Results
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35521.
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SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain. [electronic resource] by
- Liao, Y
- Anttonen, A-K
- Liukkonen, E
- Gaily, E
- Maljevic, S
- Schubert, S
- Bellan-Koch, A
- Petrou, S
- Ahonen, V E
- Lerche, H
- Lehesjoki, A-E
Producer: 20101108
In:
Neurology vol. 75
Availability: No items available.
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35522.
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35523.
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35524.
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35525.
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35526.
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35527.
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35528.
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Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. [electronic resource] by
- Veeramah, Krishna R
- Johnstone, Laurel
- Karafet, Tatiana M
- Wolf, Daniel
- Sprissler, Ryan
- Salogiannis, John
- Barth-Maron, Asa
- Greenberg, Michael E
- Stuhlmann, Till
- Weinert, Stefanie
- Jentsch, Thomas J
- Pazzi, Marjorie
- Restifo, Linda L
- Talwar, Dinesh
- Erickson, Robert P
- Hammer, Michael F
Producer: 20130906
In:
Epilepsia vol. 54
Availability: No items available.
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35529.
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35530.
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35531.
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35532.
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35533.
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35534.
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Arc expression identifies the lateral amygdala fear memory trace. [electronic resource] by
- Gouty-Colomer, L A
- Hosseini, B
- Marcelo, I M
- Schreiber, J
- Slump, D E
- Yamaguchi, S
- Houweling, A R
- Jaarsma, D
- Elgersma, Y
- Kushner, S A
Producer: 20161114
In:
Molecular psychiatry vol. 21
Availability: No items available.
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35535.
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35536.
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35537.
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Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita. [electronic resource] by
- Portaro, Simona
- Altamura, Concetta
- Licata, Norma
- Camerino, Giulia M
- Imbrici, Paola
- Musumeci, Olimpia
- Rodolico, Carmelo
- Conte Camerino, Diana
- Toscano, Antonio
- Desaphy, Jean-François
Producer: 20160520
In:
Neuromolecular medicine vol. 17
Availability: No items available.
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35538.
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35539.
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35540.
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