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Items: 1 to 20 of 190

1.

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
2.

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
3.

[Examination of very long chain fatty acids in diagnosis of x-linked adrenoleukodystrophy].

Stradomska TJ, Tylki-Szymańska A.

Pediatr Pol. 1996 Mar;71(3):197-201. Polish.

PMID:
8966090
4.

[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
5.

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
6.

[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
7.

[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
8.

Allogeneic bone marrow transplantation in adrenoleukodystrophy: clinical, pathologic, and biochemical studies.

Yeager AM, Moser HW, Tutschka PJ, Saral R, Moser AE, Kumar AA, Santos GW.

Birth Defects Orig Artic Ser. 1986;22(1):79-100. No abstract available.

PMID:
3516244
10.

[Adrenoleukodystrophy in a pair of siblings].

Rosskamp R, Fichsel H, Röder B, Conzelmann E, Hinrichs U.

Klin Padiatr. 1985 Jan-Feb;197(1):61-4. German.

PMID:
2983146
11.

Adrenoleukodystrophy.

Moser HW, Bergin A, Naidu S, Ladenson PW.

Endocrinol Metab Clin North Am. 1991 Jun;20(2):297-318. Review.

PMID:
1879401
12.

A new dietary therapy for adrenoleukodystrophy: biochemical and preliminary clinical results in 36 patients.

Moser AB, Borel J, Odone A, Naidu S, Cornblath D, Sanders DB, Moser HW.

Ann Neurol. 1987 Mar;21(3):240-9.

PMID:
2440378
13.

Adrenoleukodystrophy: a genetic, clinical, biochemical and computed tomographic study of four patients in three different families.

Dotti MT, Annunziata P, D'Amore I, Terrosi Vagnoli P, Venturi C, Federico A.

Acta Neurol (Napoli). 1987 Jun;9(3):178-90. No abstract available.

PMID:
3630789
14.

[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
15.

[Adrenoleukodystrophy: significance for genetic counseling of the determination of very long-chain fatty acids and of molecular biology].

Mathieu M, Aubourg P, Guidoux S, Epelbaum S, Benhamou P, Berquin P, Boudailliez B, Piussan C.

Ann Pediatr (Paris). 1990 Mar;37(3):157-61. French.

PMID:
2350140
16.

[Adrenomyeloneuropathy: clinical, genetic and morphologic features. Apropos of 5 cases].

Rondot P, de Recondo J, Davous P, Dubas F, Khoubesserian P.

Acta Neurol Belg. 1983 Nov-Dec;83(5):246-60. French.

PMID:
6686915
17.

[X-linked adrenoleukodystrophy--case reports of 4 patients in a family].

Dumić M, Ille J, Fumić K, Kacić-Milicić Z, Cvitanović M, Plavsić V, Spehar A, Janjanin N, Filipović-Grcić B.

Lijec Vjesn. 2002 Aug-Sep;124(8-9):258-62. Croatian.

PMID:
12587436
18.

Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.

Bezman L, Moser AB, Raymond GV, Rinaldo P, Watkins PA, Smith KD, Kass NE, Moser HW.

Ann Neurol. 2001 Apr;49(4):512-7.

PMID:
11310629
19.

[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
20.

Adrenoleukodystrophy presenting as spinocerebellar degeneration.

Nakazato T, Sato T, Nakamura T, Tsuji S, Narabayashi H.

Eur Neurol. 1989;29(4):229-34.

PMID:
2547619

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