Found: 29
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EEG profiles during general anesthesia in children: A comparative study between sevoflurane and propofol.
- Published in:
- Pediatric Anesthesia, 2019, v. 29, n. 3, p. 250, doi. 10.1111/pan.13579
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- Article
Five new TTF1/NKX2.1 mutations in brain–lung–thyroid syndrome: rescue by PAX8 synergism in one case.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2266, doi. 10.1093/hmg/ddp162
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- Article
ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.
- Published in:
- 2016
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- Publication type:
- journal article
Association of periventricular nodular heterotopia with posterior fossa cyst: a prenatal case series.
- Published in:
- Prenatal Diagnosis, 2015, v. 35, n. 4, p. 337, doi. 10.1002/pd.4543
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- Article
Clinical presentation and outcome of 20 fetuses with parvovirus B19 infection complicated by severe anemia and/or fetal hydrops.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 11, p. 1023, doi. 10.1002/pd.4413
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- Publication type:
- Article
Isolated corpus callosum agenesis: a ten-year follow-up after prenatal diagnosis (How are the children without corpus callosum at 10 years of age?).
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 3, p. 277, doi. 10.1002/pd.3824
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- Article
Main Congenital Cerebral Anomalies: How Prenatal Imaging Aids Counseling.
- Published in:
- Fetal Diagnosis & Therapy, 2014, v. 35, n. 4, p. 229, doi. 10.1159/000358519
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- Article
Main congenital cerebral anomalies: how prenatal imaging aids counseling.
- Published in:
- 2014
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- Publication type:
- journal article
Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 3, p. 307, doi. 10.1111/cge.14096
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- Publication type:
- Article
Early asymmetric inter-hemispheric transfer in the auditory network: insights from infants with corpus callosum agenesis.
- Published in:
- Brain Structure & Function, 2018, v. 223, n. 6, p. 2893, doi. 10.1007/s00429-018-1667-4
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- Article
MRI of the fetal posterior fossa.
- Published in:
- 2005
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- Publication type:
- journal article
Pontoneocerebellar hypoplasia: definition of MR features.
- Published in:
- Pediatric Radiology, 2001, v. 31, n. 9, p. 613
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- Publication type:
- Article
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
- Published in:
- Human Genetics, 2017, v. 136, n. 4, p. 463, doi. 10.1007/s00439-017-1772-0
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- Publication type:
- Article
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
- Published in:
- 2015
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- Publication type:
- journal article
Spectrum of epilepsy in terminal 1p36 deletion syndrome.
- Published in:
- Epilepsia (Series 4), 2008, v. 49, n. 3, p. 509, doi. 10.1111/j.1528-1167.2007.01424.x
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- Publication type:
- Article
Fetal Brain Injury Associated with Parvovirus B19 Congenital Infection Requiring Intrauterine Transfusion.
- Published in:
- 2019
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- Publication type:
- journal article
Patterns of Detection of Fetal Posterior Fossa Anomalies: Analysis of 81 Cases in the Second Half of Gestation.
- Published in:
- 2018
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- Publication type:
- journal article
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A ( TUBA1A).
- Published in:
- Human Mutation, 2007, v. 28, n. 11, p. 1055, doi. 10.1002/humu.20572
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- Article
Prenatal diagnosis of vermian cyst: a new type of posterior fossa cyst.
- Published in:
- Pediatric Radiology, 2023, v. 53, n. 3, p. 461, doi. 10.1007/s00247-022-05531-3
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- Publication type:
- Article
Variability of T1-weighted signal intensity of pericallosal lipomas in the fetus.
- Published in:
- 2018
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- Publication type:
- journal article
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.
- Published in:
- Brain: A Journal of Neurology, 2010, v. 133, n. 11, p. 3194, doi. 10.1093/brain/awq259
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- Article
Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutations.
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- Developmental Medicine & Child Neurology, 2019, v. 61, n. 12, p. 1439, doi. 10.1111/dmcn.14332
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- Publication type:
- Article
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
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- Human Mutation, 2018, v. 39, n. 1, p. 23, doi. 10.1002/humu.23361
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- Article
Cover Image, Volume 39, Issue 1.
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- Human Mutation, 2018, v. 39, n. 1, p. i, doi. 10.1002/humu.23372
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- Article
Agenesis of the corpus callosum and the establishment of handedness.
- Published in:
- Developmental Psychobiology, 2006, v. 48, n. 6, p. 472, doi. 10.1002/dev.20162
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- Publication type:
- Article
Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardation.
- Published in:
- Clinical Genetics, 1998, v. 53, n. 2, p. 136, doi. 10.1111/j.1399-0004.1998.tb02661.x
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- Publication type:
- Article
Epilepsy in young Tsc1<sup> +/−</sup> mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 4, p. 648, doi. 10.1111/epi.13325
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- Article
STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients.
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- Epilepsia (Series 4), 2011, v. 52, n. 10, p. 1820, doi. 10.1111/j.1528-1167.2011.03163.x
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- Publication type:
- Article
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 7, p. 1063, doi. 10.1093/hmg/7.7.1063
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- Publication type:
- Article