• A Case of Infantile Spastic Diplegia, with Tremors of the "Disseminated Sclerosis" Type
• A novel pathogenic variant in the 3' end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype?
• A prospective study of epilepsy following neonatal convulsions
• Accentuations of character in adolescents with infantile cerebral palsy
• An analysis of the gait in patients with different type of infantile cerebral paralysis
• Assessment of hearing in children with infantile cerebral palsy. Comparison of psychophysical and electrophysical examination
• Botulin toxin as treatment for spasticity and dystonia in infantile cerebral paralysis
• Botulinum toxin A in children with infantile cerebral palsy: indications and treatment concepts
• Botulinum toxin A in the treatment of infantile cerebral palsy. Taking into account multilevel, integrated treatment
• Botulinum toxin as a treatment for infantile cerebral palsy
• Botulinum toxin in infantile cerebral palsy
• Botulinum toxin in spastic infantile cerebral palsy: results in 27 cases during one year
• Carbon Modular Orthosis (Ca.M.O.): An innovative hybrid modular ankle-foot orthosis to tune the variable rehabilitation needs in hemiplegic cerebral palsy
• Central hemodynamic reactions to exercise in patients with infantile cerebral paralysis as a possibility of choosing a procedure for anesthesia and predicting its course
• Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity
• Cerebral Palsy for the Pediatric Eye Care Team Part II: Diagnosis and Treatment of Ocular Motor Deficits
• Changes in the indices of standing and walking in patients with infantile cerebral palsy under the influence of low doses of Nakom
• Characteristics and Challenges of Epilepsy in Children with Cerebral Palsy-A Population-Based Study
• Characteristics of seizures in a population-based series of mentally retarded children with active epilepsy
• Childhood neurodevelopmental disorders and maternal diabetes: A population-based cohort study
• Childhood Outcomes Following Parechovirus Infections in a US Young Infant Cohort
• Children who develop epilepsy in the first year of life: a prospective study
• Children with self-injurious behavior
• Clinical aspects of epilepsy in children with periventricular leukomalacia
• Clinical features and gene mutation analysis of patients with Niemann-Pick disease type C
• Clinical practice guidelines for the treatment of spasticity with botulinum toxin
• Clinical profile and treatment of infantile spasms using vigabatrin and ACTH--a developing country perspective
• Clinical Profile of Early Childhood Epilepsy: A Cross Sectional Study in a Tertiary Care Hospital
• Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings
• Course and treatment of progressive subacute encephalopathy caused by human immunodeficiency virus in children. The value of Botulinum toxin
• Disorders of pyruvate metabolism
• Dynamics of psychogenic depressive disorders occasioned by the birth of a sick child into a family
• Dysphagia in children with infantile cerebral palsy
• Early care and botulinum toxin. Our experience in the 21st century
• Effect of baclofen on emesis and 24-hour esophageal pH in neurologically impaired children with gastroesophageal reflux disease
• Epilepsy and related challenges in children with COL4A1 and COL4A2 mutations: A Gould syndrome patient registry
• Epilepsy in patients with spastic cerebral palsy: correlation with MRI findings at 5 years of age
• Epilepsy in rural Ugandan children: seizure pattern, age of onset and associated findings
• Evaluation of adductor myotomy versus adductor transfer to ischiadic tuber in the treatment of spastic hip in cerebral palsy
• Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus
• General movement assessment as a tool for determining the prognosis in infantile cerebral palsy in preterm infants: a systematic review
• Genetic syndrome, most likely vascular type of Ehlers-Danlos syndrome, in a 14-years old boy with extrapyramindal symptoms dominating the early childhood and growth failure
• Giant intracranial congenital hemangiopericytoma/solitary fibrous tumor: A case report and literature review
• Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania
• Guidelines for the treatment of child spasticity using botulinum toxin
• Histological differences between rootlets sectioned during selective posterior rhizotomy by two surgical techniques
• Home enteral nutrition in children--2010 nationwide survey of the Polish Society for Clinical Nutrition of Children
• Infantile cerebral palsy and neuromotor development in very low birth weight infants
• Infantile cerebral palsy of hemiplegic type; a case with pyramidal and somaesthetic deficit
• Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy
• Infantile outcome at 3 years of age among monochorionic twins with Type-II or -III selective fetal growth restriction with isolated oligohydramnios who underwent fetoscopic laser photocoagulation
• Infantile spasms: neurological and developmental follow-up--a comparison between two ethnic groups: Israeli Jews and Bedouin in the South of Israel
• Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral Neuropathy
• Juvenile Dermatomyositis and Infantile Cerebral Palsy: Aicardi-Gouteres Syndrome, Type 5, with a Novel Mutation in SAMHD1-A Case Report
• Kinesthetic characteristics of vertical stability in patients with infantile cerebral palsy
• Latent coeliac disease. Personal experience
• Long term results of stereotaxic surgery for infantile dystonia and dyskinesia
• Manual therapy for the pediatric population: a systematic review
• Mental, Neurological, and Somatic Comorbidities and Their Treatment in Persons With Intellectual Disability
• Missense mutation in the ITPR1 gene presenting with ataxic cerebral palsy: Description of an affected family and literature review
• Morphological brain damage, functional disorders and the possibilities of their treatment in children with infantile cerebral palsy
• Mortality and clinical features in cases of death among epileptic children
• Movement Analysis in Orthopedics and Trauma Surgery - Measurement Systems and Clinical Applications
• Neurologic risks caused by perinatal and neonatal problems in a provincial hospital
• Neuromuscular dysfunction of the lower urinary tract dysfunction beyond spinal cord injury and multiple sclerosis. A challenge for urologists
• New approaches in the treatment of speech disorders in children with an organic brain lesion
• New developments in spastic unilateral cerebral palsy
• Optimized therapy of spastic syndrome by combination intrathecal baclofen with botulinum toxin
• Osteopathic manipulative treatment for pediatric conditions: a systematic review
• Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients
• Perisylvian polymicrogyria, infantile spasms and arthrogryposis: the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria
• Phenotypic characterisation of 35 Colombian children with an imaging diagnosis of schizencephaly
• Phenotypic insights into ADCY5-associated disease
• Polymicrogyria: epidemiology, neurological and anatomical factors and clinical outcome in a series of 34 cases
• Prevalence and descriptive epidemiology of Lennox-Gastaut syndrome among Atlanta children
• Prevalence of neutralising antibodies in patients treated with botulinum toxin type A for spasticity
• Prompt pressure applied to peculiar points in the treatment of spasmodic infantile cerebral palsy--a report of 318 cases
• Purified cannabidiol as add-on therapy in children with treatment-resistant infantile epileptic spasms syndrome
• RAB18 Deficiency
• Relationship between 3D lower limb bone morphology and 3D gait variables in children with uni and bilateral Cerebral Palsy
• Rhythmic cortical myoclonus in Niemann-Pick disease type C
• Risk factors related to infantile spastic cerebral palsy among 145 cases
• Role of biological and social factors in mechanisms of pathologic personality formation in infantile cerebral palsy
• Role of personality reactions in the pathology of character formation in infantile cerebral palsy (clinico-psychological study)
• Studies on pediatric patients with absent auditory brainstem response (ABR) later components
• Subtalar arthrodesis-surgical management of the planovalgosity of the foot in infantile cerebral palsy.
• Surgical management of the hand in infantile spastic hemiplegia
• Surgical treatment of patients with juvenile cerebral palsy at the orthopedic clinic of the Charles University Medical School in Prague-Motol
• Surgical treatment of spinal deformity due to cerebral motor disorders using a Luque type appliance
• Symptomatic West's syndrome: specific etiological link to unexpected response to treatment
• The changing panorama of cerebral palsy in Sweden. VII. Prevalence and origin in the birth year period 1987-90
• The comprehensive pathogenetic approach to the neuro-orthopedic rehabilitation of the children of different age presenting with cerebral palsy
• The use of chronic epidural electrostimulation of the spinal cord in children with spastic diplegia--a type of infantile cerebral palsy
• The usefulness of tizanidine. A one-year follow-up of the treatment of spasticity in infantile cerebral palsy
• Therapeutic effect of the new multilevel brace orthosis on cerebral palsy gait: a case report
• Tumours in newborns and infants up to three months of life. One institution experience
• Types of diagnosis in the outpatient practice during the years 2006-2007
• Use of botulinum toxin in the preventive and palliative treatment of the hips in children with infantile cerebral palsy
• Virtual Reality-Based Intervention for Enhancing Upper Extremity Function in Children With Hemiplegic Cerebral Palsy: A Literature Review
• Visual function in children with hemiplegia in the first years of life