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Results: 1 to 20 of 97

Similar articles for PubMed (Select 9556301)

1.

Incidence of X-linked adrenoleukodystrophy and the relative frequency of its phenotypes.

Bezman L, Moser HW.

Am J Med Genet. 1998 Apr 13;76(5):415-9. Review. No abstract available.

PMID:
9556301
2.

X-linked adrenoleukodystrophy: the Australasian experience.

Kirk EP, Fletcher JM, Sharp P, Carey B, Poulos A.

Am J Med Genet. 1998 Apr 13;76(5):420-3.

PMID:
9556302
3.

X-linked adrenoleukodystrophy with non-diagnostic plasma very long chain fatty acids.

Kennedy CR, Allen JT, Fensom AH, Steinberg SJ, Wilson R.

J Neurol Neurosurg Psychiatry. 1994 Jun;57(6):759-61.

4.

X-linked adrenoleukodystrophy: phenotype distribution and expression of ALDP in Spanish kindreds.

Ruiz M, Coll MJ, Pàmpols T, Girós M.

Am J Med Genet. 1998 Apr 13;76(5):424-7.

PMID:
9556303
5.

Adrenoleukodystrophy in France: an epidemiological study.

Sereni C, Paturneau-Jouas M, Aubourg P, Baumann N, Feingold J.

Neuroepidemiology. 1993;12(4):229-33.

PMID:
8272182
6.

A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degeneration.

Dunne E, Hyman NM, Huson SM, Németh AH.

Ann Neurol. 1999 May;45(5):652-5.

PMID:
10319888
7.

X-linked adrenoleukodystrophy.

Bruyn RP.

Neurology. 1996 Apr;46(4):1192. No abstract available.

PMID:
8780135
8.

Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes.

Moser HW, Kemp S, Smith KD.

Arch Neurol. 1999 Mar;56(3):273-5. No abstract available.

PMID:
10190815
9.

Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy.

Takano H, Koike R, Onodera O, Sasaki R, Tsuji S.

Arch Neurol. 1999 Mar;56(3):295-300.

PMID:
10190819
10.

The prenatal diagnosis of X-linked adrenoleukodystrophy.

Moser AB, Moser HW.

Prenat Diagn. 1999 Jan;19(1):46-8. No abstract available.

PMID:
10073906
11.

[Adrenomyeloneuropathy--an unusual X chromosome-linked disease].

Holmberg BH, Hägg E.

Lakartidningen. 1990 Nov 14;87(46):3873-4. Swedish. No abstract available.

PMID:
2233068
12.

On the front of X-linked adrenoleukodystrophy.

Aubourg P.

Neurochem Res. 1999 Apr;24(4):515-20. Review.

PMID:
10227684
13.

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.

Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ.

Am J Hum Genet. 2002 Jun;70(6):1520-31. Epub 2002 Apr 29.

14.

[Spastic paraparesis and adrenal gland insufficiency: adrenomyeloneuropathy].

Zijlmans JM, van Marion WF.

Ned Tijdschr Geneeskd. 1987 Jan 31;131(5):208-11. Dutch. No abstract available.

PMID:
3822010
15.
16.

Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.

Dvoráková L, Storkánová G, Unterrainer G, Hujová J, Kmoch S, Zeman J, Hrebícek M, Berger J.

Hum Mutat. 2001;18(1):52-60.

PMID:
11438993
17.
18.

Epidemiology of X-linked adrenoleukodystrophy in Japan.

Takemoto Y, Suzuki Y, Tamakoshi A, Onodera O, Tsuji S, Hashimoto T, Shimozawa N, Orii T, Kondo N.

J Hum Genet. 2002;47(11):590-3.

PMID:
12436195
19.

Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Sack GH Jr, Alpern M, Webster T, Feil RP, Morrell JC, Chen G, Chen W, Caskey CT, Moser HW.

Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9489-93.

20.

X-linked adrenoleukodystrophy and haemophilia A in the same kindred.

Nogueira A, Jorge P, Dores J, Cunha M, Sousa S, Pereira I, Campos M, Justiça B, Quelhas D, Sá Miranda M.

J Inherit Metab Dis. 1993;16(3):595-8. No abstract available.

PMID:
7609460
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