Ostasiewicz, J L Huang, X Wang, et al.
Pageof 11