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Update on neuroimaging phenotypes of mid-hindbrain malformations |  SpringerLink
Update on neuroimaging phenotypes of mid-hindbrain malformations | SpringerLink

Study Finds New Gene Mutations that Lead to Enlarged Brain Size, Cancer,  Autism, Epilepsy - Neuroscience News
Study Finds New Gene Mutations that Lead to Enlarged Brain Size, Cancer, Autism, Epilepsy - Neuroscience News

Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children  with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish  an Earlier Diagnosis of PHTS in Children?
Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish an Earlier Diagnosis of PHTS in Children?

Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome -  Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online  Library
Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome - Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library

dStream Small Extremity 16ch coil | Philips
dStream Small Extremity 16ch coil | Philips

Decompressive Surgery for Craniovertebral Foramen Magnum Stenosis with  Medullary Compression in Paediatric Skeletal Dysplasia Sy
Decompressive Surgery for Craniovertebral Foramen Magnum Stenosis with Medullary Compression in Paediatric Skeletal Dysplasia Sy

Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome -  Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online  Library
Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome - Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library

Fig 1. | Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a  Series of 7 Patients | American Journal of Neuroradiology
Fig 1. | Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients | American Journal of Neuroradiology

A novel homozygous MMP2 mutation in a patient with Torg–Winchester syndrome  | Journal of Human Genetics
A novel homozygous MMP2 mutation in a patient with Torg–Winchester syndrome | Journal of Human Genetics

Frontiers | Multi-Modal Imaging to Assess the Interaction Between  Inflammation and Bone Damage Progression in Inflammatory Arthritis
Frontiers | Multi-Modal Imaging to Assess the Interaction Between Inflammation and Bone Damage Progression in Inflammatory Arthritis

Segmental Spinal Dysgenesis: Case Report and Literature Review
Segmental Spinal Dysgenesis: Case Report and Literature Review

Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome -  Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online  Library
Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome - Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library

Determinants of Indices of Cerebral Volume in Former Very Premature Infants  at Term Equivalent Age | PLOS ONE
Determinants of Indices of Cerebral Volume in Former Very Premature Infants at Term Equivalent Age | PLOS ONE

Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome -  Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online  Library
Brain magnetic resonance imaging findings in smith–lemli–opitz syndrome - Lee - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library

Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children  with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish  an Earlier Diagnosis of PHTS in Children?
Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish an Earlier Diagnosis of PHTS in Children?

Imaging of Skeletal Disorders Caused by Fibroblast Growth Factor Receptor  Gene Mutations | RadioGraphics
Imaging of Skeletal Disorders Caused by Fibroblast Growth Factor Receptor Gene Mutations | RadioGraphics

Novel mutations in the ALDH18A1 gene in complicated hereditary spastic  paraplegia with cerebellar ataxia and cognitive impairment | Journal of  Human Genetics
Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment | Journal of Human Genetics

Sarah M. Nikkel's research works | University of British Columbia -  Vancouver, Vancouver (UBC) and other places
Sarah M. Nikkel's research works | University of British Columbia - Vancouver, Vancouver (UBC) and other places

Segmental Spinal Dysgenesis
Segmental Spinal Dysgenesis

A novel FBXO28 frameshift mutation in a child with developmental delay,  dysmorphic features, and intractable epilepsy: A second gene that may  contribute to the 1q41‐q42 deletion phenotype - Balak - 2018 -
A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41‐q42 deletion phenotype - Balak - 2018 -

Segmental Spinal Dysgenesis | Ochsner Journal
Segmental Spinal Dysgenesis | Ochsner Journal

RSNA 2017: Spotlighting Some Memorable Moments
RSNA 2017: Spotlighting Some Memorable Moments

ISMRM19 Posters - Neuro
ISMRM19 Posters - Neuro

Carey-Fineman-Ziter Syndrome: A MYMK-Related Myopathy Mimicking Brainstem  Dysgenesis - IOS Press
Carey-Fineman-Ziter Syndrome: A MYMK-Related Myopathy Mimicking Brainstem Dysgenesis - IOS Press

Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children  with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish  an Earlier Diagnosis of PHTS in Children?
Cells | Free Full-Text | Cerebral MRI and Clinical Findings in Children with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish an Earlier Diagnosis of PHTS in Children?