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Items: 1 to 20 of 210

1.

Familial spastic paraparesis: an adrenoleukodystrophy phenotype?

O'Neill BP, Swanson JW, Brown FR 3rd, Griffin JW, Moser HW.

Neurology. 1985 Aug;35(8):1233-5.

2.

Familial spastic paraparesis and deafness. A new x-linked neurodegenerative disorder.

Wells CR, Jankovic J.

Arch Neurol. 1986 Sep;43(9):943-6.

PMID:
3741213
3.

Adrenoleukodystrophy: clinical and biochemical manifestations in carriers.

O'Neill BP, Moser HW, Saxena KM, Marmion LC.

Neurology. 1984 Jun;34(6):798-801.

PMID:
6539445
4.

[Adrenomyeloneuropathy. Report of two siblings and female heterozygote with spastic paraparesis].

Ibi T, Matsuoka Y, Sobue I, Matsui T, Tsuji S.

Rinsho Shinkeigaku. 1982 Nov;22(11):980-5. Japanese. No abstract available.

PMID:
7168937
5.

[A case of symptomatic adrenoleukodystrophy heterozygote manifested by spastic paraparesis of late onset].

Nemoto H, Sunohara N, Matsuda Y, Satoyoshi E, Yagishita A.

Rinsho Shinkeigaku. 1989 Jul;29(7):914-8. Review. Japanese.

PMID:
2680206
6.

[Adrenoleukomyeloneuropathy. A familial case].

Gastaut JL, Pellissier JF, Pfister B, Figarella-Branger D, Michel B.

Rev Neurol (Paris). 1988;144(5):338-46. French.

PMID:
3420352
7.

Adrenoleukodystrophy: clinical, pathological and biochemical findings in two brothers with the onset of cerebral disease in adult life.

Esiri MM, Hyman NM, Horton WL, Lindenbaum RH.

Neuropathol Appl Neurobiol. 1984 Nov-Dec;10(6):429-45.

PMID:
6527732
8.

Adrenoleukodystrophy in Israel: a genetic, clinical and biochemical study.

Chemke J, Lieberman E, Carmi R, Abarbanel Y, Costeff H, Goldhammer Y, Moser HW.

Isr J Med Sci. 1984 Dec;20(12):1123-32.

PMID:
6097565
9.

[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical spectrum, electrophysiologic and biochemical findings in 4 families].

Klemm E, Zierz S.

Nervenarzt. 1990 Apr;61(4):219-24. German. No abstract available.

PMID:
2162008
10.

Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family.

Willems PJ, Vits L, Wanders RJ, Coucke PJ, Van der Auwera BJ, Van Elsen AF, Raeymaekers P, Van Broeckhoven C, Schutgens RB, Dacremont G, et al.

Arch Neurol. 1990 Jun;47(6):665-9.

PMID:
2161209
11.

[Adult disclosure of a case of familial adrenoleukodystrophy].

Turpin JC, Paturneau-Jouas M, Sereni C, Pluot M, Baumann N.

Rev Neurol (Paris). 1985;141(4):289-95. French.

PMID:
2990005
12.

Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy.

Cotrufo R, Melone MA, Monsurro MR, Di Iorio G, Carella C, Moser HW.

Am J Med Genet. 1987 Apr;26(4):833-8.

PMID:
3591825
13.

[Familial adrenoleukodystrophy].

Le Fur JM, Le Meur F, Parent P, Toudic L, Castel Y.

J Genet Hum. 1985 Dec;33(5):427-34. French.

PMID:
4093772
14.

Identification of female carriers of adrenoleukodystrophy.

Moser HW, Moser AE, Trojak JE, Supplee SW.

J Pediatr. 1983 Jul;103(1):54-9.

PMID:
6864396
15.

[Familial spastic paraparesis: phenotypic variant of adrenoleukodystrophy].

de Andrés C, Giménez-Roldán S.

Neurologia. 1990 Jan;5(1):24-8. Spanish.

PMID:
2361026
16.

Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy.

Moser HW, Moser AE, Singh I, O'Neill BP.

Ann Neurol. 1984 Dec;16(6):628-41.

PMID:
6524872
17.

[Apropos of a familial case of adrenoleukodystrophy related to X chromosome diagnosed prenatally].

Parent P, Le Meur F, Alix D, Le Fur JM, Toudic L, Castel Y.

Pediatrie. 1987;42(4):297-301. French.

PMID:
3671029
18.

[Adrenomyeloneuropathy. 4 cases developing with the features of familial spasmodic paraplegia].

Rondot P, De Recondo J, Davous P, Dubas F, Khoubesserian P, Coignet A.

Ann Med Interne (Paris). 1984;135(7):542-7. French.

PMID:
6517427
19.

Adrenoleukodystrophy and variants. Clinical, neurophysiological and biochemical studies in patients and family members.

Goto I, Kobayashi T, Antoku Y, Tobimatsu S, Kuroiwa Y.

J Neurol Sci. 1986 Jan;72(1):103-12.

PMID:
3081689
20.

Very long-chain fatty acids in erythrocyte membrane sphingomyelin: detection of ALD hemizygotes and heterozygotes.

Tanaka K, Shimada M, Naruto T, Yamamoto H, Saeki Y, Sai H, Hirose G.

Neurology. 1986 Jun;36(6):791-5.

PMID:
3703284

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