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Infant Botulism: Review and Clinical Update

Pediatric neurology, 2015-05, Vol.52 (5), p.487-492

2015

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Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015

JAMA : the journal of the American Medical Association, 2015-12, Vol.314 (24), p.2663

2015

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Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7579

2022

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Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis

Annals of neurology, 2010-05, Vol.67 (5), p.618-624

2010

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Health-Related Quality of Life is Reduced in Pediatric Multiple Sclerosis

Pediatric neurology, 2010-08, Vol.43 (2), p.97-102

2010

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Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force

Annals of neurology, 2021-10, Vol.90 (4), p.537-538

2021

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Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions

Brain pathology (Zurich, Switzerland), 2010-11, Vol.20 (6), p.1069-1076

2010

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Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation

Pediatric radiology, 2017-06, Vol.47 (7), p.884-888

2017

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Therapeutics in Duchenne Muscular Dystrophy

NeuroRx, 2006-04, Vol.3 (2), p.225-234

Strober, Jonathan B.

2006

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Neurological symptoms in individuals with fibrodysplasia ossificans progressiva

Journal of neurology, 2012-12, Vol.259 (12), p.2636-2643

2012

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Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome

American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2767-2776

2015

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Treatment of hypokalemic periodic paralysis with topiramate

Muscle & nerve, 2011-01, Vol.43 (1), p.127-129

2011

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Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A

Molecular genetics & genomic medicine, 2018-05, Vol.6 (3), p.434-440

2018

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Recent advances in infant botulism

Pediatric neurology, 2005-03, Vol.32 (3), p.149-154

2005

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Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH 3A

Molecular genetics & genomic medicine, 2018-05, Vol.6 (3), p.434-440

2018

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Difference in disease burden and activity in pediatric patients on brain magnetic resonance imaging at time of multiple sclerosis onset vs adults

Archives of neurology (Chicago), 2009-08, Vol.66 (8), p.967

2009

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Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study

BMC neurology, 2013-11, Vol.13 (1), p.173-173, Article 173

2013

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Infant botulism, type F, presenting at 54 hours of life

Pediatric neurology, 2005-03, Vol.32 (3), p.193-196

2005

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A 41-Year-Old Man With New Headache and Altered Mental Status

Neurohospitalist, 2011-01, Vol.1 (1), p.48-54

2011

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Progressive spinal muscular atrophies

Journal of child neurology, 1999-11, Vol.14 (11), p.691-695

1999

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Topical Review: Progressive Spinal Muscular Atrophies

Journal of Child Neurology, 1999-11, Vol.14 (11), p.691-695

1999

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Parainfectious and Postinfectious Neurologic Syndromes

Principles and Practice of Pediatric Infectious Diseases, 2018, p.323-328.e1

Fifth Edition, 2018

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Congenital Myopathies

Swaiman's Pediatric Neurology, 2017, p.1123-1130

Sixth Edition, 2017

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Para- and Postinfectious Neurologic Syndromes

Principles and Practice of Pediatric Infectious Diseases, 2012, p.314-319.e1

Fourth Edition, 2012

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Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis?

Nature clinical practice. Neurology, 2007-01, Vol.3 (1), p.18-19

Strober, Jonathan B

2007

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Infant Botulism: Review and Clinical Update

Acute Flaccid Myelitis of Unknown Etiology in California, 2012-2015

Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice

Vitamin D status is associated with relapse rate in pediatric-onset multiple sclerosis

Health-Related Quality of Life is Reduced in Pediatric Multiple Sclerosis

Introducing the Child Neurology Society Leadership, Diversity, Equity, and Inclusion Task Force

Extensive FUS-Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions

Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation

Therapeutics in Duchenne Muscular Dystrophy

Neurological symptoms in individuals with fibrodysplasia ossificans progressiva

Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome

Treatment of hypokalemic periodic paralysis with topiramate

Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A

Recent advances in infant botulism

Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH 3A

Difference in disease burden and activity in pediatric patients on brain magnetic resonance imaging at time of multiple sclerosis onset vs adults

Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study

Infant botulism, type F, presenting at 54 hours of life

A 41-Year-Old Man With New Headache and Altered Mental Status

Progressive spinal muscular atrophies

Topical Review: Progressive Spinal Muscular Atrophies

Parainfectious and Postinfectious Neurologic Syndromes

Congenital Myopathies

Para- and Postinfectious Neurologic Syndromes

Do all patients with Duchenne muscular dystrophy require surgery for the correction of scoliosis?

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