Majander A - Search Results

1

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Suomalainen A, Majander A, Haltia M, Somer H, Lönnqvist J, Savontaus ML, Peltonen L. Suomalainen A, et al. Among authors: majander a. J Clin Invest. 1992 Jul;90(1):61-6. doi: 10.1172/JCI115856. J Clin Invest. 1992. PMID: 1634620 Free PMC article.

2

Childhood-Onset Leber Hereditary Optic Neuropathy-Clinical and Prognostic Insights.

Barboni P, La Morgia C, Cascavilla ML, Hong EH, Battista M, Majander A, Caporali L, Starace V, Amore G, Renzo AD, Carbonelli M, Nucci P, Jurkute N, Chen BS, Panebianco R, De Negri AM, Sadun F, Parisi V, Bandello F, Sadun AA, Carelli V, Yu-Wai-Man P. Barboni P, et al. Among authors: majander a. Am J Ophthalmol. 2023 May;249:99-107. doi: 10.1016/j.ajo.2022.12.014. Epub 2022 Dec 18. Am J Ophthalmol. 2023. PMID: 36543315

3

Disorders associated with multiple deletions of mitochondrial DNA.

Haltia M, Suomalainen A, Majander A, Somer H. Haltia M, et al. Among authors: majander a. Brain Pathol. 1992 Apr;2(2):133-9. doi: 10.1111/j.1750-3639.1992.tb00681.x. Brain Pathol. 1992. PMID: 1341954 Review.

4

Benzodiazepine sensitivity in Leber's hereditary optic neuroretinopathy.

Nikoskelainen E, Asola M, Kalimo H, Savontaus ML, Majander A. Nikoskelainen E, et al. Among authors: majander a. Lancet. 1992 Nov 14;340(8829):1223-4. doi: 10.1016/0140-6736(92)92925-6. Lancet. 1992. PMID: 1359290 No abstract available.

5

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

Suomalainen A, Paetau A, Leinonen H, Majander A, Peltonen L, Somer H. Suomalainen A, et al. Among authors: majander a. Lancet. 1992 Nov 28;340(8831):1319-20. doi: 10.1016/0140-6736(92)92496-3. Lancet. 1992. PMID: 1360038

6

[Mitochondrial diseases].

Pihko H, Suomalainen A, Somer H, Haltia M, Majander A. Pihko H, et al. Among authors: majander a. Duodecim. 1992;108(6):578-90. Duodecim. 1992. PMID: 1366118 Review. Finnish. No abstract available.

7

[Short stature and calcium deposits in the brain of an 8-year-old girl].

Pihko H, Suomalainen A, Majander A, Wallden T. Pihko H, et al. Among authors: majander a. Duodecim. 1992;108(6):603-6. Duodecim. 1992. PMID: 1366121 Finnish. No abstract available.

8

Gene defects in Leber hereditary optic neuroretinopathy.

Savontaus ML, Huoponen K, Majander A, Aula P, Nikoskelainen EK. Savontaus ML, et al. Among authors: majander a. Biochim Biophys Acta. 1992 Jul 17;1101(2):204-5. Biochim Biophys Acta. 1992. PMID: 1633186 Review. No abstract available.

9

Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion.

Majander A, Suomalainen A, Vettenranta K, Sariola H, Perkkiö M, Holmberg C, Pihko H. Majander A, et al. Pediatr Res. 1991 Oct;30(4):327-30. doi: 10.1203/00006450-199110000-00007. Pediatr Res. 1991. PMID: 1956715

10

Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON).

Majander A, Huoponen K, Savontaus ML, Nikoskelainen E, Wikström M. Majander A, et al. FEBS Lett. 1991 Nov 4;292(1-2):289-92. doi: 10.1016/0014-5793(91)80886-8. FEBS Lett. 1991. PMID: 1959619 Free article.

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