Co-Authors
This is a "connection" page, showing publications co-authored by Cathrine Constantacos and Janel Hunter.
Connection Strength
0.741
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Constantacos C, Hunter JD, Walsh ET, South AM. Rare PHEX variant with insidious presentation leads to a delayed diagnosis of X-linked hypophosphatemia. BMJ Case Rep. 2021 May 19; 14(5).
Score: 0.198
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Hunter JD, Staton H, Constantacos C, Walsh ET, Crudo DF. Pathogenicity of a glucokinase gene mutation and description of its clinical phenotype. Pediatr Diabetes. 2020 09; 21(6):942-944.
Score: 0.185
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Walsh ET, Hunter JD, Crudo DF, Constantacos C. Sinusitis, an under-reported adverse effect in children treated with radioactive iodine therapy and review of the current literature. J Pediatr Endocrinol Metab. 2020 Jan 28; 33(1):171-173.
Score: 0.181
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Bharill SA, Hunter JD, Walsh ET, Crudo DF, Constantacos C. Pediatric stroke as the presenting symptom of new-onset type 1 diabetes mellitus without DKA: case report and literature review. J Pediatr Endocrinol Metab. 2019 Sep 25; 32(9):1035-1037.
Score: 0.177