10th International Child Neurology Congress (ICNC)

Abstracts (HTML) List of Authors

Laan, L. A. E. M.

MOYAMOYA SYNDROME ASSOCIATED WITH ALTERNATING HEMIPLEGIA

Lachhwani, D.

OUTCOME IN INFANTS PRESENTING WITH MIGRATING PARTIAL SEIZURES

Lacy, M.

NEUROCOGNITIVE CORRELATES OF GROUP MEMBERSHIP: A COMPARISON OF HYDROCEPHALUS PATIENTS SHUNTED WITHIN THE FIRST YEAR OF LIFE AND NORMAL CONTROLS

Lagae, L.

ANTENATAL MATERNAL ANXIETY IS ASSOCIATED WITH SPECIFIC IMPAIRMENTS IN COGNITIVE FUNCTIONING AT AGE 17
ASSOCIATION BETWEEN ERP-WAVEFORMS IN A GAMBLING TASK AND ANTENATAL MATERNAL ANXIETY: ADOLESCENTS OF ANXIOUS MOTHERS SHOW DIFFERENT FRONTAL LOBE FUNCTIONING
HOME OBSERVATION OF SEIZURES IN EPILEPTIC CHILDREN: RESULTS OF A FLEMISCH STUDY
OPTOTYPE AND GRATING VISUAL ACUITY IN CHILDREN WITH VISUAL PERCEPTUAL IMPAIRMENT

Lagos, R.

ISQUEMIC STROKE SECONDARY TO ARTERIAL DISSECTION

Lai, H.

CLINICAL STUDY ON BENIGN INFANTILE CONVULSIONS ASSOCIATED WITH MILD GASTROENTERITIS
EFFECTS OF BENIGN AUDITORY STIMULSTION ON CEREBRAL OXIDATIVE METABOLISM AND CEREBRAL BLOOD FLOW IN PRETERM INFANTS

Lalli, C.

NEUROBIOLOGICAL CAUSES OF MILD MENTAL RETARDATION: THE ROLE OF ADENOSINE DEAMINASE POLYMORPHISM

Lam, C. W.

GALACTORRHEA-A STRONG CLINICAL CLUE TOWARDS THE DIAGNOSIS OF NEUROTRANSMITTER DISEASE
DYT1 MUTATION: FROM ASYMPTOMATIC CARRIER TO STIFF MAN SYNDROME

Lambson, L.

PHENOTYPIC VARIABILITY IN NARP (NEUROGENIC MUSCLE WEAKNESS ATAXIA RETINITIS PIGMENTOSA): CORRELATION WITH LEVELS OF MUTANT MITOCHONDRIAL DNA IN BLOOD

Lamhonwah, A. M.

OCTN3 IS A MAMMALIAN PEROXISOMAL MEMBRANE CARNITINE TRANSPORTER: IMPLICATIONS FOR PEROXISOMAL DISORDERS
NOVEL LOCALIZATION OF OCTN1, AN ORGANIC CATION/CARNITINE TRANSPORTER, TO MAMMALIAN MITOCHONDRIA: IMPLICATIONS FOR CARNITINE-RESPONSIVE ENCEPHALOPATHY AND MYOPATHY

Laridon, A.

INTRATHECAL BACLOFEN (ITB TM) THERAPY FOR SPASTIC CHILDREN: 7 YEARS OF EXPERIENCE

Larouche, A.

PRO-INFLAMMATORY CYTOKINES IN THE PATHOGENESIS OF BRAIN INJURIES FOLLOWING PERINATAL INFECTION AND ANOXIA

Larsson, B.

HHEADACHE IN SWEDISH SCHOOL CHILDREN – A FOLLOW-UP STUDY

Larysz-Brysz, M.

IS FOCAL CORTICAL DYSPLASIA TYPE IIB THE FOCAL FORM OF TUBEROUS SCLEROSIS COMPLEX?

Latimer, E.

NEONATAL FLUOXETINE WITHDRAWAL SYNDROME – A MOVEMENT DISORDER SECONDARY TO MATERNAL USE DURING PREGNANCY

Latorre, R.

CALVARIAL TUBERCULOSIS IN AN ADOLESCENT GIRL WITH NEUROFIBROMATOSIS TYPE 1

Lau, K. S.

IDENTIFYING PRENATAL, PERINATAL AND ENVIRONMENTAL RISK FACTORS FOR AUTISM SPECTRUM DISORDER (ASD): A CASECONTROL STUDY

Laurell, K.

HHEADACHE IN SWEDISH SCHOOL CHILDREN – A FOLLOW-UP STUDY

Lavenstein, B.

NEONATAL FLUOXETINE WITHDRAWAL SYNDROME – A MOVEMENT DISORDER SECONDARY TO MATERNAL USE DURING PREGNANCY
ANALYSIS OF THE WORKFORCE CRISIS IN CHILD NEUROLOGY IN THE UNITED STATES

Lavoie, É

HEMIMEGACEREBELLUM: A REPORT OF ONE CASE

Law, M.

DETERMINANTS OF QUALITY OF LIFE IN SCHOOL AGE CHILDREN WITH CEREBRAL PALSY

Lawrenson, J.

SYDENHAM'S CHOREA: A NEW APPROACH TO AN OLD DISEASE

Lawton, L.

BONE DENSITY INTERPRETATION IN CHILDREN WITH CEREBRAL PALSY

Lazar, A.

SECKEL SYNDROME AND EPILEPSY

Lazeyras, F.

EARLY MODIFICATIONS OF AMPLITUDE-INTEGRATED EEG IN PREMATURE INFANTS

Lecoutre, N.

EFFECTS OF EXERCISE TRAINING ON CARDIORESPIRATORY REQUIREMENT IN CHIDREN WITH NEUROMUSCULAR DISORDER

Lee, D. C.

ISOLATION AND CHARACTERIZATION OF STEM/ PROGENITOR CELLS FROM HUMAN AMNION – POSSIBLE APPLICATION OF NEURAL REPAIR IN THE FUTURE

Lee, E. J.

NEUROPROTECTIVE EFFECT OF MAGNOLOL ON ORGANOTYPIC HIPPOCAMPAL SLICE CULTURES

Lee, H. F.

CLINICAL MANIFESTATIONS OF MITOCHONDRIAL DISEASES IN INFANTS AND CHILDREN
MRI FINDINGS OF MITOCHONDRIAL DISEASES IN INFANTS AND CHILDREN

Lee, H. M.

DENERVATION AFFECTS THE EXPRESSION OF PGC-1 ALPHA AND MITOCHONDRIAL BIOGENESIS

Lee, H. Y.

A MOUSE MODEL OF PAROXYSMAL NON-KINESIGENIC DYSKINESIA (PNKD)

Lee, M. Y.

NEUROPROTECTIVE EFFECT OF MAGNOLOL ON ORGANOTYPIC HIPPOCAMPAL SLICE CULTURES

Lee, S. H.

SAFETY AND EFFICACY OF THE 'BOTOX®-MULTI-MUSCLE-CONCEPT' (B-MMOCONCEPT) IN CHILDREN WITH CEREBRAL PALSY

Lee, W. T.

LOW CSF FOLATE IN CHILDREN WITH PSYCHOMOTOR RETARDATION
LONG-TERM FOLLOW-UP OF MECP2-KNOCKOUT MICE USING MAGNETIC RESONANCE TECHNIQUES
CONGENITAL ADRENAL HYPERPLASIA IN A PATIENT WITH DUCHENNE MUSCULAR DYSTROPHY
DETERMINATION OF BRAIN DEATH IN CHILDREN IN TAIWAN
PROTHROMBOTIC DISORDERS IN CHILDREN WITH ISCHEMIC STROKE IN TAIWAN
PLASMA CGRP LEVELS IN THE DIAGNOSIS OF PEDIATRIC MIGRAINE

Legido, A.

NEUROLEPTIC MALIGNANT SYNDROME IN CHILDREN

Lehwald, L.

SLEEP DISTURBANCE IN PEDIATRIC CHRONIC DAILY HEADACHE PATIENTS

Lei, K.

CHEMICAL CHAPERONE THERAPY FOR GAUCHER DISEASE: N-OCTYL-BETA-VALIENAMINE INCREASES THE CELLULAR ACTIVITY OF NOT ONLY F213I BUT ALSO N188S BETAGLUCOCEREBROSIDASES

Leitner, Y.

THE DEVELOPMENTAL OUTCOME OF MILD VENTRICULOMEGALY DIAGNOSED BY PRENATAL MAGNETIC RESONANCE IMAGING (MRI)
CEREBRAL PALSY – MEDICAL, FUNCTIONAL, EDUCATIONAL AND PSYCHOSOCIAL LONGTERM OUTCOME

Lelard, T.

NATURE OF MOTOR DISORDER AND DYNAMIC PLANTAR PRESSURE DISTRIBUTION MEASUREMENT IN CHILDREN WITH CEREBRAL PALSY

Lema, P.

IMPACT OF PREVENTING PROLONGED FEBRILE SEIZURES IN THE PREDISPOSED BRAIN

Lemieux, B.

CLINICAL SPECTRUM OF MYOTONIC DYSTROPHY IN CHILDREN

Lemire, E.

CREE LEUKOENCEPHALOPATHY: ANOTHER CAUSE OF A “TIGROID” PATTERN OF DEMYELINATION
PERIPHERAL NERVE INVOLVEMENT IN A CHILD WITH CREE LEUKODYSTROPHY

Lemka, M.

AGENESIS OF CORPUS CALLOSUM – CLINICS AND GENETICS
ANTIPHOSPHOLIPID ANTIBODIES IN CHILDREN MIGRAINE

Leonard, H.

ATOMOXETINE TREATMENT OF ADHD IN CHILDREN WITH COMORBID TOURETTE SYNDROME

Leonard, N. J.

FAMILIAL CEREBRAL PALSY: RECURRENCE OF CEREBRAL PALSY IN THE PRESENCE OF MULTIPLE RISK FACTORS

Leresche, N.

BASIC MECHANISMS OF ABSENCE SEIZURES

Lerman-Sagie, T.

IN UTERO IDENTIFICATION OF COMMISSURAL ANOMALIES – THE EXPERIENCE OF THE FETAL NEUROLOGY MULTIDISCIPLINARY CLINIC
DEVELOPMENTAL COORDINATION DISORDER IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER: CHARACTERIZATION OF THE PROBLEM AND THE IMPACT OF PHYSICAL THERAPY INTERVENTION
NOVEL SHORT-CHAIN ACYL-COA DEHYDROGENASE GENE MUTATION (319 C>T) PRESENTS WITH HYPOTONIA, DEVELOPMENTAL DELAY, MULTICORE MYOPATHY AND CLINICAL HETEROGENEITY AND IS CANDIDATE FOUNDER MUTATION IN ASHKENAZI JEWS
ASSOCIATION OF PARIETO-OCCIPITAL POLYMICROGYRIA, CHIARI MALFORMATION TYPE 1 AND SYRINGOMYELIA

Leshner, R.

A CINRG PILOT TRIAL OF OXATOMIDE IN STEROID-NAÏVE DUCHENNE MUSCULAR DYSTROPHY

Leung, L. S.

EARLY-LIFE SEIZURES INDUCED BY GABAB–RECEPTOR ANTAGONIST INCREASE HIPPOCAMPAL KINDLING SUSCEPTIBILITY IN ADULT RATS

Leuzzi, V.

IDENTIFICATION OF THE CRITICAL LOCUS IN A NEW FORM OF LEUCODYSTROPHY WITH PROGRESSIVE ATAXIA, DEAFNESS, AND CARDIOMYOPATHY

Lev, D.

IN UTERO IDENTIFICATION OF COMMISSURAL ANOMALIES – THE EXPERIENCE OF THE FETAL NEUROLOGY MULTIDISCIPLINARY CLINIC

Levi-Hakeini, O.

CEREBRAL PALSY – MEDICAL, FUNCTIONAL, EDUCATIONAL AND PSYCHOSOCIAL LONGTERM OUTCOME

Levine, L. R.

EFFECTS OF LONGER-TERM ATOMOXETINE TREATMENT IN ADOLESCENTS WITH ADHD

Lev Lev, D.

ASSOCIATION OF PARIETO-OCCIPITAL POLYMICROGYRIA, CHIARI MALFORMATION TYPE 1 AND SYRINGOMYELIA

Levy, A.

STEREOTYPIES IN RETT SYNDROME – ANALYSIS OF 65 PORTUGUESE PATIENTS

Lewin-Kowalik, J.

IS FOCAL CORTICAL DYSPLASIA TYPE IIB THE FOCAL FORM OF TUBEROUS SCLEROSIS COMPLEX?

Lewis, D.

ATOMOXETINE TREATMENT OF ADHD IN CHILDREN WITH COMORBID TOURETTE SYNDROME

Li, D.

MAGNETIC RESONANCE IMAGING CRITERIA FOR THE DIAGNOSIS OF CHILDHOOD MULTIPLE SCLEROSIS

Li, J.

SUCCESSFUL PROPHYLAXIS OF FEBRILE CONVULSION WITH TOPIRAMATE

Li, K.

BOLD FMRI IN INFANTS AND YOUNG CHILDREN WITH SUSPECTED VISUAL IMPAIRMENT

Li, M.

GENE DELIVERY INTO PRIMARY CEREBRAL CORTICAL NEURONS BY LENTIVIRAL VECTOR

Li, W. H.

CLINICAL AND IMMUNOLOGICAL STUDIES OF JUVENILE MYASTHENIA GRAVIS

Li, X.

SURVIVAL MOTOR NEURON PROTEIN (SMN) DEPLETION IN NEURONAL CELLS BY siRNA INHIBITION: AN IN VITRO MODEL FOR SMA
INFLUENCES OF AGE AND THE DURATION OF STATUS CONVULSION ON INTRACELLULAR CYTOCHROME C RELEASE IN HIPPOCAMPUS
CORRELATIVE FACTORS OF NEURONAL APOPTOSIS IN HIPPOCAMPUS AFTER STATUS CONVULSION

Li, Z.

SHORT-TERM AND LONG-TERM EFFECTS OF EARLY SEIZURES ON DEVELOPING BRAIN

Liang, J.

NOVEL MUTATIONS IN THE ABCD1 GENE OF TWO TAIWANESE PATIENTS WITH ADRENOLEUKODYSTROPHY
THE CLINICAL AND THE ICTAL VIDEO-EEG CHARACTERISTICS OF 28 CASES WITH INFANTILE SPASMS
CLINICAL CHARACTERISTICS, ETIOLOGY, EEG AND PROGNOSIS OF 12 PATIENTS WITH INFANTILE SPASMS AND PARTIAL SEIZURES

Liang, K. C.

POTENTIATION OF LEARNING IMPAIRMENT OF ACETAZOLAMIDE BY AMILORIDE IN RATS

Liao, W. J.

DENERVATION AFFECTS THE EXPRESSION OF PGC-1 ALPHA AND MITOCHONDRIAL BIOGENESIS

Licht, D.

PRE-OPERATIVE MRI ABNORMALITIES ARE COMMON IN FULL-TERM INFANTS WITH SEVERE CHD AND RESEMBLE LESIONS IN PRE-TERM INFANTS

Liendo, S.

DEVELOPMENT OF VLBW PREMATURES IN THE SECOND YEAR OF LIFE

Lillakas, L.

THE VESTIBULO-OCULAR REFLEX IN CHIARI TYPE II MALFORMATION
THE VESTIBULO-OCULAR REFLEX IN CHILDREN

Lillywhite, L. M.

COGNITIVE DYSFUNCTION AND THE DISTRIBUTION OF SPIKE ACTIVITY IN BECTS

Limperopoulos, C.

THE VULNERABLE IMMATURE CEREBELLUM: CONSEQUENCES FOR SURVIVORS FOLLOWING EARLY LIFE INJURY

Lin, J. J.

NEUROLOGIC OUTCOMES IN CHILDREN WITH ENTEROVIRUS 71-RELATED CARDIOPULMONARY FAILURE AFTER EXTRACORPOREAL MEMBRANE OXYGENATION: PROGNOSTIC VALUE OF SERUM NEURON SPECIFIC ENOLASE

Lin, K. L.

LOW DOSE VIGABATRIN FOR THE TREATMENT OF INFANTILE SPASMS
RETROSPECTIVE STUDY OF MITOCHONDRIAL DISORDER IN CHILDHOOD
NEUROLOGIC OUTCOMES IN CHILDREN WITH ENTEROVIRUS 71-RELATED CARDIOPULMONARY FAILURE AFTER EXTRACORPOREAL MEMBRANE OXYGENATION: PROGNOSTIC VALUE OF SERUM NEURON SPECIFIC ENOLASE

Linder, M.

CONSTRAINT INDUCED MOVEMENT THERAPY IN CONGENITAL HEMIPARESIS III: FMRI REVEALS INCREASED ACTIVATION IN PRIMARY SENSORIMOTOR CORTEX (M1S1)
CONSTRAINT-INDUCED MOVEMENT THERAPY IN PATIENTS WITH CONGENITAL HEMIPARESIS DUE TO STROKE

Linder, S.

ATOMOXETINE TREATMENT OF ADHD IN CHILDREN WITH COMORBID TOURETTE SYNDROME

Lindor, N.

VANISHING WHITE MATTER DISEASE WITH NEUTROPENIA: A CASE REPORT WITH SERIAL MRI AND EEG CORRELATION

Lingappa, L.

ACUTE ENCEPHALOPATHY WITH SEVERE BRAINSTEM INVOLVEMENT – IS IT ONE ENTITY

Linnankivi, T.

POSTERIOR LISSENCEPHALY, PONTINE HYPOPLASIA, CEREBELLAR CORTICAL DYSGENESIS AND WHITE MATTER HYPERINTENSITY. TWO CASES WITH COBBLE STONE CORTEX AND ONE WITHOUT

Lissens, W.

DIAGNOSTICS IN MITOCHONDRIAL DISEASES: THE NEED OF COLLABORATION BETWEEN CLINICIAN AND RESEARCH LABORATORIES
AMINOACYLASE I DEFICIENCY: A NEW INBORN ERROR OF METABOLISM LOCATED IN THE PROTEIN DEGRADATION PATHWAY OF N-ACETYLATED PROTEINS

Liu, C. H.

CLINICAL ANALYSIS OF DEVELOPMENTAL DELAY IN COMBINED INTERVENTION CLINIC

Liu, G.

BOLD FMRI IN INFANTS AND YOUNG CHILDREN WITH SUSPECTED VISUAL IMPAIRMENT

Liu, X. Y.

USING FUNCTIONAL CANDIDATE GENE STRATEGY TO STUDY CHILDHOOD ABSENCE EPILEPSY GENE

Liu, Y.

EFFECT OF CHOLECYSTOKININ-8 ON IN VITRO CULTURED RAT CORTICAL NEURONS AGAINST APOPTOSIS AND EXPRESSION OF NERVE GROWTH FACTOR

Liu, Z.

SHORT-TERM AND LONG-TERM EFFECTS OF EARLY SEIZURES ON DEVELOPING BRAIN

Liu, Z. H.

IMPROVING QUALITY OF LIFE OF CHILDREN WITH CEREBRAL PALSY WITH ACUPUNCTURE THERAPY
CEREBRAL PALSY WITH SPEECH DISORDER TREATED BY ACUPUNCTURE COMBINED WITH SPEECH THERAPY

Liu, Z. S.

EVALUATION OF THE EMOTION QUESTION, ADAPTIVE BEHAVIOR AND VISUAL PERCEPTION IN CHILDREN WITH TIC DISORDERS

Lo, P.

ISOLATED INTRACRANIAL HYPERTENSION AS A LATE MANIFESTATION OF SINUS VENOUS COMPRESSION SECONDARY TO A DEPRESSED SKULL FRACTURE

Lobo Antunes, N.

STEREOTYPIES IN RETT SYNDROME – ANALYSIS OF 65 PORTUGUESE PATIENTS

Lodygensky, G.

EARLY MODIFICATIONS OF AMPLITUDE-INTEGRATED EEG IN PREMATURE INFANTS

Logan, W.

EFFECT OF ACETAZOLAMIDE IN MOYAMOYA DISEASE
PREDICTORS OF DYSTONIA IN CHILDHOOD BASAL GANGLIA STROKE

Loizzo, A. L.

IDENTIFICATION OF THE CRITICAL LOCUS IN A NEW FORM OF LEUCODYSTROPHY WITH PROGRESSIVE ATAXIA, DEAFNESS, AND CARDIOMYOPATHY

Lokesh, L.

SPINAL MUSCULAR ATROPHY -ROLE OF PATHOLOGY IN DIAGNOSIS

Lonnqvist, T.

CATASTROPHIC EPILEPSY IN PATIENTS WITH INFANTILE ONSET SPINOCEREBELLAR ATAXIA (IOSCA), A NUCLEAR MITOCHONDRIAL DISORDER

Lopez-Gutierrez, J. C.

ABSENCE OF CAROTID AND VERTEBRAL ARTERIES, AND PERSISTENCE OF EMBRYONIC ARTERIES ASSOCIATED WITH CUTANEOUS HEMANGIOMAS
OBSTETRIC BRACHIAL PALSY. ROLE OF BOTULINUM TOXIN TYPE-A IN EARLY TREATMENT

López-Marín, L.

LEVETIRACETAM AS ADD-ON THERAPY IN 25 CHILDREN WITH MYOCLONIC EPILEPSY

Lopez-Pereira, P.

NEUROFIBROMATOSIS TYPE 1 (NF1) AND NEUROFIBROMAS OF THE EXTERNAL GENITALIA: PRESENTATION IN 3 PATIENTS

Loukas, A.

HOW DO MUTATIONS IN VOLTAGE-GATED SODIUM CHANNELS CAUSE EPILEPSY?

Lovic, A.

OBSTETRIC BRACHIAL PALSY. ROLE OF BOTULINUM TOXIN TYPE-A IN EARLY TREATMENT

Low, L.

6-PYRUVOYL-TETRAHYDROPTERIN SYNTHASE DEFICIENCY: THE CLINICAL SPECTRUM IN 3 CHINESE PATIENTS

Lowry, N.

CREE LEUKOENCEPHALOPATHY: ANOTHER CAUSE OF A “TIGROID” PATTERN OF DEMYELINATION
PERIPHERAL NERVE INVOLVEMENT IN A CHILD WITH CREE LEUKODYSTROPHY

Lu, C.

PERCEIVED ACCURACY OF INFORMATION SOURCES CONSULTED BY FAMILIES WHOSE CHILDREN HAVE EPILEPSY

Lu, J. F.

NOVEL MUTATIONS IN THE ABCD1 GENE OF TWO TAIWANESE PATIENTS WITH ADRENOLEUKODYSTROPHY

Lu, J. J.

USING FUNCTIONAL CANDIDATE GENE STRATEGY TO STUDY CHILDHOOD ABSENCE EPILEPSY GENE

Luaces, R. P.

ABSENCE OF CAROTID AND VERTEBRAL ARTERIES, AND PERSISTENCE OF EMBRYONIC ARTERIES ASSOCIATED WITH CUTANEOUS HEMANGIOMAS

Luan, Z.

CHEMICAL CHAPERONE THERAPY FOR GAUCHER DISEASE: N-OCTYL-BETA-VALIENAMINE INCREASES THE CELLULAR ACTIVITY OF NOT ONLY F213I BUT ALSO N188S BETAGLUCOCEREBROSIDASES
BOLD FMRI IN INFANTS AND YOUNG CHILDREN WITH SUSPECTED VISUAL IMPAIRMENT

Ludovici, A.

SINGLE-VOXEL H1 MR SPECTROSCOPY OF NORMAL APPEARING WHITE MATTER IN PATIENTS WITH TUBEROUS SCLEROSIS

Lujic, L.

L-2-OH-GLUTARIC ACIDURIA – REPORT ON NEUROIMAGING FINDINGS IN 3 CASES

Lund, A. M.

A DANISH THREE-YEAR PROSPECTIVE TRIAL OF NEWBORN SCREENING FOR INBORN ERRORS OF METABOLISM USING TANDEM MASS SPECTROMETRY

Lux, A.

THE UNITED KINGDOM INFANTILE SPASMS STUDY: NEURODEVELOPMENTAL OUTCOME AT 4.2 YEARS OF AGE

Lžičařová, E.

NEUROENDOSCOPIC TREATMENT OF ARACHNOIDAL CYSTS IN CHILDREN