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Author/Creator Hurley, Annette

1. Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss. (8th December 2017)

Authors:
Umrigar, Ayesha; Musso, Amanda; Mercer, Danielle; Hurley, Annette; Glausier, Cassondra; Bakeer, Mona; Marble, Michael; Hicks, Chindo; Tsien, Fern
Journal:
SAGE open medical case reports
Issue:
Volume 5(2017)
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Record Type:
Journal Article
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3. Letter to the Editor: An Affront to Scientific Inquiry Re. Issue 6 (November 2018)

Authors:
Iliadou, Vasiliki (Vivian); Chermak, Gail D.; Bamiou, Doris-Eva; Rawool, Vishakha Waman; Ptok, Martin; Purdy, Suzanne; Jutras, Benoît; Moncrieff, Deborah; Stokkereit Mattsson, Tone; Ferre, Jeanane M.; Fox, Cydney; Grech, Helen; Geffner, Donna; Hedjever, Mladen; Bellis, Teri James; Nimatoudis, Ioa...
Journal:
Ear and hearing
Issue:
Volume 39:Issue 6(2018)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗