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Procalcitonin, a high acute phase reactant in antiepileptic hypersentivity syndrome in pediatric age. [electronic resource] by
- Cantarín-Extremera, Verónica
- Castaño-De La Mota, Cristina
- Alvarez-Coca, Javier
- Rojas, Mariluz Ruiz-Falcó
- Gutierrez-Solana, Luis González
- García Peñas, Juan José
- Martínez-Pérez, Jorge
- Duat-Rodríguez, Anna
- López-Marín, Laura
- Losada-Del Pozo, Rebeca
Producer: 20120612
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 16
Availability: No items available.
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4.
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Vanishing white matter disease in a spanish population. [electronic resource] by
- Turón-Viñas, Eulàlia
- Pineda, Mercè
- Cusí, Victòria
- López-Laso, Eduardo
- Del Pozo, Rebeca Losada
- Gutiérrez-Solana, Luis González
- Moreno, David Conejo
- Sierra-Córcoles, Concha
- Olabarrieta-Hoyos, Naiara
- Madruga-Garrido, Marcos
- Aguirre-Rodríguez, Javier
- González-Álvarez, Verónica
- O'Callaghan, Mar
- Muchart, Jordi
- Armstrong-Moron, Judith
Producer: 20140804
In:
Journal of central nervous system disease vol. 6
Availability: No items available.
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5.
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Urinary sulphatoxymelatonin as a biomarker of serotonin status in biogenic amine-deficient patients. [electronic resource] by
- Batllori, Marta
- Molero-Luis, Marta
- Arrabal, Luisa
- Heras, Javier de Las
- Fernandez-Ramos, Joaquín-Alejandro
- Gutiérrez-Solana, Luis González
- Ibáñez-Micó, Salvador
- Domingo, Rosario
- Campistol, Jaume
- Ormazabal, Aida
- Sedel, Frederic
- Opladen, Thomas
- Zouvelou, Basiliki
- Pons, Roser
- Garcia-Cazorla, Angels
- Lopez-Laso, Eduardo
- Artuch, Rafael
Producer: 20190802
In:
Scientific reports vol. 7
Availability: No items available.
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Clinical, biochemical, and molecular studies in pyridoxine-dependent epilepsy. Antisense therapy as possible new therapeutic option. [electronic resource] by
- Pérez, Belén
- Gutiérrez-Solana, Luis González
- Verdú, Alfonso
- Merinero, Begoña
- Yuste-Checa, Patricia
- Ruiz-Sala, Pedro
- Calvo, Rocio
- Jalan, Anil
- Marín, Laura López
- Campos, Oscar
- Ruiz, Maria Ángeles
- San Miguel, Marta
- Vázquez, Maria
- Castro, Margarita
- Ferrer, Isaac
- Navarrete, Rosa
- Desviat, Lourdes Ruiz
- Lapunzina, Pablo
- Ugarte, Magdalena
- Pérez-Cerdá, Celia
Producer: 20130402
In:
Epilepsia vol. 54
Availability: No items available.
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7.
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Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. [electronic resource] by
- Li, Rong
- Johnson, Anne B
- Salomons, Gajja
- Goldman, James E
- Naidu, Sakkubai
- Quinlan, Roy
- Cree, Bruce
- Ruyle, Stephanie Z
- Banwell, Brenda
- D'Hooghe, Marc
- Siebert, Joseph R
- Rolf, Cristin M
- Cox, Helen
- Reddy, Alyssa
- Gutiérrez-Solana, Luis González
- Collins, Amanda
- Weller, Roy O
- Messing, Albee
- van der Knaap, Marjo S
- Brenner, Michael
Producer: 20050425
In:
Annals of neurology vol. 57
Availability: No items available.
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8.
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A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteins. [electronic resource] by
- Navarro-Sastre, Aleix
- Tort, Frederic
- Stehling, Oliver
- Uzarska, Marta A
- Arranz, José Antonio
- Del Toro, Mireia
- Labayru, M Teresa
- Landa, Joseba
- Font, Aida
- Garcia-Villoria, Judit
- Merinero, Begoña
- Ugarte, Magdalena
- Gutierrez-Solana, Luis Gonzalez
- Campistol, Jaume
- Garcia-Cazorla, Angels
- Vaquerizo, Julian
- Riudor, Encarnació
- Briones, Paz
- Elpeleg, Orly
- Ribes, Antonia
- Lill, Roland
Producer: 20120221
In:
American journal of human genetics vol. 89
Availability: No items available.
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