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Academic Journal

Autism Genetics: Over 100 Risk Genes and Counting

Subjects: Autism Spectrum Disorder; Genetics; Exome Sequencing

  • Source: Pediatric Neurology Briefs; Vol. 34 (2020); 13 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-34

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Academic Journal

Neurotransmitters and Sodium Channelopathies; Possible Link?

Subjects: Seizures; Channelopathy; SCN2A

  • Source: Pediatric Neurology Briefs; Vol 31, No 03 | Nov 2017; 7 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-31-3

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Academic Journal

Genetic Testing Requires NGS and Sanger Methodologies

Subjects: NGS; Sanger; SCN1A

  • Source: Pediatric Neurology Briefs; Vol 30, No 09 | Sep 2016; 36 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-30-9

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Academic Journal

Clinical and Molecular Characterization of ALG1-CDG

Subjects: Asparagine-Linked Glycosylation Protein 1; CDG; Carbohydrate-Deficient Transferrin

  • Source: Pediatric Neurology Briefs; Vol 30, No 02 | Feb 2016; 14 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-30-2

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Academic Journal

Alternating Hemiplegia and Cardiac Dysrhythmia

Subjects: Alternating Hemiplegia of Childhood; ATP1A3; SUDEP

  • Source: Pediatric Neurology Briefs; Vol 29, No 09 | Sep 2015; 71 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-29-9

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Academic Journal

De Novo Mutations in Patients with Ataxic CP

Subjects: Cerebral Palsy; Ataxia; Genetics

  • Source: Pediatric Neurology Briefs; Vol 29, No 08 | Aug 2015; 62 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-29-8

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Academic Journal

Gene Identification in Alternating Hemiplegia

Subjects: Alternating Hemiplegia of Childhood; Disease-Associated Gene; Emotional Stress

  • Source: Pediatric Neurology Briefs; Vol 26, No 09 | Sep 2012; 69-69 ; 2166-6482 ; 1043-3155 ; 10.15844/pedneurbriefs-26-9

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