John Kamholz

John Kamholz

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John Kamholz

John Kamholz

Publications by authors named "John Kamholz"

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The effects of chronic Δ-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) use on cerebral glucose metabolism in multiple sclerosis: a pilot study.

Appl Physiol Nutr Metab 2020 Apr 16;45(4):450-452. Epub 2019 Dec 16.

Department of Health and Human Physiology, University of Iowa, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.1139/apnm-2019-0634DOI Listing
April 2020

Increased leg muscle fatigability during 2 mA and 4 mA transcranial direct current stimulation over the left motor cortex.

Exp Brain Res 2020 Feb 9;238(2):333-343. Epub 2020 Jan 9.

Department of Health and Human Physiology, University of Iowa, E432 Field House, Iowa City, IA, 52242, USA.

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http://dx.doi.org/10.1007/s00221-019-05721-wDOI Listing
February 2020

The Tolerability and Efficacy of 4 mA Transcranial Direct Current Stimulation on Leg Muscle Fatigability.

Brain Sci 2019 Dec 23;10(1). Epub 2019 Dec 23.

Department of Health and Human Physiology, University of Iowa, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.3390/brainsci10010012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017217PMC
December 2019

Transcranial Direct Current Stimulation (tDCS) to Improve Gait in Multiple Sclerosis: A Timing Window Comparison.

Front Hum Neurosci 2019 28;13:420. Epub 2019 Nov 28.

Department of Health and Human Physiology, University of Iowa, Iowa City, IA, United States.

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http://dx.doi.org/10.3389/fnhum.2019.00420DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893177PMC
November 2019

Author response to Dr. Aziz-"Statin use and delayed onset of Huntington disease".

Mov Disord 2019 05;34(5):763-764

Carver College of Medicine at the University of Iowa, Department of Psychiatry, Iowa City, Iowa, USA.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/mds.27678
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http://dx.doi.org/10.1002/mds.27678DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521849PMC
May 2019

Statin use and delayed onset of Huntington's disease.

Mov Disord 2019 02 21;34(2):281-285. Epub 2018 Dec 21.

Department of Psychiatry, Carver College of Medicine at the University of Iowa, Iowa City, Iowa, USA.

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http://dx.doi.org/10.1002/mds.27591DOI Listing
February 2019

Comparing Risperidone and Olanzapine to Tetrabenazine for the Management of Chorea in Huntington Disease: An Analysis from the Enroll-HD Database.

Mov Disord Clin Pract 2019 Feb 30;6(2):132-138. Epub 2018 Nov 30.

Department of Neurology The University of Iowa Hospitals and Clinics Iowa City IA United States.

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http://dx.doi.org/10.1002/mdc3.12706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384174PMC
February 2019

Comparing Risperidone and Olanzapine to Tetrabenazine for the Management of Chorea in Huntington Disease: An Analysis from the Enroll-HD Database.

Mov Disord Clin Pract 2019 Feb 30;6(2):132-138. Epub 2018 Nov 30.

Department of Neurology The University of Iowa Hospitals and Clinics Iowa City IA United States.

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http://dx.doi.org/10.1002/mdc3.12706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384174PMC
February 2019

Spinal Cord Infarction Presenting as a Hemicord Syndrome: Report of 2 Cases.

J Stroke Cerebrovasc Dis 2018 Jun 13;27(6):e107-e109. Epub 2018 Feb 13.

Neurology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

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http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2018.01.003DOI Listing
June 2018

Insertion of proteolipid protein into mitochondria but not DM20 regulates metabolism of cells.

Neurosci Lett 2018 06 2;678:90-98. Epub 2018 May 2.

Wayne State University School of Medicine Department of Anatomy and Cell Biology, Detroit, MI, 48201, USA. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2018.05.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975245PMC
June 2018

exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E.

Ann Clin Transl Neurol 2017 04 12;4(4):236-245. Epub 2017 Mar 12.

Department of Neurology Neuromuscular Division University of Iowa Hospitals and Clinics Iowa City Iowa; Department of Neurology Neurogenetics Division University of Iowa Hospitals and Clinics Iowa City Iowa.

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http://dx.doi.org/10.1002/acn3.395DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376752PMC
April 2017

Abl2 kinase phosphorylates Bi-organellar regulator MNRR1 in mitochondria, stimulating respiration.

Biochim Biophys Acta Mol Cell Res 2017 Feb 30;1864(2):440-448. Epub 2016 Nov 30.

Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bbamcr.2016.11.029DOI Listing
February 2017

Substance abuse may hasten motor onset of Huntington disease: Evaluating the Enroll-HD database.

Neurology 2017 Feb 1;88(9):909-915. Epub 2017 Feb 1.

From the Departments of Pharmaceutical Care (J.L.S.), Neurology (J.L.S., J.A.K., S.M.E.F., J.S.P., P.C.N.), Psychiatry (J.A.K., D.J.M., J.S.P., P.C.N.), and Pediatrics (P.C.N.), The University of Iowa Hospitals and Clinics, Iowa City.

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http://dx.doi.org/10.1212/WNL.0000000000003661DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331869PMC
February 2017

Role of Pulmonary Evaluation in Diagnosis of Neurosarcoidosis.

Sarcoidosis Vasc Diffuse Lung Dis 2016 Oct 7;33(3):209-215. Epub 2016 Oct 7.

Detroit Medical Center/Wayne State University.

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October 2016

Novel pathologic findings in patients with Pelizaeus-Merzbacher disease.

Neurosci Lett 2016 08 17;627:222-32. Epub 2016 May 17.

Center for Molecular Medicine and Genetics, Wayne State University, School of Medicine, Detroit, MI 48201, United States; Department of Anatomy and Cell Biology, Wayne State University, School of Medicine, Detroit, MI 48201, United States.

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https://linkinghub.elsevier.com/retrieve/pii/S03043940163034
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http://dx.doi.org/10.1016/j.neulet.2016.05.028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948744PMC
August 2016

Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2-p12) deletion.

Muscle Nerve 2015 Nov 19;52(5):905-8. Epub 2015 Jun 19.

Department of Neurology, Carver College of Medicine, University of Iowa, 200 Hawkins Drive, Iowa City, Iowa, 52246, USA.

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http://dx.doi.org/10.1002/mus.24713DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596757PMC
November 2015

Diffusion tensor imaging of patients with proteolipid protein 1 gene mutations.

J Neurosci Res 2014 Dec 23;92(12):1723-32. Epub 2014 Aug 23.

Department of Neuroscience, University of Toledo, Toledo, Ohio; Center of Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan.

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http://dx.doi.org/10.1002/jnr.23458DOI Listing
December 2014

Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher disease.

J Neurol Sci 2013 Dec 30;335(1-2):75-81. Epub 2013 Aug 30.

Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, United States; Department of Neurosciences & Neurology, University of Toledo College of Medicine, Toledo, OH 43614, United States.

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http://dx.doi.org/10.1016/j.jns.2013.08.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969727PMC
December 2013

Proteolipid protein dimerization at cysteine 108: Implications for protein structure.

Neurosci Res 2012 Oct 10;74(2):144-55. Epub 2012 Aug 10.

Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, United States.

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http://dx.doi.org/10.1016/j.neures.2012.07.009DOI Listing
October 2012

Crystal structure of the extracellular domain of human myelin protein zero.

Proteins 2012 Jan 4;80(1):307-13. Epub 2011 Oct 4.

Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

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http://dx.doi.org/10.1002/prot.23164DOI Listing
January 2012

Predicting the unpredictable.

Authors:
John Kamholz

Ann Neurol 2009 Apr;65(4):480

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http://dx.doi.org/10.1002/ana.21650DOI Listing
April 2009

Differential distribution of neuregulin in human brain and spinal fluid.

Brain Res 2009 Mar 29;1258:1-11. Epub 2008 Dec 29.

Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI 48201 , USA.

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http://dx.doi.org/10.1016/j.brainres.2008.12.047DOI Listing
March 2009

Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations.

Hum Mol Genet 2008 Jul 12;17(13):1877-89. Epub 2008 Mar 12.

Department of Neurosciences, Ophthalmology and Genetics, Universityof Genova, 16132 Genova, Italy.

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http://dx.doi.org/10.1093/hmg/ddn083DOI Listing
July 2008

Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKC alpha.

J Cell Biol 2007 May 14;177(4):707-16. Epub 2007 May 14.

Department of Biological Sciences, The University of Iowa, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.1083/jcb.200608060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064215PMC
May 2007

T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.

Ann Neurol 2006 Feb;59(2):358-64

Department of Neurology and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI 48201, USA.

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http://dx.doi.org/10.1002/ana.20777DOI Listing
February 2006

Neuronal cell injury precedes brain atrophy in multiple sclerosis.

Neurology 2005 Jan;64(1):176; author reply 176

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http://dx.doi.org/10.1212/wnl.64.1.176DOI Listing
January 2005

CNS myelin paranodes require Nkx6-2 homeoprotein transcriptional activity for normal structure.

J Neurosci 2004 Dec;24(50):11215-25

Brookdale Center for Molecular Biology, Mount Sinai School of Medicine, New York, New York, 10029, USA.

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http://dx.doi.org/10.1523/JNEUROSCI.3479-04.2004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730372PMC
December 2004

Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene.

Neurology 2004 Jul;63(1):194; author reply 194

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http://dx.doi.org/10.1212/wnl.63.1.194DOI Listing
July 2004

Phenotypic clustering in MPZ mutations.

Brain 2004 Feb 7;127(Pt 2):371-84. Epub 2004 Jan 7.

Department of Neurology, Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan, USA.

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http://dx.doi.org/10.1093/brain/awh048DOI Listing
February 2004

Role of TC21/R-Ras2 in enhanced migration of neurofibromin-deficient Schwann cells.

Oncogene 2004 Jan;23(2):368-78

Department of Cell Biology, Neurobiology and Anatomy, University of Cincinnati, College of Medicine, 3125 Eden Ave., Cincinnati, OH 45267-0521, USA.

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http://dx.doi.org/10.1038/sj.onc.1207075DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854497PMC
January 2004

Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy.

Ann Neurol 2003 Mar;53(3):354-65

Department of Neurology and Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.

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http://dx.doi.org/10.1002/ana.10466DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744322PMC
March 2003

Nk6, a novel Drosophila homeobox gene regulated by vnd.

Mech Dev 2002 Aug;116(1-2):105-16

Department of Pathology, University of Michigan, Ann Arbor 48109, USA.

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http://dx.doi.org/10.1016/s0925-4773(02)00155-7DOI Listing
August 2002

Hereditary motor and sensory neuropathies: a biological perspective.

Lancet Neurol 2002 Jun;1(2):110-8

Department of Neurology and the Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.

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http://dx.doi.org/10.1016/s1474-4422(02)00042-xDOI Listing
June 2002

TGFbeta1 modulates the phenotype of Schwann cells at the transcriptional level.

Mol Cell Neurosci 2002 Mar;19(3):307-19

Department of Neurology, Wayne State University, Elliman Building 3206, 421 East Canfield, Detroit, Michigan 48201, USA.

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http://dx.doi.org/10.1006/mcne.2001.1094DOI Listing
March 2002

Overcoming Cellular Immunity to Prolong Adenoviral-Mediated Gene Expression in Sciatic Nerve.

Ann N Y Acad Sci 1999 Oct;883(1):397-414

Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan 48201, USADepartment of Pediatrics, Division of Pediatric Neurology, Wayne State University School of Medicine, Detroit, Michigan 48201, USAInstitute of Neurology, University of Milan, IRCCS, Ospedale Maggiore Policlinico, Milan, ItalyCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08601.xDOI Listing
October 1999

The Absence of Myelin P Protein Produces a Novel Molecular Phenotype in Schwann Cell.

Ann N Y Acad Sci 1999 Oct;883(1):281-293

Institute of Neurology, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, ItalyDepartment of Neurology, Wayne State University, Detroit, Michigan 48201, USACenter for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, USADepartment of Neurology, University Hospital, Limoges, France.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08590.xDOI Listing
October 1999

Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations.

Ann N Y Acad Sci 1999 Oct;883(1):351-365

Department of Neurology, Wayne State University School of Medicine, 4201 St. Antoine Boulevard, 8C UHC, Detroit, Michigan 48201, USACenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, 521 East Canfield, 3216 Scott Hall, Detroit, Michigan 48201, USADepartment of Neurology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USADepartment of Physical Medicine and Rehabilitation, University of Washington School of Medicine, Seattle, Washington 98195, USADepartment of Neurology, University Hospital, Limoges F-87042, FranceSection of Neurology, Mayo Clinic, Scottsdale, Arizona 85259, USADepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana 46202, USADepartment of Neurology, University of Washington School of Medicine, Seattle, Washington 98195, USADepartment of Neurosciences, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08597.xDOI Listing
October 1999

Correlation between Weakness and Axonal Loss in Patients with CMT1A.

Ann N Y Acad Sci 1999 Oct;883(1):490-492

Department of Neurology, 421 East Canfield, 3124 Elliman Building, Detroit, Michigan 48201, USA.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08618.xDOI Listing
October 1999

Introduction to the Third International Symposium on Charcot-Marie-Tooth Disorders.

Ann N Y Acad Sci 1999 Oct;883(1):xiii-xviii

Department of Neurology, Wayne State University School of Medicine, 421 East Canfield Avenue, 3124 Elliman Bulding, Detroit, Michigan 48201, USADepartment of Neurology, Columbia University, 710 West 168th Street, Unit 157, New York, New York 10032, USA.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08559.xDOI Listing
October 1999

Regulation of Myelin-Specific Gene Expression: Relevance to CMT1.

Ann N Y Acad Sci 1999 Oct;883(1):91-108

Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan 48201, USAGraduate Program in Molecular Biology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USAInstitute of Neurology, University of Milan, IRCCS, Ospedale Maggiore, Policlinico, Milan, ItalyCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

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http://dx.doi.org/10.1111/j.1749-6632.1999.tb08572.xDOI Listing
October 1999