Found: 17
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Sensory Processing Difficulties Correlate With Disease Severity and Quality of Life Among Children With Migraine.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00448
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- Publication type:
- Article
Prognostic Parameters of Acute Transverse Myelitis in Children.
- Published in:
- Journal of Child Neurology, 2020, v. 35, n. 14, p. 999, doi. 10.1177/0883073820947512
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- Publication type:
- Article
Development of Infants With Idiopathic External Hydrocephalus.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 8, p. 1044, doi. 10.1177/0883073814553273
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- Publication type:
- Article
Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1.
- Published in:
- European Journal of Pediatrics, 2015, v. 174, n. 2, p. 199, doi. 10.1007/s00431-014-2366-7
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- Publication type:
- Article
Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri.
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 2, p. 361, doi. 10.3390/brainsci13020361
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- Publication type:
- Article
High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome.
- Published in:
- Children, 2023, v. 10, n. 7, p. 1122, doi. 10.3390/children10071122
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- Publication type:
- Article
Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia.
- Published in:
- Journal of Neurology, 2014, v. 261, n. 11, p. 2165, doi. 10.1007/s00415-014-7457-x
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- Publication type:
- Article
Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology.
- Published in:
- 2019
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- Publication type:
- journal article
Kyphoscoliosis peptidase ( KY) mutation causes a novel congenital myopathy with core targetoid defects.
- Published in:
- 2016
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- Publication type:
- Letter
Methylphenidate Induction of Complex Visual Hallucinations.
- Published in:
- Journal of Child Neurology, 2009, v. 24, n. 8, p. 1005, doi. 10.1177/0883073808331357
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- Publication type:
- Article
Vertebral Artery Dissection and Posterior Stroke in a Child.
- Published in:
- Journal of Child Neurology, 2008, v. 23, n. 5, p. 568, doi. 10.1177/0883073807313038
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- Publication type:
- Article
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 251, doi. 10.1007/s10048-016-0491-3
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- Publication type:
- Article
Reply to: The many faces of TUBB4A mutations.
- Published in:
- 2014
- By:
- Publication type:
- Letter
Erratum to: Expansion of the spectrum of TUBB4A-related disorders: A new phenotype associated with a novel mutation in the TUBB4A gene.
- Published in:
- 2014
- By:
- Publication type:
- Erratum
Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene.
- Published in:
- Neurogenetics, 2014, v. 15, n. 2, p. 107, doi. 10.1007/s10048-014-0392-2
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- Publication type:
- Article
Sensory processing patterns affect headache severity among adolescents with migraine.
- Published in:
- Journal of Headache & Pain, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s10194-020-01119-0
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- Publication type:
- Article
An Update on the Ketogenic Diet, 2012.
- Published in:
- Rambam Maimonides Medical Journal, 2012, v. 3, n. 1, p. 1, doi. 10.5041/RMMJ.10072
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- Publication type:
- Article