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A C Toback

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Digestive Diseases and Sciences|September 1, 1984
Splenic torsion. An unusual cause of splenomegalyA C Toback, D M Steece, M D Kaye
Cutis|September 1, 1987
Eruptive vellus hair cystsJ L Held, J E Andrew, A C Toback
The Journal of Clinical Investigation|May 1, 1987
Immunochemical study of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyriaH Fujita, S Sassa, A C Toback, et al.
Journal of the American Academy of Dermatology|November 1, 1986
Severe chronic photosensitivity in association with acquired immunodeficiency syndromeA C Toback, J Longley, A C Cardullo, 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.
The Journal of Investigative Dermatology|May 1, 1994
Molecular defects of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyriaK Meguro, H Fujita, N Ishida, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Digestive Diseases and Sciences|September 1, 1984
Splenic torsion. An unusual cause of splenomegalyA C Toback, D M Steece, M D Kaye
Cutis|September 1, 1987
Eruptive vellus hair cystsJ L Held, J E Andrew, A C Toback
The Journal of Clinical Investigation|May 1, 1987
Immunochemical study of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyriaH Fujita, S Sassa, A C Toback, et al.
Journal of the American Academy of Dermatology|November 1, 1986
Severe chronic photosensitivity in association with acquired immunodeficiency syndromeA C Toback, J Longley, A C Cardullo, 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.
The Journal of Investigative Dermatology|May 1, 1994
Molecular defects of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyriaK Meguro, H Fujita, N Ishida, et al.
Pageof 2