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A comprehensive serum lipidome profiling of amyotrophic lateral sclerosis. [electronic resource] by
- FernÁndez-Eulate, Gorka
- Ruiz-Sanz, JosÉ Ignacio
- Riancho, Javier
- ZufirÍa, Monica
- GereÑu, Gorka
- FernÁndez-TorrÓn, Roberto
- Poza-Aldea, Juan JosÉ
- Ondaro, Jon
- Espinal, Juan Bautista
- GonzÁlez-ChinchÓn, Gonzalo
- Zulaica, Miren
- Ruiz-Larrea, Maria BegoÑa
- LÓpez De Munain, Adolfo
- Gil-Bea, Francisco Javier
Producer: 20210609
In:
Amyotrophic lateral sclerosis & frontotemporal degeneration vol. 21
Availability: No items available.
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Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease. [electronic resource] by
- Gutiérrez Gutiérrez, Gerardo
- Díaz-Manera, Jordi
- Almendrote, Míriam
- Azriel, Sharona
- Eulalio Bárcena, José
- Cabezudo García, Pablo
- Camacho Salas, Ana
- Casanova Rodríguez, Carlos
- Cobo, Ana María
- Díaz Guardiola, Patricia
- Fernández-Torrón, Roberto
- Gallano Petit, María Pía
- García Pavía, Pablo
- Gómez Gallego, María
- Gutiérrez Martínez, Antonio José
- Jericó, Ivonne
- Kapetanovic García, Solange
- López de Munaín Arregui, Adolfo
- Martorell, Loreto
- Morís de la Tassa, Germán
- Moreno Zabaleta, Raúl
- Muñoz-Blanco, José Luis
- Olivar Roldán, Juana
- Pascual Pascual, Samuel Ignacio
- Peinado Peinado, Rafael
- Pérez, Helena
- Poza Aldea, Juan José
- Rabasa, María
- Ramos, Alba
- Rosado Bartolomé, Alfredo
- Rubio Pérez, Miguel Ángel
- Urtizberea, Jon Andoni
- Zapata-Wainberg, Gustavo
- Gutiérrez-Rivas, Eduardo
Producer: 20200903
In:
Medicina clinica vol. 153
Availability: No items available.
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Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy. [electronic resource] by
- Böhm, Johann
- Biancalana, Valérie
- Dechene, Elizabeth T
- Bitoun, Marc
- Pierson, Christopher R
- Schaefer, Elise
- Karasoy, Hatice
- Dempsey, Melissa A
- Klein, Fabrice
- Dondaine, Nicolas
- Kretz, Christine
- Haumesser, Nicolas
- Poirson, Claire
- Toussaint, Anne
- Greenleaf, Rebecca S
- Barger, Melissa A
- Mahoney, Lane J
- Kang, Peter B
- Zanoteli, Edmar
- Vissing, John
- Witting, Nanna
- Echaniz-Laguna, Andoni
- Wallgren-Pettersson, Carina
- Dowling, James
- Merlini, Luciano
- Oldfors, Anders
- Bomme Ousager, Lilian
- Melki, Judith
- Krause, Amanda
- Jern, Christina
- Oliveira, Acary S B
- Petit, Florence
- Jacquette, Aurélia
- Chaussenot, Annabelle
- Mowat, David
- Leheup, Bruno
- Cristofano, Michele
- Poza Aldea, Juan José
- Michel, Fabrice
- Furby, Alain
- Llona, Jose E Barcena
- Van Coster, Rudy
- Bertini, Enrico
- Urtizberea, Jon Andoni
- Drouin-Garraud, Valérie
- Béroud, Christophe
- Prudhon, Bernard
- Bedford, Melanie
- Mathews, Katherine
- Erby, Lori A H
- Smith, Stephen A
- Roggenbuck, Jennifer
- Crowe, Carol A
- Brennan Spitale, Allison
- Johal, Sheila C
- Amato, Anthony A
- Demmer, Laurie A
- Jonas, Jessica
- Darras, Basil T
- Bird, Thomas D
- Laurino, Mercy
- Welt, Selman I
- Trotter, Cynthia
- Guicheney, Pascale
- Das, Soma
- Mandel, Jean-Louis
- Beggs, Alan H
- Laporte, Jocelyn
Producer: 20120906
In:
Human mutation vol. 33
Availability: No items available.
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