Herman and Faye Sarkowsky Endowed Chair, Head, Division of Pediatric Neurology, University of Washington
Neurology
Dr. Sidney M. Gospe Jr., MD
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Sidney M. Gospe Jr. practices Neurology. He attended Duke University School of Medicine. Duke University School of Medicine is a one of the best medicals schools. Duke University School of Medicine has a rank of 8 in research and a 29 in primary care He has 2 awards "Top MD" and "Super Doctor". Sidney Gospe is a published doctor as well. He has 74 publications published. The latest was: Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.
Publications
- Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine.
- Corpus Callosum Diffusion and Connectivity Features in High Functioning Subjects With Pyridoxine-Dependent Epilepsy.
- Callosal alterations in pyridoxine-dependent Epilepsy.
- Pyridoxine or pyridoxal-5'-phosphate for neonatal Epilepsy: The distinction just got murkier.
- Pathology of Inherited Manganese Transporter Deficiency.
- A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.
- Glial localization of antiquitin: Implications for pyridoxine-dependent Epilepsy.
- Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis.
- Truncating CLCN1 mutations in myotonia congenita: Variable patterns of inheritance.
- Preliminary investigation of the use of newborn dried blood spots for screening pyridoxine-dependent Epilepsy by LC-MS/MS.
- Evidence-Based Decision Support for Neurological Diagnosis Reduces Errors and Unnecessary Workup.
- Epilepsy due to 20q13.33 subtelomere deletion masquerading as pyridoxine-dependent Epilepsy.
- Natural history of pyridoxine-dependent Epilepsy: tools for prognostication.
- Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man.
- Pyridoxine dependent Epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up.
- Biomarkers aiding diagnosis of atypical presentation of pyridoxine-dependent Epilepsy.
- Redefining outcome of first seizures by acute illness.
- Clinical and genetic characterization of manifesting carriers of DMD mutations.
- Pyridoxine-dependent Epilepsy and pyridoxine phosphate oxidase deficiency: unique clinical symptoms and non-specific EEG characteristics.
- Neonatal vitamin-responsive epileptic encephalopathies.
- Simultaneous determination of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate and pipecolic acid by LC-MS/MS for pyridoxine-dependent seizures and folinic ac...
- Clinical features and the management of pyridoxine-dependent and pyridoxine-responsive seizures: review of 63 North American cases submitted to a patient registry.
- Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients.
- Neuromuscular hip dysplasia in Charcot-Marie-Tooth disease type 1A.
- Exposure to environmental tobacco smoke during pregnancy in rats yields less effect on indices of brain cell number and size than does postnatal exposure.
- Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.
- Variable presentation of nemaline myopathy: novel mutation of alpha actin gene.
- Pyridoxine-dependent seizures: new genetic and biochemical clues to help with diagnosis and treatment.
- Nonhuman primate models of intrauterine cytomegalovirus infection.
- Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures.
- Hospital pharmacy and emergency department availability of parenteral pyridoxine.
- Nonfebrile illness seizures: a unique seizure category?
- Seizures, syncope, or breath-holding presenting to the pediatric neurologist--when is the etiology a life-threatening arrhythmia?
- Pyridoxine-dependent seizures and cognition in adulthood.
- Pyridoxine-dependent seizures: findings from recent studies pose new questions.
- Paraparesis, hypermanganesaemia, and polycythaemia: a novel presentation of cirrhosis.
- Glutamate decarboxylase is not genetically linked to pyridoxine-dependent seizures.
- Prenatal exposure to toluene results in abnormal neurogenesis and migration in rat somatosensory cortex.
- Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.
- Longitudinal MRI findings in pyridoxine-dependent seizures.
- Current perspectives on pyridoxine-dependent seizures.
- Toluene abuse embryopathy: longitudinal neurodevelopmental effects of prenatal exposure to toluene in rats.
- Fulminant demyelinating neuropathy mimicking cerebral death.
- Effects of environmental tobacco smoke exposure in utero and/or postnatally on brain development.
- Multiple organ failure after ingestion of pennyroyal oil from herbal tea in two infants.
- Development of a rat model of toluene-abuse embryopathy.
- Spinal arteriovenous malformation presenting as meningitis.
- Behavioral and neurochemical changes in folate-deficient mice.
- Transient cortical blindness in an infant exposed to methamphetamine.
- Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination.
- Fatal infantile polyarteritis nodosa with predominant central nervous system involvement.
- The effects of high-dose toluene on embryonic development in the rat.
- Cerebrospinal fluid 5-hydroxyindoleacetic acid and homovanillic acid in the pediatric opsoclonus-Myoclonus syndrome.
- Stable-isotope dilution GC-MS for determination of toluene in submilliliter volumes of whole blood.
- Reduced GABA synthesis in pyridoxine-dependent seizures.
- Nutritional factors and anticonvulsant therapies: effect on growth in children with Epilepsy.
- Brain injury and protective effects of hypothermia using triphenyltetrazolium chloride in neonatal rat.
- Visual evoked potentials and visual processing in stimulant drug-exposed infants.
- Brainstem bilirubin toxicity in the newborn primate may be promoted and reversed by modulating PCO2.
- Electroencephalography laboratory diagnosis of prolonged QT interval.
- Measurement of spontaneous rotational movement (circling) in normal children.
- Acute vincristine neurotoxicity in the presence of hereditary motor and sensory neuropathy type I.
- Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene.
- Hereditary long Q-T syndrome presenting as Epilepsy: electroencephalography laboratory diagnosis.
- Drug-induced dystonia in neuronal ceroid-lipofuscinosis.
- Myeloradiculopathy associated with wasp sting.
- Nemaline myopathy associated with hypertrophic cardiomyopathy.
- Life-threatening congestive heart failure as the presentation of centronuclear myopathy.
- Central nervous system distribution of inhaled toluene.
- Infantile spasms following near-drowning: a report of two cases.
- Studies of dopamine pharmacology in molluscs.
- Pharmacological studies of a novel dopamine-sensitive receptor mediating burst-firing inhibition of neurosecretory cell R 15 in Aplysia californica.
- Dopamine inhibits burst-firing of neurosecretory cell R 15 in Aplysia californica: establishment of a dose-response relationship.
Schools
Duke University School Of Medicine
Baylor College Of Med
Procedures Preformed
- EEG (Electroencephalogram)
Conditions Treated
- Chorea (Excluding Huntington's Chorea)
- Convulsions
- Epilepsy
- Headache
- View All
Doctors Specialties
- Pediatric Neurology
- Pediatrics
- Neurology
Accepted Insurances
Awards
- Top MD
- Super Doctor
Education
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Baylor College of Medicine -
Duke University School of Medicine
Hospital
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Seattle Children's Hospital -
University of Washington Medical Center -
UW Medicine/Harborview Medical Center
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