Craniosynostosis Secondary to Rickets: Manifestations on Computed Tomography

por Wang, Page I., Marcus, Jeffrey R., Fuchs, Herbert E., Mukundan, Srinivasan
Publicado 2015

Pediatric Giant Prolactinoma Presenting With Acute Obstructive Hydrocephalus and Intracranial Hypertension

por Hendrix, Grace, Benjamin, Robert, MacIver, Nancie, Barboriak, Daniel P, Fuchs, Herbert, Gumus Balikcioglu, Pinar
Publicado 2021

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

por Markunas, Christina A., Soldano, Karen, Dunlap, Kaitlyn, Cope, Heidi, Asiimwe, Edgar, Stajich, Jeffrey, Enterline, David, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G., Ashley-Koch, Allison E.
Publicado 2013

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

por Markunas, Christina A, Lock, Eric, Soldano, Karen, Cope, Heidi, Ding, Chien-Kuang C, Enterline, David S, Grant, Gerald, Fuchs, Herbert, Ashley-Koch, Allison E, Gregory, Simon G
Publicado 2014

Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation

por Lock, Eric F, Soldano, Karen L, Garrett, Melanie E, Cope, Heidi, Markunas, Christina A, Fuchs, Herbert, Grant, Gerald, Dunson, David B, Gregory, Simon G, Ashley-Koch, Allison E
Publicado 2015