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American Journal of Human Genetics|June 29, 2002
Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding nogginDavid J Brown, Theresa B Kim, Elizabeth M Petty, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 7, 2003
Characterization of a stapes ankylosis family with a NOG mutationDavid J Brown, Theresa B Kim, Elizabeth M Petty, et al.
Pediatric Radiology|January 6, 2020
The continuous lure of pediatric radiologyPeter J Strouse, Erin K Romberg, Delma Y Jarrett, et al.
International Journal of Behavioral Medicine|January 29, 2016
The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell DiseaseC R Jonassaint, M C Beach, J A Haythornthwaite, et al.
Contemporary Clinical Trials|December 21, 2020
Trial design of comparing patient-specific versus weight-based protocols to treat vaso-occlusive episodes in sickle cell disease (COMPARE-VOE)Stephanie O Ibemere, Sarah B Dubbs, Huiman X Barnhart, et al.
Blood Advances|June 20, 2020
American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic painAmanda M Brandow, C Patrick Carroll, Susan Creary, et al.
Proteomics. Clinical Applications|April 29, 2021
Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell diseaseEboni I Lance, Lisa M Faulcon, Zongming Fu, et al.
American Journal of Hematology|October 28, 2014
Health-related quality of life in children with sickle cell anemia: impact of blood transfusion therapyLauren M Beverung, John J Strouse, Monica L Hulbert, et al.
Plos One|December 7, 2013
Chikungunya as a cause of acute febrile illness in southern Sri LankaMegan E Reller, Ufuoma Akoroda, Ajith Nagahawatte, et al.
Blood|November 30, 2023
Deciphering and disrupting PIEZO1-TMEM16F interplay in hereditary xerocytosisPengfei Liang, Yang Zhang, Yui Chun S Wan, et al.
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