MILHORAT Thomas | Department of Neurosurgery, The Chiari Institute, Harvey Cushing Institutes of Neuroscience, North S
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概要
- 同名の論文著者
- Department of Neurosurgery, The Chiari Institute, Harvey Cushing Institutes of Neuroscience, North Sの論文著者
関連著者
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Nishikawa Misao
Department of Neurosurgery, Osaka city University Graduate School of Medicine
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Nishikawa Misao
Department Of Neurosurgery Osaka City University Graduate School Of Medicine
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Nishikawa Misao
Department Of Neurosurgery The Chiari Institute Harvey Cushing Institutes Of Neuroscience North Shor
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MILHORAT Thomas
Department of Neurosurgery, The Chiari Institute, Harvey Cushing Institutes of Neuroscience, North S
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BOLOGNESE Paolo
Department of Neurosurgery, The Chiari Institute, Harvey Cushing Institutes of Neuroscience, North S
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MCDONNELL Nazli
Medical Genetics, NIH National Institute on Aging
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FRANCOMANO Clair
Harvey Institute for Medical Genetics, Greater Baltimore Medical Center
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Francomano Clair
Harvey Institute For Medical Genetics Greater Baltimore Medical Center
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Mcdonnell Nazli
Medical Genetics Nih National Institute On Aging
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Bolognese Paolo
Department Of Neurosurgery The Chiari Institute Harvey Cushing Institutes Of Neuroscience North Shor
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Milhorat Thomas
Department Of Neurosurgery The Chiari Institute Harvey Cushing Institutes Of Neuroscience North Shor
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Nishikawa Misao
Department Of Neurosurgery Osaka City General Hospital
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Milhorat Thomas
Department Of Neurosurgery North Shore University Hospital
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Bolognese Paolo
Department Of Neurosurgery North Shore University Hospital
著作論文
- Tethered Cord Syndrome : Preliminary Report of Clinical Features and Morphometric Analysis on Association of Chiari Malformation Type I
- Occipito-atlanto-axial Hypermobility : Clinical Features and Dynamic Analysis of Cranial Settling and Posterior Gliding of Occipital Condyle : Part 2 : Findings in Patients with Post-traumatic Condition
- Occipito-atlanto-axial Hypermobility : Clinical Features and Dynamic Analysis of Cranial Settling and Posterior Gliding of Occipital Condyle : Part 1 : Findings in Patients with Hereditary Disorders of Connective Tissue and Ehlers-Danlos Syndrome