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Neuropathological analysis of an adult case of the Cornelia de Lange syndrome

https://doi.org/10.1007/s00401-002-0562-4
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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archderm.1966.01600240068011openalex-snapshot
Cutaneous Manifestations of the Cornelia de Lange Syndrome
inferredcites →https://doi.org/10.1002/ajmg.1320470704openalex-snapshot
Clinical variability within Brachmann‐de Lange syndrome: A proposed classification system
inferredcites →https://doi.org/10.1002/ana.410050311openalex-snapshot
Alzheimer neurofibrillary tangles in diseases other than senile and presenile dementia
inferredcites →https://doi.org/10.1007/bf00272831openalex-snapshot
Partial trisomy 3q
inferredcites →https://doi.org/10.1007/bf00304630openalex-snapshot
Differential distribution of neurofibrillary tangles in the cerebral cortex of dementia pugilistica and Alzheimer's disease cases
inferredcites →https://doi.org/10.1007/bf00307688openalex-snapshot
Alzheimer neuropathology in non-Down's syndrome mentally retarded adults
inferredcites →https://doi.org/10.1007/bf00308476openalex-snapshot
A comparative study of histological and immunohistochemical methods for neurofibrillary tangles and senile plaques in Alzheimer's disease
inferredcites →https://doi.org/10.1007/bf00308819openalex-snapshot
Neuropathological observations in a case of autism presenting with self-injury behavior
inferredcites →https://doi.org/10.1007/bf00308912openalex-snapshot
Pathological proteins Tau 64 and 69 are specifically expressed in the somatodendritic domain of the degenerating cortical neurons during Alzheimer's disease
inferredcites →https://doi.org/10.1007/bf00308927openalex-snapshot
Correlation between microscopical changes and Tau 64 and 69 biochemical detection in senile dementia of the Alzheimer type
inferredcites →https://doi.org/10.1007/s004010050571openalex-snapshot
Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome
inferredcites →https://doi.org/10.1007/s004010051066openalex-snapshot
Neuronal cytoskeletal changes are an early consequence of repetitive head injury
inferredcites →https://doi.org/10.1016/0165-5876(96)01339-0openalex-snapshot
Temporal bone and brain stem histopathological findings in Cornelia de Lange syndrome
inferredcites →https://doi.org/10.1016/s0022-3476(63)80234-6openalex-snapshot
The Cornelia de Lange syndrome
inferredcites →https://doi.org/10.1016/s0022-3476(78)81077-4openalex-snapshot
The association of chromosome 3 duplication and the Correlia de Lange syndrome
inferredcites →https://doi.org/10.1016/s0197-4580(97)00047-xopenalex-snapshot
Prevalence, Incidence and Duration of Braak’s Stages in the General Population: Can We Know?
inferredcites →https://doi.org/10.1017/s0033291700049588openalex-snapshot
The aftermath of boxing
inferredcites →https://doi.org/10.1097/00019052-200110000-00005openalex-snapshot
Congenital myopathies and congenital muscular dystrophies
inferredcites →https://doi.org/10.1111/j.1651-2227.1969.tb04748.xopenalex-snapshot
PATHOLOGICAL FEATURES IN THE DE LANGE SYNDROME
inferredcites →https://doi.org/10.1111/j.1651-2227.1984.tb09947.xopenalex-snapshot
Partial Trisomy 3q (3q25→qter) Syndrome in Two Siblings
inferredcites →https://doi.org/10.1136/adc.38.200.349openalex-snapshot
Typus Degenerativus Amstelodamensis
inferredcites →https://doi.org/10.1136/jmg.27.6.405openalex-snapshot
Cornelia de Lange syndrome with ring chromosome 3.
inferredcites →https://doi.org/10.1148/88.1.101openalex-snapshot
Roentgenology of the Brachmann-De Lange Syndrome
inferredcites →https://doi.org/10.2214/ajr.100.1.27openalex-snapshot
SKELETAL CHANGES IN THE CORNELIA DE LANGE SYNDROME

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3985603openalex-extracted
STAG2 Promotes the Myelination Transcriptional Program in Oligodendrocytes
inferred← citeshttps://doi.org/10.1002/0471695998.mgs013openalex-snapshot
C ornelia de L ange Syndrome
inferred← citeshttps://doi.org/10.1002/9780470893159.ch15openalex-snapshot
Cornelia de Lange Syndrome
inferred← citeshttps://doi.org/10.1002/9781119432692.ch15openalex-snapshot
CORNELIA DE LANGE SYNDROME
inferred← citeshttps://doi.org/10.1002/ajmg.a.31757openalex-snapshot
Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance
inferred← citeshttps://doi.org/10.1002/ajmg.a.34329openalex-snapshot
Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature
inferred← citeshttps://doi.org/10.1002/ajmg.a.36573openalex-snapshot
Autism traits in children and adolescents with Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.c.30137openalex-snapshot
Natural history of aging in Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.c.31503openalex-snapshot
Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment
inferred← citeshttps://doi.org/10.1007/978-3-031-76269-7_18openalex-snapshot
Cornelia de Lange Syndrome
inferred← citeshttps://doi.org/10.1007/s00247-015-3300-5openalex-snapshot
Neuroimaging features of Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.1007/s10803-020-04617-xopenalex-snapshot
Repetitive and Self-injurious Behaviors in Children with Cornelia de Lange Syndrome
inferred← citeshttps://doi.org/10.1007/s12565-020-00567-7openalex-snapshot
Regulation and dysregulation of spatial chromatin structure in the central nervous system
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00173-7openalex-snapshot
Pathways—Cohesinopathies
inferred← citeshttps://doi.org/10.1038/ng1363openalex-snapshot
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.1038/s41576-018-0031-0openalex-snapshot
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
inferred← citeshttps://doi.org/10.1097/yco.0000000000000311openalex-snapshot
Behavioral and psychiatric manifestations in Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.1111/j.1399-0004.2009.01271.xopenalex-snapshot
Cornelia de Lange syndrome, cohesin, and beyond
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2010.05718.xopenalex-snapshot
Impact of nuclear organization and dynamics on epigenetic regulation in the central nervous system: implications for neurological disease states
inferred← citeshttps://doi.org/10.1186/s11689-017-9208-7openalex-snapshot
Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance
inferred← citeshttps://doi.org/10.1186/s11689-019-9269-xopenalex-snapshot
Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis
inferred← citeshttps://doi.org/10.1186/s13023-017-0723-0openalex-snapshot
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome
inferred← citeshttps://doi.org/10.5336/pediatr.2018-59617openalex-snapshot
Neurodevelopment Physiotherapy in Cornelia de Lange Syndrome
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