Publications by authors named "Michael Partington"

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Commentary on "Causes of death among people with myelomeningocele: A multi-institutional 47-year retrospective study" by Szymanski et al.
Michael D Partington

J Pediatr Rehabil Med· January 2024

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Symptomatic spinal arachnoid cyst with spastic diplegia secondary to cerebral palsy: illustrative case.
Andrew Guillotte, Abdul-Rahman Alkiswani, Kathryn A Keeler, Michael D Partington

J Neurosurg Case Lessons· November 2023

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First-time tethered cord release among adults with myelomeningocele: an analysis of people in the National Spina Bifida Patient Registry.
Mark S Dias, Ming Wang, Menglu Liang, Elias B Rizk, Robin Bowman, Michael D Partington

J Neurosurg Spine· October 2023

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Editorial. The elusive fibrofatty filum holy grail.
Jeffrey P Blount, Michael D Partington

J Neurosurg Pediatr· March 2023

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Significant brainstem dysfunction in neonates with myelomeningoceles: a comparison of prenatal versus postnatal closure.
Paul A Grabb, Emmanuel J Vlastos, Paige A Lundy, Michael B Partington

J Neurosurg Pediatr· May 2022

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Estimating the prevalence of neurosurgical interventions in adults with spina bifida using the Health Facts data set: implications for transition planning and the development of adult clinics.
Joseph S Domino, Paige Lundy, Earl F Glynn, Michael Partington

J Neurosurg Pediatr· April 2022

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Neurosurgery guidelines for the care of people with spina bifida.
Jeffrey P Blount, Robin Bowman, Mark S Dias, Betsy Hopson, Michael D Partington

J Pediatr Rehabil Med· October 2021

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Expression of and correlational patterns among neuroinflammatory, neuropeptide, and neuroendocrine molecules from cerebrospinal fluid in cerebral palsy.
Cory J Goracke-Postle, Chantel C Burkitt, Angela Panoskaltsis-Mortari, Michael Ehrhardt, George L Wilcox, Michael Partington

BMC Neurol· October 2021

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Tethered spinal cord among individuals with myelomeningocele: an analysis of the National Spina Bifida Patient Registry.
Mark S Dias, Ming Wang, Elias B Rizk, Robin Bowman, Michael D Partington

J Neurosurg Pediatr· July 2021

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Intrathoracic migration of ventriculo-peritoneal shunt via Morgagni hernia.
Paige A Lundy, Michael D Partington, Chad A Tuchek, David M Garcia

Childs Nerv Syst· January 2021

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Musculoskeletal Pain Outcomes Pre- and Post Intrathecal Baclofen Pump Implant in Children With Cerebral Palsy: A Prospective Cohort Study.
Chantel C Barney, Alyssa M Merbler, Jean Stansbury, Linda E Krach, Michael Partington

Arch Rehabil Res Clin Transl· June 2020

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Intracranial subdural empyemas and epidural abscesses in children.
Paige Lundy, Christian Kaufman, David Garcia, Michael D Partington, Paul A Grabb

J Neurosurg Pediatr· July 2019

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Retinal Findings in Young Children With Increased Intracranial Pressure From Nontraumatic Causes.
Angell Shi, Abhaya Kulkarni, Kenneth W Feldman, Avery Weiss, Emily A McCourt, Michael Partington

Pediatrics· February 2019

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Decompression for Chiari malformation type II in individuals with myelomeningocele in the National Spina Bifida Patient Registry.
Irene Kim, Betsy Hopson, Inmaculada Aban, Elias B Rizk, Mark S Dias, Michael D Partington

J Neurosurg Pediatr· December 2018

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Treated hydrocephalus in individuals with myelomeningocele in the National Spina Bifida Patient Registry.
Irene Kim, Betsy Hopson, Inmaculada Aban, Elias B Rizk, Mark S Dias, Michael D Partington

J Neurosurg Pediatr· December 2018

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Congenital Brain and Spinal Cord Malformations and Their Associated Cutaneous Markers.
Mark Dias, Michael Partington,

Pediatrics· October 2015

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Neurolysis alone as the treatment for neuroma-in-continuity with more than 50% conduction in infants with upper trunk brachial plexus birth palsy.
Emily Andrisevic, Marshall Taniguchi, Michael D Partington, Julie Agel, Ann E Van Heest

J Neurosurg Pediatr· February 2014

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Injected contrast study fails to demonstrate catheter-pump connector tear.
Linda E Krach, Michael D Partington

J Pediatr Rehabil Med· October 2012

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CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.
Anna Hackett, Patrick S Tarpey, Andrea Licata, James Cox, Annabel Whibley, Michael Partington

Eur J Hum Genet· May 2010

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Clinical study of two brothers with a novel 33 bp duplication in the ARX gene.
Michelle K Demos, Tod Fullston, Michael W Partington, Jozef Gécz, William T Gibson

Am J Med Genet A· July 2009

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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
Patrick S Tarpey, Raffaella Smith, Erin Pleasance, Annabel Whibley, Sarah Edkins, Michael Partington

Nat Genet· May 2009

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Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
Lane J Jaeckle Santos, Chao Xing, Robert B Barnes, Lesley C Ades, Andre Megarbane, Michael Partington

Hum Genet· June 2008

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Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
Guy Froyen, Mark Corbett, Joke Vandewalle, Irma Jarvela, Owen Lawrence, Michael Partington

Am J Hum Genet· February 2008

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Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
Michael Field, Patrick S Tarpey, Raffaella Smith, Sarah Edkins, Sarah O'Meara, Michael Partington

Am J Hum Genet· August 2007

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Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
Patrick S Tarpey, F Lucy Raymond, Sarah O'Meara, Sarah Edkins, Jon Teague, Michael Partington

Am J Hum Genet· February 2007

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