Search Results - "Feller, Ana"

  • Showing 1 - 7 results of 7
Refine Results
  1. 1

    Treatment with TRIAC in pediatric patients with MCT8 by Gazek, Natalia, Feller, Ana L, Vaiani, Elisa, Di Palma, Isabel, Savransky, Andrea, Ramírez, Pablo, Marino, Roxana, Pérez Garrido, Natalia, Lazzati, Juan M, Herzovich, Viviana, Dujovne, Noelia

    Published in Archivos argentinos de pediatría (01-12-2023)
    “…Monocarboxylate transporters (MCTs) allow the cellular entry of thyroid hormones, especially into the central nervous system (CNS), where they are crucial for…”
    Get full text
    Journal Article
  2. 2

    Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study by Lourdes, Vega-Hanna, Mario, Sanz-Cuesta, Didac, Casas-Alba, Mercè, Bolasell, Loreto, Martorell, Leticia, Pías, Lucia, Feller Ana, Martínez-Monseny, Antonio Federico, Mercedes, Serrano

    Published in Frontiers in pediatrics (13-06-2023)
    “…Sotos Syndrome (SS, OMIM#117550) is a heterogeneous genetic condition, recognized by three main clinical features present in most cases: overgrowth with…”
    Get full text
    Journal Article
  3. 3

    Characterization of a cohort of patients with hypercalcemia in a tertiary pediatric hospital by Feller, Ana, Aziz, Mariana, Gil, Silvia, Ciaccio, Marta, Vaiani, Elisa, Viterbo, Gisela

    Published in Archivos argentinos de pediatría (01-12-2024)
    “…Introduction. Hypercalcemia is infrequent in pediatrics, of diverse etiology, and with multiorgan morbidity. Objective. Describe the etiology, biochemistry,…”
    Get full text
    Journal Article
  4. 4

    Intrathyroidal neurofibroma, a case report by Feller, Ana, De Guevara, Deborah, Herzovich, Viviana, Dujovne, Noelia, Ciaccio, Marta, Gazek, Natalia

    Published in Archivos argentinos de pediatría (17-10-2024)
    “…Neurofibromatosis type 1 (NF1) is the most common neurocutaneous disease. It is characterized by café-au-lait spots, melanocytic hamartomas of the iris,…”
    Get full text
    Journal Article
  5. 5

    ABCD syndrome, an uncommon cause of hypercalcemia in pediatrics by Feller, Ana, Aziz, Mariana, Gil, Silvia, Blanco, Agustina, Garavaglia, Mariano, Paz, Marcos, Steinbrun, Silvina, Grignoli, María, Vezzani, Clarisa, Barcala, Consuelo, Ciaccio, Marta, Viterbo, Gisela

    Published in Archivos argentinos de pediatría (01-12-2024)
    “…ABCD syndrome (ABnormal Calcium, Calcinosis, and Creatinine in Down syndrome) is characterized by an association of hypercalcemia, hypercalciuria,…”
    Get full text
    Journal Article
  6. 6

    Tratamiento con TRIAC en pacientes pediátricos con deficiencia de MCT8 by Gazek, Natalia, Feller, Ana L., Vaiani, Elisa, Di Palma, Isabel, Savransky, Andrea, Ramírez, Pablo, Marino, Roxana, Pérez Garrido, Natalia, Lazzati, Juan M., Herzovich, Viviana, Dujovne, Noelia

    Published in Archivos argentinos de pediatría (01-12-2023)
    “…RESUMEN Los transportadores de monocarboxilatos (MCT) permiten el ingreso celular de hormonas tiroideas, especialmente en el sistema nervioso central (SNC),…”
    Get full text
    Journal Article
  7. 7