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Alternating Hemiplegia of Childhood
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Fucosidosis Revisited:A Review of 77 Patients
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A Follow-up Study of Intractable Seizures in Childhood
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Rett Syndrome:Natural History and Management
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Overview of Phenylketonuria
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The Tuberous Sclerosis Complex
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Prader-Willi and Angelman Syndromes
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Fetal Alcohol Syndrome and Fetal Alcohol Effects
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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A Clinical Study of Noonan Syndrome
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
Alternating Hemiplegia of Childhood
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Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
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Hazards of Oral Anticoagulants During Pregnancy
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
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Transition to Adult Care for Children with Chronic Neurological Disorders
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009
Extension of the Clinical Spectrum of Danon Disease
Neurol 70:1358-1359, van der Kooi,A.J.,et al, 2008
Mirror Writing: Neurological Reflections on an Unusual Phenomenon
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Angelman Syndrome Revisited
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Phenylketonuria
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Developmental Neurotoxivity of Industrial Chemicals
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Gray Matter Heterotopia
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Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999
New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999
Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998
Bilirubin Metabolism and Kernicterus
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Startle Provoked Epileptic Seizures:Features in 19 Patients
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
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Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Neurologic Abnormalities in Murderers
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993
Neuroleptics, Learning Disability, and the Community:Some History and Mystery
BMJ 307:184-187, Manchester,D., 1993
Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
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Hypomelanosis of Ito
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992
Twinning and Neurologic Morbisity
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Angelman Syndrome: Clinical Profile
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