Carrier erythrocyte entrapped thymidine phosphorylas etherapy for MNGIE

被引：75

作者：

Moran, N. F. ^{[1
,2
]}

Bain, M. D. ^{[3
]}

Muqit, M. M. K. ^{[4
]}

Bax, B. E. ^{[3
]}

机构：

[1] Kent & Canterbury Hosp, Canterbury CT1 3NG, Kent, England

[2] Kings Coll Hosp London, London, England

[3] Univ London, Dept Child Hlth, Div Clin & Dev Sci, London WC1E 7HU, England

[4] Inst Neurol, Inst Mol Neurosci, London WC1N 3BG, England

来源：

NEUROLOGY | 2008年 / 71卷 / 09期

关键词：

D O I：

10.1212/01.wnl.0000324602.97205.ab

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：686 / 688

页数：6

共 7 条

[1]

Survival of human carrier erythrocytes in vivo [J].

Bax, BE ;

Bain, MD ;

Talbot, PJ ;

Parker-Williams, EJ ;

Chalmers, RA .

CLINICAL SCIENCE, 1999, 96 (02) :171-178

[2]

Bax BE, 2000, ADV EXP MED BIOL, V486, P47

[3]

A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency [J].

Bax, Bridget E. ;

Bain, Murray D. ;

Fairbanks, Lynette D. ;

Webster, A. David B. ;

Ind, Philip W. ;

Hershfield, Michael S. ;

Chalmers, Ronald A. .

EUROPEAN JOURNAL OF HAEMATOLOGY, 2007, 79 (04) :338-348

[4]

Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE [J].

Hirano, M. ;

Marti, R. ;

Casali, C. ;

Tadesse, S. ;

Uldrick, T. ;

Fine, B. ;

Escolar, D. M. ;

Valentino, M. L. ;

Nishino, I. ;

Hesdorffer, C. ;

Schwartz, J. ;

Hawks, R. G. ;

Martone, D. L. ;

Cairo, M. S. ;

DiMauro, S. ;

Stanzani, M. ;

Garvin, J. H., Jr. ;

Savage, D. G. .

NEUROLOGY, 2006, 67 (08) :1458-1460

[5]

MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY (MNGIE) - CLINICAL, BIOCHEMICAL, AND GENETIC FEATURES OF AN AUTOSOMAL RECESSIVE MITOCHONDRIAL DISORDER [J].

HIRANO, M ;

SILVESTRI, G ;

BLAKE, DM ;

LOMBES, A ;

MINETTI, C ;

BONILLA, E ;

HAYS, AP ;

LOVELACE, RE ;

BUTLER, I ;

BERTORINI, TE ;

THRELKELD, AB ;

MITSUMOTO, H ;

SALBERG, LM ;

ROWLAND, LP ;

DIMAURO, S .

NEUROLOGY, 1994, 44 (04) :721-727

[6]

Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiency [J].

Martí, R ;

Nishigaki, Y ;

Hirano, M .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (01) :14-18

[7]

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder [J].

Nishino, I ;

Spinazzola, A ;

Hirano, M .

SCIENCE, 1999, 283 (5402) :689-692

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