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Isohanni, P
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1

RWD131 A Nationwide Feasibility Study and Study Concept to ..:

Kyttälä, M. ; Auranen, M. ; Vesikansa, A...
Value in Health.  26 (2023)  12 - p. S529 , 2023
Link: https://doi.org/10.1016/..
 
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2

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A ..:

Isohanni, P. ; Carroll, C. ; Suomalainen, A..
European Journal of Paediatric Neurology.  21 (2017)  - p. e137-e138 , 2017
Link: https://doi.org/10.1016/..
 
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3

A new phenotype of RYR1-myopathy: Mild dominant calf myopat..:

Jokela, M. ; Isohanni, P. ; Penttilä, S..
Neuromuscular Disorders.  26 (2016)  - p. S136 , 2016
Link: https://doi.org/10.1016/..
 
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4

PP03.4 – 2660: Recurrent metabolic crises and mitochondrial..:

Isohanni, P. ; Linnankivi, T. ; Honarmand, S....
European Journal of Paediatric Neurology.  19 (2015)  - p. S37 , 2015
Link: https://doi.org/10.1016/..
 
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5

Leukoencephalopathy with brainstem and spinal cord involvem..:

van Berge, L. ; Hamilton, E. M. ; Linnankivi, T....
Brain.  137 (2014)  4 - p. 1019-1029 , 2014
Link: https://doi.org/10.1093/..
 
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6

O20 – 1660 Leigh syndrome: a multicenter study of natural h..:

Sofou, K ; de Coo, IF ; de Angst, IB...
European Journal of Paediatric Neurology.  17 (2013)  - p. S7 , 2013
Link: https://doi.org/10.1016/..
 
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7

Dominant encephalopathy mimicking mitochondrial disease:

Lönnqvist, T. ; Isohanni, P. ; Valanne, L....
Neurology.  76 (2011)  1 - p. 101-103 , 2011
Link: https://doi.org/10.1212/..
 
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8

P16.12 Phenotypes associated with a novel lamin A/C mutatio..:

Pihko, H. ; Isohanni, P. ; Paetau, A..
European Journal of Paediatric Neurology.  15 (2011)  - p. S98 , 2011
Link: https://doi.org/10.1016/..
 
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9

POLG1manifestations in childhood:

Isohanni, P. ; Hakonen, A.H. ; Euro, L....
Neurology.  76 (2011)  9 - p. 811-815 , 2011
Link: https://doi.org/10.1212/..
 
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10

Distribution of Campylobacter jejuni isolates from Turkey F..:

Perko‐Mäkelä, P. ; Alter, T. ; Isohanni, P...
Zoonoses and Public Health.  58 (2011)  6 - p. 388-398 , 2011
Link: https://doi.org/10.1111/..
 
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11

Thymidine kinase 2 mutations in autosomal recessive progres..:

Tyynismaa, H. ; Sun, R. ; Ahola-Erkkila, S....
Human Molecular Genetics.  21 (2011)  1 - p. 66-75 , 2011
Link: https://doi.org/10.1093/..
 
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12

Wines as possible meat marinade ingredients possess antimic..:

Isohanni, P. ; Alter, T. ; Saris, P..
Poultry Science.  89 (2010)  12 - p. 2704-2710 , 2010
Link: https://doi.org/10.3382/..
 
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13

Thymidine kinase 2 defects can cause multi-tissue mtDNA dep..:

Gotz, A. ; Isohanni, P. ; Pihko, H....
Brain.  131 (2008)  11 - p. 2841-2850 , 2008
Link: https://doi.org/10.1093/..
 
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14

Recessive Twinkle mutations in early onset encephalopathy w..:

Hakonen, A. H. ; Isohanni, P. ; Paetau, A....
Brain.  130 (2007)  11 - p. 3032-3040 , 2007
Link: https://doi.org/10.1093/..
 
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15

NMO02 Myopathy caused by mitochondrial thymidine kinase (TK..:

Isohanni, P. ; Götz, A. ; Marjavaara, S....
European Journal of Paediatric Neurology.  11 (2007)  - p. 37 , 2007
Link: https://doi.org/10.1016/..
 
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