U R Alapati|M B Poh-Fitzpatrick - JoVE Visualize

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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.

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.

Archives of Dermatology|April 1, 1985

Quinidine photosensitivityR B Armstrong, E E Leach, G Whitman, et al.

Archives of Dermatology|September 1, 1992

Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.

Hepatology (Baltimore, Md.)|December 1, 1989

Interaction of hemopexin, albumin and liver fatty acid-binding protein with protoporphyrinE Knobler, M B Poh-Fitzpatrick, D Kravetz, et al.

The Journal of Investigative Dermatology|July 27, 1999

Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase geneX Wang, L Yang, L Kurtz, et al.

The New England Journal of Medicine|March 12, 1987

Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineageA C Toback, S Sassa, M B Poh-Fitzpatrick, et al.

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Showing results (41-50 of 54) with videos related to

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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.

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.

Archives of Dermatology|April 1, 1985

Quinidine photosensitivityR B Armstrong, E E Leach, G Whitman, et al.

Archives of Dermatology|September 1, 1992

Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.

Hepatology (Baltimore, Md.)|December 1, 1989

Interaction of hemopexin, albumin and liver fatty acid-binding protein with protoporphyrinE Knobler, M B Poh-Fitzpatrick, D Kravetz, et al.

The Journal of Investigative Dermatology|July 27, 1999

Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase geneX Wang, L Yang, L Kurtz, et al.

The New England Journal of Medicine|March 12, 1987

Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineageA C Toback, S Sassa, M B Poh-Fitzpatrick, et al.

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