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Search Results - Linares-Pardo, Ian
Search Results - Linares-Pardo, Ian
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A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotype
by
Ballester‐Lopez, Alfonsina
,
Koehorst, Emma
,
Almendrote, Miriam
,
Martínez‐Piñeiro, Alicia
,
Lucente, Giuseppe
,
Linares‐Pardo, Ian
,
Núñez‐Manchón, Judit
,
Guanyabens, Nicolau
,
Cano, Antoni
,
Lucia, Alejandro
,
Overend, Gayle
,
Cumming, Sarah A.
,
Monckton, Darren G.
,
Casadevall, Teresa
,
Isern, Irina
,
Sánchez‐Ojanguren, Josep
,
Planas, Albert
,
Rodríguez‐Palmero, Agustí
,
Monlleó‐Neila, Laura
,
Pintos‐Morell, Guillem
,
Ramos‐Fransi, Alba
,
Coll‐Cantí, Jaume
,
Nogales‐Gadea, Gisela
Published in
Human mutation
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Manifesting heterozygotes in McArdle disease: a myth or a reality—role of statins
by
Núñez-Manchón, Judit
,
Ballester-Lopez, Alfonsina
,
Koehorst, Emma
,
Linares-Pardo, Ian
,
Coenen, Daniëlle
,
Ara, Ignacio
,
Rodriguez-Lopez, Carlos
,
Ramos-Fransi, Alba
,
Martínez-Piñeiro, Alicia
,
Lucente, Giuseppe
,
Almendrote, Miriam
,
Coll-Cantí, Jaume
,
Pintos-Morell, Guillem
,
Santos-Lozano, Alejandro
,
Arenas, Joaquin
,
Martín, Miguel Angel
,
de Castro, Mauricio
,
Lucia, Alejandro
,
Santalla, Alfredo
,
Nogales-Gadea, Gisela
Published in
Journal of inherited metabolic disease
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Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1
by
Ballester-Lopez, Alfonsina
,
Koehorst, Emma
,
Linares-Pardo, Ian
,
Núñez-Manchón, Judit
,
Almendrote, Miriam
,
Lucente, Giuseppe
,
Arbex, Andrea
,
Puente, Carles Puente
,
Lucia, Alejandro
,
Monckton, Darren G.
,
Cumming, Sarah A.
,
Pintos-Morell, Guillem
,
Coll-Cantí, Jaume
,
Ramos-Fransi, Alba
,
Martínez-Piñeiro, Alicia
,
Nogales-Gadea, Gisela
Published in
Genes
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Correction to: Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins
by
Núñez-Manchón, Judit
,
Ballester-Lopez, Alfonsina
,
Koehorst, Emma
,
Linares-Pardo, Ian
,
Coenen, Daniëlle
,
Ara, Ignacio
,
Rodriguez-Lopez, Carlos
,
Ramos-Fransi, Alba
,
Martínez-Piñeiro, Alicia
,
Lucente, Giuseppe
,
Almendrote, Miriam
,
Coll-Cantí, Jaume
,
Pintos-Morell, Guillem
,
Santos-Lozano, Alejandro
,
Arenas, Joaquin
,
Martín, Miguel Angel
,
de Castro, Mauricio
,
Lucia, Alejandro
,
Santalla, Alfredo
,
Nogales-Gadea, Gisela
Published in
Journal of inherited metabolic disease
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The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1
by
Ballester-Lopez, Alfonsina
,
Linares-Pardo, Ian
,
Koehorst, Emma
,
Núñez-Manchón, Judit
,
Pintos-Morell, Guillem
,
Coll-Cantí, Jaume
,
Almendrote, Miriam
,
Lucente, Giuseppe
,
Arbex, Andrea
,
Magaña, Jonathan J
,
Murillo-Melo, Nadia M
,
Lucia, Alejandro
,
Monckton, Darren G
,
Cumming, Sarah A
,
Ramos-Fransi, Alba
,
Martínez-Piñeiro, Alicia
,
Nogales-Gadea, Gisela
Published in
Genes
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An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epi...
by
Koehorst, Emma
,
Odria, Renato
,
Capó, Júlia
,
Núñez-Manchón, Judit
,
Arbex, Andrea
,
Almendrote, Miriam
,
Linares-Pardo, Ian
,
Natera-de Benito, Daniel
,
Saez, Verónica
,
Nascimento, Andrés
,
Ortez, Carlos
,
Rubio, Miguel Ángel
,
Díaz-Manera, Jordi
,
Alonso-Pérez, Jorge
,
Lucente, Giuseppe
,
Rodriguez-Palmero, Agustín
,
Ramos-Fransi, Alba
,
Martínez-Piñeiro, Alicia
,
Nogales-Gadea, Gisela
,
Suelves, Mònica
Published in
Biomedicines
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Three-dimensional imaging in myotonic dystrophy type 1: Linking molecular alterations with disease phenotype
by
Ballester-Lopez, Alfonsina
,
Núñez-Manchón, Judit
,
Koehorst, Emma
,
Linares-Pardo, Ian
,
Almendrote, Miriam
,
Lucente, Giuseppe
,
Guanyabens, Nicolau
,
Lopez-Osias, Marta
,
Suárez-Mesa, Adrián
,
Hanick, Shaliza Ann
,
Chojnacki, Jakub
,
Lucia, Alejandro
,
Pintos-Morell, Guillem
,
Coll-Cantí, Jaume
,
Martínez-Piñeiro, Alicia
,
Ramos-Fransi, Alba
,
Nogales-Gadea, Gisela
Published in
Neurology. Genetics
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