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Journal Abstract Search
199 related items for PubMed ID: 2721023
1. Dual porphyria in double heterozygotes with porphobilinogen deaminase and uroporphyrinogen decarboxylase deficiencies. Doss MO. Clin Genet; 1989 Feb; 35(2):146-51. PubMed ID: 2721023 [Abstract] [Full Text] [Related]
3. Familial porphyria cutanea tarda: the pattern of porphyrins formed from porphobilinogen by hemolysates. Alleman MA, Wilson JH, van den Berg JW, Edixhoven-Bosdijk A, van Gastel-Quist LM. Clin Chem; 1982 May; 28(5):1144-7. PubMed ID: 7074894 [Abstract] [Full Text] [Related]
4. Steady-state levels of uroporphyrinogen decarboxylase mRNA in lymphoblastoid cell lines from patients with familial porphyria cutanea tarda and their relatives. Hansen JL, Pryor MA, Kennedy JB, Kushner JP. Am J Hum Genet; 1988 Jun; 42(6):847-53. PubMed ID: 3369447 [Abstract] [Full Text] [Related]
11. Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family. Lazaro P, de Salamanca RE, Elder GH, Villaseca ML, Chinarro S, Jaqueti G. Br J Dermatol; 1984 May; 110(5):613-7. PubMed ID: 6722030 [Abstract] [Full Text] [Related]
18. [Early forms of porphyria cutanea tarda. Apropos of 2 cases with a study of familial enzymatic deficiency and definition of the mode of genetic transmission]. Herrero C, Muniesa AM, Lecha M, Elder GH, Mascaro JM. Ann Dermatol Venereol; 1984 May 29; 111(11):973-8. PubMed ID: 6524816 [Abstract] [Full Text] [Related]