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Neurosurgery|April 5, 2018

Origin of Syrinx Fluid in Syringomyelia: A Physiological StudyJohn D Heiss, Katie Jarvis, René K Smith, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|May 31, 2019

Trial of magnetic resonance-guided putaminal gene therapy for advanced Parkinson's diseaseJohn D Heiss, Codrin Lungu, Dima A Hammoud, et al.

European Journal of Human Genetics : EJHG|June 23, 2019

Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencingAnthony M Musolf, Winson S C Ho, Kyle A Long, et al.

Pediatric Neurology|May 28, 2018

A Multidisciplinary Consensus for Clinical Care and Research Needs for Sturge-Weber SyndromeAlejandro J De la Torre, Aimee F Luat, Csaba Juhász, et al.

Neurology. Genetics|April 28, 2020

Neuraxial dysraphism in <i>EPAS1-</i>associated syndrome due to improper mesenchymal transitionJared S Rosenblum, Anthony J Cappadona, Davis P Argersinger, et al.

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Showing results (11-20 of 15) with videos related to

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You have reached the last page of results.This site can display upto 15 results.

Neurosurgery|April 5, 2018

Origin of Syrinx Fluid in Syringomyelia: A Physiological StudyJohn D Heiss, Katie Jarvis, René K Smith, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|May 31, 2019

Trial of magnetic resonance-guided putaminal gene therapy for advanced Parkinson's diseaseJohn D Heiss, Codrin Lungu, Dima A Hammoud, et al.

European Journal of Human Genetics : EJHG|June 23, 2019

Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencingAnthony M Musolf, Winson S C Ho, Kyle A Long, et al.

Pediatric Neurology|May 28, 2018

A Multidisciplinary Consensus for Clinical Care and Research Needs for Sturge-Weber SyndromeAlejandro J De la Torre, Aimee F Luat, Csaba Juhász, et al.

Neurology. Genetics|April 28, 2020

Neuraxial dysraphism in <i>EPAS1-</i>associated syndrome due to improper mesenchymal transitionJared S Rosenblum, Anthony J Cappadona, Davis P Argersinger, et al.

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