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KURENAI TANJI, M.D.
M.D.
Neuropathology Physician
NPI: 1952438863IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology Physician
Pathology — Anatomic Pathology
Code: 207ZP0101X
231053-1(NY)
Neuropathology PhysicianPrimary
Pathology — Neuropathology
Code: 207ZN0500X
231053-1(NY)
Education
OTHER
Class of 1984
Research & Publications (20)
Light microscopic methods to visualize mitochondria on tissue sections.
PMID 18929660·Methods·2008
6-review
Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria.
PMID 17445692·Methods Cell Biol·2007
6-review
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction.
PMID 12471464·Acta Neuropathol·2003
5-case
Optical imaging techniques (histochemical, immunohistochemical, and in situ hybridization staining methods) to visualize mitochondria.
PMID 11381601·Methods Cell Biol·2001
7-preclinical
Neuropathological features of mitochondrial disorders.
PMID 11735377·Semin Cell Dev Biol·2001
6-review
Kearns-sayre syndrome: oncocytic transformation of choroid plexus epithelium.
PMID 11018246·J Neurol Sci·2000
5-case
Two-dimensional finite elements model for boron management in agroforestry sites.
PMID 19184495·Environ Monit Assess·2010
8-other
Effect of sound intensity on tonotopic fMRI maps in the unanesthetized monkey.
PMID 19631273·Neuroimage·2010
7-preclinical
Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice.
PMID 19028666·Hum Mol Genet·2009
7-preclinical
Retinoic acid-inducible gene-I is constitutively expressed and involved in IFN-gamma-stimulated CXCL9-11 production in intestinal epithelial cells.
PMID 19201382·Immunol Lett·2009
8-other
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegia.
PMID 19285865·Neuromuscul Disord·2009
5-case
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.
PMID 18504129·Neuromuscul Disord·2008
7-preclinical
Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance.
PMID 18467430·Hum Mol Genet·2008
7-preclinical
Maturation process of TDP-43-positive neuronal cytoplasmic inclusions in amyotrophic lateral sclerosis with and without dementia.
PMID 18560845·Acta Neuropathol·2008
8-other
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
PMID 18332249·Arch Neurol·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 622 W 168TH ST, PH1564W
NEW YORK, NY 10032 - Phone
- (212) 305-7399
Quick Facts
- NPI
- 1952438863
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 42
- Publications
- 20
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