Search Results - "Deyanira González Devia"

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    Sellar Gangliocytoma: Case Report and Review of an Extremely Rare Tumour by Quiroga-Padilla, Pedro José, González-Devia, Deyanira, Andrade, Rafael, Escalante, Paola, Jiménez-Hakim, Enrique

    Published in Case reports in neurology (19-07-2021)
    “…Abstract Sellar gangliocytomas (SGs) are rare, well-differentiated, low-grade neoplasias that commonly present along with a pituitary adenoma (PA). We describe…”
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    Journal Article
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    Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3′ untranslated region of the aldolase B gene by Morales-Alvarez, Martha Catalina, Ricardo-Silgado, Maria Laura, Lemus, Hernan Nicolas, González-Devia, Deyanira, Mendivil, Carlos O

    Published in SAGE open medical case reports (01-01-2019)
    “…Hereditary fructose intolerance, caused by mutations in the ALDOB gene, is an unusual cause of hypoglycemia. ALDOB encodes the enzyme aldolase B, responsible…”
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    Journal Article
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    TIROSEC: Molecular, Clinical and Histopathological Profile of Papillary Thyroid Carcinoma in a Colombian Cohort by Cruz-Romero, Sergio D., González, Sebastián, Juez, José Y., Becerra, David S., Baldión, Ana M., Hakim, José A., González-Devia, Deyanira, Perdomo, Sandra, Rodríguez-Urrego, Paula A.

    Published in Advances in therapy (01-02-2024)
    “…Introduction In Colombia, thyroid cancer ranks among the highest incidences, yet our population lacks studies on its molecular profile. This study aims to…”
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    Journal Article
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    Intermittent Fasting as a Trigger of Ketoacidosis in a Patient With Stable, Long-term Type 1 Diabetes by Fernández-Cardona, Alejandra, González-Devia, Deyanira, Mendivil, Carlos O

    Published in Journal of the Endocrine Society (01-10-2020)
    “…Abstract Diabetic ketoacidosis (DKA) is an acute complication of type 1 diabetes (T1DM) with a high morbidity and mortality. Diabetic ketoacidosis is usually…”
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    Journal Article
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    Unusual Course of an Aggressive Pituitary Prolactinoma: Case Report and Review of the Literature by Pérez Pinzón, Juliana, González-Devia, Deyanira, Kattah Calderón, William, López Panqueva, Rocío del Pilar, Jiménez Hakim, Enrique

    Published in Case reports in neurology (01-01-2019)
    “…Pituitary carcinomas are rare tumors with heterogeneous behaviors. Their carcinogenesis is still unknown. Consequently, treatment is multimodal and not…”
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    Potential contribution of Helicobacter pylori proteins in the pathogenesis of type 1 gastric neuroendocrine tumor and urticaria. In silico approach by Sánchez Caraballo, Andrés, Guzmán, Yenny, Sánchez, Jorge, Munera, Marlon, Garcia, Elizabeth, Gonzalez-Devia, Deyanira

    Published in PloS one (25-04-2023)
    “…Helicobacter pylori has been linked to several diseases such as chronic urticaria, gastritis, and type 1 gastric neuroendocrine tumors (type 1 gNET). Although…”
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    Herramientas para el abordaje diagnóstico de los tumores neuroendocrinos de páncreas by Yenny Fernanda Guzmán, Rocío del Pilar López, Alonso Vera, Deyanira González Devia

    Published in Revista colombiana de cirugía (01-06-2019)
    “…Introducción. Los tumores neuroendocrinos de páncreas son relativamente raros y heterogéneos. Sin embargo, su incidencia se ha incrementado a nivel mundial,…”
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    Journal Article
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    Prognostic factors for recurrence in patients with papillary thyroid carcinoma by Hakim Tawil, José Antonio, Rojas, María Fernanda, Santivañez, Juan José, León, Leonardo, González Devia, Deyanira

    Published in Ear, nose, & throat journal (21-02-2023)
    “…The prognostic factors for tumor recurrence and mortality of patients diagnosed with Papillary Thyroid Carcinoma (PTC) with immediate surgery in Colombia has…”
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    Case report: desensitization of hypersensitivity against the antisense oligonucleotide volanesorsen by Isaac, Rafael H, Gonzalez-Devia, Deyanira, Mendivil, Carlos O, Chapman, Edgardo

    Published in Frontiers in allergy (08-06-2023)
    “…Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder that causes extremely elevated plasma triglyceride levels, with…”
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    Journal Article
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    A 17-Year-Old Male with a Small Bowel Neuroendocrine Tumor (NET): Flushing Differential Diagnosis by Forero Molina, Maria Alejandra, Garcia-Gomez, Elizabeth, MD, Gonzalez-Devia, Deyanira, MD, Duperly, Rafael García, MD, Torres, Alonso Vera, MD

    Published in Journal of allergy and clinical immunology (01-02-2016)
    “…Small bowel NETs are related to serotonin hypersecretion causing flushing, diarrhea, abdominal pain, bronchoconstriction and heart involvement (carcinoid…”
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    Journal Article
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    A 17-year-old male with a Small Bowel Neuroendocrine Tumor: flushing differential diagnosis by Forero Molina, Maria Alejandra, Garcia, Elizabeth, Gonzalez-Devia, Deyanira, García-Duperly, Rafael, Vera, Alonso

    Published in The World Allergy Organization journal (04-09-2017)
    “…Neuroendocrine tumors (NETs) are heterogeneous neoplasms that originate from cells with a secretory function. Small bowel NETs (SB-NETs) are related to…”
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    A 17-year-old male with a Small Bowel Neuroendocrine Tumor: flushing differential diagnosis by Maria Alejandra Forero Molina, Elizabeth Garcia, Deyanira Gonzalez-Devia, Rafael García-Duperly, Alonso Vera

    Published in The World Allergy Organization journal (01-01-2017)
    “…Background Neuroendocrine tumors (NETs) are heterogeneous neoplasms that originate from cells with a secretory function. Small bowel NETs (SB-NETs) are related…”
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    Journal Article
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