Results
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1061.
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1062.
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1063.
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1064.
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1065.
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1066.
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1067.
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Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family. [electronic resource] by
- de la Peña, P
- Bornstein, B
- del Hoyo, P
- Fernández-Moreno, M A
- Martín, M A
- Campos, Y
- Gómez-Escalonilla, C
- Molina, J A
- Cabello, A
- Arenas, J
- Garesse, R
Producer: 20011101
In:
Neurology vol. 57
Availability: No items available.
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1068.
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1069.
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1070.
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1071.
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1072.
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1073.
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1074.
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1075.
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1076.
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Evaluation of diagnostic NOTCH3 immunostaining in CADASIL. [electronic resource] by
- Lesnik Oberstein, Saskia A J
- van Duinen, Sjoerd G
- van den Boom, Rivka
- Maat-Schieman, Marion L C
- van Buchem, Mark A
- van Houwelingen, Hans C
- Hegeman-Kleinn, Ingrid M
- Ferrari, Michel D
- Breuning, Martijn H
- Haan, Joost
Producer: 20031001
In:
Acta neuropathologica vol. 106
Availability: No items available.
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1077.
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1078.
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1079.
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1080.
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Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation. [electronic resource] by
- Tuominen, S
- Juvonen, V
- Amberla, K
- Jolma, T
- Rinne, J O
- Tuisku, S
- Kurki, T
- Marttila, R
- Pöyhönen, M
- Savontaus, M L
- Viitanen, M
- Kalimo, H
Producer: 20010830
In:
Stroke vol. 32
Availability: No items available.
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