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M B Poh-Fitzpatrick

Showing results (61-70 of 83) with videos related to

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Archives of Dermatology|August 1, 1974
Rapid quantitative assay for erythrocyte porphyrinsM B Poh-Fitzpatrick, S Piomelli, P Young, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1992
Distribution of erythrocyte free porphyrin content in erythropoietic protoporphyriaM Sassaroli, R da Costa, H Väänänen, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 1, 1991
Urinary porphyrin excretion in normal children and adultsK E Bloom, E F Zaider, L J Morledge, et al.
The Journal of Clinical Investigation|April 1, 1982
Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyriaS Sassa, G L Zalar, M B Poh-Fitzpatrick, et al.
Hepatology (Baltimore, Md.)|May 1, 1983
Cholic acid amelioration of light and electron microscopic hepatic lesions in experimental protoporphyriaJ H Lefkowitch, K C Feng-Chen, J A Sklar, 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.
Analytical Biochemistry|October 1, 1979
Quantitative determination of hemoglobin and cytochemical staining for peroxidase using 3,3',5,5'-tetramethylbenzidine dihydrochloride, a safe substitute for benzidineH H Liem, F Cardenas, M Tavassoli, et al.
The New England Journal of Medicine|April 17, 1986
Complete suppression of the symptoms of congenital erythropoietic porphyria by long-term treatment with high-level transfusionsS Piomelli, M B Poh-Fitzpatrick, C Seaman, et al.
Clinical and Experimental Dermatology|August 24, 1999
Mutations in the translation initiation codon of the protoporphyrinogen oxidase gene underlie variegate porphyriaJ Frank, J A McGrath, M B Poh-Fitzpatrick, et al.
Journal of the American Academy of Dermatology|May 1, 1996
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infantJ L Huang, E Zaider, P Roth, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Archives of Dermatology|August 1, 1974
Rapid quantitative assay for erythrocyte porphyrinsM B Poh-Fitzpatrick, S Piomelli, P Young, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1992
Distribution of erythrocyte free porphyrin content in erythropoietic protoporphyriaM Sassaroli, R da Costa, H Väänänen, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 1, 1991
Urinary porphyrin excretion in normal children and adultsK E Bloom, E F Zaider, L J Morledge, et al.
The Journal of Clinical Investigation|April 1, 1982
Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyriaS Sassa, G L Zalar, M B Poh-Fitzpatrick, et al.
Hepatology (Baltimore, Md.)|May 1, 1983
Cholic acid amelioration of light and electron microscopic hepatic lesions in experimental protoporphyriaJ H Lefkowitch, K C Feng-Chen, J A Sklar, 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.
Analytical Biochemistry|October 1, 1979
Quantitative determination of hemoglobin and cytochemical staining for peroxidase using 3,3',5,5'-tetramethylbenzidine dihydrochloride, a safe substitute for benzidineH H Liem, F Cardenas, M Tavassoli, et al.
The New England Journal of Medicine|April 17, 1986
Complete suppression of the symptoms of congenital erythropoietic porphyria by long-term treatment with high-level transfusionsS Piomelli, M B Poh-Fitzpatrick, C Seaman, et al.
Clinical and Experimental Dermatology|August 24, 1999
Mutations in the translation initiation codon of the protoporphyrinogen oxidase gene underlie variegate porphyriaJ Frank, J A McGrath, M B Poh-Fitzpatrick, et al.
Journal of the American Academy of Dermatology|May 1, 1996
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infantJ L Huang, E Zaider, P Roth, et al.
Pageof 9