Results
|
1.
|
Molecular characterization of familial hypercholesterolemia in Spain: identification of 39 novel and 77 recurrent mutations in LDLR. [electronic resource] by
- Mozas, Pilar
- Castillo, Sergio
- Tejedor, Diego
- Reyes, Gilberto
- Alonso, Rodrigo
- Franco, Miguel
- Saenz, Pedro
- Fuentes, Francisco
- Almagro, Fátima
- Mata, Pedro
- Pocoví, Miguel
Producer: 20041025
In:
Human mutation vol. 24
Availability: No items available.
|
|
2.
|
Impact of low-density lipoprotein receptor mutational class on carotid atherosclerosis in patients with familial hypercholesterolemia. [electronic resource] by
- Junyent, Mireia
- Gilabert, Rosa
- Jarauta, Estíbaliz
- Núñez, Isabel
- Cofán, Montserrat
- Civeira, Fernando
- Pocoví, Miguel
- Mallén, Miguel
- Zambón, Daniel
- Almagro, Fátima
- Vega, Juan
- Tejedor, Diego
- Ros, Emilio
Producer: 20100415
In:
Atherosclerosis vol. 208
Availability: No items available.
|
|
3.
|
Value of the Definition of Severe Familial Hypercholesterolemia for Stratification of Heterozygous Patients. [electronic resource] by
- Pérez-Calahorra, Sofia
- Sánchez-Hernández, Rosa María
- Plana, Núria
- Marco-Benedi, Victoria
- Pedro-Botet, Juan
- Almagro, Fátima
- Brea, Angel
- Ascaso, Juan Francisco
- Lahoz, Carlos
- Civeira, Fernando
Producer: 20170524
In:
The American journal of cardiology vol. 119
Availability: No items available.
|
|
4.
|
Effect of LDL cholesterol, statins and presence of mutations on the prevalence of type 2 diabetes in heterozygous familial hypercholesterolemia. [electronic resource] by
- Climent, Elisenda
- Pérez-Calahorra, Sofía
- Marco-Benedí, Victoria
- Plana, Nuria
- Sánchez, Rosa
- Ros, Emilio
- Ascaso, Juan F
- Puzo, Jose
- Almagro, Fátima
- Lahoz, Carlos
- Civeira, Fernando
- Pedro-Botet, Juan
Producer: 20190215
In:
Scientific reports vol. 7
Availability: No items available.
|
|
5.
|
|
|
6.
|
Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia. [electronic resource] by
- Civeira, Fernando
- Ros, Emilio
- Jarauta, Estibaliz
- Plana, Nuria
- Zambon, Daniel
- Puzo, Jose
- Martinez de Esteban, Juan P
- Ferrando, Juan
- Zabala, Sergio
- Almagro, Fatima
- Gimeno, Jose A
- Masana, Luis
- Pocovi, Miguel
Producer: 20090106
In:
The American journal of cardiology vol. 102
Availability: No items available.
|
|
7.
|
Effect of lipid-lowering treatment in cardiovascular disease prevalence in familial hypercholesterolemia. [electronic resource] by
- Perez-Calahorra, Sofía
- Laclaustra, Martín
- Marco-Benedí, Victoria
- Lamiquiz-Moneo, Itziar
- Pedro-Botet, Juan
- Plana, Núria
- Sanchez-Hernandez, Rosa M
- Amor, Antonio J
- Almagro, Fátima
- Fuentes, Francisco
- Suarez-Tembra, Manuel
- Civeira, Fernando
Producer: 20200603
In:
Atherosclerosis vol. 284
Availability: No items available.
|
|
8.
|
Clinical and molecular characteristics of homozygous familial hypercholesterolemia patients: Insights from SAFEHEART registry. [electronic resource] by
- Alonso, Rodrigo
- Díaz-Díaz, Jose Luis
- Arrieta, Francisco
- Fuentes-Jiménez, Francisco
- de Andrés, Raimundo
- Saenz, Pedro
- Ariceta, Gema
- Vidal-Pardo, José I
- Almagro, Fatima
- Argueso, Rosa
- Prieto-Matos, Pablo
- Miramontes, José P
- Pintó, Xavier
- Rodriguez-Urrego, Johana
- Perez de Isla, Leopoldo
- Mata, Pedro
Producer: 20171009
In:
Journal of clinical lipidology vol. 10
Availability: No items available.
|
|
9.
|
Homozygous Familial Hypercholesterolemia in Spain: Prevalence and Phenotype-Genotype Relationship. [electronic resource] by
- Sánchez-Hernández, Rosa M
- Civeira, Fernando
- Stef, Marianne
- Perez-Calahorra, Sofía
- Almagro, Fátima
- Plana, Nuria
- Novoa, Francisco J
- Sáenz-Aranzubía, Pedro
- Mosquera, Daniel
- Soler, Cristina
- Fuentes, Francisco J
- Brito-Casillas, Yeray
- Real, Jose T
- Blanco-Vaca, Francisco
- Ascaso, Juan F
- Pocovi, Miguel
Producer: 20171030
In:
Circulation. Cardiovascular genetics vol. 9
Availability: No items available.
|
|
10.
|
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach. [electronic resource] by
- Versmissen, Jorie
- Oosterveer, Daniëlla M
- Yazdanpanah, Mojgan
- Dehghan, Abbas
- Hólm, Hilma
- Erdman, Jeanette
- Aulchenko, Yurii S
- Thorleifsson, Gudmar
- Schunkert, Heribert
- Huijgen, Roeland
- Vongpromek, Ranitha
- Uitterlinden, André G
- Defesche, Joep C
- van Duijn, Cornelia M
- Mulder, Monique
- Dadd, Tony
- Karlsson, Hróbjartur D
- Ordovas, Jose
- Kindt, Iris
- Jarman, Amelia
- Hofman, Albert
- van Vark-van der Zee, Leonie
- Blommesteijn-Touw, Adriana C
- Kwekkeboom, Jaap
- Liem, Anho H
- van der Ouderaa, Frans J
- Calandra, Sebastiano
- Bertolini, Stefano
- Averna, Maurizio
- Langslet, Gisle
- Ose, Leiv
- Ros, Emilio
- Almagro, Fátima
- de Leeuw, Peter W
- Civeira, Fernando
- Masana, Luis
- Pintó, Xavier
- Simoons, Maarten L
- Schinkel, Arend F L
- Green, Martin R
- Zwinderman, Aeilko H
- Johnson, Keith J
- Schaefer, Arne
- Neil, Andrew
- Witteman, Jacqueline C M
- Humphries, Steve E
- Kastelein, John J P
- Sijbrands, Eric J G
Producer: 20151022
In:
European journal of human genetics : EJHG vol. 23
Availability: No items available.
|