Detalhe da pesquisa
1.
Highlighting the Dystonic Phenotype Related to GNAO1.
Mov Disord
; 37(7): 1547-1554, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35722775
2.
Screening for neurodevelopmental disorders in children with congenital heart disease.
Eur J Pediatr
; 180(4): 1157-1167, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33119792
3.
Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons.
Am J Hum Genet
; 99(2): 511-20, 2016 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27453579
4.
Use of EEG in neonatal hypoxic-ischemic encephalopathy: A French survey of current practice and perspective for improving health care.
Neurophysiol Clin
; 53(1): 102883, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37229978
5.
Differentiating Genetic Forms of Pontocerebellar Hypoplasia From Acquired Lesions Resembling Pontocerebellar Hypoplasia: Clinical, Neurodevelopmental, and Imaging Insight From 19 Extremely Premature Patients.
J Child Neurol
; 38(10-12): 622-630, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37731326
6.
Recanalization Treatments for Pediatric Acute Ischemic Stroke in France.
JAMA Netw Open
; 5(9): e2231343, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36107427
7.
Ultrasound diagnosis, management and prognosis in a consecutive series of 27 cases of fetal hydrops following maternal parvovirus B19 infection.
Fetal Diagn Ther
; 30(1): 41-7, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21502743
8.
Comparison of seizure reduction and serum fatty acid levels after receiving the ketogenic and modified Atkins diet.
Seizure
; 18(5): 359-64, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19196525
9.
The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
Neurogenetics
; 9(4): 277-85, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18685874
10.
Unusual clinical features in infantile Spinal Muscular Atrophies.
Brain Dev
; 30(3): 169-78, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17804187
11.
Phenotypic variability of prenatally presenting Gaucher's disease.
Prenat Diagn
; 33(10): 1004-6, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23749476
12.
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
Hum Mutat
; 28(11): 1055-64, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17584854
13.
Postmeningitis subdural fluid collection in infants: changing pattern and indications for surgery.
J Neurosurg
; 104(6 Suppl): 383-7, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16776372
14.
Amniotic bands and associated polymicrogyria: In favor of a unique ischemic cause.
Eur J Obstet Gynecol Reprod Biol
; 236: 252-254, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30955893
15.
Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient.
Orphanet J Rare Dis
; 7: 18, 2012 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22452838
16.
LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity.
Arch Neurol
; 66(8): 1007-15, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19667223
17.
Antenatal diagnosis of a third ventricular mass: fetus in fetu or teratoma?
Childs Nerv Syst
; 24(8): 887-91, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18493782
18.
French general practitioners' management of children's migraine headaches.
Headache
; 47(9): 1282-92, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17927644