Arama Sonuçları - Celia Pérez‐Cerdá
- Gösterilen 1 - 13 sonuçlar arası kayıtlar. 13
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Pharmacological Chaperoning: A Potential Treatment for PMM2-CDG Yazar: Patricia Yuste‐Checa, Sandra Brasil, Alejandra Gámez, Jarl Underhaug, Lourdes R. Desviat, Magdalena Ugarte, Celia Pérez‐Cerdá, Aurora Martı́nez, Belén Pérez
Baskı/Yayın Bilgisi 2016Artigo -
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The molecular landscape of propionic acidemia and methylmalonic aciduria in Latin America Yazar: Belén Pérez, Celia J. Angaroni, Rocío Sánchez-Alcudia, B. Merinero, Celia Pérez‐Cerdá, Norma Spécola, Pilar Rodríguez‐Pombo, Moacır Wajner, Raquel Dodelson de Kremer, Verónica Cornejo, Lourdes R. Desviat, Magdalena Ugarte
Baskı/Yayın Bilgisi 2010Artigo -
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The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism Yazar: M. Esther Gallardo, Lourdes R. Desviat, José Manuel Rodríguez Rodríguez, Jorge Esparza-Gordillo, Celia Pérez‐Cerdá, Belén Pérez, Pilar Rodríguez‐Pombo, Olga Criado‐García, Raúl Sanz, D. Holmes Morton, K. Michael Gibson, Thuy Le, Antònia Ribes, Santiago Rodrı́guez de Córdoba, Magdalena Ugarte, Miguel Á. Peñalva
Baskı/Yayın Bilgisi 2001Artigo -
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Clinical, biochemical, and molecular studies in pyridoxine‐dependent epilepsy. Antisense therapy as possible new therapeutic option Yazar: Belén Pérez, Luis González Gutiérrez‐Solana, Alfonso Verdú, B. Merinero, Patricia Yuste‐Checa, Pedro Ruiz‐Sala, Rocío Calvo, Anil Jalan, Laura López Marín, Oscar Campos, María Ángeles Ruiz, Marta San Miguel, María Eugenia Vázquez, Margarita Castro, Isaac Ferrer, Rosa Navarrete, Lourdes R. Desviat, Pablo Lapunzina, Magdalena Ugarte, Celia Pérez‐Cerdá
Baskı/Yayın Bilgisi 2013Artigo -
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Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment Yazar: Mercedes Serrano, Víctor de Diego, Jordi Muchart, Daniel Cuadras, Ana Felipe‐Rucián, Alfons Macaya, Ramón Velázquez, M. Pilar Poo, Carmen Fons, M. Mar O’Callaghan, Àngels García‐Cazorla, Cristina Martínez Boix, Bernabé Robles, Francisco Antonio Martínez-Carratalá, M. Girós, Paz Briones, Laura Gort, Rafael Artuch, Celia Pérez‐Cerdá, Jaak Jaeken, Belen Pérez, Belén Pérez‐Dueñas
Baskı/Yayın Bilgisi 2015Artigo -
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The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT Yazar: Curtis R. Coughlin, Michael A. Swanson, Kathryn E. Kronquist, Cécile Acquaviva, Tim Hutchin, Pilar Rodríguez‐Pombo, Marja-Leena Väisänen, Elaine Spector, Geralyn Creadon‐Swindell, Ana M. Brás-Goldberg, Elisa Rahikkala, Jukka S. Moilanen, Vincent Mahieu, Gert Matthijs, Irene Bravo‐Alonso, Celia Pérez‐Cerdá, Magdalena Ugarte, Christine Vianey‐Saban, Gunter Scharer, Johan L.K. Van Hove
Baskı/Yayın Bilgisi 2016Artigo -
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Stroke-Like Episodes and Cerebellar Syndrome in Phosphomannomutase Deficiency (PMM2-CDG): Evidence for Hypoglycosylation-Driven Channelopathy Yazar: Mercè Izquierdo-Serra, Antonio Federico Martínez‐Monseny, Laura López, Julia Carrillo-García, Albert Edo, Juan Darío Ortigoza‐Escobar, Oscar Coyoli García, Ramón Cancho‐Candela, M L Carrasco-Marina, Luis Gutiérrez-Solana, Daniel Cuadras, Jordi Muchart, Raquel Montero, Rafael Artuch, Celia Pérez‐Cerdá, Belen Pérez, Belén Pérez‐Dueñas, Alfons Macaya, José M. Fernández‐Fernández, Mercedes Serrano
Baskı/Yayın Bilgisi 2018Artigo -
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Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia Yazar: Matthias R. Baumgartner, Friederike Hörster, Carlo Dionisi‐Vici, Göknur Haliloğlu, Daniela Karall, Kimberly A. Chapman, Martina Huemer, Michel Hochuli, Murielle Assoun, Diana Ballhausen, Alberto Burlina, Brian Fowler, Sarah C. Grünert, Stephanie Grünewald, Tomáš Honzík, B. Merinero, Celia Pérez‐Cerdá, Sabine Scholl‐Bürgi, Flemming Skovby, Frits A. Wijburg, Anita MacDonald, Diego Martinelli, Jörn Oliver Sass, Vassili Valayannopoulos, Anupam Chakrapani
Baskı/Yayın Bilgisi 2014Revisão -
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Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases Yazar: Elena Martín‐Hernández, Luis Aldámiz‐Echevarría, E. Castejón-Ponce, Consuelo Pedrón‐Giner, María L. Couce, Juliana Serrano-Nieto, Guillem Pintos‐Morell, Amaya Bélanger-Quintana, Mercedes Martínez‐Pardo, María Teresa García‐Silva, Pilar Quijada‐Fraile, Isidro Vitoria, Jaime Dalmau, Rosa A. Lama‐More, María Amor Bueno-Delgado, Mirella del Toro-Riera, Inmaculada García‐Jiménez, Concepción Sierra-Córcoles, Mónica Ruiz‐Pons, Luis Peña Quintana, Inmaculada Vives‐Piñera, Ana Heloneida de Araújo Morais, Elena Balmaseda‐Serrano, Silvia Meavilla, Pablo Sanjurjo-Crespo, Celia Pérez‐Cerdá
Baskı/Yayın Bilgisi 2014Artigo -
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CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation Yazar: Jos C. Jansen, Sebahattin Çirak, Monique van Scherpenzeel, Sharita Timal, Janine Reunert, Stephan Rust, Belén Pérez, Dorothée Vicogne, Peter Krawitz, Yoshinao Wada, Angel Ashikov, Celia Pérez‐Cerdá, Celia Medrano, Andrea Arnoldy, Alexander Hoischen, Karin Huijben, Gerry Steenbergen, Dulce Quelhas, Luísa Diogo, Daisy Rymen, Jaak Jaeken, Nathalie Guffon, David Cheillan, Lambertus P. van den Heuvel, Yusuke Maeda, Olaf Kaiser, Ulrike Schara, Patrick Gerner, Marjolein A.W. van den Boogert, Adriaan G. Holleboom, Marie‐Cécile Nassogne, Étienne Sokal, Jody Salomon, Geert van den Bogaart, Joost P.H. Drenth, Martijn A. Huynen, Joris A. Veltman, Ron A. Wevers, Éva Morava, Gert Matthijs, François Foulquier, Thorsten Marquardt, Dirk J. Lefeber
Baskı/Yayın Bilgisi 2016Artigo -
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Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2 Yazar: Óscar Rubio Cabezas, Sarah E. Flanagan, Horia Stanescu, Elena García‐Martínez, Richard Caswell, Hana Lango Allen, Montserrat Antón-Gamero, Jesús Argente, Anna-Marie Bussell, André W. Brändli, Chris Cheshire, Elizabeth Crowne, Simona Dumitriu, Robert Drynda, Julian Hamilton‐Shield, Wesley Hayes, Alexis Hofherr, Daniela Iancu, Naomi Issler, Craig Jefferies, Peter M. Jones, Matthew B. Johnson, Anne Kesselheim, Enriko Klootwijk, M Koettgen, Wendy Lewis, José María Martos, Monika Mozere, Jill T. Norman, Vaksha Patel, Andrew Parrish, Celia Pérez‐Cerdá, Jesús Pozo, Sofia Rahman, Neil J. Sebire, Mehmet Tekman, Peter D. Turnpenny, William van’t Hoff, Daan H.H.M. Viering, Michael N. Weedon, Patricia D. Wilson, Lisa M. Guay‐Woodford, Robert Kleta, Khalid Hussain, Sian Ellard, Detlef Böckenhauer
Baskı/Yayın Bilgisi 2017Artigo
Arama Araçları:
İlgili Konular
Biology
Gene
Medicine
Biochemistry
Internal medicine
Amino acid
Genetics
Chemistry
Enzyme
Gastroenterology
Mutation
Allele
Ataxia
Cell biology
Computational biology
Encephalopathy
Endocrinology
Environmental health
Glycosylation
Hyperammonemia
Methylmalonic acid
Methylmalonic acidemia
Methylmalonic aciduria
Mutant
Newborn screening
Pediatrics
Phenotype
Population
Propionic acidemia
Proteostasis