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

Por Dobyns, William B.
Publicado em 1997

Malformations of cortical development: clinical features and genetic causes

Por Guerrini, Renzo, Dobyns, William B.
Publicado no Lancet Neurol (2014)

An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome

Por Moog, Ute, Dobyns, William B.
Publicado no Am J Med Genet C Semin Med Genet (2018)

Infantile hydrocephalus: a review of epidemiology, classification and causes

Por Tully, Hannah M, Dobyns, William B
Publicado no Eur J Med Genet (2014)

Malformations of cortical development and epilepsy

Por Leventer, Richard J., Guerrini, Renzo, Dobyns, William B.
Publicado em 200

Malformations of Cortical Development and Epilepsy

Por Barkovich, A. James, Dobyns, William B., Guerrini, Renzo
Publicado no Cold Spring Harb Perspect Med (2015)

Reply to Hsueh YP et al.

Por Nambot, Sophie, Hevner, Robert F., Dobyns, William B.
Publicado no 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...

Por Ashwal, Stephen, Michelson, David, Plawner, Lauren, Dobyns, William B.
Publicado em 2009

A developmental and genetic classification for midbrain-hindbrain malformations

Por Barkovich, A. James, Millen, Kathleen J., Dobyns, William B.
Publicado em 2009

A genetic and biologic classification of infantile spasms

Por Paciorkowski, Alex R., Thio, Liu Lin, Dobyns, William B.
Publicado em 2011

Genetic Basis of Brain Malformations

Por Parrini, Elena, Conti, Valerio, Dobyns, William B., Guerrini, Renzo
Publicado no 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...

Por Gripp, Karen W., Hopkins, Elisabeth, Doyle, Daniel, Dobyns, William B.
Publicado no Am J Med Genet A (2010)

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

Por O’Driscoll, Mark , Dobyns, William B. , van Hagen, Johanna M. , Jeggo, Penny A. 
Publicado em 2007

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

Por Haverfield, Eden V, Whited, Amanda J, Petras, Kristin S, Dobyns, William B, Das, Soma
Publicado em 2009

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

Por Judkins, Alexander R., Martinez, Daniel, Ferreira, Pamela, Dobyns, William B., Golden, Jeffrey A.
Publicado em 2011

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

Por Oegema, Renske, Barkovich, A. James, Mancini, Grazia M.S., Guerrini, Renzo, Dobyns, William B.
Publicado no Neurology (2019)

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

Por Barkovich, A. James, Guerrini, Renzo, Kuzniecky, Ruben I., Jackson, Graeme D., Dobyns, William B.
Publicado em 2012

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

Por Tully, Hannah M., Wenger, Tara L., Kukull, Walter A., Doherty, Dan, Dobyns, William B.
Publicado no Neurosurg Focus (2016)

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

Por Ma, Mandy, Adams, Heather R., Seltzer, Laurie E., Dobyns, William B., Paciorkowski, Alex R.
Publicado no J Pediatr (2016)

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

Por Rajab, Anna, Aldinger, Kimberly A., El-Shirbini, Hisham Ali, Dobyns, William B., Ross, M. Elizabeth
Publicado em 2009