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Sudden Death, Febrile Seizures, and Hippocampal and Temporal Lobe Maldevelopment in Toddlers: A New Entity.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 6, p. 455, doi. 10.2350/08-09-0542.1
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- Article
Sudden Death in Toddlers Associated with Developmental Abnormalities of the Hippocampus: A Report of Five Cases.
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- Pediatric & Developmental Pathology, 2007, v. 10, n. 3, p. 208, doi. 10.2350/06-08-0144.1
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- Article
Epilepsy-Induced Microarchitectural Changes in the Brain.
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- Pediatric & Developmental Pathology, 2005, v. 8, n. 6, p. 607, doi. 10.1007/s10024-005-0054-3
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- Article
Evidence of increased cell proliferation in the hippocampus in children with Ammon's horn sclerosis.
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- Pathology International, 2007, v. 57, n. 2, p. 76, doi. 10.1111/j.1440-1827.2006.02060.x
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- Article
International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods.
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- Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1315, doi. 10.1111/epi.12220
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- Publication type:
- Article
Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias.
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- Epilepsia (Series 4), 2012, v. 53, n. 8, p. 1341, doi. 10.1111/j.1528-1167.2012.03508.x
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- Article
The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission.
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- Epilepsia (Series 4), 2011, v. 52, n. 1, p. 158, doi. 10.1111/j.1528-1167.2010.02777.x
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- Article
Memory, Emotional and Vocational Impairments before and after Anterior Temporal Lobectomy for Complex Partial Seizures.
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- Epilepsia (Series 4), 2006, v. 47, n. 11, p. 1922, doi. 10.1111/j.1528-1167.2006.00812.x
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- Article
Seizure Control and Cognitive Outcome after Temporal Lobectomy: A Comparison of Classic Ammon's Horn Sclerosis, Atypical Mesial Temporal Sclerosis, and Tumoral Pathologies.
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- Epilepsia (Series 4), 2003, v. 44, n. 3, p. 387, doi. 10.1046/j.1528-1157.2003.33902.x
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- Article
Interaction of reelin signaling and Lis1 in brain development.
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- Nature Genetics, 2003, v. 35, n. 3, p. 270, doi. 10.1038/ng1257
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- Article
Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.
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- Nature Genetics, 2002, v. 32, n. 2, p. 267, doi. 10.1038/ng987
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- Article
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
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- Nature Genetics, 2001, v. 28, n. 3, p. 232, doi. 10.1038/90067
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- Article
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome.
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- Nature Genetics, 1999, v. 22, n. 1, p. 15, doi. 10.1038/8722
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- Article
Cytogenetic demonstration of gene amplification in a primary intracranial germ cell tumor.
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- Genes, Chromosomes & Cancer, 1993, v. 6, n. 1, p. 61, doi. 10.1002/gcc.2870060112
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- Article
What is it? Case 2, 1988. Congenital mental retardation and juvenile parkinsonism.
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- Movement Disorders, 1988, v. 3, n. 4, p. 352, doi. 10.1002/mds.870030413
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- Article
What is it? Case 3, 1988. Progressive myoclonic epilepsy, dementia, and blindness in a young girl.
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- Movement Disorders, 1988, v. 3, n. 4, p. 362, doi. 10.1002/mds.870030414
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- Publication type:
- Article
Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome.
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- Journal of Neuroscience, 2006, v. 26, n. 1, p. 319, doi. 10.1523/JNEUROSCI.2623-05.2006
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- Article
Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?
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- EMBO Journal, 2007, v. 26, n. 22, p. 4732, doi. 10.1038/sj.emboj.7601885
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- Article
Mixed Neuronal-Glial Tumors (Gangliogliomas) in Children.
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- Pediatric Neurosurgery, 1996, v. 24, n. 6, p. 306, doi. 10.1159/000121060
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- Article
Postradiation Meningioma in a Child.
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- Pediatric Neurosurgery, 1988, v. 14, n. 6, p. 319, doi. 10.1159/000120412
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- Article
Congenital Arachnoid Cysts in Children.
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- Pediatric Neurosurgery, 1989, v. 15, n. 5, p. 223, doi. 10.1159/000120473
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- Article
Hemispherectomy for Sturge-Weber Syndrome.
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- Pediatric Neurosurgery, 1979, v. 5, n. 3, p. 233, doi. 10.1159/000119821
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- Article
Hippocampal malformation associated with sudden death in early childhood: a neuropathologic study.
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- Forensic Science, Medicine & Pathology, 2016, v. 12, n. 1, p. 14, doi. 10.1007/s12024-015-9731-3
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- Article
Response to Letter to the Editor from Ackerman MJ, et al.
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- 2016
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- Publication type:
- Letter
Sudden unexpected death in early childhood: general observations in a series of 151 cases.
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- Forensic Science, Medicine & Pathology, 2016, v. 12, n. 1, p. 4, doi. 10.1007/s12024-015-9724-2
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- Article
White matter spongiosis with vigabatrin therapy for infantile spasms.
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- Epilepsia (Series 4), 2018, v. 59, n. 4, p. e40, doi. 10.1111/epi.14032
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- Article
Shaken infant syndrome: developmental neuropathology, progressive cortical dysplasia, and epilepsy.
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- Acta Neuropathologica, 2002, v. 103, n. 4, p. 321, doi. 10.1007/s00401-001-0470-z
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- Article
Globoid cell leukodystrophy: comparison of neuropathology with magnetic resonance imaging.
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- Acta Neuropathologica, 1994, v. 88, n. 1, p. 26, doi. 10.1007/BF00294356
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- Article
Comparison of Ethanol Versus Formalin Fixation on Preservation of Histology and RNA in Laser Capture Microdissected Brain Tissues.
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- Brain Pathology, 2004, v. 14, n. 2, p. 175, doi. 10.1111/j.1750-3639.2004.tb00050.x
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- Article
Pediatric Brain Tumors: Introduction.
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- Brain Pathology, 2003, v. 13, n. 3, p. 373, doi. 10.1111/j.1750-3639.2003.tb00036.x
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- Article
Activation of mammalian target of rapamycin in cytomegalic neurons of human cortical dysplasia.
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- Annals of Neurology, 2006, v. 60, n. 4, p. 420
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- Article
Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutation.
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- Annals of Neurology, 2003, v. 54, n. 3, p. 398
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- Article
CMT4A: Identification of a Hispanic GDAP1 founder mutation.
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- Annals of Neurology, 2003, v. 53, n. 3, p. 400
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- Article
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
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- BMC Pediatrics, 2002, v. 2, p. 12, doi. 10.1186/1471-2431-2-12
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- Article
The neurological mutant quaking<sup>viable</sup> is Parkin deficient.
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- Mammalian Genome, 2004, v. 15, n. 3, p. 210, doi. 10.1007/s00335-003-2333-5
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- Article
Dentate gyrus abnormalities in sudden unexplained death in infants: morphological marker of underlying brain vulnerability.
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- Acta Neuropathologica, 2015, v. 129, n. 1, p. 65, doi. 10.1007/s00401-014-1357-0
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- Publication type:
- Article
A Cluster Classification for Histologic Diagnoses of CNS Tumors in an Epidemiologic Study.
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- Neuroepidemiology, 1990, v. 9, n. 1, p. 2, doi. 10.1159/000110747
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- Article
A Good Relationship With Neuropathology.
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- Journal of Child Neurology, 2010, v. 25, n. 5, p. 644, doi. 10.1177/0883073810362761
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- Article
Neuropathology of Rett Syndrome.
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- Journal of Child Neurology, 2005, v. 20, n. 9, p. 747, doi. 10.1177/08830738050200090901
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- Publication type:
- Article
Survey of MeCP2 in the Rett Syndrome and the Non-Rett Syndrome Brain.
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- Journal of Child Neurology, 2003, v. 18, n. 10, p. 683, doi. 10.1177/08830738030180100601
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- Article
Antineuronal Nuclei Immunohistochemical Staining Patterns in Childhood Ependymomas.
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- Journal of Child Neurology, 2001, v. 16, n. 8, p. 548, doi. 10.2310/7010.2001.16878
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- Article
Multicore Myopathy, Microcephaly, Aganglionosis, and Short Stature.
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- Journal of Child Neurology, 1994, v. 9, n. 3, p. 275, doi. 10.1177/088307389400900309
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- Publication type:
- Article
Determination of Gangliosides in Six Human Primary Medulloblastomas.
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- Journal of Neurochemistry, 1990, v. 55, n. 4, p. 1322, doi. 10.1111/j.1471-4159.1990.tb03142.x
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- Article
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.
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- Human Molecular Genetics, 2007, v. 16, n. 15, p. 1802, doi. 10.1093/hmg/ddm128
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- Article
Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior.
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- Human Molecular Genetics, 2006, v. 15, n. 21, p. 3241, doi. 10.1093/hmg/ddl402
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- Article
Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy.
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- Human Molecular Genetics, 2005, v. 14, n. 11, p. 1539, doi. 10.1093/hmg/ddi162
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- Article
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.
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- Human Molecular Genetics, 2004, v. 13, n. 21, p. 2679, doi. 10.1093/hmg/ddh282
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- Article
Insight into Rett syndrome: MeCP2levels display tissue- and cell-specific differences and correlatewith neuronal maturation.
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- Human Molecular Genetics, 2002, v. 11, n. 2, p. 115, doi. 10.1093/hmg/11.2.115
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- Article
Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoA.
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- Human Molecular Genetics, 2000, v. 9, n. 4, p. 477, doi. 10.1093/hmg/9.4.477
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- Article
Fatal Group A Streptococcal Meningitis and Toxic Shock-Like Syndrome: Case Report.
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- Clinical Infectious Diseases, 1994, v. 18, n. 1, p. 91
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- Publication type:
- Article