Resultats de la cerca - Heikki Rantala
- Mostrar 1 - 5 resultats de 5
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Viral infections and recurrences of febrile convulsions per Heikki Rantala, M Uhari, Hanna Tuokko
Publicat 1990Artigo -
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Homozygous W748S mutation in the <i>POLG1</i> gene in patients with juvenile‐onset Alpers syndrome and status epilepticus per Johanna Uusimaa, Reetta Hinttala, Heikki Rantala, Markku Päivärinta, Riitta Herva, Matias Röyttä, Heidi K. Soini, Jukka S. Moilanen, Anne M. Remes, Ilmo E. Hassinen, Kari Majamaa
Publicat 2008Artigo -
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Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy per Mikko Muona, Ryosuke Ishimura, Anni Laari, Yoshinobu Ichimura, Tarja Linnankivi, Riikka Keski‐Filppula, Riitta Herva, Heikki Rantala, Anders Paetau, Minna Pöyhönen, Miki Obata, Takefumi Uemura, Thomas Karhu, Norihisa Bizen, Hirohide Takebayashi, Shane McKee, Michael Parker, Nadia Akawi, Jeremy F. McRae, Matthew E. Hurles, Outi Kuismin, Mitja Kurki, Anna‐Kaisa Anttonen, Keiji Tanaka, Aarno Palotie, Satoshi Waguri, Anna‐Elina Lehesjoki, Masaaki Komatsu
Publicat 2016Artigo
Eines de cerca:
Matèries relacionades
Medicine
Epilepsy
Neuroscience
Psychiatry
Biology
Gene
Genetics
Pediatrics
Psychology
Anesthesia
Anticonvulsant
Computer science
Coupling (piping)
Dysfunctional family
Encephalopathy
Febrile convulsions
Hemodynamics
Intensive care medicine
Internal medicine
Lennox–Gastaut syndrome
Materials science
Metallurgy
Mitochondrial DNA
Mutation
Nuclear magnetic resonance
Physics
Point mutation
Programming language
Resting state fMRI
SIGNAL (programming language)