117 related articles for article (PubMed ID: 821788)
1. Menkes' kinky hair syndrome: a genetic disease involving copper.
Holtzman NA
Fed Proc; 1976 Sep; 35(11):2276-80. PubMed ID: 821788
[TBL] [Abstract][Full Text] [Related]
2. Regulation of copper metabolism in the mottled mouse.
Packman S
Arch Dermatol; 1987 Nov; 123(11):1545-1547a. PubMed ID: 3674914
[TBL] [Abstract][Full Text] [Related]
3. [Mice with mottled mutation--a model for defective copper metabolism in humans].
Lenartowicz M
Postepy Hig Med Dosw; 1998; 52(5):527-41. PubMed ID: 9857676
[TBL] [Abstract][Full Text] [Related]
4. Hepatic copper metabolism in a mouse model for Menkes' kinky hair syndrome.
Castillo RO; Thaler MM; O'Toole C; Packman S
Pediatr Res; 1990 May; 27(5):492-6. PubMed ID: 2345676
[TBL] [Abstract][Full Text] [Related]
5. Genetic diseases of copper metabolism.
Prohaska JR
Clin Physiol Biochem; 1986; 4(1):87-93. PubMed ID: 3514056
[TBL] [Abstract][Full Text] [Related]
6. Congenital copper deficiency: copper therapy and dopamine-beta-hydroxylase activity in the mottled (brindled) mouse.
Wenk G; Suzuki K
J Neurochem; 1983 Dec; 41(6):1648-52. PubMed ID: 6644305
[TBL] [Abstract][Full Text] [Related]
7. Menkes kinky-hair syndrome. An inherited defect in the intestinal absorption of copper with widespread effects.
Danks DM; Stevens BJ; Campkell PE; Cartwright EC; Gillespie JM; Townley RR; Blomfield J; Turner BB; Mayne V; Walker-Smith JA
Birth Defects Orig Artic Ser; 1974; 10(10):132-7. PubMed ID: 4462625
[No Abstract] [Full Text] [Related]
8. Genetic defects of iron transport.
Bannerman RM
Fed Proc; 1976 Sep; 35(11):2281-5. PubMed ID: 782924
[TBL] [Abstract][Full Text] [Related]
9. [Copper pathology (author's transl)].
Mallet B; Romette J; Di Costanzo JD
Nouv Presse Med; 1982 Jan; 11(4):271-4. PubMed ID: 7058150
[TBL] [Abstract][Full Text] [Related]
10. Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects.
Danks DM; Campbell PE; Stevens BJ; Mayne V; Cartwright E
Pediatrics; 1972 Aug; 50(2):188-201. PubMed ID: 5045349
[No Abstract] [Full Text] [Related]
11. [Copper level and metallothionein-like Cu-binding protein in cultured skin fibroblasts from patients with Menkes' disease and Wilson's disease].
Sato M; Hayashi A; Ito H; Tojo M; Arima M
No To Shinkei; 1984 Nov; 36(11):1063-8. PubMed ID: 6525319
[TBL] [Abstract][Full Text] [Related]
12. Menkes kinky hair disease. A defect in metallothionein metabolism?
Garnica AD; Frias JL; Easley JF; Rennert OM
Birth Defects Orig Artic Ser; 1974; 10(8):149-55. PubMed ID: 4458824
[No Abstract] [Full Text] [Related]
13. Inborn errors of trace metal metabolism.
Aggett PJ
Br J Hosp Med; 1987 Sep; 38(3):190-6, 200-1. PubMed ID: 3315073
[TBL] [Abstract][Full Text] [Related]
14. [Clinical aspects of Menkes syndrome].
Kolb HJ; Guthoff T
Monatsschr Kinderheilkd; 1987 Dec; 135(12):827-31. PubMed ID: 3437907
[TBL] [Abstract][Full Text] [Related]
15. Kinky hair disease.
Menkes JH
Pediatrics; 1972 Aug; 50(2):181-3. PubMed ID: 5045346
[No Abstract] [Full Text] [Related]
16. [The onset of psychiatric disorders and Wilson's disease].
Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
[TBL] [Abstract][Full Text] [Related]
17. [Menkès disease. Study of copper-dependent enzymes].
Rohmer A; Krug JP; Mennesson M; Mandel P; Mack G; Zawislak R
Pediatrie; 1977; 32(5):447-56. PubMed ID: 889620
[No Abstract] [Full Text] [Related]
18. Metallothionein gene regulation in Menkes' syndrome.
Hamer DH
Arch Dermatol; 1987 Oct; 123(10):1384a-1385a. PubMed ID: 3662572
[TBL] [Abstract][Full Text] [Related]
19. Prenatal and postnatal diagnosis of diseases of copper metabolism.
Chan WY; Rennert OM
Ann Clin Lab Sci; 1982; 12(5):372-80. PubMed ID: 6753725
[TBL] [Abstract][Full Text] [Related]
20. [Disturbances in copper homeostasis are the main cause of serious human diseases].
Bandorowicz-Pikuła J; Pikuła S
Postepy Biochem; 1997; 43(4):281-7. PubMed ID: 9572080
[No Abstract] [Full Text] [Related]
[Next] [New Search]