Search Results - Ramos Luza, Erika

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    A rare and unique genetic complementing CREBBP plus ASH1L mutations presenting as an mixed Menke-Hennekam- Rubistein-Taybi-ASH1L syndrome with autistic phenotype case report

    A rare and unique genetic complementing CREBBP plus ASH1L mutations presenting as an mixed Menke-Hennekam- Rubistein-Taybi-ASH1L syndrome with autistic phenotype case report by Trillo Alvarez, Wolfgang, Medina Suárez, Joshua, Calderón Paiva, Gabriel, Gonzales Romero, Patrick, Ramos Luza, Erika, Escalante Ortiz, Jonatan, Delgado Villanueva, Luis, Valdivia Pino, Juan, Gomez Azcue, Angela

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    Propriospinal myoclonus as presentation of primary autoimmune cerebellar ataxia case series

    Propriospinal myoclonus as presentation of primary autoimmune cerebellar ataxia case series by Alvarez, Wolfgang Trillo, Suárez, Joshua Medina, Paiva, Gabriel Calderón, Romero, Patrick Gonzales, Mercado, Adriana Escalante, Rosado, Pierina Bermejo, Torreblanca, Linda Chávez, Quispe, Angelica Flores, Medina, Andrea Ancasi, Luza, Erika Ramos

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