Professor of Neurology, University Tex Houston
Neurology
Dr. Ian J. Butler, MD
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Dr. Ian J. Butler is an expert in the field of Neurology. He over the years received 2 awards: "Top Doctors:SE Texas" and "Super Doctor". Ian J. Butler is a published MD. He published 101 publications, including: 'Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic flu...'
Publications
- Cardiac asystole during head up tilt (HUTT) in children and adolescents: is this benign physiology?
- Oculomotor executive function abnormalities with increased tic severity in Tourette Syndrome.
- Biogenic amine metabolism in juvenile neurocardiogenic Syncope with dysautonomia.
- Transient tonic upgaze deviation: a neuro-ophthalmological complication of acute cerebellitis.
- Severe narrowing of left cavernous carotid artery associated with Fusobacterium necrophorum infection.
- Secondary Erythromelalgia Successfully Treated With Intravenous Immunoglobulin.
- Glucose Transporter Type I Deficiency Causing Mitochondrial Dysfunction.
- Incidence of papilledema and obesity in children diagnosed with idiopathic ''benign'' intraCranial hypertension: case series and review.
- Diffusion tensor tractography of the human Brain cortico-ponto-cerebellar pathways: a quantitative preliminary study.
- Rapamycin reduces seizure frequency in Tuberous sclerosis complex.
- FIRST: a practical approach to the causes and management of febrile seizures.
- Regression of subependymal giant cell astrocytoma with rapamycin in Tuberous sclerosis complex.
- Neurologic complications associated with respiratory syncytial virus.
- Poliomyelitis-like Syndrome in a child with West Nile virus infection.
- Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations.
- Trigeminal myokymia in a young girl.
- Language dysfunction in epileptic conditions.
- Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation.
- Lumbar Spinal stenosis causing congenital clubfoot.
- Neurologic manifestations of achondroplasia.
- Are abused babies protected from further abuse?
- Transplantation of adrenal medullary tissue to caudate nucleus using stereotactic techniques.
- Data-directed scan sequence for the general assignment of C-glycosylflavone O-glycosides in plant extracts by liquid chromatography-ion trap mass spectrometry.
- Electron microscopy in the diagnosis of lysosomal storage diseases.
- Patterns of electromagnetic activity recorded from neoplastic tissue.
- The incidence of severe physical child abuse in Wales.
- Neonatal myasthenia gravis in the infant of a myasthenic mother in remission.
- The role of acetylcholine receptor antibodies in the pathogenesis of myasthenia gravis.
- Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.
- SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
- CMT4A: identification of a Hispanic GDAP1 founder mutation.
- Electroencephalogram discharges in atypical cognitive development.
- Sphenoid sinusitis masquerading as migraine Headaches in children.
- Respiratory syncytial virus.
- Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase gene.
- Encephalopathy associated with respiratory syncytial virus bronchiolitis.
- Recurrent isolated ptosis in presumed ophthalmoplegic Migraine of childhood.
- Pulmonary hypoplasia in the myogenin null mouse embryo.
- Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathies.
- Rapid-onset Dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two families.
- Rolandic type cerebral Palsy in children as a pattern of hypoxic-ischemic injury in the full-term neonate.
- Cerebrospinal fluid homovanillic acid levels in rapid-onset Dystonia-parkinsonism.
- Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies.
- X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP).
- Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family.
- Autosomal dominant torsion Dystonia with onset in infancy.
- In vivo microdialysis and gas chromatography/mass spectrometry for studies on release of N-acetylaspartlyglutamate and N-acetylaspartate in rat Brain hypothalamus.
- Severity of medical and neurologic complications as a determinant of neurodevelopmental outcome at 6 and 12 months in very low birth weight infants.
- Variable phenotype of rapid-onset Dystonia-parkinsonism.
- Proton magnetic resonance imaging and spectroscopic studies of the pathogenesis and treatment of juvenile dermatomyositis.
- Cerebrovascular Disorders of childhood.
- Rapid-onset Dystonia-parkinsonism.
- Proton magnetic resonance spectroscopic studies of hypertrophied muscle. Effect of botulinum toxin treatment.
- Cerebrospinal fluid studies in the Rett Syndrome: biogenic amines and beta-endorphins.
- Movement Disorders of children.
- The behavioral sciences and issues in child neurology and developmental pediatrics.
- Persistent unilateral tibialis anterior muscle hypertrophy with complex repetitive discharges and myalgia: report of two unique cases and response to botulinum toxin.
- Xeroderma pigmentosum and Cockayne Syndrome: overlapping clinical and biochemical phenotypes.
- Malignant hyperthermia: skeletal muscle defect(s) predisposing to labile Ca2+ regulation?
- A congenital myasthenic Syndrome refractory to acetylcholinesterase inhibitors.
- Diencephalic Syndrome revisited.
- Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic flu...
- Kearns-Sayre Syndrome. A review of a multisystem disorder of children and young adults.
- Effect of drugs on rat Brain, cerebrospinal fluid and blood GABA content.
- Biogenic amine metabolism in Tourette Syndrome.
- Gilles de la Tourette Syndrome: further studies and thoughts.
- Chronic progressive poliomyelitis secondary to vaccination of an immunodeficient child.
- Combined immunodeficiency and vaccine-related poliomyelitis in a child with cartilage-hair hypoplasia.
- Long-term treatment of juvenile Huntington''s chorea with dipropylacetic acid.
- Bone marrow in the Batten-Vogt Syndrome.
- A disorder of biogenic amines in dihydropteridine reductase deficiency.
- Biogenic amine synthesis defect in dihydropteridine reductase deficiency.
- Dihydropteridine reductase deficiency variant of phenylketonuria: a disorder of neurotransmitters.
- Neuropsychological characteristics of children with Tourette Syndrome: evidence for a nonverbal learning disability?
- Treatment-resistant eosinophilic polymyositis in a child.
- D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction.
- Amoxapine overdose in a young man: a transient mitochondrial Abnormality?
- Chronology of neurochemical alterations induced by GABA agonist administration.
- Central core disease and malignant hyperthermia Syndrome.
- Catecholamines in rat Brain following postnatal undernutrition and nutritional rehabilitation.
- Clinical symptomatology, CSF neurotransmitter metabolites, and serum haloperidol levels in Tourette Syndrome.
- A dominantly inherited Syndrome with continuous motor neuron discharges.
- Cervical myelopathy due to dural compression in mucopolysaccharidosis.
- Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphate.
- Neurologic manifestations of Ehlers-Danlos Syndrome.
- Short-latency somatosensory evoked potentials in the management of patients with achondroplasia.
- Long-term neurological sequelae in achondroplasia.
- Germ-cell Tumors of the diencephalon.
- Dopaminergic dsyfunction in Tourette Syndrome.
- Age effect on dopamine and serotonin metabolite levels in cerebroSpinal fluid.
- CSF neurotransmitter studies. An infant with ascorbic acid-responsive tyrosinemia.
- X-linked mental retardation with fragile site at band Xq2800.
- Neurotransmitter defects and treatment of Disorders of hyperphenylalaninemia.
- Tourette's Syndrome. Some new concepts.
- Neurologic handicaps after low oestriol excretions in pregnancy.
- Central nervous system infections.
- Congenital hypomyelinating Neuropathy.
- Prenatal and postnatal hypothyroidism abolishes lesion-induced noradrenergic sprouting in the adult rat.
- Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards.
- Foramen magnum stenosis in homozygous achondroplasia.
Schools
University Of Adelaide School Of Medicine Faculty Of Health Sciences
Adelaide Chldns Hospital
Grt Ormond St Hospital
Royal Chldns Hospital
University Wales
Johns Hopkins Hospital
Conditions Treated
- Ataxia
- Brachial Plexus Palsy
- Brain Injury
- Cerebral Palsy
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Doctors Specialties
- Pediatric Neurology
- Neurology
Accepted Insurances
Awards
- Top Doctors:SE Texas
- Super Doctor
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