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2. A variant of adrenomyeloneuropathy in a family with adrenoleukodystrophy and adrenomyeloneuropathy. Simpson DA; Pawlak AM; Nigro MA; Wishnow R J Am Osteopath Assoc; 1994 Sep; 94(9):745-8, 751-2. PubMed ID: 7995738 [TBL] [Abstract][Full Text] [Related]
3. Linkage of adrenoleukodystrophy to a polymorphic DNA probe. Aubourg PR; Sack GH; Meyers DA; Lease JJ; Moser HW Ann Neurol; 1987 Apr; 21(4):349-52. PubMed ID: 2883927 [TBL] [Abstract][Full Text] [Related]
4. Incidence of X-linked adrenoleukodystrophy and the relative frequency of its phenotypes. Bezman L; Moser HW Am J Med Genet; 1998 Apr; 76(5):415-9. PubMed ID: 9556301 [No Abstract] [Full Text] [Related]
5. [Familial deficiency of C7 associated with adrenomyeloneuropathy]. Pelletier J; Pestre P; ali Chérif A; Drancourt M; Gallais H; Khalil R Rev Neurol (Paris); 1994; 150(1):78-80. PubMed ID: 7801048 [TBL] [Abstract][Full Text] [Related]
6. [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. PubMed ID: 3671029 [TBL] [Abstract][Full Text] [Related]
7. [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. PubMed ID: 8966090 [TBL] [Abstract][Full Text] [Related]
8. X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes. Berger J; Molzer B; Faé I; Bernheimer H Biochem Biophys Res Commun; 1994 Dec; 205(3):1638-43. PubMed ID: 7811247 [TBL] [Abstract][Full Text] [Related]
10. [Familial adrenoleukodystrophy]. Le Fur JM; Le Meur F; Parent P; Toudic L; Castel Y J Genet Hum; 1985 Dec; 33(5):427-34. PubMed ID: 4093772 [TBL] [Abstract][Full Text] [Related]
11. Progressive neurologic deterioration in a nine-year-old white male. Barness LA; Chandra S; Kling P; Laxova R; Allen DB; Gilbert-Barness E Am J Med Genet; 1990 Dec; 37(4):489-503. PubMed ID: 2260594 [No Abstract] [Full Text] [Related]
12. [Adrenomyeloneuropathy and adrenoleukodystrophy: genetic identity and detection. Apropos of a family]. Labauge P; Ducros A; Khalaf K; Pages M; Blard JM Ann Med Interne (Paris); 1994; 145(1):53-5. PubMed ID: 8192283 [No Abstract] [Full Text] [Related]
13. Adrenomyeloneuropathy and hypothyroidism. A 15 year follow-up case report. Laureti S; Lucarelli M; Santeusanio F; Casucci G Recenti Prog Med; 1992 Feb; 83(2):67-72. PubMed ID: 1502421 [TBL] [Abstract][Full Text] [Related]
14. X-linked adrenoleukodystrophy: the Australasian experience. Kirk EP; Fletcher JM; Sharp P; Carey B; Poulos A Am J Med Genet; 1998 Apr; 76(5):420-3. PubMed ID: 9556302 [TBL] [Abstract][Full Text] [Related]
15. [X-linked adrenoleukodystrophy--2 case reports]. Dumić M; Ille J; Plavsić V; Filipović-Grcić B; Vrljicak K; Barisić N; Roscher A Lijec Vjesn; 1998; 120(1-2):19-23. PubMed ID: 9650481 [TBL] [Abstract][Full Text] [Related]
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17. [Adrenomyeloneuropathy and adrenoleukodystrophy. Description of a family with neurological and psychiatric syndromes and implication for the differential diagnosis of the paraspastic symptoms]. Klemm E; Fröscher W Med Klin (Munich); 1991 Aug; 86(8):390-3. PubMed ID: 1921903 [No Abstract] [Full Text] [Related]