Showing 1 - 9 results of 9 for search 'Teresa Collazo', query time: 0.03s Refine Results
  1. 1
    Estudio molecular de anemia falciforme. Frecuencia de los alelos βS y βC en pacientes estudiados en el año 2010

    Estudio molecular de anemia falciforme. Frecuencia de los alelos βS y βC en pacientes estudiados en el año 2010 by Ismael Aramís Cervera García, Marisleivis García Heredia, Teresa Collazo Mesa

    Published 2012-11-01
    Get full text
    Article
  2. 2
    Introducción del diagnóstico molecular de la hemocromatosis tipo 1 en Cuba

    Introducción del diagnóstico molecular de la hemocromatosis tipo 1 en Cuba by Ismael Aramís Cervera García, Marileivis García Heredia, Teresa Collazo Mesa

    Published 2013-06-01
    Get full text
    Article
  3. 3
    GJB6-D13S1830 and GJB6-D13S1854 Deletions in Patients with non-Syndromic Prelingual Deafness

    GJB6-D13S1830 and GJB6-D13S1854 Deletions in Patients with non-Syndromic Prelingual Deafness by Mercedes Arceo Álvarez, Estela Morales Peralta, Yuledmi Perdomo Chacón, Teresa Collazo Mesa

    Published 2024-08-01
    Get full text
    Article
  4. 4
    Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients

    Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients by Antonio Alejandro Esperón Álvarez, Inés Virginia Noa Hechavarría, Ixchel López Reyes, Teresa Collazo Mesa

    Published 2024-03-01
    Get full text
    Article
  5. 5
    Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency

    Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency by Taimí Barrueta Ordóñez, Teresa Collazo Mesa, Paulina Lantigua Cruz, Adrián de Jesús González Navarro, Tania Espinosa Reyes

    Published 2019-02-01
    Get full text
    Article
  6. 6
    Genotype-Phenotype Correlation in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in Cuba

    Genotype-Phenotype Correlation in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in Cuba by Tania Mayvel Espinosa Reyes, Teresa Collazo Mesa, Paulina Arasely Lantigua Cruz, Adriana Agramonte Machado, Emma Domínguez Alonso, Henrik Falhammar

    Published 2021-01-01
    Get full text
    Article
  7. 7
    Identificación del polimorfismo c.2448-25G>A en pacientes con diagnóstico clínico de la enfermedad de Wilson

    Identificación del polimorfismo c.2448-25G>A en pacientes con diagnóstico clínico de la enfermedad de Wilson by Yulia Clark Feoktistova, Caridad Ruenes Domech, Elsa F García Bacallao, Teresa Collazo Mesa, Zoe Robaina Jiménez, Hilda Roblejo Balbuena

    Published 2015-11-01
    Get full text
    Article
  8. 8
    Challenging Diagnosis of Invasive Sinus Aspergillosis Mimicking Gradenigo’s Syndrome in an Elderly Patient with T-Cell Lymphoma

    Challenging Diagnosis of Invasive Sinus Aspergillosis Mimicking Gradenigo’s Syndrome in an Elderly Patient with T-Cell Lymphoma by Victoria Ramos de Ascanio, Gloria Liaño-Esteso, David Roldán, Teresa Collazo-Lorduy, Sara Martínez-Flores, José Ángel Hernández-Rivas, Isabel González-Gascón-y-Marín

    Published 2023-12-01
    Get full text
    Article
  9. 9
    Detección del polimorfismo T991T en familias cubanas con diagnóstico clínico de la enfermedad de Wilson

    Detección del polimorfismo T991T en familias cubanas con diagnóstico clínico de la enfermedad de Wilson by Yulia Clark Feoktistova, Caridad Ruenes Domech, Elsa F. García Bacallao, Teresa Collazo Mesa, Hilda Roblejo Balbuena, Estela Morales Peralta, Iliana Clark Feoktistova, Zoe Robaina Jiménez

    Published 2017-02-01
    Get full text
    Article

Search Tools: