Home

tengeri Lil Szeminárium nikkel mri Szánalmas Kimerülés úszó

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

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

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?

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

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?

Frontiers | Reductions in Corpus Callosum Volume Partially Mediate Effects  of Prenatal Alcohol Exposure on IQ
Frontiers | Reductions in Corpus Callosum Volume Partially Mediate Effects of Prenatal Alcohol Exposure on IQ

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

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

Megalencephaly-capillary malformation syndrome and associated  hydrocephalus: treatment options and revision of the literature |  SpringerLink
Megalencephaly-capillary malformation syndrome and associated hydrocephalus: treatment options and revision of the literature | SpringerLink

Brain magnetic resonance imaging findings in Smith-Lemli-Opitz syndrome. -  Abstract - Europe PMC
Brain magnetic resonance imaging findings in Smith-Lemli-Opitz syndrome. - Abstract - Europe PMC

ISMRM19 Posters - Neuro
ISMRM19 Posters - Neuro

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 -

Megalencephaly-capillary malformation syndrome and associated  hydrocephalus: treatment options and revision of the literature |  SpringerLink
Megalencephaly-capillary malformation syndrome and associated hydrocephalus: treatment options and revision of the literature | SpringerLink

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

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

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

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

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

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

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

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

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

Frontiers | Case report: PLPHP deficiency, a rare but important cause of  B6-responsive disorders: A report of three novel individuals and review of  51 cases
Frontiers | Case report: PLPHP deficiency, a rare but important cause of B6-responsive disorders: A report of three novel individuals and review of 51 cases

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

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

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?

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