10th International Child Neurology Congress (ICNC)

Abstracts (HTML) List of Authors

Paavonen, J.

PITFALLS IN THE CURRENT MANAGEMENT OF TRAUMATIC BRAIN INJURIES IN CHILDREN – THE STOCKHOLM EXPERIENCE
COMPARISON OF THE DIAGNOSTIC TOOLS FOR ASPERGER SYNDROME

Packer, R. J.

STATE-OF-THE-ART TREATMENT OF TUMORS OF THE NERVOUS SYSTEM IN CHILDHOOD

Paczkowski, M.

ATOMOXETINE TREATMENT FOR PEDIATRIC PATIENTS WITH ADHD AND COMORBID ANXIETY

Paderova, K.

EARLY ONSET MS – A RETROSPECTIVE STUDY

Paetau, A.

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

Pahs, G.

LEVETIRACETAM FOR THE TREATMENT OF “NOT SO BENIGN” IDIOPATHIC PARTIAL EPILEPSIES OF CHILDHOOD

Painter, M.

ANALYSIS OF THE WORKFORCE CRISIS IN CHILD NEUROLOGY IN THE UNITED STATES

Pakula-Kosciesza, I.

USEFULNESS OF BRAIN MRI IN DIAGNOSIS OF NBIA IN PKAN AND NON-PKAN PATIENTS

Pal, D. K.

SPEECH AND LANGUAGE DISORDERS AGGREGATE IN ROLANDIC EPILEPSY FAMILIES
AUTOSOMAL DOMINANT TRANSMISSION OF CENTROTEMPORAL SPIKES IN ROLANDIC EPILEPSY FAMILIES
NO EXCESS OF NEUROIMAGING ABNORMALITIES ASSOCIATED WITH ROLANDIC EPILEPSY

Palmarino, M.

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

Paloscia, C.

NEUROPSYCHOLOGICAL ENDOPHENOTYPES IN ADHD: NEUROCOGNITIVE DEFICITS IN ADHD PATIENTS AND THEIR PARENTS
NEUROCOGNITIVE ENDOPHENOTYPES OF ADHD

Pan, H.

USING FUNCTIONAL CANDIDATE GENE STRATEGY TO STUDY CHILDHOOD ABSENCE EPILEPSY GENE
THE GENOTYPE AND PHENOTYPE STUDIES OF 40 CHINESE PATIENTS WITH X-ALD
GENE DELIVERY INTO PRIMARY CEREBRAL CORTICAL NEURONS BY LENTIVIRAL VECTOR

Pandey, R. M.

A RANDOMIZED CONTROLLED TRIAL TO COMPARE EFFICACY OF ORAL CLOBAZAM WITH ORAL DIAZEPAM FOR PROPHYLAXIS OF FEBRILE SEIZURES

Panousopoulou, C.

FETAL BRAIN MRI FINDINGS IN TWO CASES OF PYRUVATE DEHYDROGENASE DEFICIENCY

Papademetris, X.

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

Papavasiliou, A.

CHANGES IN CARS SCORES AND SHORT SENSORY PROFILE IN AUTISTIC CHILDREN INVOLVED IN PSYCHOEDUCATIONAL ACTIVITIES – A PILOT STUDY

Paquier, P. F.

FUNCTIONAL OUTCOME AFTER LOW-GRADE ASTROCYTOMA TREATMENT IN CHILDHOOD

Parano, P.

PANDAS IN AUTISTIC PATIENTS
MALIGNANT HYPERTENSION IN TUBEROUS SCLEROSIS: AN ASSOCIATION WITH ADULTTYPE POLYCYSTIC KIDNEY DISEASE

Parascandalo, R.

SEPIAPTERIN REDUCTASE DEFICIENCY: A CONGENITAL DOPA-RESPONSIVE MOTOR AND COGNITIVE DISORDER

Parmiggiani, S.

OUTCOME AT 4 YEARS OF AGE IN CHILDREN WITH NEONATAL HYPOXIC-ISCHEMIC ENCEPHALOPATHY TREATED WITH HYPOTHERMIA

Paro-Panjan, D.

NEONATAL SLEEP MYOCLONUS – A BENIGN SHAKING DURING NEONATAL PERIOD

Parreira, S. L.

STEROID THERAPY IN BRAZILIAN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY
DUCHENNE MUSCULAR DYSTROPHY AND STEROID THERAPY: EVALUATION OF PATIENTS' MOTOR PERFORMANCE

Pascual, J.

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

Pascual-Castroviejo, I.

CUTANEOUS HEMANGIOMAS AND PERSISTENCE OF EMBRYONIC VASCULARIZATION
NEUROFIBROMATOSIS TYPE 1 (NF1) AND SPINAL NEUROFIBROMAS. PRESENTATION IN 26 PATIENTS
MIGRATION AND ORGANIZATION NEURONAL DISORDERS ASSOCIATED WITH FACIAL HEMANGIOMA AND VASCULAR MALFORMATION: PRESENTATION OF 5 PATIENTS
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

Pascual-Pascual, S. I.

CONGENITAL MYASTHENIC SYNDROMES
CUTANEOUS HEMANGIOMAS AND PERSISTENCE OF EMBRYONIC VASCULARIZATION
NEUROFIBROMATOSIS TYPE 1 (NF1) AND NEUROFIBROMAS OF THE EXTERNAL GENITALIA: PRESENTATION IN 3 PATIENTS
NEUROFIBROMATOSIS TYPE 1 (NF1) AND SPINAL NEUROFIBROMAS. PRESENTATION IN 26 PATIENTS
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

Pasini, A.

NEUROPSYCHOLOGICAL ENDOPHENOTYPES IN ADHD: NEUROCOGNITIVE DEFICITS IN ADHD PATIENTS AND THEIR PARENTS
NEUROCOGNITIVE ENDOPHENOTYPES OF ADHD

Passchier, J.

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

Passos-Bueno, M. R.

ELEVATED SERUM T3 IS A MARKER FOR X-LINKED MENTAL RETARDATION/”CEREBRAL PALSY” SYNDROME CAUSED BY MUTATION IN MONOCARBOXYLATE TRANSPORTER-8

Patel, K. M.

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

Patenaude, Y.

HEMIMEGACEREBELLUM: A REPORT OF ONE CASE

PeBenito, R.

CALVARIAL TUBERCULOSIS IN AN ADOLESCENT GIRL WITH NEUROFIBROMATOSIS TYPE 1

Pedemonte, M.

MUTATIONS IN POMT1 AND POMGNT1 IN ITALIAN CHILDREN WITH CMD
MYOPATHIC FORM OF VERY-LONG CHAIN ACYL-COA DEHYDROGENASE (VLCAD) DEFICIENCY DIAGNOSED BY BIOCHEMICAL AND GENETIC ANALYSIS FROM DRIED BLOOD SPOT. IDENTIFICATION OF TWO NOVEL MUTATIONS

Peduto, M. D. C.

STEROID THERAPY IN BRAZILIAN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY
DUCHENNE MUSCULAR DYSTROPHY AND STEROID THERAPY: EVALUATION OF PATIENTS' MOTOR PERFORMANCE

Pelham, W.

THE FIRST SUMMER TREATMENT PROGRAM FOR CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER IN KURUME CITY, JAPAN

Penney, S.

PROGNOSIS FOLLOWING CLINICAL NEONATAL SEIZURES: RESULTS FROM A POPULATION BASED COHORT 14 YEARS LATER

Percy, A.

RETT SYNDROME: CURRENT STATUS AND NEW DIRECTIONS

Perea de Posadas, M.

NEUROMUSCULAR DISEASES: CHILDREN, EPIDEMIOLOGIC, ARGENTINIEN

Pernikova, I.

TREATMENT RESULTS OF CHILDREN WITH HIGH RISK MEDULOBLASTOMA. A SINGLE CENTER EXPERIENCE

Perrier, J.

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

Pessoa, A.

SPASTIC PARAPLEGIA WITH THIN CORPUS CALLOSUM AND MENTAL RETARDATION (SPG11): CLINICAL AND GENETIC STUDY IN 10 PATIENTS

Peterson, E. B.

CREATING A NEURO-PATIENT RESOURCE CENTRE

Petroukhin, A.

POST-TRAUMATIC EPILEPSY IN CHILDREN AFTER CLOSED HEAD INJURY

Petruzzi, M. J.

LACK OF ASSOCIATION OF THROMBOPHILIC POLYMORPHISMS WITH PERINATAL STROKE: A CASE CONTROL STUDY

Phillips, A.

MRI FINDINGS INFORM NEURODEVELOPMENTAL OUTCOMES IN INDIVIDUALS WITH AGENESIS OF THE CORPUS CALLOSUM (ACC): ANALYSIS OF A PROSPECTIVE COHORT

Piemonte, F.

LATE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS AND ITS VARIANTS

Pierre, E.

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

Pietrani, M.

BRAIN MRI 3 D/CT FUSION FOR SUBDURAL AND DEPTH ELECTRODES PLACEMENT IN EPILEPSY SURGERY

Pihko, H.

POSTERIOR LISSENCEPHALY, PONTINE HYPOPLASIA, CEREBELLAR CORTICAL DYSGENESIS AND WHITE MATTER HYPERINTENSITY. TWO CASES WITH COBBLE STONE CORTEX AND ONE WITHOUT
CATASTROPHIC EPILEPSY IN PATIENTS WITH INFANTILE ONSET SPINOCEREBELLAR ATAXIA (IOSCA), A NUCLEAR MITOCHONDRIAL DISORDER

Pikova, J.

EARLY ONSET MS – A RETROSPECTIVE STUDY

Pilarska, E.

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

Pinci, M.

LEVETIRACETAM AS INITIAL MONOTHERAPHY FOR IDIOPATHIC GENERALIZED EPILEPSY

Ping, L.

THE GENOTYPE AND PHENOTYPE STUDIES OF 40 CHINESE PATIENTS WITH X-ALD

Pizzatti, T.

OUTCOME AT 4 YEARS OF AGE IN CHILDREN WITH NEONATAL HYPOXIC-ISCHEMIC ENCEPHALOPATHY TREATED WITH HYPOTHERMIA

Plesca, 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

Pogliani, L.

OUTCOME AT 4 YEARS OF AGE IN CHILDREN WITH NEONATAL HYPOXIC-ISCHEMIC ENCEPHALOPATHY TREATED WITH HYPOTHERMIA

Polcari, A.

ABNORMAL VISUAL CORTICAL DEVELOPMENT IN YOUNG WOMEN WITH A HISTORY OF REPEATED CHILDHOOD SEXUAL ABUSE: A VOXEL-BASED MORPHOMETRIC STUDY

Polsky, D.

ANALYSIS OF THE WORKFORCE CRISIS IN CHILD NEUROLOGY IN THE UNITED STATES

Pomeroy, S. P.

SUCCESSFUL TREATMENT OF SEVERE MYCOPLASMA BRAINSTEM ENCEPHALITIS WITH PLASMAPHARESIS

Pontigon, A. M.

DIAGNOSTIC DELAYS IN ACUTE PEDIATRIC ARTERIAL ISCHEMIC STROKE

Poon, W. K.

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

Poor Avanjy, S. H. H.

CORRELATION OF NEUROLOGICAL DEFICITS AND NEUROIMAGING FINDINGS IN CEREBRAL PALSY

Porfirio, C.

NEUROPSYCHOLOGICAL ENDOPHENOTYPES IN ADHD: NEUROCOGNITIVE DEFICITS IN ADHD PATIENTS AND THEIR PARENTS
NEUROCOGNITIVE ENDOPHENOTYPES OF ADHD

Poulin, C.

DETERMINANTS OF QUALITY OF LIFE IN SCHOOL AGE CHILDREN WITH CEREBRAL PALSY
SICKLE CELL CRISIS PRESENTING AS A NUMB CHIN SYNDROME IN A CHILD
SIMULTANEOUS GUILLAIN-BARRE SYNDROME AND ACUTE DEMYELINATING ENCEPHALOMYELITIS IN THE PEDIATRIC POPULATION

Powers, J.

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

Prachi, D.

BASELINE COGNITIVE PERFORMANCE IN ASYMPTOMATIC BOYS WITH X-ALD WHO LATER DEVELOP CEREBRAL DISEASE

Pranzatelli, M.

CHARACTERIZING NEUROCOGNITIVE AND BEHAVIORAL FUNCTIONING IN PEDIATRIC OPSOCLONUS-MYOCLONUS SYNDROME (OMS)

Prasad, A.

CELLULAR BIOENERGETICS AND CEREBRAL DYSMORPHOGENESIS: LESSONS FROM AMISH MICROCEPHALY
OUTCOME VARIABLES OF STATUS EPILEPTICUS IN A PEDIATRIC INTENSIVE CARE UNIT
RISK FACTORS FOR THE DEVELOPMENT OF HOLOPROSENCEPHALY: A MANITOBA-BASED CASE-CONTROL STUDY
PHENOTYPIC VARIABILITY IN CRANIOFACIAL AND ORGAN SYSTEM DEVELOPMENT IN HOLOPROSENCEPHALY
PRESCRIBING PRACTICES IN CHILDHOOD EPILEPSY: USE OF A POPULATION HEALTH CARE DRUG DATABASE

Prasad, C.

CELLULAR BIOENERGETICS AND CEREBRAL DYSMORPHOGENESIS: LESSONS FROM AMISH MICROCEPHALY
RISK FACTORS FOR THE DEVELOPMENT OF HOLOPROSENCEPHALY: A MANITOBA-BASED CASE-CONTROL STUDY
PHENOTYPIC VARIABILITY IN CRANIOFACIAL AND ORGAN SYSTEM DEVELOPMENT IN HOLOPROSENCEPHALY

Prayer, D.

LATERALIZING AND LOCALIZING VALUE OF DIFFERENT IMAGING MODALITIES IN CHILDREN WITH CORTICAL MALFORMATIONS

Price, A. E.

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

Price, V.

MANGANESE-INDUCED PARKINSONISM IN CHILDHOOD

Prieur, B.

MICTURITION-INDUCED REFLEX EPILEPSY: A PEDIATRIC CASE AND REVIEW OF THE LITERATURE

Primec, Z. R.

DURATION OF HYPSARRHYTHMIA OVER THREE WEEKS CORRELATES WITH LOWER MENTAL OUTCOME

Procak Psaros, C.

EXECUTIVE FUNCTIONS IN CHILDREN WITH NEUROFIBROMATOSIS 1 (NF1)

Prohorova, A.

APPLICATION OF CEREBROLYSIN IN REMOTE PERIOD OF AN EASY CEREBRO-CRANIAL TRAUMA IN CHILDREN
PECULIARITIES OF CEREBRAL HEMODYNAMIC IN CHILDREN WITH POSTTRAUMATIC EPILEPSY

Prokisch, H.

USEFULNESS OF BRAIN MRI IN DIAGNOSIS OF NBIA IN PKAN AND NON-PKAN PATIENTS

Pronk, J. C.

PATHOGENESIS AND MOLECULAR BIOLOGY OF LEUKODYSTROPHIES

Ptacek, L. J.

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

Puric, D.

INITIAL CLINICAL AND MRI FINDINGS IN SUBACUTE SCLEROSING PANENCEPHALITIS (SSPE)

Pyykkonen, B. A.

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