Successful treatment of highly recurrent facial baroparesis in a frequent high-altitude traveler: a case report

por Caffrey, Jason P., Adams, Jason W., Costantino, Isabel, Klepper, Kristin, Kari, Elina, Brown, Lori A.
Publicado 2020

Compound heterozygous mutations in MASP1 in a deaf child with absent cochlear nerves

por Kari, Elina, Schrauwen, Isabelle, Llaci, Lorida, Fisher, Laurel M., Go, John L., Naymik, Marcus, Knowles, James A., Huentelman, Matthew J., Friedman, Rick A.
Publicado 2017

A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing loss

por Kari, Elina, Llaci, Lorida, Go, John L., Naymik, Marcus, Knowles, James A., Leal, Suzanne M., Rangasamy, Sampath, Huentelman, Matthew J., Friedman, Rick A., Schrauwen, Isabelle
Publicado 2019