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Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Subjects: Ataxia; Calcium Channels, L-Type; Long QT syndrome

  • Source: Genetics in MedicineGenetics in Medicine, Nature Publishing Group, 2021, 23 (10), pp.1922-1932. ⟨10.1038/s41436-021-01232-8⟩Genet MedGenetics in Medicine, 2021, 23 (10),

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Neonatal and neurodevelopmental outcomes in preterm infants according to maternal body mass index: A prospective cohort study

Subjects: Pediatrics; Neonatal intensive care unit; Physiology

  • Source: PLoS ONEPLoS ONE, Public Library of Science, 2019, 14 (12), pp.e0225027. ⟨10.1371/journal.pone.0225027⟩PLoS ONE, Vol 14, Iss 12, p e0225027 (2019)Plos One 12 (14), e0225027.

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From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand?

Subjects: Biopsychosocial model; Motor disorder; 030506 rehabilitation

  • Source: Annals of Physical and Rehabilitation MedicineAnnals of Physical and Rehabilitation Medicine, Elsevier Masson, 2019, ⟨10.1016/j.rehab.2019.07.003⟩Annals of Physical and Rehabilitation

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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

Subjects: Male; Movement disorders; Adolescent

  • Source: Brain, vol. 133, no. 3, pp. 655-670Brain, 133, 655-70Brain, 133, 655-670. Oxford University PressBrainBrain, 133(Part 3), 655-670. Oxford University PressBrain, 133, Pt

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