Results 131 to 140 of about 11,195 (218)

Author response for "Executive functions in agenesis of the corpus callosum: Working memory and sustained attention in the BTBR inbred mouse strain"

, 2020
Loren A. Martin, Fang‐Wei Hsu, Brooke Herd, Michael Gregg, Hannah A. Sample, Jason Kaplan   +5 more
openalex   +1 more source

A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report. [PDF]

Medicine (Baltimore)
Cao GH, Zhang AQ, Dong Y, Fan LL, Yin JY, Tang LL, Li YL.   +6 more
europepmc   +1 more source

Clinical outcomes and neurodevelopmental outcome of prenatally diagnosed agenesis of corpus callosum in single center of Korea. [PDF]

Obstet Gynecol Sci, 2017
Kim SE, Jang HI, Chang KH, Sung JH, Lee J, Lee J, Choi SJ, Oh SY, Roh CR, Kim JH.   +9 more
europepmc   +1 more source

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

, 2013
Samin A. Sajan, Liliana Fernández, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Mari Wakahiro, Susan L. Christian, Jean‐Baptiste Rivière, Christopher T. Sullivan, Jyotsna Sudi, Michael J. Herriges, Alexander Paciorkowski, A. James Barkovich, Joseph Glessner, Kathleen J. Millen, Håkon Håkonarson, William B. Dobyns, Elliott H. Sherr   +17 more
openalex   +2 more sources

Glial interactions in the formation and plasticity of the corpus callosum. [PDF]

Front Cell Neurosci
Czyrska J, Ziętek MM, Bernat A, Sampino S.   +3 more
europepmc   +1 more source

A case of central sleep apnea in an adult with agenesis of the corpus callosum. [PDF]

Respir Med Case Rep
Cabriada-Nuño V, Castro-Quintas S, Urrutia-Gajate A, Tijero-Merino B.   +3 more
europepmc   +1 more source

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum. [PDF]

Mol Syndromol, 2015
Shetty M, Srikanth A, Kadandale J, Hegde S.   +3 more
europepmc   +1 more source

Agenesis of corpus callosum

, 2017
openaire   +1 more source

Assessing the clinical application value of SNP-array in fetal central nervous system malformations. [PDF]

Hum Genomics
Li W, Su J, Lu W, Tang X, Zhou C, Lan Y, Wei Y, Huang L, Luo J, Ou S, Tan S, Wei S, Jiang Y, Su J, Wang L, Huang M, Luo J, Huang P.   +17 more
europepmc   +1 more source

Reverse Shapiro Syndrome Presenting as Fever of Unknown Origin: A Case Report and Review of the Literature. [PDF]

Cureus
Kotsi E, Thomas K, Palkopoulou M, Papavdi M, Kaparou P, Pelekanos A, Deutsch M, Vassilopoulos D, Koullias E.   +8 more
europepmc   +1 more source