Congenital malformations of the brain: Pathological, embryological, clinical, radiological, and genetic aspects

Autor Dobyns, William B.
Vydáno 1997

Malformations of cortical development: clinical features and genetic causes

Autor Guerrini, Renzo, Dobyns, William B.
Vydáno v Lancet Neurol (2014)

An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome

Autor Moog, Ute, Dobyns, William B.
Vydáno v Am J Med Genet C Semin Med Genet (2018)

Infantile hydrocephalus: a review of epidemiology, classification and causes

Autor Tully, Hannah M, Dobyns, William B
Vydáno v Eur J Med Genet (2014)

Malformations of cortical development and epilepsy

Autor Leventer, Richard J., Guerrini, Renzo, Dobyns, William B.
Vydáno 200

Malformations of Cortical Development and Epilepsy

Autor Barkovich, A. James, Dobyns, William B., Guerrini, Renzo
Vydáno v Cold Spring Harb Perspect Med (2015)

Reply to Hsueh YP et al.

Autor Nambot, Sophie, Hevner, Robert F., Dobyns, William B.
Vydáno v Eur J Hum Genet (2020)

Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the...

Autor Ashwal, Stephen, Michelson, David, Plawner, Lauren, Dobyns, William B.
Vydáno 2009

A developmental and genetic classification for midbrain-hindbrain malformations

Autor Barkovich, A. James, Millen, Kathleen J., Dobyns, William B.
Vydáno 2009

A genetic and biologic classification of infantile spasms

Autor Paciorkowski, Alex R., Thio, Liu Lin, Dobyns, William B.
Vydáno 2011

Genetic Basis of Brain Malformations

Autor Parrini, Elena, Conti, Valerio, Dobyns, William B., Guerrini, Renzo
Vydáno v Mol Syndromol (2016)

High Incidence of Progressive Postnatal Cerebellar Enlargement in Costello Syndrome: Brain Overgrowth Associated with HRAS Mutations as the Likely Cause of Structural Brain and Spi...

Autor Gripp, Karen W., Hopkins, Elisabeth, Doyle, Daniel, Dobyns, William B.
Vydáno v Am J Med Genet A (2010)

Cellular and Clinical Impact of Haploinsufficiency for Genes Involved in ATR Signaling

Autor O’Driscoll, Mark , Dobyns, William B. , van Hagen, Johanna M. , Jeggo, Penny A. 
Vydáno 2007

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

Autor Haverfield, Eden V, Whited, Amanda J, Petras, Kristin S, Dobyns, William B, Das, Soma
Vydáno 2009

Polymicrogyria Includes Fusion of the Molecular Layer and Decreased Neuronal Populations, But Normal Cortical Laminar Organization

Autor Judkins, Alexander R., Martinez, Daniel, Ferreira, Pamela, Dobyns, William B., Golden, Jeffrey A.
Vydáno 2011

Subcortical heterotopic gray matter brain malformations: Classification study of 107 individuals

Autor Oegema, Renske, Barkovich, A. James, Mancini, Grazia M.S., Guerrini, Renzo, Dobyns, William B.
Vydáno v Neurology (2019)

A developmental and genetic classification for malformations of cortical development: update 2012

Autor Barkovich, A. James, Guerrini, Renzo, Kuzniecky, Ruben I., Jackson, Graeme D., Dobyns, William B.
Vydáno 2012

Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage

Autor Tully, Hannah M., Wenger, Tara L., Kukull, Walter A., Doherty, Dan, Dobyns, William B.
Vydáno v Neurosurg Focus (2016)

Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies

Autor Ma, Mandy, Adams, Heather R., Seltzer, Laurie E., Dobyns, William B., Paciorkowski, Alex R.
Vydáno v J Pediatr (2016)

Recessive Developmental Delay, Small Stature, Microcephaly and Brain Calcifications with Locus on Chromosome 2

Autor Rajab, Anna, Aldinger, Kimberly A., El-Shirbini, Hisham Ali, Dobyns, William B., Ross, M. Elizabeth
Vydáno 2009