Showing 1 - 16 results of 16 for search '"enfermedades genéticas."', query time: 0.02s Refine Results
  1. 1
    Diagnosis of Methyl Malonicaciduria from 2013 to 2018

    Diagnosis of Methyl Malonicaciduria from 2013 to 2018 by Alina Concepción Álvarez, Ivette Camayd Viera, Norma Elena de León Ojeda, Alina García García, Laritza Martínez Rey, Daniel Quintana Hernández

    Published 2020-02-01
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  2. 2
    Alternativas diagnósticas y terapéuticas para las porfirias hepáticas agudas en adultos, desde una perspectiva actual

    Alternativas diagnósticas y terapéuticas para las porfirias hepáticas agudas en adultos, desde una perspectiva actual by Holmes Rafael Algarín Lara, Elber Luis Osorio Rodríguez, Jhonny Jesus Patiño Patiño, Angie Paola Tavera Medina, Edwin Guevara Romero

    Published 2021-12-01
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  3. 3
    Enfermedades esqueléticas de causa genética: experiencia en un servicio de referencia nacional

    Enfermedades esqueléticas de causa genética: experiencia en un servicio de referencia nacional by Estela Morales Peralta, Gretell Huertas Pérez

    Published 2021-01-01
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  4. 4
    Síndrome de Marfan. Presentación de un caso

    Síndrome de Marfan. Presentación de un caso by Laydamí Rodríguez Amador, Idioel Abreu La Rosa, Héctor Javier Cruz de los Santos, Lorena Álvarez Fernández, Ana Laura Taillacq Suárez, Roberto Lloveras Casañas

    Published 2022-07-01
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  5. 5
    Costello Syndrome. A case report

    Costello Syndrome. A case report by Yadelis Maldonado Martínez, Alexander Torres Molina, Diorgis Duran Lobaina

    Published 2014-06-01
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  6. 6
    Noonan's Syndrome. Case Report

    Noonan's Syndrome. Case Report by Mirsa Rosas Hernández, Elba Daisy Rivas Rodríguez, Raúl E. Silva Silva

    Published 2015-04-01
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  7. 7
    Prader-Willi Syndrome. About a Case

    Prader-Willi Syndrome. About a Case by Carlos Enrique Cruz Carrazana, Claudia García Carrazana

    Published 2021-04-01
    Subjects: “…enfermedades genéticas congénitas…”
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  8. 8
    Essentials of diagnosis and prevention of genetic diseases in the primary health care.

    Essentials of diagnosis and prevention of genetic diseases in the primary health care. by Julia Surí González, María Antonia Ocaña Gil, María del Rosario Liriano Ricabal, Luisa Días Requeiro, Antonio Masót Rangel, Sonia González Sosa

    Published 2009-07-01
    Subjects: “…enfermedades genéticas congénitas…”
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  9. 9
    La hipocalcemia severa, una emergencia endocrina de difícil manejo

    La hipocalcemia severa, una emergencia endocrina de difícil manejo by Amanda Páez Talero

    Published 2024-12-01
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  10. 10
    Síndrome de Axenfeld-Rieger. Presentación de un caso

    Síndrome de Axenfeld-Rieger. Presentación de un caso by Armando Rafael Milanés Armengol, Kattia Molina Castellanos, Yusnavy Lozano Curbelo, Marla Milanés Molina, Ángel Miguel Ojeda Leal

    Published 2020-12-01
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  11. 11
    Genetic factors for breast carcinogenesis

    Genetic factors for breast carcinogenesis by Pedro Enrique Miguel-Soca, Ivis Argüelles González, Marisol Peña González

    Published 2016-12-01
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  12. 12
    Diagnóstico molecular de distrofia muscular de Duchenne/Becker en una familia sin antecedentes patológicos de la enfermedad

    Diagnóstico molecular de distrofia muscular de Duchenne/Becker en una familia sin antecedentes patológicos de la enfermedad by Ivonne Martín Hernández, Alejandro Ariosa Olea, Mariesky Zayas Guillot, Tatiana Zaldívar Vaillant, Celia Rosa Soto Pérez-Stable

    Published 2018-10-01
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  13. 13
    Marfan Syndrome: Regarding Two Cases

    Marfan Syndrome: Regarding Two Cases by Elsy Roxana Geroy Moya, María Quiñones Hernández, Anaelys Acosta Hernández

    Published 2020-02-01
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  14. 14
    Neurofibromatosis type 1 or Von Recklinghausen's disease. A case report

    Neurofibromatosis type 1 or Von Recklinghausen's disease. A case report by Marisleidy Denis Rodríguez, Miguel Alejandro Pulido Gutiérrez, Thaimi Conde Cueto, Luis Omar López Hurtado

    Published 2023-05-01
    Subjects: “…neurofibromatosis 1, enfermedad genética…”
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  15. 15
    Síndrome de Cohen. Presentación de un caso

    Síndrome de Cohen. Presentación de un caso by Elayne Esther Santana Hernández, Victor Jesús Tamayo Chang

    Published 2014-04-01
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  16. 16
    Airway approach in a pediatric patient with Noonan syndrome. Presentation of a case

    Airway approach in a pediatric patient with Noonan syndrome. Presentation of a case by Dayane García Jiménez, Rolando Javier Álvarez Pérez, Robin Fajardo Alcalá, Ivanis Idael Corría Milán

    Published 2025-01-01
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