Search Results - "Nunes, Vania S"

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    Global anaesthesia-related cardiac arrest rates in children: a systematic review and meta-analysis by Tiradentes, Teofilo Augusto A, Einav, Sharon, Braz, Jose R C, Nunes-Nogueira, Vania S, Betini, Marluci, Corrente, Jose E, Braz, Mariana G, Braz, Leandro G

    Published in British journal of anaesthesia : BJA (01-11-2023)
    “…Neonates and infants have a higher perioperative risk of cardiac arrest and mortality than adults. The Human Development Index (HDI) ranges from 0 to 1,…”
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    Journal Article
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    Intrasellar Chondroid Chordoma : A Case Report by Hirosawa, Renata Midori, Nunes, Vania S., Zanini, Marco Antonio, Castro, Ana Valéria B., Santos, Antonio B. A., França, Mariana M., Fabris, Viciany Erique

    Published in ISRN endocrinology (01-01-2011)
    “…Chordomas are tumors derived from cells that are remnants of the notochord, particularly from its proximal and distal extremes, they are mainly midline and…”
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    Conservative management of pituitary tumor apoplexy by Santos, Antonio Benigno A, França, Mariana M, Hirosawa, Renata M, Marivo, Mônica, Zanini, Marco A, Nunes, Vania S

    “…Pituitary tumor apoplexy is a rare neuroendocrine syndrome resulting, in most cases, from hemorrhage or infarctation of a pre-existing pituitary adenoma…”
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    Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency by Cruz, Juliana B, Nunes, Vania S, Clara, Sueli A, Perone, Denise, Kopp, Peter, Nogueira, Célia R

    “…The present study aimed at evaluating the PROP1 and HESX1 genes in a group of patients with septo-optic dysplasia (SOD) and pituitary hormone deficiency…”
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    Possible association between Carney complex and multiple endocrine neoplasia type 1 phenotypes by Nunes, Vania S, Chang, Cláudia V, Mazeto, Gláucia M F S, Marques, Mariângela E A, Castro, Ana Valéria B, Nogueira, Célia R

    “…Carney Complex (CNC) and Multiple Endocrine Neoplasia type 1 (MEN1) are forms of multiple endocrine neoplasia of dominant autosomal inheritance. Diagnosis of…”
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