10th International Child Neurology Congress (ICNC)

Abstracts (HTML) Autorenliste

D'Amico, A.

MUTATIONS IN POMT1 AND POMGNT1 IN ITALIAN CHILDREN WITH CMD

D'Arceuil, H.

AXONAL ABNORMALITIES IN THE BRAIN OF THE ABCD1 KNOCKOUT MOUSE, AN ANIMAL MODEL OF X-LINKED ADRENOLEUKODYSTROPHY

D'Argenzio, L.

ROLE OF -850 TNF-Á AND PSEN1 IN DOWN SYNDROME-RELATED DEMENTIA

D'Cruz, O. N. F.

EFFICACY OF LEVETIRACETAM IN STIMULUS-SENSITIVE (REFLEX) EPILEPSY

Daana, M.

LAMOTRIGINE OVERDOSE IN A CHILD

Dabscheck, G.

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

Dagenais, L.

COMMUNICATING A DIAGNOSIS OF CEREBRAL PALSY: AN ANALYSIS OF CAREGIVER SATISFACTION & STRESS

Damen, L.

EFFECTIVENESS OF INTERVENTIONS IN CHILDREN WITH MIGRAINE

Danchaivijitr, N.

CLASSIFICATION AND EVOLUTION OF CEREBRAL ARTERIOPATHIES IN CHILDHOOD ARTERIAL ISCHAEMIC STROKE

da Paz, J. A.

SPINAL CORD AFFECTION IN LEIGH SYNDROME IN 4 PATIENTS

Darke, K.

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

Das, R.

PHOTOMODULATION OF CYTOCHROME OXIDASE
AMANTADINE FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) IN CHILDREN WITH EPILEPSY: A NOVEL TREATMENT

Davidson, A.

SEIZURES IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Davidzon, G.

THE CLINICAL SPECTRUM OF MTDNA DEPLETION DUE TO MUTATIONS IN THE THYMIDINE KINASE (TK2) GENE

Davis, E.

RELIABILITY AND VALIDITY OF THE CEREBRAL PALSY QUALITY OF LIFE QUESTIONNAIRE FOR CHILDREN (CP QOL- Child)

Davis, M.

THE MORAL EXPERIENCE OF FAMILIES WITH CHILDREN REQUIRING ASSISTED-VENTILATION AT HOME

Davitoiu, A. M.

NEURONAL MIGRATION DISORDERS – CORRELATION BETWEEN CLINICAL AND NEUROIMAGING FEATURES
INFANTILE SPASMS IN TUBEROUS SCLEROSIS
ETIOLOGICAL AND NEUROIMAGISTIC ASPECTS IN INFANTILE SPASMS
A RARE CASE OF INFANTILE SPASMS – AICARDI SYNDROME
A PRACTICAL APPROACH TO BOURNEVILLE TUBEROUS SCLEROSIS

DeBassio, W.

AMANTADINE FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) IN CHILDREN WITH EPILEPSY: A NOVEL TREATMENT

De Borchgrave, V.

LONGITUDINAL ELECTROENCEPHALO-CLINICAL EVOLUTION IN 4 PATIENTS WITH RASMUSSEN ENCEPHALITIS

De Buyst, J.

THE LOGISTIC SCORE: A CRITERION FOR HYPOTHERMIA AFTER BIRTH ASPHYXIA?

de Crespigny, A.

AXONAL ABNORMALITIES IN THE BRAIN OF THE ABCD1 KNOCKOUT MOUSE, AN ANIMAL MODEL OF X-LINKED ADRENOLEUKODYSTROPHY

Degirmenci, Y.

HALLERVORDEN-SPATZ SYNDROME WITH THE ONSET OF JAW OPENING DYSTONIA

deGrauw, T.

BRAIN HISTOPATHOLOGY IN LEUKOENCEPHALOPATHY DUE TO MLC1 GENE MUTATION

del Carmen, M.

NEUROMUSCULAR DISEASES: CHILDREN, EPIDEMIOLOGIC, ARGENTINIEN

de Lissovoy, G.

COST-EFFECTIVENESS OF INTRATHECAL BACLOFEN THERAPY FOR TREATMENT OF SEVERE SPASTICITY ASSOCIATED WITH CEREBRAL PALSY

De los Santos, C.

SEPTO-OPTIC DYSPLASIA – A CLINICAL SPECTRUM DEFINITION IN 54 CASES

De Maeght, G.

HOME OBSERVATION OF SEIZURES IN EPILEPTIC CHILDREN: RESULTS OF A FLEMISCH STUDY

Dematteo, C.

DEVELOPMENTAL PATHWAY OF COGNITIVE RECOVERY FROM PAEDIATRIC ACQUIRED BRAIN INJURY (ABI)

De Meirleir, L.

DIAGNOSTIC APPROACH TO MITOCHONDRIAL DISORDERS
ENZYME REPLACEMENT THERAPY IN MPS1
DIAGNOSTICS IN MITOCHONDRIAL DISEASES: THE NEED OF COLLABORATION BETWEEN CLINICIAN AND RESEARCH LABORATORIES
DELAYED NEUROMOTOR DEVELOPMENT COMBINED WITH ALBINISM AND INCREASED VERY LONG CHAIN FATTY ACIDS
AMINOACYLASE I DEFICIENCY: A NEW INBORN ERROR OF METABOLISM LOCATED IN THE PROTEIN DEGRADATION PATHWAY OF N-ACETYLATED PROTEINS
DUPLICATION OF MECP2 IN A GIRL WITH RETT SYNDROME VARIANT

Deming, D.

CLINICAL FACTORS ASSOCIATED WITH POSTMORTEM CNS ABNORMALITIES FOLLOWING CARDIAC TRANSPLANTATION

Demos, M.

ELECTRO-CLINICAL STUDY OF FOUR FIRST NATIONS FAMILIES WITH BENIGN FAMILIAL INFANTILE SEIZURES
A NOVEL KCNA1 MUTATION CAUSES EPISODIC ATAXIA TYPE 1 WITH PERSISTENT CEREBELLAR DEFICITS

Dennis, M.

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

Deonna, T.

EPILEPTIC STEREOTYPIES

De Praeter, C.

AMINOACYLASE I DEFICIENCY: A NEW INBORN ERROR OF METABOLISM LOCATED IN THE PROTEIN DEGRADATION PATHWAY OF N-ACETYLATED PROTEINS

Deprez, C.

COULD CYTOKINES ALTER NEUROVEGETATIVE FUNCTIONS IN THE BRAINSTEM? IMPLICATIONS FOR SIDS

De Raedemaeker, M.

DUPLICATION OF MECP2 IN A GIRL WITH RETT SYNDROME VARIANT

Dericco, A.

NEURORADIOLOGIC CORRELATION IN MÖBIUS SYNDROME AND CENTRAL RESPIRATORY DISFUNCTION

de Sagun, R.

CALVARIAL TUBERCULOSIS IN AN ADOLESCENT GIRL WITH NEUROFIBROMATOSIS TYPE 1

Desai, F.

SEIZURES IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Deshpande, N.

PHENOTYPIC VARIABILITY IN CRANIOFACIAL AND ORGAN SYSTEM DEVELOPMENT IN HOLOPROSENCEPHALY

de Sousa, C.

IMMUNE MEDIATED CHOREA ENCEPHALOPATHY AND PARVOVIRUS INFECTION
INVESTIGATION OF SUSPECTED PAEDIATRIC NON-ACCIDENTAL HEAD INJURY

Detke, H. C.

ATOMOXETINE IN ADOLESCENTS WITH ADHD AND COMORBID DEPRESSION

Detre, J.

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

deVeber, G.

EFFECT OF ACETAZOLAMIDE IN MOYAMOYA DISEASE
DIFFUSION RESTRICTION IN REMOTE DESCENDING CORTICOSPINAL TRACTS PREDICTS MOTOR OUTCOME IN NEONATAL ARTERIAL ISCHEMIC STROKE
A DECADE IN THE MAKING: THE HISTORY OF NORTH AMERICA'S FIRST PAEDIATRIC STROKE PROGRAM
USE OF CLOPIDOGREL IN PEDIATRIC ARTERIAL ISCHEMIC STROKE: SAFETY AND ADVERSE EFFECTS
DIAGNOSTIC DELAYS IN ACUTE PEDIATRIC ARTERIAL ISCHEMIC STROKE

DeVeber, G.

CEREBRAL SINOVENOUS THROMBOSIS IN CHILDREN: A STUDY OF SAFETY OF ANTICOAGULANT THERAPY

De Vivo, D. C.

GLUCOSE TRANSPORTER TYPE I DEFICIENCY SYNDROME (GLUT 1 DS)
THE CLINICAL SPECTRUM OF MTDNA DEPLETION DUE TO MUTATIONS IN THE THYMIDINE KINASE (TK2) GENE
AMINOGLYCOSIDE ENHANCEMENT OF GLUCOSE TRANSPORT IN GLUT1 DEFICIENCY SYNDROME

Dezoete, A.

PREDICTION OF OUTCOME IN PRETERM INFANTS USING COTSIDE TWO-CHANNEL EEG MONITORING

Dhaunchak, A.

TRANSGENIC MODELS OF HUMAN LEUKODYSTROPHIES: INSIGHT INTO PATHOMECHANISMS

Diamond, G.

PSEUDONEUROLOGICAL SYNDROME IN INSTITUTIONALIZED INFANTS PRIOR TO BONDING AND ADOPTION

Dias, A.

STEREOTYPIES IN RETT SYNDROME – ANALYSIS OF 65 PORTUGUESE PATIENTS

Dias, K.

STEREOTYPIES IN RETT SYNDROME – ANALYSIS OF 65 PORTUGUESE PATIENTS

Dickson, R.

A REVIEW OF THE ABUSE LIABILITY OF ATOMOXETINE, A NONSTIMULANT PHARMACOTHERAPY FOR ADHD
LONG-TERM ATOMOXETINE ADMINISTRATION FOR YOUNG CHILDREN WITH ATTENTION-DEFICIT/HYPERACTIVITY DISORDER

Diez, B.

CEREBRAL INFARCTION LINKED TO GERMINAL TUMOR

Di Giandomenico, S.

SACS MUTATIONS IN AUTOSOMAL RECESSIVE SPASTIC ATAXIAS

Dilenge, M. E.

SIMULTANEOUS GUILLAIN-BARRE SYNDROME AND ACUTE DEMYELINATING ENCEPHALOMYELITIS IN THE PEDIATRIC POPULATION

DiMauro, S.

THERAPEUTIC APPROACHES TO MITOCHONDRIAL ENCEPHALOMYOPATHIES
THE CLINICAL SPECTRUM OF MTDNA DEPLETION DUE TO MUTATIONS IN THE THYMIDINE KINASE (TK2) GENE

Dimova, P.

CSWS: DIAGNOSTIC, THERAPEUTIC AND PROGNOSTIC ISSUES IN SIX CHILDREN TREATED WITH CORTICOSTEROIDS
CHARACTERISTICS OF RARE NEUROLOGICAL COMPLICATIONS OF VARICELLA INFECTION IN CHILDREN

Dinopoulos, A.

BRAIN HISTOPATHOLOGY IN LEUKOENCEPHALOPATHY DUE TO MLC1 GENE MUTATION
INTRACRANIAL SUBDURAL EFFUSIONS AND RETINAL HEMORRHAGES, SIMULATING CHILD ABUSE, IN A PATIENT DIAGNOSED WITH GLUTARIC ACIDURIA TYPE II
STEROIDS AND IVIG IN EBV-RELATED PEDIATRIC GUILLAIN-BARRE SYNDROME

Di Palma, L.

SEPTO-OPTIC DYSPLASIA – A CLINICAL SPECTRUM DEFINITION IN 54 CASES

Dirks, P.

EFFECT OF ACETAZOLAMIDE IN MOYAMOYA DISEASE

Di Taranto, P.

OUTCOME FOLLOWING EARLY NEUROSURGICAL MANAGEMENT OF BRACHIAL PLEXUS BIRTH INJURIES: AN ANALYSIS OF 100 CONSECUTIVE CASES

Djordjevic, V.

INHERITED THROMBOPHILIA AS A RISK FACTOR FOR STROKE IN SERBIAN CHILDREN

Djuranovic, V.

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

Do, T.

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

Dom, L.

HOME OBSERVATION OF SEIZURES IN EPILEPTIC CHILDREN: RESULTS OF A FLEMISCH STUDY

Domanska-Pakiela, D.

ROLE OF EEG IN PREDICTION OF EPILEPSY IN INFANTS WITH TUBEROUS SCLEROSIS COMPLEX

Domenievitz, D.

LONG-TERM EFFECT OF REPEATED INJECTIONS OF BOTULINUM TOXIN IN CHILDREN WITH CEREBRAL PALSY – A PROSPECTIVE STUDY

Donner, E.

PREDICTORS OF POST-SURGICAL SEIZURE FREEDOM IN CHILDREN WITH NORMAL MRI AND INTRACTABLE EPILEPSY
LIFE AFTER VNS: PARENTS' PERSPECTIVES OF QUALITY OF LIFE IN CHILDREN WITH DEVELOPMENTAL DELAY AND EPILEPSY AFTER IMPLANTATION OF A VAGAL NERVE STIMULATOR
SURGICAL TREATMENT FOR ACUTE SYMPTOMATIC REFRACTORY STATUS EPILEPTICUS USING MAGNETOENCEPHALOGRAPHY
EEG AND VIDEO-EEG IN CHILDREN WITH AUTISM AND STARING SPELLS
SPATIO-TEMPORAL CHANGES OF ICTAL HIGH FREQUENCY OSCILLATIONS IN PEDIATRIC NEOCORTICAL EPILEPSY

Donohue, P.

THE RELATIONSHIP BETWEEN NEUROMATURATION PRIOR TO TERM AND TODDLER MOTOR ABILITIES

Dooley, J.

MANGANESE-INDUCED PARKINSONISM IN CHILDHOOD
CANADIAN ADOLESCENTS WITH MIGRAINE: IMPAIRED HEALTH-RELATED QUALITY OF LIFE
THE EPIDEMIOLOGY OF EPILEPTIC ENCEPHALOPATHIES

Dorta, N.

SPEECH AND LANGUAGE DISORDERS AGGREGATE IN ROLANDIC EPILEPSY FAMILIES

Dosch, H. M.

T CELL PROLIFERATION AGAINST MYELIN, PANCREATIC, AND DIETARY ANTIGENS IN CHILDREN: AUTOIMMUNITY IS DETECTABLE EARLY IN CNS DEMYELINATION AND TYPE I DIABETES

Douste, K.

EVALUATION OF IRON DEFICIENCY AND ADHD INTER RELATION SHIP IN PEDIATRIC NEUROLOGY OUT PATIENT

Doutrellot, P. L.

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

Dower, N.

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

Drachman, D. B.

NEW AND OLD STRATEGIES IN THE TREATMENT OF MYASTHENIA GRAVIS

Dragomir, D.

NEURONAL MIGRATION DISORDERS – CORRELATION BETWEEN CLINICAL AND NEUROIMAGING FEATURES
INFANTILE SPASMS IN TUBEROUS SCLEROSIS
ETIOLOGICAL AND NEUROIMAGISTIC ASPECTS IN INFANTILE SPASMS
SECKEL SYNDROME AND EPILEPSY
A RARE CASE OF INFANTILE SPASMS – AICARDI SYNDROME
A PRACTICAL APPROACH TO BOURNEVILLE TUBEROUS SCLEROSIS

Drake, J.

SURGICAL TREATMENT FOR ACUTE SYMPTOMATIC REFRACTORY STATUS EPILEPTICUS USING MAGNETOENCEPHALOGRAPHY

Drouin, R.

CLINICAL SPECTRUM OF MYOTONIC DYSTROPHY IN CHILDREN
ISOLATED UNILATERAL DIAPHRAGMATIC PARALYSIS AS INITIAL NEONATAL MANIFESTATION OF MULTI-MINICORE MYOPATHY

Du, J. C.

LOW CSF FOLATE IN CHILDREN WITH PSYCHOMOTOR RETARDATION

Dubey, P.

ANNUAL DISABILITY PROGRESSION IN PURE ADRENOMYELONEUROPATHY PATIENTS

Dubowitz, V.

THERAPEUTIC INNOVATIONS IN THE NEUROMUSCULAR DISORDERS

Duckrow, R.

CORRELATION OF MAGNETIC RESONANCE SPECTROSCOPIC IMAGING AND INTRACRANIAL EEG LOCALIZATION OF SEIZURES

Duffner, P.

THE TREATMENT OF INFANTS AND VERY YOUNG CHILDREN WITH BRAIN TUMORS: THE U.S. COOPERATIVE GROUP EXPERIENCE: 1986–2006
LACK OF ASSOCIATION OF THROMBOPHILIC POLYMORPHISMS WITH PERINATAL STROKE: A CASE CONTROL STUDY

Duffy, F.

HIGH DOSE DIAZEPAM (HDD) IN CHILDHOOD-ONSET EPILEPTIC ENCEPHALOPATHIES WITH SLEEP ACTIVATED EEG (EESA_EEG)

Duivenvoorden, H.

QUALITY OF LIFE IN CHILDREN WITH HEADACHE IN A DUTCH GENERAL HOSPITAL COMPARED WITH A COHORT OF HEALTHY CHILDREN

Dumas, F.

COMMUNICATING A DIAGNOSIS OF CEREBRAL PALSY: AN ANALYSIS OF CAREGIVER SATISFACTION & STRESS

Dumitrescu, C.

NEUROPSYCHOLOGICAL PROFILE DIFFERENCES SUPPORT DIAGNOSTIC DIVERGENCE BETWEEN ASPERGERS SYNDROME AND NONVERBAL LEARNING DISORDER

Duncan, J.

CORRELATION OF MAGNETIC RESONANCE SPECTROSCOPIC IMAGING AND INTRACRANIAL EEG LOCALIZATION OF SEIZURES

Dunkel, I.

DIFFUSE CNS GERM CELL NEOPLASM PRESENTING WITH PROGRESSIVE ENCEPHALOPATHY: 3 CASES

Dunn, D.

PROBLEMS WITH ATTENTION IN CHILDREN WITH EPILEPSY
SEIZURE RISK IN PATIENTS WITH ADHD TREATED WITH ATOMOXETINE
ATOMOXETINE TREATMENT OF ADHD IN CHILDREN WITH COMORBID TOURETTE SYNDROME

Dunn, R. J.

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

Durity, F.

ATYPICAL PRESENTATION OF SPINAL CORD TUMORS IN CHILDREN

Durkin, M. S.

GLOBAL HEALTLH PRIORITIES AND THE PREVENTION OF NEURODEVELOPMENTAL DISABILITIES

Durning, S.

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

Durr, A.

SACS MUTATIONS IN AUTOSOMAL RECESSIVE SPASTIC ATAXIAS