Marc C. Patterson researcher
Patterson, Marc C.
VIAF ID: 311801552 (Personal)
Permalink: http://viaf.org/viaf/311801552
Preferred Forms
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Works
Title | Sources |
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A 19-month-old girl of South Indian parents presented to a general pediatric clinic for evaluation of global developmental regression | |
Angelman's syndrome: clinical and electroencephalographic findings. | |
Broad screening test for sphingolipid-storage diseases. | |
Cerebellar leukoencephalopathy: most likely histiocytosis-related | |
Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome | |
Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7. | |
Co-morbidity of Sanfilippo syndrome type C and D-2-hydroxyglutaric aciduria | |
Cognitive impairment occurs in children and adolescents with multiple sclerosis: results from a United States network | |
Consensus statement on preventive and symptomatic care of leukodystrophy patients | |
Correction: Disease and patient characteristics in NP-C patients: findings from an international disease registry | |
Correlations between in vitro dissolution, in vivo bioavailability and hypoglycaemic effect of oral glibenclamide | |
Disease specific therapies in leukodystrophies and leukoencephalopathies | |
Editorial comment: Ataxia, ophthalmoplegia, and impairment of consciousness in a 19 month-old American boy | |
Editorial comment: Cerebellar ataxia, vertical supranuclear gaze palsy, sensorineural deafness, epilepsy, dementia and hallucinations in an adolescent male | |
Epidural hematoma in a patient on pegylated-L-asparginase therapy | |
Epilepsy in children--when should we think neurometabolic disease? | |
The frequency of non-epileptic spells in children: results of video-EEG monitoring in a tertiary care center. | |
From stargazing chicks to seizing infants: thiamine deficiency redux | |
IGF system in children with congenital disorders of glycosylation. | |
In memoriam: Manuel Rodriguez Gomez, MD July 4, 1928 - January 21, 2006 | |
Inborn errors of metabolism for child neurology residents. | |
Jeavons Syndrome: Clinical Features and Response to Treatment | |
Limbic encephalitis associated with anti-GAD antibody and common variable immune deficiency | |
Long-term outcome of symptomatic infantile spasms established by video-electroencephalography (EEG) monitoring. | |
The long-term outcomes of presymptomatic infants transplanted for Krabbe disease: report of the workshop held on July 11 and 12, 2008, Holiday Valley, New York | |
Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms | |
Measuring to improve: a new rating scale for Batten disease | |
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene | |
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation | |
Movers and shakers: diagnosing neurotransmitter diseases with CSF | |
Neurology of inherited glycosylation disorders | |
Neurotransmitter abnormalities and response to supplementation in SPG11. | |
Newborn screening for Krabbe disease: the New York State model. | |
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis | |
Niemann-Pick type C Suspicion Index tool: analyses by age and association of manifestations. | |
The pathophysiology and mechanisms of NP-C disease. | |
Peer review fraud-it's not big and it's not clever | |
Pompe disease diagnosis and management guideline. | |
Posterior reversible encephalopathy syndrome and hemorrhage associated with tacrolimus in a pediatric heart transplantation recipient. | |
Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease. | |
Proton magnetic resonance spectroscopy as a probe into the pathophysiology of autism spectrum disorders (ASD): a review. | |
Quo vadis: the re-definition of "inborn metabolic diseases" | |
Response to immunotherapy in a 20-month-old boy with anti-NMDA receptor encephalitis | |
Scurvy and rickets masked by chronic neurologic illness: revisiting "psychologic malnutrition". | |
Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion | |
Subclinical seizures in children diagnosed with localization-related epilepsy: clinical and EEG characteristics. | |
Teaching neuroimages: call it as you see it: evolution of bilateral striatal necrosis. | |
Therapy of Niemann-Pick disease, type C. | |
Too Old for a Diaper! A Child With Diaper Changing-Induced Seizures. | |
An unusual presentation of copper metabolism disorder and a possible connection with Niemann-Pick type C. | |
Upośledzenie umysłowe : co kryje X? | |
The US Network of Pediatric Multiple Sclerosis Centers: Development, Progress, and Next Steps | |
Views of recently first-certified US child neurologists on their residency training. | |
Violent recurrent ballism associated with infections in two children with static encephalopathy | |
Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective. |