Suchergebnisse - "Ruiz-Casares, Eva"

PubPharm (11)

1

Pilot Study on the Prevalence of Diamine Oxidase Gene Variants in Patients with Symptoms of Histamine Intolerance

enthalten in: Nutrients | 2024

von Duelo, A. | Comas-Basté, O. | Sánchez-Pérez, S. | +4

2

Lower Urinary Tract Symptoms (LUTS) as a New Clinical Presentation of Histamine Intolerance : A Prevalence Study of Genetic Diamine Oxidase Deficiency

enthalten in: Journal of clinical medicine | 2023

von Ponce Díaz-Reixa, J. | Aller Rodríguez, M. | Martínez Breijo, S. | +9

3

Prevalence of Genetic Diamine Oxidase (DAO) Deficiency in Female Patients with Fibromyalgia in Spain

enthalten in: Biomedicines | 2023

von Okutan, G. | Ruiz Casares, E. | Perucho Alcalde, T. | +6

4

Cumulative effect of AOC1 gene variants on symptoms and pathological conditions in adult women with fibromyalgia : a pilot study

enthalten in: Frontiers in genetics | 2023

von Okutan, G. | Perucho Alcalde, T. | Ruiz Casares, E. | +7

5

Genetic profile in genes associated with muscle injuries and injury etiology in professional soccer players

enthalten in: Frontiers in genetics | 2022

von Maestro, A. | Del Coso, J. | Aguilar-Navarro, M. | +6

6

Liver prometastatic reaction : Stimulating factors and responsive cancer phenotypes

enthalten in: Seminars in cancer biology | 2021

von Vidal-Vanaclocha, F. | Crende, O. | García de Durango, C. | +14

7

Recommendations to report and interpret HLA genetic findings in coeliac disease

enthalten in: Revista espanola de enfermedades digestivas | 2018

von Núñez, C. | Garrote, J. | Arranz, E. | +7

8

Familial porphyria cutanea tarda in Spain : characterization of eight novel mutations in the UROD gene and haplotype analysis of the common p.G281E mutation

enthalten in: Gene | 2013

von Gómez-Abecia, S. | Morán-Jiménez, M. | Ruiz-Casares, E. | +5

9

Familial porphyria cutanea tarda in Spain: Characterization of eight novel mutations in the UROD gene and haplotype analysis of the common p.G281E mutation

enthalten in: Gene | 2013

von Gómez-Abecia, S. | Morán-Jiménez, M. | Ruiz-Casares, E. | +5

10

Phenotypic variability in Marfan syndrome in a family with a novel nonsense FBN1 gene mutation

enthalten in: Revista espanola de cardiologia (English ed.) | 2012

von Díaz de Bustamante, A. | Ruiz-Casares, E. | Darnaude, M. | +2