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PubPharm (106)
1
Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant
enthalten in:
Clinical genetics
| 2023
von
Hautakangas, M.
|
Widgren, P.
|
Korpelainen, P.
| +12
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2
Novel human lymph node-derived matrix supports the adhesion of metastatic oral carcinoma cells
enthalten in:
BMC cancer
| 2023
von
Naakka, E.
|
Wahbi, W.
|
Tiikkaja, R.
| +13
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3
Novel human lymph node-derived matrix supports the adhesion of metastatic oral carcinoma cells
enthalten in:
BMC cancer
| 2023
von
Naakka, E.
|
Wahbi, W.
|
Tiikkaja, R.
| +13
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4
Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease
enthalten in:
Frontiers in neuroscience
| 2023
von
Tallgren, A.
|
Kager, L.
|
O'Grady, G.
| +15
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5
Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant
enthalten in:
Clinical Genetics
| 2023
von
Hautakangas, M.
|
Widgren, P.
|
Korpelainen, P.
| +12
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6
Priming protects the spinal cord in an experimental aortic occlusion model
enthalten in:
The Journal of thoracic and cardiovascular surgery
| 2022
von
Honkanen, H.
|
Mustonen, C.
|
Herajärvi, J.
| +6
CommentIn: J Thorac Cardiovasc Surg. 2022 Sep;164(3):811-813. - PMID 33131887
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7
Spinal cord injury during selective cerebral perfusion and segmental artery occlusion : an experimental study
enthalten in:
Interactive cardiovascular and thoracic surgery
| 2022
von
Honkanen, H.
|
Mustonen, C.
|
Tuominen, H.
| +3
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8
Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction
enthalten in:
The Journal of allergy and clinical immunology
| 2021
von
Kaustio, M.
|
Nayebzadeh, N.
|
Hinttala, R.
| +34
ErratumIn: J Allergy Clin Immunol. 2021 Dec;148(6):1603. - PMID 34872653
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9
Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease
enthalten in:
Molecular medicine (Cambridge, Mass.)
| 2020
von
Hiltunen, A.
|
Kangas, S.
|
Ohlmeier, S.
| +10
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10
Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease
enthalten in:
Molecular medicine
| 2020
von
Hiltunen, A.
|
Kangas, S.
|
Ohlmeier, S.
| +10
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Acta neuropathologica
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BBB damage
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