Detalhe da pesquisa
1.
Uncommon Causes of Nontraumatic Intracerebral Hemorrhage.
Stroke
; 55(5): 1416-1427, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38572651
2.
Cerebral arteriopathies of childhood and stroke - A focus on systemic arteriopathies and pediatric fibromuscular dysplasia (FMD).
Vasc Med
; 29(3): 328-341, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38898630
3.
Long-term clinical and radiological trajectories of craniocervical vasculopathy in children with PHACE syndrome.
Dev Med Child Neurol
; 2024 Apr 10.
Artigo
Inglês
| MEDLINE | ID: mdl-38597798
4.
Predictors of disease course and long-term outcomes of idiopathic intracranial hypertension in children and adolescents.
Eur J Pediatr
; 182(11): 5137-5147, 2023 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-37691042
5.
Neurosurgical aspects of Noonan syndrome.
Childs Nerv Syst
; 39(4): 849-856, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36847963
6.
Monogenic Causes of Apparently Idiopathic Perinatal Intracranial Hemorrhage.
Ann Neurol
; 89(4): 813-822, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33527515
7.
Use of Intraoperative Neuronavigation to Identify Transdural Collaterals in Moyamoya Vasculopathy: A Simple Way to Make It Safer.
Pediatr Neurosurg
; 57(4): 287-294, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35697008
8.
Current trends in pediatric moyamoya: a survey of international practitioners.
Childs Nerv Syst
; 37(6): 2011-2023, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33694129
9.
Cherry-Red Spot in Tay-Sachs Disease.
N Engl J Med
; 386(26): e72, 2022 06 30.
Artigo
Inglês
| MEDLINE | ID: mdl-35767441
10.
VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis.
Neurogenetics
; 20(4): 187-195, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31418091
11.
The safety, tolerability, and effectiveness of PTL-101, an oral cannabidiol formulation, in pediatric intractable epilepsy: A phase II, open-label, single-center study.
Epilepsy Behav
; 98(Pt A): 233-237, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31394352
12.
Mechanism of Hyponatremia in Community-Acquired Pneumonia: Does B-type Natriuretic Peptide Play a Causative Role?
Pediatr Emerg Care
; 34(9): 641-646, 2018 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-27383523
13.
Homozygous mutation, p.Pro304His, in IDH3A, encoding isocitrate dehydrogenase subunit is associated with severe encephalopathy in infancy.
Neurogenetics
; 18(1): 57-61, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28058510
14.
Sleep Disturbances in Adolescents With Idiopathic Intracranial Hypertension.
Pediatr Neurol
; 142: 39-46, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36905761
15.
Utility of genetic testing in children with leukodystrophy.
Eur J Paediatr Neurol
; 45: 29-35, 2023 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-37267771
16.
Efficacy of Medical Cannabis for Treatment of Refractory Epilepsy in Children and Adolescents with Emphasis on the Israeli Experience.
Isr Med Assoc J
; 19(2): 76-78, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-28457054
17.
Ivy sign: a diagnostic and prognostic biomarker for pediatric moyamoya.
J Neurosurg Pediatr
; 29(4): 458-466, 2022 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34972077
18.
The Genetic Landscape of Ischemic Stroke in Children - Current Knowledge and Future Perspectives.
Semin Pediatr Neurol
; 44: 100999, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36456039
19.
Cannabidiol-enriched oil in children and adults with treatment-resistant epilepsy-does tolerance exist?
Brain Dev
; 43(1): 89-96, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-32713661
20.
Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A).
Stem Cell Res
; 51: 102178, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33482465