Kurenai Tanji

Kurenai Tanji

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Kurenai Tanji

Kurenai Tanji

Publications by authors named "Kurenai Tanji"

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Bioavailability and cytosolic kinases modulate response to deoxynucleoside therapy in TK2 deficiency.

EBioMedicine 2019 Aug 2;46:356-367. Epub 2019 Aug 2.

Department of Neurology, H. Houston Merritt Neuromuscular Research Center, Columbia University Medical Center, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ebiom.2019.07.037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710986PMC
August 2019

Demyelinating Neuropathy in a Patient Treated With Revusiran for Transthyretin (Thr60Ala) Amyloidosis.

J Clin Neuromuscul Dis 2019 Mar;20(3):120-128

Division of Neuropathology, Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY.

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http://dx.doi.org/10.1097/CND.0000000000000242DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392216PMC
March 2019

Three-Dimensional Analysis of Mitochondrial Crista Ultrastructure in a Patient with Leigh Syndrome by In Situ Cryoelectron Tomography.

iScience 2018 Aug 20;6:83-91. Epub 2018 Jul 20.

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA 15213, USA; Department of Cell Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA. Electronic address:

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http://dx.doi.org/10.1016/j.isci.2018.07.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137323PMC
August 2018

Epilepsy surgery for epileptic encephalopathy as a sequela of herpes simplex encephalitis: case report.

J Neurosurg Pediatr 2017 Jul 28;20(1):56-63. Epub 2017 Apr 28.

Department of Neurology, Division of Child Neurology, Columbia University Medical Center, New York.

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http://dx.doi.org/10.3171/2017.3.PEDS16632DOI Listing
July 2017

Clinical Reasoning: A 58-year-old man with progressive ptosis and walking difficulty.

Neurology 2017 07;89(1):e1-e5

From the Departments of Neurology (P.-H.K., K.T., S.-H.K.) and Pathology and Cell Biology (K.T.), Columbia University, New York, NY; and the Department of Neurology (P.-H.K., R.Y.L.), Buddhist Tzu Chi General Hospital, Hualien, Taiwan.

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http://dx.doi.org/10.1212/WNL.0000000000004064DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496515PMC
July 2017

Demyelinating neuropathy in genetically confirmed acute intermittent porphyria.

Muscle Nerve 2015 Nov 2;52(5):916-7. Epub 2015 Jul 2.

Department of Pathology & Cell Biology, Division of Neuropathology, Columbia University Medical Center, New York.

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http://doi.wiley.com/10.1002/mus.24733
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http://dx.doi.org/10.1002/mus.24733DOI Listing
November 2015

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Orphanet J Rare Dis 2015 Oct 15;10:135. Epub 2015 Oct 15.

CHU Nantes, Service de Génétique Médicale, Unité de Génétique Moléculaire, 9 quai Moncousu, 44093, Nantes CEDEX 1, France.

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http://link.springer.com/content/pdf/10.1186%2Fs13023-015-03
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http://www.ojrd.com/content/10/1/135
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http://dx.doi.org/10.1186/s13023-015-0352-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608180PMC
October 2015

Bortezomib-associated demyelinating neuropathy--clinical and pathologic features.

J Clin Neuromuscul Dis 2015 Jun;16(4):202-9

*Department of Neurology, Columbia Neuropathy Research Center, The Neurological Institute of New York, Columbia University Medical Center, New York, NY; †Division of Neuropathology, Department of Pathology and Cell Biology, Neuromuscular Pathology Laboratory, Columbia University College of Physicians and Surgeons, New York, NY; ‡Division of Neuromuscular Medicine, Department of Neurology, The University of Oklahoma Health Sciences Center, Oklahoma, OK.

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http://dx.doi.org/10.1097/CND.0000000000000077DOI Listing
June 2015

Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish.

Muscle Nerve 2015 May 17;51(5):767-72. Epub 2015 Feb 17.

Department of Neurology, Columbia University, 180 Fort Washington Avenue, New York, New York, 10032, USA.

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http://dx.doi.org/10.1002/mus.24528DOI Listing
May 2015

Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM gene.

Muscle Nerve 2014 Aug;50(2):292-5

Department of Neurology, Columbia University Medical Center, College of Physicians & Surgeons, 630 West 168th Street, New York, New York, USA.

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http://dx.doi.org/10.1002/mus.24262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107085PMC
August 2014

Peripheral T-cell lymphoma emerging in a patient with aggressive polymyositis: molecular evidence for neoplastic transformation of an oligoclonal T-cell infiltrate.

Acta Neuropathol 2013 Oct 13;126(4):595-601. Epub 2013 Aug 13.

Division of Neuropathology, Department of Pathology and Cell Biology, Columbia University Medical Center and New York Presbyterian Hospital, 630 W. 168th Street, PH15-124, New York, 10032, USA,

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http://link.springer.com/content/pdf/10.1007/s00401-013-1164
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http://link.springer.com/10.1007/s00401-013-1164-z
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http://dx.doi.org/10.1007/s00401-013-1164-zDOI Listing
October 2013

Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance.

Dev Cell 2013 Sep 19;26(6):591-603. Epub 2013 Sep 19.

Department of Medicine, College of Physicians and Surgeons, Columbia University, 630 West 168(th) Street, New York, NY 10032, USA; Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, 630 West 168(th) Street, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.devcel.2013.08.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798056PMC
September 2013

Muscle and nerve biopsies: techniques for the neurologist and neurosurgeon.

Clin Neurol Neurosurg 2013 Aug 13;115(8):1206-14. Epub 2013 Jun 13.

Department of Neurological Surgery, Columbia University Medical Center, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.clineuro.2013.05.008DOI Listing
August 2013

Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.

Brain 2013 May 29;136(Pt 5):1508-17. Epub 2013 Mar 29.

Research Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca, VHIR, Universitat Autònoma de Barcelona, Passeig Vall d'Hebron, 119-129 08035 Barcelona, Spain.

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http://dx.doi.org/10.1093/brain/awt074DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634201PMC
May 2013

The many clinical faces of cytochrome c oxidase deficiency.

Adv Exp Med Biol 2012 ;748:341-57

Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.

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http://dx.doi.org/10.1007/978-1-4614-3573-0_14DOI Listing
September 2012

Congenital megaconial myopathy due to a novel defect in the choline kinase Beta gene.

Arch Neurol 2012 May;69(5):657-61

Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.

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http://dx.doi.org/10.1001/archneurol.2011.2333DOI Listing
May 2012

Morphological assessment of mitochondrial respiratory chain function on tissue sections.

Authors:
Kurenai Tanji

Methods Mol Biol 2012 ;837:181-94

Neuromuscular Pathology Laboratory, Division of Neuropathology, Department of Pathology and Cell Biology, Columbia University, New York, NY, USA.

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http://link.springer.com/10.1007/978-1-61779-504-6_12
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http://dx.doi.org/10.1007/978-1-61779-504-6_12DOI Listing
April 2012

Loss of myelin-associated glycoprotein in kearns-sayre syndrome.

Arch Neurol 2012 Apr;69(4):490-9

Mitochondrial Research Group, Institute for Aging and Health, Newcastle University, Framlington Place, Newcastle upon Tyne, United Kingdom.

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http://dx.doi.org/10.1001/archneurol.2011.2167DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672633PMC
April 2012

Spinal cord bypass surgery with intercostal and spinal accessory nerves: an anatomical feasibility study in human cadavers.

J Neurosurg Spine 2012 Feb 2;16(2):178-86. Epub 2011 Dec 2.

Department of Neurological Surgery, Columbia University Medical Center, New York, USA.

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http://dx.doi.org/10.3171/2011.9.SPINE10378DOI Listing
February 2012

Restricted diffusion in a thrombosed anterior cerebral artery aneurysm mimicking a dermoid cyst.

J Neuroimaging 2012 Jan 21;22(1):85-8. Epub 2010 Jun 21.

Department of Neurology and Radiology, St. Lukes Roosevelt Hospital, New York, NY 10025, USA.

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http://dx.doi.org/10.1111/j.1552-6569.2010.00495.xDOI Listing
January 2012

MERRF and Kearns-Sayre overlap syndrome due to the mitochondrial DNA m.3291T>C mutation.

Muscle Nerve 2011 Sep;44(3):448-51

Department of Neurology, Columbia University Medical Center, 630 West 168th Street, P&S 4-423, New York, New York 10032, USA.

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http://doi.wiley.com/10.1002/mus.22149
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http://dx.doi.org/10.1002/mus.22149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197731PMC
September 2011

Primitive neuroectodermal tumors of the spine: a comprehensive review with illustrative clinical cases.

Neurosurg Focus 2011 Jan;30(1):E1

Department of Neurological Surgery, Columbia University Medical Center, New York, New York, USA.

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http://thejns.org/doi/10.3171/2010.10.FOCUS10217
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http://dx.doi.org/10.3171/2010.10.FOCUS10217DOI Listing
January 2011

Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease.

Am J Pathol 2010 Nov 23;177(5):2541-8. Epub 2010 Sep 23.

Department of Genetics and Development, P&S 4-449, Columbia University Medical Center, 630 W. 168th St., New York, NY 10032, USA.

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http://dx.doi.org/10.2353/ajpath.2010.100229DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966810PMC
November 2010

The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegia.

Neuromuscul Disord 2009 Apr 13;19(4):297-9. Epub 2009 Mar 13.

Department of Neurology, Columbia University Medical Center, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.nmd.2009.01.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699630PMC
April 2009

Light microscopic methods to visualize mitochondria on tissue sections.

Methods 2008 Dec 16;46(4):274-80. Epub 2008 Oct 16.

Department of Pathology, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.ymeth.2008.09.027DOI Listing
December 2008

A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.

J Neurol Sci 2008 Jul 7;270(1-2):23-7. Epub 2008 Mar 7.

Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.

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http://dx.doi.org/10.1016/j.jns.2008.01.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6195319PMC
July 2008

Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.

Neuromuscul Disord 2008 Jun 27;18(6):453-9. Epub 2008 May 27.

Departamento de Bioquímica, Hospital Universitario Puerta de Hierro, Instituto de Investigaciones Biomédicas, CSIC-UAM, CIBERER, ISCiii, Madrid, Spain.

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http://www.ant-tnsjournal.com/Mag_Files/18-4/dw2009111916284
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http://linkinghub.elsevier.com/retrieve/pii/S096089660800097
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http://dx.doi.org/10.1016/j.nmd.2008.04.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891825PMC
June 2008

Amyotrophic lateral sclerosis with ragged-red fibers.

Arch Neurol 2008 Mar;65(3):403-6

Department of Neurology, Columbia University Medical Center, 3-317 Russ Berrie Medical Science Pavilion, 1150 St Nicholas Ave, New York, NY 10032, USA.

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http://dx.doi.org/10.1001/archneurol.2007.65DOI Listing
March 2008

A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.

Pediatr Res 2007 May;61(5 Pt 1):622-4

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.

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http://dx.doi.org/10.1203/pdr.0b013e3180459f2dDOI Listing
May 2007

Use of stents to treat intracranial cerebrovascular disease.

Annu Rev Med 2007 ;58:107-22

Columbia University College of Physicians & Surgeons, New York, New York 10032, USA.

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http://dx.doi.org/10.1146/annurev.med.58.121205.100631DOI Listing
April 2007

The transformation of pediatric gliomatosis cerebri to cerebellar glioblastoma multiforme presenting as supra- and infratentorial acute disseminated encephalomyelitis. Case report.

J Neurosurg 2005 Jan;102(1 Suppl):72-7

Department of Neurological Surgery, Columbia College of Physicians and Surgeons, Neurological Institute of New York, New York 10032, USA.

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http://dx.doi.org/10.3171/ped.2005.102.1.0072DOI Listing
January 2005

Fatal infantile neuromuscular presentation of glycogen storage disease type IV.

Neuromuscul Disord 2004 Apr;14(4):253-60

Department of Neurology, College of Physicians and Surgeons, Columbia University, 4-420, 630 West 168th Street, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.nmd.2003.12.006DOI Listing
April 2004

Clinicopathological review: cord compression secondary to a lesion of the cervical spine in an 11-year-old girl.

Neurosurgery 2004 Apr;54(4):934-7; discussion 938

Department of Neurological Surgery, Columbia-Presbyterian Medical Center, Columbia University, 710 West 168th Street, New York, NY 10032-3784, USA.

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http://dx.doi.org/10.1227/01.neu.0000116139.82435.c4DOI Listing
April 2004

Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.

J Child Neurol 2004 Apr;19(4):258-61

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

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http://dx.doi.org/10.1177/088307380401900403DOI Listing
April 2004

Multicystic encephalomalacia after first-trimester intrauterine fetal death in monochorionic twins.

Am J Obstet Gynecol 2004 Feb;190(2):563-5

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Columbia Presbyterian Medical Center, Columbia University, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/s0002-9378(03)00824-xDOI Listing
February 2004

Mitochondrial DNA dysfunction in oncocytic hepatocytes.

Liver Int 2003 Oct;23(5):397-403

Department of Pathology, College of Physicians and Surgeons, Columbia University, NY, New York 10032, USA.

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October 2003

Histopathological evaluation of middle cerebral artery after percutaneous intracranial transluminal angioplasty.

Stroke 2003 Sep 7;34(9):e170-3. Epub 2003 Aug 7.

Doris & Stanley Tananbaum Stroke Center, Neurological Institute, New York Presbyterian Hospital, Columbia University, 710 W 168th St, Box 131, New York, NY 10032, USA.

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http://dx.doi.org/10.1161/01.STR.0000086764.86787.9CDOI Listing
September 2003

The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction.

Acta Neuropathol 2003 Jan 7;105(1):69-75. Epub 2002 Sep 7.

Department of Pathology of the College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.

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http://link.springer.de/link/service/journals/00401/contents
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http://dx.doi.org/10.1007/s00401-002-0604-yDOI Listing
January 2003

Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.

Muscle Nerve 2002 Nov;26(5):597-607

Department of Neurology, Columbia University College of Physicians & Surgeons, 630 West 168th Street, New York, New York 10032, USA.

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http://dx.doi.org/10.1002/mus.10194DOI Listing
November 2002

Clinical features and genetics of myoclonic epilepsy with ragged red fibers.

Adv Neurol 2002 ;89:217-29

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, New York, USA.

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October 2002

Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.

Am J Hum Genet 2002 Sep 31;71(3):679-83. Epub 2002 Jul 31.

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY, 10032, USA.

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http://dx.doi.org/10.1086/342482DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC379205PMC
September 2002