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X
Holme, E.
660  Ergebnisse:
Personensuche X
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1

Incidence and risk factors for major bleeding among patient..:

Samuelsen, P ; Eggen, A.E ; Steigen, T...
European Heart Journal.  41 (2020)  Supplement_2 - p. , 2020
Link: https://doi.org/10.1093/..
 
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2

OP5 – 2696: Pyruvate dehydrogenase complex deficiency: Phen..:

Sofou, K. ; Kollberg, G. ; Mitsis, M....
European Journal of Paediatric Neurology.  19 (2015)  - p. S2 , 2015
Link: https://doi.org/10.1016/..
 
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3

Characterization and review of MTHFD1 deficiency: four new ..:

Burda, P. ; Kuster, A. ; Hjalmarson, O....
Journal of Inherited Metabolic Disease.  38 (2015)  5 - p. 863-872 , 2015
Link: https://doi.org/10.1007/..
 
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4

PP6.6 – 1797 Isolated complex I deficiency and atypical cli..:

Björkman, K ; Sofou, K ; Darin, N...
European Journal of Paediatric Neurology.  17 (2013)  - p. S46 , 2013
Link: https://doi.org/10.1016/..
 
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5

Subnormal levels of POL A cause inefficient initiation of l..:

Roos, S. ; Macao, B. ; Fuste, J. M....
Human Molecular Genetics.  22 (2013)  25 - p. 5295-5295 , 2013
Link: https://doi.org/10.1093/..
 
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6

Ekbom's syndrome of photomyoclonus, cerebellar ataxia and c..:

Träff, J. ; Holme, E. ; Ekbom, K..
Acta Neurologica Scandinavica.  92 (2009)  5 - p. 394-397 , 2009
Link: https://doi.org/10.1111/..
 
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7

Molecular basis of infantile reversible cytochrome c oxidas..:

Horvath, R. ; Kemp, J. P. ; Tuppen, H. A. L....
Brain.  132 (2009)  11 - p. 3165-3174 , 2009
Link: https://doi.org/10.1093/..
 
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8

M.P.1.12 Progressive encephalopathy and complex I deficienc..:

Moslemi, A. ; Darin, N. ; Tulinius, M...
Neuromuscular Disorders.  17 (2007)  9-10 - p. 771 , 2007
Link: https://doi.org/10.1016/..
 
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9

M.P.3.06 Genotypes and phenotypes associated with Alpers sy..:

Tulinius, M. ; Kollberg, G. ; Moslemi, A....
Neuromuscular Disorders.  17 (2007)  9-10 - p. 829 , 2007
Link: https://doi.org/10.1016/..
 
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10

ETFDH mutations as a major cause of riboflavin-responsive m..:

Olsen, R. K. J. ; Olpin, S. E. ; Andresen, B. S....
Brain.  130 (2007)  8 - p. 2045-2054 , 2007
Link: https://doi.org/10.1093/..
 
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11

Deficiency of mitochondrial ATP synthase of nuclear genetic..:

Sperl, W. ; Ješina, P. ; Zeman, J....
Neuromuscular Disorders.  16 (2006)  12 - p. 821-829 , 2006
Link: https://doi.org/10.1016/..
 
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12

G.P.3 07 Mitochondrial myopathy with exercise intolerance a..:

Moslemi, A.R. ; Darin, N. ; Kolberg, G....
Neuromuscular Disorders.  16 (2006)  9-10 - p. 661 , 2006
Link: https://doi.org/10.1016/..
 
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13

Mitochondrial myopathy with exercise intolerance and retina..:

Darin, N. ; Kollberg, G. ; Moslemi, A-R....
Neuromuscular Disorders.  16 (2006)  8 - p. 504-506 , 2006
Link: https://doi.org/10.1016/..
 
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14

A novel mutation in the mitochondrial tRNAPhe gene associat..:

Moslemi, A.-R. ; Lindberg, C. ; Toft, J....
Neuromuscular Disorders.  14 (2004)  1 - p. 46-50 , 2004
Link: https://doi.org/10.1016/..
 
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15

Reversibility of cirrhotic regenerative liver nodules upon ..:

Crone, J ; Möslinger, D ; Bodamer, OA...
Acta Paediatrica.  92 (2003)  5 - p. 625-628 , 2003
Link: https://doi.org/10.1111/..
 
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