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

Tekijä Dobyns, William B.
Julkaistu 1997

Malformations of cortical development: clinical features and genetic causes

Tekijä Guerrini, Renzo, Dobyns, William B.
Julkaisussa Lancet Neurol (2014)

An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome

Tekijä Moog, Ute, Dobyns, William B.
Julkaisussa Am J Med Genet C Semin Med Genet (2018)

Infantile hydrocephalus: a review of epidemiology, classification and causes

Tekijä Tully, Hannah M, Dobyns, William B
Julkaisussa Eur J Med Genet (2014)

Malformations of cortical development and epilepsy

Tekijä Leventer, Richard J., Guerrini, Renzo, Dobyns, William B.
Julkaistu 200

Malformations of Cortical Development and Epilepsy

Tekijä Barkovich, A. James, Dobyns, William B., Guerrini, Renzo
Julkaisussa Cold Spring Harb Perspect Med (2015)

Reply to Hsueh YP et al.

Tekijä Nambot, Sophie, Hevner, Robert F., Dobyns, William B.
Julkaisussa 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...

Tekijä Ashwal, Stephen, Michelson, David, Plawner, Lauren, Dobyns, William B.
Julkaistu 2009

A developmental and genetic classification for midbrain-hindbrain malformations

Tekijä Barkovich, A. James, Millen, Kathleen J., Dobyns, William B.
Julkaistu 2009

A genetic and biologic classification of infantile spasms

Tekijä Paciorkowski, Alex R., Thio, Liu Lin, Dobyns, William B.
Julkaistu 2011

Genetic Basis of Brain Malformations

Tekijä Parrini, Elena, Conti, Valerio, Dobyns, William B., Guerrini, Renzo
Julkaisussa 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...

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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