Search Results - Vaya Montaña, A

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  1. 1
    C0147: Homocysteine Levels in Patients with Primary and Secondary Raynaud’s Phenomenon. Its Association with Microangiopathy Severity

    C0147: Homocysteine Levels in Patients with Primary and Secondary Raynaud’s Phenomenon. Its Association with Microangiopathy Severity by Vaya Montaña, A, Alis, R, Ricart, J.M, Todolí, J, Calvo, J

    Published in Thrombosis research
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  2. 2
    C0117: Metabolic Alterations in Morbid Obesity. Influence on the Haemorheological Profile

    C0117: Metabolic Alterations in Morbid Obesity. Influence on the Haemorheological Profile by Vaya Montaña, A, Suescun Giménez, M, Hernández-Mijares, A, Solá Izquierdo, E, Cámara Gómez, R, Romagnoli, M, Bautista, D, Laiz Marro, B

    Published in Thrombosis research
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  3. 3
    C0115: Red Blood Cell Distribution Width is Associated with Increased Risk of Cryptogenic Stroke

    C0115: Red Blood Cell Distribution Width is Associated with Increased Risk of Cryptogenic Stroke by Vaya Montaña, A, Hernandez Martí, V, Rivera Soria, L, Luis Hernandez Tintorer, J, España Furio, F, Lago Martin, A, Bautista, D

    Published in Thrombosis research
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  4. 4
    C0118: Thrombophilic Mutations in Ocular Behçet’s Disease with Posterior Segment Involvement

    C0118: Thrombophilic Mutations in Ocular Behçet’s Disease with Posterior Segment Involvement by Vayá Montaña, A, Suescun Giménez, M, España, E, España Furió, F, Ricart Vayá, J.M

    Published in Thrombosis research
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  5. 5
    Thalassemic trait caused by IVS II-1 (GAEA) mutation detected in a Spanish family

    Thalassemic trait caused by IVS II-1 (GAEA) mutation detected in a Spanish family by Moreno Miralles, I, Vaya Montaña, A, Rosatelli, M C, Mameli, C, Bolufer Gilabert, P

    Published in Haematologica (Roma)
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  6. 6
    Thalassemic trait caused by IVS II-1 (GAEA) mutation detected in a Spanish family

    Thalassemic trait caused by IVS II-1 (GAEA) mutation detected in a Spanish family by Moreno Miralles, I, Vaya Montaña, A, Rosatelli, M C, Mameli, C, Bolufer Gilabert, P

    Published in Haematologica
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  7. 7
    20210G/A mutation of prothrombin gene in a patient with deep venous thrombosis ad pulmonary embolism without other risk factors of thrombosis

    20210G/A mutation of prothrombin gene in a patient with deep venous thrombosis ad pulmonary embolism without other risk factors of thrombosis by de la Cuadra, P, Nauffal, M D, Vayá Montaña, A, Martínez, M A, Perpiñá, M

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  8. 8
    Mutación 20210G/A del gen de la protrombina en un paciente con trombosis venosa profunda y embolia pulmonar sin otros factores de riesgo trombótico

    Mutación 20210G/A del gen de la protrombina en un paciente con trombosis venosa profunda y embolia pulmonar sin otros factores de riesgo trombótico by de la Cuadra, P., Nauffal, M.D., Vayá Montaña, A., Martínez, M.A., Perpiñá, M.

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  9. 9
    Impact of contralateral and ipsilateral reference tissue selection on self-referencing differential spectroscopy for breast cancer detection

    Impact of contralateral and ipsilateral reference tissue selection on self-referencing differential spectroscopy for breast cancer detection by Leproux, Anais, Cerussi, Albert E, Tanamai, Vaya W, Durkin, Amanda F, Compton, Montana, Tromberg, Bruce J, Gratton, Enrico

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  10. 10
    Thalassemlc trait caused by IVS II-1 (G→A) mutation detected in a Spanish family

    Thalassemlc trait caused by IVS II-1 (G→A) mutation detected in a Spanish family by MORENO MIRALLES, Isabel, VAYA MONTANA, Amparo, ROSATELLI, Maria Cristina, MAMELI, Carmen, BOLUFER GILABERT, Pascual

    Published in Haematologica (Roma)
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