Showing 1 - 5 results of 5 for search 'Luz María Sánchez-Sánchez', query time: 0.04s Refine Results
  1. 1
    IFITM5-related (type V) osteogenesis imperfecta with evidence of perinatal involvement: A case report

    IFITM5-related (type V) osteogenesis imperfecta with evidence of perinatal involvement: A case report by Valentina Martínez-Montoya, Miguel Angel Fonseca-Sánchez, Gerardo Fabian-Morales, Ramiro Vega-Gamas, Gloria Eugenia Queipo-García, Luis Felipe León-Madero, Luz María Sánchez-Sánchez

    Published 2024-06-01
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  2. 2
    Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature

    Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature by Aidé Tamara Staines-Boone, Caroline Deswarte, Edna Venegas Montoya, Edna Venegas Montoya, Luz María Sánchez-Sánchez, Jorge Alberto García Campos, Teodoro Muñiz-Ronquillo, Jacinta Bustamante, Francisco J. Espinosa-Rosales, Saul Oswaldo Lugo Reyes

    Published 2017-05-01
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  3. 3
    Case Report: DOCK8 Deficiency Without Hyper-IgE in a Child With a Large Deletion

    Case Report: DOCK8 Deficiency Without Hyper-IgE in a Child With a Large Deletion by Edna Venegas-Montoya, Aidé Tamara Staines-Boone, Luz María Sánchez-Sánchez, Jorge Alberto García-Campos, Rubén Antonio Córdova-Gurrola, Yuridia Salazar-Galvez, David Múzquiz-Zermeño, María Edith González-Serrano, Saul O. Lugo Reyes

    Published 2021-06-01
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  4. 4
    P019: Mexican Clinical and Molecular Registry of mucopolysaccharidosis type VII

    P019: Mexican Clinical and Molecular Registry of mucopolysaccharidosis type VII by Ma Dolores Hernandez, Jaime Asael Lopez Valdez, Cristian Mauritanya Muñoz Sánchez, Estefania Duran Sanchez, Maria Angelica Ramirez Hernandez, Alma Delia Vázquez de la Serna, Adriana Ruiz Herrera, Claudia Rivera Acuña, Beatriz Adriana Llamas Guillen, Luz María Sánchez Sánchez, Alondra Deras Martínez, Carmen Amor Avila Rejón, José Elias García Ortíz, Laura Flores

    Published 2023-01-01
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  5. 5
    Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease

    Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease by Valentina Martinez‐Montoya, Luz María Sánchez‐Sánchez, Roberto Sandoval‐Pacheco, Diana Mónica Anaya Castro, Carmen Araceli Arellano‐Valdez, Carmen Amor Ávila‐Rejón, Pedro Alejandro Aguilar‐Juárez, Martín Espino‐Pluma, Cruz Antonio González‐Santillanes, Rosa Isela Martínez‐Segovia, Dorian Olmos‐Morfin, Ofelia Padilla‐De laTorre, Ishar Solís‐Sánchez, Mónica Vázquez‐Del Mercado Espinosa, Camilo Ernesto Villarroel‐Cortés, Jesús Salvador Velarde‐Félix, Jaime López‐Valdez, Julio Olaiz‐Urbina, Edgar Ricárdez‐Marcial, Imelda Vergara‐Sánchez, Pablo Radillo‐Díaz, Ekaterina Kazakova, Beatriz De la Fuente‐Cortez, Luz delCarmen Marquez‐Quiróz, Benjamín Torres‐Octavo, Rubicel Diaz‐Martinez

    Published 2024-07-01
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