Detalhe da pesquisa
1.
The Utility of Early Brain MRI for Patients with Neurofibromatosis Type 1 and Optic Pathway Glioma: A Long-Term Follow-Up in a Tertiary Referral Hospital.
Neuropediatrics
; 53(5): 370-375, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35381604
2.
Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years.
Neuropediatrics
; 51(6): 440-444, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32629522
3.
Sensory processing patterns affect headache severity among adolescents with migraine.
J Headache Pain
; 21(1): 48, 2020 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32375649
4.
Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology.
BMC Pediatr
; 19(1): 484, 2019 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31823772
5.
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.
Neurogenetics
; 17(4): 251-257, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27631729
6.
Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1.
Eur J Pediatr
; 174(2): 199-203, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027832
7.
Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene.
Neurogenetics
; 15(2): 107-13, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24526230
8.
Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri.
Brain Sci
; 13(2)2023 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36831904
9.
High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome.
Children (Basel)
; 10(7)2023 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37508619
10.
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN.
J Med Genet
; 48(6): 383-9, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21493957
11.
Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects.
Acta Neuropathol
; 132(3): 475-8, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27484770
12.
[Infantile spasms and modified hypsarrhythmia].
Harefuah
; 150(4): 373-7, 418, 417, 2011 Apr.
Artigo
em Hebraico
| MEDLINE | ID: mdl-22164920
13.
Prognostic Parameters of Acute Transverse Myelitis in Children.
J Child Neurol
; 35(14): 999-1003, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32808576
14.
Reply to: The many faces of TUBB4A mutations.
Neurogenetics
; 15(2): 83, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24659298
15.
Sensory Processing Difficulties Correlate With Disease Severity and Quality of Life Among Children With Migraine.
Front Neurol
; 10: 448, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31178812
16.
Vertebral artery dissection and posterior stroke in a child.
J Child Neurol
; 23(5): 568-71, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18281617
17.
Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test.
J Clin Neurol
; 14(2): 153-157, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29629523
18.
Thick Corpus Callosum in Children.
J Clin Neurol
; 13(2): 170-174, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28406584
19.
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.
Neuromuscul Disord
; 27(2): 136-140, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28024842
20.
Development of Infants With Idiopathic External Hydrocephalus.
J Child Neurol
; 30(8): 1044-7, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25348416