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Anomalous development of brain structure and function in spina bifida myelomeningocele

Developmental disabilities research reviews, 2010, Vol.16 (1), p.23-30

2010

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Intermittent Horner Syndrome: An Uncommon Occurrence

Journal of neuro-ophthalmology, 2024-03, Vol.44 (1), p.e136-e137

Salman, Michael S

2024

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Epidemiology of Cerebellar Diseases and Therapeutic Approaches

Cerebellum (London, England), 2018-02, Vol.17 (1), p.4-11

Salman, Michael S.

2018

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Neuroimaging Features in Children with Optic Nerve Hypoplasia and Septo-Optic-Pituitary Dysplasia

Canadian journal of neurological sciences, 2024-05, Vol.51 (3), p.416-424

2024

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Acute Neurological Complications in Pediatric Diabetic Ketoacidosis

Canadian journal of neurological sciences, 2024-09, p.1-3

2024

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Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis

Frontiers in neurology, 2017-05, Vol.8, p.190

2017

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Persistence of Infantile-Onset Saccade Initiation Delay (Congenital Ocular Motor Apraxia): An Update on a Young Adult

Canadian journal of neurological sciences, 2024-03, Vol.51 (2), p.310-311

2024

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The Role of the Pediatric Cerebellum in Motor Functions, Cognition, and Behavior: A Clinical Perspective

Neuroimaging clinics of North America, 2016-08, Vol.26 (3), p.317-329

2016

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Head Thrusts in Two Children With Unusual Neuroimaging Findings

Journal of neuro-ophthalmology, 2022-03, Vol.42 (1), p.e427-e429

2022

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Risk factors in children with optic nerve hypoplasia and septo‐optic dysplasia

Developmental medicine and child neurology, 2024-01, Vol.66 (1), p.106-116

2024

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Cerebellar malformations in children: determining long‐term neurological outcomes

Developmental medicine and child neurology, 2019-03, Vol.61 (3), p.289-290

2019

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Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression

Annals of neurology, 2017-03, Vol.81 (3), p.419-429

2017

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Ophthalmic and Neuroimaging Associations In Optic Nerve Hypoplasia/Septo-Optic-Pituitary Dysplasia

Canadian journal of neurological sciences, 2024-01, p.1-7

2024

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Ketogenic Diet in Alpers-Huttenlocher Syndrome

Pediatric neurology, 2009-04, Vol.40 (4), p.314-316

2009

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Visual acuity outcomes in children with optic nerve hypoplasia and septo-optic-pituitary dysplasia

Pediatric neurology, 2023-12, Vol.149, p.167-175

2023

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Gastroschisis and septo‐optic‐pituitary dysplasia: Is there an association?

Journal of paediatrics and child health, 2024-07, Vol.60 (7), p.294-298

2024

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Prolonged Survival and Serial Magnetic Resonance Imaging/Magnetic Resonance Spectroscopy Changes in Infantile Krabbe Disease

Pediatric neurology, 2012-10, Vol.47 (4), p.299-302

2012

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Acquired Microcephaly in a Patient with HECW2 Mutation

Canadian journal of neurological sciences, 2021-05, Vol.48 (3), p.435-437

2021

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Infantile-Onset Saccade Initiation Delay (Congenital Ocular Motor Apraxia)

Current neurology and neuroscience reports, 2015-05, Vol.15 (5), p.24-24, Article 24

Salman, Michael S.

2015

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Segmental Myoclonus and Epilepsy in a Child with GAD 65 Antibodies

Canadian journal of neurological sciences, 2022-01, Vol.49 (1), p.136-139

2022

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Can Latent Class Analysis Be Used to Improve the Diagnostic Process in Pediatric Patients with Chronic Ataxia?

Cerebellum (London, England), 2017-04, Vol.16 (2), p.348-357

2017

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Assessing Children with Poor Coordination Can Be Tricky – A Review on Ataxia and Ataxia Mimickers and a Study of Three Children with Severe Epilepsy

Journal of multidisciplinary healthcare, 2021-11, Vol.14, p.3331-3341

2021

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Congenital Cranial Dysinnervation Disorder: An Unusual Phenotype With Multiple Cranial Neuropathies and Novel Neuroimaging Findings

Journal of neuro-ophthalmology, 2019-09, Vol.39 (3), p.348-351

2019

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Selected Ophthalmological Features in Children with Septo-Optic Dysplasia and Optic Nerve Hypoplasia

Neuro-ophthalmology (Amsterdam : Aeolus Press. 1980), 2022-11, Vol.46 (6), p.367-374

2022

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Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

Anomalous development of brain structure and function in spina bifida myelomeningocele

Intermittent Horner Syndrome: An Uncommon Occurrence

Epidemiology of Cerebellar Diseases and Therapeutic Approaches

Neuroimaging Features in Children with Optic Nerve Hypoplasia and Septo-Optic-Pituitary Dysplasia

Acute Neurological Complications in Pediatric Diabetic Ketoacidosis

Eyelid Retraction in Isolated Unilateral Congenital Blepharoptosis

Persistence of Infantile-Onset Saccade Initiation Delay (Congenital Ocular Motor Apraxia): An Update on a Young Adult

The Role of the Pediatric Cerebellum in Motor Functions, Cognition, and Behavior: A Clinical Perspective

Head Thrusts in Two Children With Unusual Neuroimaging Findings

Risk factors in children with optic nerve hypoplasia and septo‐optic dysplasia

Cerebellar malformations in children: determining long‐term neurological outcomes

Genetics and genotype–phenotype correlations in early onset epileptic encephalopathy with burst suppression

Ophthalmic and Neuroimaging Associations In Optic Nerve Hypoplasia/Septo-Optic-Pituitary Dysplasia

Ketogenic Diet in Alpers-Huttenlocher Syndrome

Visual acuity outcomes in children with optic nerve hypoplasia and septo-optic-pituitary dysplasia

Gastroschisis and septo‐optic‐pituitary dysplasia: Is there an association?

Prolonged Survival and Serial Magnetic Resonance Imaging/Magnetic Resonance Spectroscopy Changes in Infantile Krabbe Disease

Acquired Microcephaly in a Patient with HECW2 Mutation

Infantile-Onset Saccade Initiation Delay (Congenital Ocular Motor Apraxia)

Segmental Myoclonus and Epilepsy in a Child with GAD 65 Antibodies

Can Latent Class Analysis Be Used to Improve the Diagnostic Process in Pediatric Patients with Chronic Ataxia?

Assessing Children with Poor Coordination Can Be Tricky – A Review on Ataxia and Ataxia Mimickers and a Study of Three Children with Severe Epilepsy

Congenital Cranial Dysinnervation Disorder: An Unusual Phenotype With Multiple Cranial Neuropathies and Novel Neuroimaging Findings

Selected Ophthalmological Features in Children with Septo-Optic Dysplasia and Optic Nerve Hypoplasia

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