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Adriano Jiménez‐Escrig

Hospital Universitario Ramon y Cajal

23H指数
94论文数
4.5K被引数
收录论文 19
发表时间
α-Secretase nonsense mutation (ADAM10 Tyr167*) in familial Alzheimer's disease家族性阿尔茨海默氏病中的 α-分泌酶无义突变 (ADAM10 Tyr167 *)
err2020-10-31
err15
errOAAI
errAguero, Pablo; Sainz, Maria Jose; Garcia-Ayllon, Maria-Salud; Saez-Valero, Javier; Tellez, Raquel; Guerrero-Lopez, Rosa; Perez-Perez, Julian; Jimenez-Escrig, Adriano; Gomez-Tortosa, Estrella
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Teaching Video NeuroImages: Palatal myoclonus in leukodystrophies: A clinical sign orienting to Alexander disease
err2020-01-14
err0
errOAAI
errMartinez-Poles, Javier; Escribano-Paredes, Jose Bernardo; Garcia-Madrona, Sebastian; Nedkova-Hristova, Velina; Jimenez-Escrig, Adriano
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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
err2019-10-29
err42
errOAAI
errBandres-Ciga, Sara; Ahmed, Sarah; Sabir, Marya S.; Blauwendraat, Cornelis; Adarmes-Gomez, Astrid D.; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fatima; Carrion-Claro, Mario; Gomez-Garre, Pilar; Jesus, Silvia; Labrador-Espinosa, Miguel A.; Macias, Daniel; Mendez-del-Barrio, Carlota; Perinan-Tocino, Teresa; Tejera-Parrado, Cristina; Vargas-Gonzalez, Laura; Diez-Fairen, Monica; Alvarez, Ignacio; Pablo Tartari, Juan; Buongiorno, Mariateresa; Aguilar, Miquel; Gorostidi, Ana; Alberto Bergareche, Jesus; Mondragon, Elisabet; Vinagre-Aragon, Ana; Croitoru, Ioana; Ruiz-Martinez, Javier; Dols-Icardo, Oriol; Kulisevsky, Jaime; Marin-Lahoz, Juan; Pagonabarraga, Javier; Pascual-Sedano, Berta; Ezquerra, Mario; Camara, Ana; Compta, Yaroslau; Fernandez, Manel; Fernandez-Santiago, Ruben; Munoz, Esteban; Tolosa, Eduard; Valldeoriola, Francesc; Gonzalez-Aramburu, Isabel; Sanchez Rodriguez, Antonio; Sierra, Maria; Menendez-Gonzalez, Manuel; Blazquez, Marta; Garcia, Ciara; Martin, Esther Suarez-San; Garcia-Ruiz, Pedro; Carlos Martinez-Castrillo, Juan; Vela-Desojo, Lydia; Ruz, Clara; Javier Barrero, Francisco; Escamilla-Sevilla, Francisco; Minguez-Castellanos, Adolfo; Cerdan, Debora; Tabernero, Cesar; Gomez Heredia, Maria Jose; Perez Errazquin, Francisco; Romero-Acebal, Manolo; Feliz, Cici; Luis Lopez-Sendon, Jose; Mata, Marina; Martinez Torres, Irene; Kim, Jonggeol Jeffrey; Dalgard, Clifton L.; Brooks, Janet; Saez-Atienzar, Sara; Raphael Gibbs, J.; Jorda, Rafael; Botia, Juan A.; Bonet-Ponce, Luis; Morrison, Karen E.; Clarke, Carl; Tan, Manuela; Morris, Huw; Edsall, Connor; Hernandez, Dena; Simon-Sanchez, Javier; Nalls, Mike A.; Scholz, Sonja W.; Jimenez-Escrig, Adriano; Duarte, Jacinto; Vives, Francisco; Duran, Raquel; Hoenicka, Janet; Alvarez, Victoria; Infante, Jon; Jose Marti, Maria; Clarimon, Jordi; Lopez de Munain, Adolfo; Pastor, Pau; Mir, Pablo; Singleton, Andrew
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PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progression
err2019-04-01
err30
PREAI
errDarling, Alejandra; Aguilera-Albesa, Sergio; Aisha Tello, Cristina; Serrano, Mercedes; Tomas, Miguel; Camino-Leon, Rafael; Fernandez-Ramos, Joaquin; Jimenez-Escrig, Adriano; Poo, Pilar; O'Callaghan, Mar; Ortez, Carlos; Nascimento, Andres; Fernandez Mesaque, Ramon Candau; Madruga, Marcos; Arrabal, Luisa; Roldan, Susana; Gomez-Martin, Hilario; Garrido, Cristina; Temudo, Teresa; Jou-Munoz, Cristina; Muchart, Jordi; Huisman, Thierry A. G. M.; Poretti, Andrea; Lupo, Vincenzo; Espinos, Carmen; Perez-Duenas, Belen
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RNA-Seq blood transcriptome profiling in familial attention deficit and hyperactivity disorder (ADHD)
err2018-12-01
err11
PREAI
errLorenzo, Gustavo; Braun, Jorge; Munoz, Gonzalo; Casarejos, Maria J.; Bazan, Eulalia; Jimenez-Escrig, Adriano
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A novel ATTR L32V mutation causes familial amyloid polyneuropathy in a Bolivian family
err2017-07-27
err3
PREAI
errMartinez-Ulloa, Pedro L.; Vallejo, Manuela; Corral, Inigo; Garcia-Barragan, Nuria; Alcazar, Alberto; Martinez-Alonso, Emma; Martinez-Poles, Javier; Pian, Hector; Jimenez-Escrig, Adriano
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Optimal excitation and emission wavelengths to analyze amino acids and optimize neurotransmitters quantification using precolumn OPA-derivatization by HPLC
err2015-02-18
err51
errOAAI
errPerucho, J.; Gonzalo-Gobernado, R.; Bazan, E.; Casarejos, M. J.; Jimenez-Escrig, A.; Asensio, M. J.; Herranz, A. S.
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Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of cerebrotendinous xanthomatosis
err2012-07-31
err5
errOAAI
errTaboada, Maria; Martinez, Diego; Pilo, Belen; Jimenez-Escrig, Adriano; Robinson, Peter N.; Sobrido, Maria J.
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Effects of Intravenous Administration of Human Umbilical Cord Blood Stem Cells in 3-Acetylpyridine-Lesioned Rats
err2012-01-01
err6
errOAAI
errCalatrava-Ferreras, Lucia; Gonzalo-Gobernado, Rafael; Herranz, Antonio S.; Reimers, Diana; Montero Vega, Teresa; Jimenez-Escrig, Adriano; Richart Lopez, Luis Alberto; Bazan, Eulalia
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Clinical-Genetic Correlations in Familial Alzheimer's Disease Caused by Presenilin 1 Mutations早老素1突变引起的家族性阿尔茨海默病的临床-遗传相关性
err2010-01-28
err50
PREAI
errGomez-Tortosa, Estrella; Barquero, Sagrario; Baron, Manuel; Gil-Neciga, Eulogio; Castellanos, Fernando; Zurdo, Martin; Manzano, Sagrario; Munoz, David G.; Jimenez-Huete, Adolfo; Rabano, Alberto; Jose Sainz, M.; Guerrero, Rosa; Gobernado, Isabel; Perez-Perez, Julian; Jimenez-Escrig, Adriano
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Histocompatibility class I and II antigens in extensive kindred with Sneddon's syndrome and related hypercoagulation disorders
err2007-01-01
err2
PREAI
errLousa, Manuel; Pardo, Ana; Arnaiz-Villena, Antonio; Jimenez-Escrig, Adriano; Gobernado, Jose
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A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes
errBRAIN
IF11.7
err2005-04-20
err10
PREAI
errJimenez-Escrig, A; Gomez-Tortosa, E; Baron, M; Rabano, A; Arcos-Burgos, M; Palacios, LG; Yusta, A; Anta, P; Perez, I; Hierro, M; Munoz, DG; Barquero, S
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Patient with amusia and frontotemporal degeneration with familiar history
err2004-07-01
err0
PREAI
errBarquero, MS; Jiménez-Escrig, A; Gómez-Tortosa, E; Barón, M; Payno, MA; Villanueva, C; Rábano, A; Muñoz, D
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Variability in age at onset within siblings with familial Alzheimer's disease:: Results from the Genodem Project
err2004-07-01
err0
PREAI
errGómez-Tortosa, E; Barón, M; Jiménez-Escrig, A; Sainz, MJ; Manzano, S; Payno, M; Barquero, MS
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A large multigenerational pedigree of autosomal dominant late-onset definite Alzheimer's disease implies novel genetic causes
err2004-07-01
err0
PREAI
errJimenez-Escrig, A; Gomez-Tortosa, E; Baron, M; Rabano, A; Muñoz, P; Perez, I; David, M; Barquero, MS
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Oculo-auricular phenomenon secondary to vestibular dysfunction
err2002-05-21
err2
PREAI
errJiménez-Escrig, A; San-Millan, JM; Barón, M
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ANTIGANGLIOSIDE ANTIBODIES IN TOXIC OIL SYNDROME
err1995-07-01
err0
errOAAI
errINIGUEZ, C; JIMENEZESCRIG, A; GOBERNADO, J; DEBLAS, G; NOCITO, M; DELVILLAR, ML; GONZALEZPORQUE, P
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CUT-OFF SELECTION IN ANTIACETYLCHOLINE RECEPTOR ANTIBODY DETERMINATION
err1994-08-01
err0
errOAAI
errMARTINEZCASTRILLO, JC; ORENSANZ, LM; JIMENEZESCRIG, A; SOMOZA, E
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