Detalhe da pesquisa
1.
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
Brain
; 141(3): 698-712, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29365063
2.
Whole-exome sequencing reveals a novel missense mutation in the MARS gene related to a rare Charcot-Marie-Tooth neuropathy type 2U.
J Peripher Nerv Syst
; 23(2): 138-142, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29582526
3.
Frequency of pediatric migraine with aura in a clinic-based sample.
Headache
; 56(1): 113-7, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26790850
4.
Clinical Profile of Attention Deficit Hyperactivity Disorder: Impact of Ethnic and Social Diversities in Israel.
Isr Med Assoc J
; 18(6): 322-5, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27468523
5.
Pediatric mixed headache -The relationship between migraine, tension-type headache and learning disabilities - in a clinic-based sample.
J Headache Pain
; 17: 42, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27102119
6.
The Clinical Characteristics of ADHD Diagnosed in Adolescents in Comparison With Younger Children.
J Atten Disord
; 24(8): 1125-1131, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28367712
7.
Pseudotumor Cerebri Syndrome: From Childhood to Adulthood Risk Factors and Clinical Presentation.
J Child Neurol
; 35(5): 311-316, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31928127
8.
Clinical spectrum and medical treatment of children with electrical status epilepticus in sleep (ESES).
Epilepsia
; 50(6): 1517-24, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19054417
9.
Delayed language development due to infantile thiamine deficiency.
Dev Med Child Neurol
; 51(8): 629-34, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19191836
10.
Handedness in patients with developmental coordination disorder.
J Child Neurol
; 23(2): 151-4, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18079311
11.
Vigabatrin, lamotrigine, topiramate and serum carnitine levels.
Pediatr Neurol
; 39(1): 18-21, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18555168
12.
Typical absence epilepsy presenting prior to age of 3 years: an uncommon form of idiopathic generalized epilepsy.
Eur J Paediatr Neurol
; 11(6): 346-52, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17500018
13.
Differential stimulant response on attention in children with comorbid anxiety and oppositional defiant disorder.
J Child Neurol
; 22(5): 538-42, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17690058
14.
Childhood epilepsy with occipital paroxysms: difficulties in distinct segregation into either the early-onset or late-onset epilepsy subtypes.
J Child Neurol
; 22(5): 588-92, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17690066
15.
Childhood-onset idiopathic intracranial hypertension: relation of sex and obesity.
Pediatr Neurol
; 36(4): 247-9, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17437908
16.
A novel mutation of the CLN8 gene: is there a Mediterranean phenotype?
Pediatr Neurol
; 36(6): 411-3, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17560505
17.
The Role of Prematurity in Patients With Hemiplegic Cerebral Palsy.
J Child Neurol
; 31(6): 678-82, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26500242
18.
The clinical profile of children with ADHD that require OROS-methylphenidate combined with shorter-acting formulations.
Atten Defic Hyperact Disord
; 7(4): 313-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25838111
19.
The neurologic profile of children and adolescents with inflammatory bowel disease.
J Child Neurol
; 30(5): 551-7, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24700662
20.
Clinical characteristics of autism spectrum disorder in Israel: impact of ethnic and social diversities.
Biomed Res Int
; 2015: 962093, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25984535