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Results: 7

Related Articles by Review for PubMed (Select 8554662)

1.

Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene.

De Meirleir L, Seneca S, Lissens W, Schoentjes E, Desprechins B.

Pediatr Neurol. 1995 Oct;13(3):242-6.

PMID:
8554662
2.

Familial dystonia and choreoathetosis in three generations associated with bilateral striatal necrosis.

Craver RD, Duncan MC, Nelson JS.

J Child Neurol. 1996 May;11(3):185-8. Review.

PMID:
8734018
3.

A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.

Odièvre MH, Chretien D, Munnich A, Robinson BH, Dumoulin R, Masmoudi S, Kadhom N, Rötig A, Rustin P, Bonnefont JP.

Hum Mutat. 2005 Mar;25(3):323-4. Review.

PMID:
15712224
4.

[Bilateral infantile striatal necrosis].

Capa García L, Herranz Fernández JL, Arteaga Manjón-Cabeza R, Abadi A.

An Esp Pediatr. 1991 Jul;35(1):55-8. Review. Spanish. No abstract available.

PMID:
1772173
5.

[Complex V deficiency].

Matsumoto H, Nishino I.

Nihon Rinsho. 2002 Apr;60 Suppl 4:495-8. Review. Japanese. No abstract available.

PMID:
12013922
6.

Hypoxanthine-guanine phosphoribosyltransferase deficiency.

Sorensen LB, Pepe P.

Bull Rheum Dis. 1970 Dec;21(4):621-5. Review. No abstract available.

PMID:
5532393
7.

[Dementia, chorea].

Watanabe M, Ohkoshi N.

Nihon Rinsho. 2002 Apr;60 Suppl 4:321-4. Review. Japanese. No abstract available.

PMID:
12013876
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