Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes. - Wikidata - wikimedia - TriplyDB

Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes.

Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes.

http://www.wikidata.org/entity/Q38174078

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Clinical features and neuroimaging (CT and MRI) findings in presumed Zika virus related congenital infection and microcephaly: retrospective case series study Visual and Motor Deficits in Grown-up Mice with Congenital Zika Virus Infection Nonmicrocephalic Infants with Congenital Zika Syndrome Suspected Only after Neuroimaging Evaluation Compared with Those with Microcephaly at Birth and Postnatally: How Large Is the Zika Virus "Iceberg"?Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome Cockayne syndrome: Clinical features, model systems and pathways.Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva.Patterns and pathways of calcification in the developing brain.Nervous System Injury and Neuroimaging of Zika Virus Infection.Encephalopathies with intracranial calcification in children: clinical and genetic characterization

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P2860

Intracranial calcification in childhood: a review of aetiologies and recognizable phenotypes.

http://www.wikidata.org/entity/Q38174078

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Developmental Medicine and Child Neurology

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Dan Warren

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John H Livingston

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Stavros Stivaros

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P2860

Susceptibility-Weighted MR Imaging: A Review of Clinical Applications in Children

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Two brothers with findings resembling congenital intrauterine infection-like syndrome (pseudo-TORCH syndrome)

Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ

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612-626

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10.1111/DMCN.12359

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