Surgery for Petroclival Meningiomas: A Comprehensive Review of Outcomes in the Skull Base Surgery Era

Por DiLuna, Michael L., Bulsara, Ketan R.
Publicado em 2010

Complications from cervical intra‐arterial heroin injection

Por DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H
Publicado em 2007

Complications from cervical intra-arterial heroin injection

Por DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H
Publicado em 2009

KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein

Por Gunel, Murat, Laurans, Maxwell S. H., Shin, Dana, DiLuna, Michael L., Voorhees, Jennifer, Choate, Keith, Nelson-Williams, Carol, Lifton, Richard P.
Publicado em 2002

COL4A1 Mutation in Preterm Intraventricular Hemorrhage

Por Bilguvar, Kaya, DiLuna, Michael L., Bizzarro, Matthew J., Bayri, Yasar, Schneider, Karen C., Lifton, Richard P., Gunel, Murat, Ment, Laura R.
Publicado em 2009

Mapping a Mendelian Form of Intracranial Aneurysm to 1p34.3-p36.13

Por Nahed, Brian V., Seker, Askin, Guclu, Bulent, Ozturk, Ali K., Finberg, Karin, Hawkins, Abigail A., DiLuna, Michael L., State, Matthew, Lifton, Richard P., Gunel, Murat
Publicado em 2005

Malignant Cerebellar Edema Subsequent to Accidental Prescription Opioid Intoxication in Children

Por Duran, Daniel, Messina, Robert D., Beslow, Lauren A., Montejo, Julio D., Karimy, Jason K., Gavankar Furey, Charuta, Sheridan, Alison D., Sze, Gordon, Yarman, Yanki, DiLuna, Michael L., Kahle, Kristopher T.
Publicado no Front Neurol (2017)

Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation

Por Duran, Daniel, Jin, Sheng Chih, DeSpenza, Tyrone, Nelson-Williams, Carol, Cogal, Andrea G, Abrash, Elizabeth W, Harris, Peter C, Lieske, John C, Shimshak, Serena JE, Mane, Shrikant, Bilguvar, Kaya, DiLuna, Michael L, Günel, Murat, Lifton, Richard P, Kahle, Kristopher T
Publicado no Hum Genome Var (2016)

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

Por State, Matthew W., Greally, John M., Cuker, Adam, Bowers, Peter N., Henegariu, Octavian, Morgan, Thomas M., Gunel, Murat, DiLuna, Michael, King, Robert A., Nelson, Carol, Donovan, Abigail, Anderson, George M., Leckman, James F., Hawkins, Trevor, Pauls, David L., Lifton, Richard P., Ward, David C.
Publicado em 2003

Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles

Por Timberlake, Andrew T, Choi, Jungmin, Zaidi, Samir, Lu, Qiongshi, Nelson-Williams, Carol, Brooks, Eric D, Bilguvar, Kaya, Tikhonova, Irina, Mane, Shrikant, Yang, Jenny F, Sawh-Martinez, Rajendra, Persing, Sarah, Zellner, Elizabeth G, Loring, Erin, Chuang, Carolyn, Galm, Amy, Hashim, Peter W, Steinbacher, Derek M, DiLuna, Michael L, Duncan, Charles C, Pelphrey, Kevin A, Zhao, Hongyu, Persing, John A, Lifton, Richard P
Publicado no eLife (2016)

Abstract 24: Two Locus Inheritance of Non-Syndromic Midline Craniosynostosis Via Rare SMAD6 and Common BMP2 Alleles

Por Timberlake, Andrew T., Choi, Jungmin, Zaidi, Samir, Lu, Qiongshi, Nelson-Williams, Carol, Brooks, Eric D., Bilguvar, Kaya, Tikhonova, Irina, Mane, Shrikant, Yang, Jenny F., Sawh-Martinez, Rajendra, Persing, Sarah, Zellner, Elizabeth G., Loring, Erin, Chuang, Carolyn, Galm, Amy, Hashim, Peter W., Steinbacher, Derek, DiLuna, Michael L., Duncan, Charles C., Pelphrey, Kevin A., Zhao, Hongyu, Persing, John A., Lifton, Richard P.
Publicado no Plast Reconstr Surg Glob Open (2017)