Similar articles for PMID: 5829335

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Sex-linked neurodegenerative disease associated with monilethrix.

Bray PF. Bray PF. Pediatrics. 1965 Sep;36(3):417-20. Pediatrics. 1965. PMID: 5829335 No abstract available.

Menkes kinky hair disease. A defect in metallothionein metabolism?

Garnica AD, Frias JL, Easley JF, Rennert OM. Garnica AD, et al. Birth Defects Orig Artic Ser. 1974;10(8):149-55. Birth Defects Orig Artic Ser. 1974. PMID: 4458824 No abstract available.

Kinky hair disease.

Menkes JH. Menkes JH. Pediatrics. 1972 Aug;50(2):181-3. Pediatrics. 1972. PMID: 5045346 No abstract available.

[The kinky-hair syndrome of Menkes (author's transl)].

Dorn G, Neuhäuser G, Heye D, Kielhorn A. Dorn G, et al. Klin Padiatr. 1973 Nov;185(6):480-9. Klin Padiatr. 1973. PMID: 4798675 German. No abstract available.

[Letter: Original anomalies in a new case of Menkes's disease].

Louis J, Blanckaert D, Desbonnets P, Farriaux JP, Fontaine G. Louis J, et al. Nouv Presse Med. 1975 Apr 12;4(15):1138. Nouv Presse Med. 1975. PMID: 1134937 French. No abstract available.

[A patient with kinky hair disease (Menke's disease)].

Van de Kamp JJ, Oving H, Giesbets MA. Van de Kamp JJ, et al. Ned Tijdschr Geneeskd. 1975 Mar 29;119(13):505-10. Ned Tijdschr Geneeskd. 1975. PMID: 1168863 Dutch. No abstract available.

A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region.

Hamel BC, Wesseling P, Renier WO, van den Helm B, Ropers HH, Kremer H, Mariman EC. Hamel BC, et al. J Med Genet. 1999 Feb;36(2):140-3. J Med Genet. 1999. PMID: 10051014 Free PMC article.

Kinky hair syndrome: response to copper therapy.

Bucknall WE, Haslam RH, Holtzman NA. Bucknall WE, et al. Pediatrics. 1973 Nov;52(5):653-7. Pediatrics. 1973. PMID: 4744662 No abstract available.

["Kinky hair"-syndrome. Menkes' syndrome].

Vestermark S, Vraa-Jensen J. Vestermark S, et al. Ugeskr Laeger. 1973 May 28;135(22):1081. Ugeskr Laeger. 1973. PMID: 4757102 Danish. No abstract available.

Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation.

Turner G, Partington M, Kerr B, Mangelsdorf M, Gecz J. Turner G, et al. Am J Med Genet. 2002 Nov 1;112(4):405-11. doi: 10.1002/ajmg.10714. Am J Med Genet. 2002. PMID: 12376946

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