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Items: 1 to 20 of 51

1.

Mitochondrial neurogastrointestinal encephalomyopathy mimicking anorexia nervosa.

Feddersen B, DE LA Fontaine L, Sass JO, Lutz J, Abicht A, Klopstock T, Verma IC, Meisenzahl E, Pogarell O.

Am J Psychiatry. 2009 Apr;166(4):494-5. doi: 10.1176/appi.ajp.2008.08101525. No abstract available.

PMID:
19339372
2.

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.

Hirano M, Nishigaki Y, Martí R.

Neurologist. 2004 Jan;10(1):8-17. Review.

PMID:
14720311
3.

[MNGIE (mitochondrial neurogastrointestinal encephalomyopathy)].

Nishino I.

Ryoikibetsu Shokogun Shirizu. 2001;(36):160-3. Review. Japanese. No abstract available.

PMID:
11596354
4.

Relapsing neuropathy in an 18-year-old woman.

Ginsberg L, Schapira AH, Taanman JW.

Lancet Neurol. 2007 Feb;6(2):192-8. Review. No abstract available.

PMID:
17239807
5.

MNGIE: from nuclear DNA to mitochondrial DNA.

Nishino I, Spinazzola A, Hirano M.

Neuromuscul Disord. 2001 Jan;11(1):7-10. Review.

PMID:
11166160
6.

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): biochemical features and therapeutic approaches.

Lara MC, Valentino ML, Torres-Torronteras J, Hirano M, Martí R.

Biosci Rep. 2007 Jun;27(1-3):151-63. Review.

PMID:
17549623
7.

[Mitochondrial Neuro-Gastro-Intestinal Encephalopathy (MNGIE): When and how to suspect it in front of an atypical anorexia nervosa?]

Danjou M, Guardia D, Geoffroy PA, Seguy D, Cottencin O.

Encephale. 2016 Dec;42(6):574-579. doi: 10.1016/j.encep.2016.05.002. Epub 2016 Jun 28. Review. French.

PMID:
27371119
8.

Mitochondrial encephalopathy.

Longo N.

Neurol Clin. 2003 Nov;21(4):817-31. Review.

PMID:
14743651
9.

[Genetic diseases of the mitochondrial DNA in humans].

Solano A, Playán A, López-Pérez MJ, Montoya J.

Salud Publica Mex. 2001 Mar-Apr;43(2):151-61. Review. Spanish.

PMID:
11381844
10.

[MNGIE--thymidine phosphorylase deficiency].

Nishino I, Hirano M.

Nihon Rinsho. 2002 Apr;60 Suppl 4:349-52. Review. Japanese. No abstract available.

PMID:
12013883
11.

Digestive smooth muscle mitochondrial myopathy in patients with mitochondrial-neuro-gastro-intestinal encephalomyopathy (MNGIE).

Blondon H, Polivka M, Joly F, Flourie B, Mikol J, Messing B.

Gastroenterol Clin Biol. 2005 Aug-Sep;29(8-9):773-8. Review.

12.

Mitochondrial myopathy diagnosis.

Shoffner JM.

Neurol Clin. 2000 Feb;18(1):105-23. Review.

PMID:
10658170
13.

[ARCO (autosomal recessive cardiomyopathy and ophthalmoplegia)].

Goto Y.

Ryoikibetsu Shokogun Shirizu. 2001;(36):170-1. Review. Japanese. No abstract available.

PMID:
11596359
14.

[Mitochondrial diseases].

Nagel JD, Haverkamp F, Lentze MJ.

Klin Padiatr. 1997 Nov-Dec;209(6):345-56. Review. German.

PMID:
9445918
15.

[Diagnostic investigations of mitochondrial diseases with neurological symptoms].

Auré K, Lombès A.

Rev Neurol (Paris). 2007 Feb;163(2):254-63. Review. French.

PMID:
17351548
16.

[Encephalomyopathy].

Nakase H.

Nihon Rinsho. 2002 Apr;60 Suppl 4:501-3. Review. Japanese. No abstract available.

PMID:
12013925
17.

Cellular models for pathogenesis in mitochondrial diseases.

Di Donato S.

Curr Opin Neurol. 1996 Dec;9(6):469-72. Review. No abstract available.

PMID:
9007407
18.

Mitochondrial disorders.

DiMauro S, Tanji K.

Jpn J Hum Genet. 1997 Dec;42(4):473-87. Review.

PMID:
9560947
19.

[Mitochondrial encephalopathies].

Castro-Gago M, Novo-Rodríguez MI, Pintos-Martínez E, Campos Y, Arenas J, Eirís-Puñal J.

Rev Neurol. 2000 Aug 1-15;31(3):263-82. Review. Spanish.

PMID:
10996928
20.

The ophthalmologic manifestations of mitochondrial disease.

Johns DR.

Semin Ophthalmol. 1995 Dec;10(4):295-302. Review.

PMID:
10160216

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