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

von Dobyns, William B.
Veröffentlicht 1997

Malformations of cortical development: clinical features and genetic causes

von Guerrini, Renzo, Dobyns, William B.
Veröffentlicht in Lancet Neurol (2014)

An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome

von Moog, Ute, Dobyns, William B.
Veröffentlicht in Am J Med Genet C Semin Med Genet (2018)

Infantile hydrocephalus: a review of epidemiology, classification and causes

von Tully, Hannah M, Dobyns, William B
Veröffentlicht in Eur J Med Genet (2014)

Malformations of cortical development and epilepsy

von Leventer, Richard J., Guerrini, Renzo, Dobyns, William B.
Veröffentlicht 200

Malformations of Cortical Development and Epilepsy

von Barkovich, A. James, Dobyns, William B., Guerrini, Renzo
Veröffentlicht in Cold Spring Harb Perspect Med (2015)

Reply to Hsueh YP et al.

von Nambot, Sophie, Hevner, Robert F., Dobyns, William B.
Veröffentlicht in 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...

von Ashwal, Stephen, Michelson, David, Plawner, Lauren, Dobyns, William B.
Veröffentlicht 2009

A developmental and genetic classification for midbrain-hindbrain malformations

von Barkovich, A. James, Millen, Kathleen J., Dobyns, William B.
Veröffentlicht 2009

A genetic and biologic classification of infantile spasms

von Paciorkowski, Alex R., Thio, Liu Lin, Dobyns, William B.
Veröffentlicht 2011

Genetic Basis of Brain Malformations

von Parrini, Elena, Conti, Valerio, Dobyns, William B., Guerrini, Renzo
Veröffentlicht in 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...

von Gripp, Karen W., Hopkins, Elisabeth, Doyle, Daniel, Dobyns, William B.
Veröffentlicht in Am J Med Genet A (2010)

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

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

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

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

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

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

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

von Oegema, Renske, Barkovich, A. James, Mancini, Grazia M.S., Guerrini, Renzo, Dobyns, William B.
Veröffentlicht in Neurology (2019)

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

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

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

von Tully, Hannah M., Wenger, Tara L., Kukull, Walter A., Doherty, Dan, Dobyns, William B.
Veröffentlicht in Neurosurg Focus (2016)

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

von Ma, Mandy, Adams, Heather R., Seltzer, Laurie E., Dobyns, William B., Paciorkowski, Alex R.
Veröffentlicht in J Pediatr (2016)

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

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