134 related articles for article (PubMed ID: 866144)
21. [Acute intermittent porphyria. Detection of asymptomatic carriers of the genetic defect].
Grandchamp B; Grelier M; Nordmann Y
Nouv Presse Med; 1975 Jun; 4(24):1801-2. PubMed ID: 1161481
[TBL] [Abstract][Full Text] [Related]
22. Acute hereditary coproporphyria induced by the androgenic/anabolic steroid methandrostenolone (Dianabol).
Lane PR; Massey KL; Worobetz LJ; Jutras MN; Hull PR
J Am Acad Dermatol; 1994 Feb; 30(2 Pt 2):308-12. PubMed ID: 8294588
[TBL] [Abstract][Full Text] [Related]
23. [Hereditary coproporphyria].
Gregor A; Kostrzewska E; Zywiecka M
Pol Arch Med Wewn; 1981 Jul; 66(1):25-31. PubMed ID: 7291025
[No Abstract] [Full Text] [Related]
24. A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells.
Gross U; Gerlach R; Kühnel A; Seifert V; Doss MO
J Inherit Metab Dis; 2003; 26(6):565-70. PubMed ID: 14605502
[TBL] [Abstract][Full Text] [Related]
25. A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family.
Susa S; Daimon M; Yamamori I; Kondo M; Yamatani K; Sasaki H; Kato T
J Hum Genet; 1998; 43(3):182-4. PubMed ID: 9747031
[TBL] [Abstract][Full Text] [Related]
26. A molecular, enzymatic and clinical study in a family with hereditary coproporphyria.
Gross U; Puy H; Meissauer U; Lamoril J; Deybach JC; Doss M; Nordmann Y; Doss MO
J Inherit Metab Dis; 2002 Aug; 25(4):279-86. PubMed ID: 12227458
[TBL] [Abstract][Full Text] [Related]
27. The inherited enzymatic defect in porphyria variegata.
Deybach JC; de Verneuil H; Nordmann Y
Hum Genet; 1981; 58(4):425-8. PubMed ID: 7327566
[TBL] [Abstract][Full Text] [Related]
28. Hereditary coproporphyria and variegate porphyria in Denmark.
With TK
Dan Med Bull; 1983 Mar; 30(2):106-12. PubMed ID: 6851678
[No Abstract] [Full Text] [Related]
29. [Hereditary coproporphyria. 7 cases].
Jaeger A; Tempe JD; Geisler F; Nordmann Y; Mantz JM
Nouv Presse Med; 1975 Nov; 4(39):2783-7. PubMed ID: 1196884
[TBL] [Abstract][Full Text] [Related]
30. Molecular defects of the coproporphyrinogen oxidase gene in hereditary coproporphyria.
Sassa S; Kondo M; Taketani S; Nomura N; Furuyama K; Akagi R; Nagai T; Terajima M; Galbraith RA; Fujita H
Cell Mol Biol (Noisy-le-grand); 1997 Feb; 43(1):59-66. PubMed ID: 9074789
[TBL] [Abstract][Full Text] [Related]
31. [Hereditary coproporphyria in the Federal Republic of Germany (author's transl)].
Doss M; von Tiepermann R; Verspohl F
J Clin Chem Clin Biochem; 1978 Sep; 16(9):519-24. PubMed ID: 712343
[No Abstract] [Full Text] [Related]
32. [Hydroa vacciniforme type eruption disclosing hereditary coproporphyria].
Jeanmougin M; Pedreiro J; Manciet JR; Moulin JP; Civatte J
Ann Dermatol Venereol; 1988; 115(11):1236-8. PubMed ID: 3239925
[No Abstract] [Full Text] [Related]
33. [9 cases of hepatic coproporphyria (hereditary coproporphyria)].
Sasaki H; Kaneko K; Tsuneyama H; Hattori A; Aida M
Saishin Igaku; 1970 Sep; 25(9):1978-95. PubMed ID: 5458521
[No Abstract] [Full Text] [Related]
34. [Hereditary coproporphyria (Hepatic coproporphyria), Erythropoietic coproporphyria].
Kiso S; Kawata S; Kashihara T; Tamura S; Matsuzawa Y
Nihon Rinsho; 1995 Jun; 53(6):1433-7. PubMed ID: 7616659
[TBL] [Abstract][Full Text] [Related]
35. Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.
Schreiber WE; Zhang X; Senz J; Jamani A
Hum Mutat; 1997; 10(3):196-200. PubMed ID: 9298818
[TBL] [Abstract][Full Text] [Related]
36. [An acute attack of hereditary coproporphyria concomitant with severe generalized polyneuropathy and respiratory insufficiency].
Piradov MA; Avdiunina IA; Alferova VP; Pustovoĭt IaS; Pivnik AV; Karpova IV; Popov AA; Selivanov VV; Kim AV; Rider FK
Anesteziol Reanimatol; 2003; (3):64-7. PubMed ID: 12918208
[No Abstract] [Full Text] [Related]
37. Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria.
Wiman A; Floderus Y; Harper P
J Hum Genet; 2002; 47(8):407-12. PubMed ID: 12181641
[TBL] [Abstract][Full Text] [Related]
38. Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.
Lamoril J; Puy H; Whatley SD; Martin C; Woolf JR; Da Silva V; Deybach JC; Elder GH
Am J Hum Genet; 2001 May; 68(5):1130-8. PubMed ID: 11309681
[TBL] [Abstract][Full Text] [Related]
39. Activities of delta-aminolevulinic acid synthetase in the liver and bone marrow of hepatic coproporphyria (hereditary coproporphyria).
Sasaki H; Kaneko K; Tsuneyama H
Acta Med Biol (Niigata); 1969 Sep; 17(2):97-9. PubMed ID: 5349574
[No Abstract] [Full Text] [Related]
40. Homozygous case of hereditary coproporphyria.
Grandchamp B; Phung N; Nordmann Y
Lancet; 1977 Dec 24-31; 2(8052-8053):1348-9. PubMed ID: 74745
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
