Professor of Neurology, University Tenn College of Medicine
Neurology
Dr. Mark Ledoux, MD
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Mark Ledoux works in the field of Neurology. He researched medicine at University of Alabama Medical Center. University of Alabama Medical Center is ranked 37/17 in Research/PrimaryCare. He received 2 awards: "Memphis Magazine: Top Doctors" and "CMS Meaningful Use Stage 1 Certification". Mark Ledoux has written publications. He has 86 publications published with PubMed. The lastest publication is: 'Single-unit activity of cerebellar nuclear cells in the awake genetically dystonic rat.' He accepts all Medicare patients.
Publications
- Blepharospasm in a multiplex African-American pedigree.
- Treatment of myoclonus-Dystonia syndrome with tetrabenazine.
- Recent advances in the genetics of Dystonia.
- A rare sequence variant in intron 1 of THAP1 is associated with primary Dystonia.
- Pathogenic variants in TUBB4A are not found in primary Dystonia.
- Emerging common molecular pathways for primary Dystonia.
- FUS in familial Essential tremor - The search for common causes is still on.
- Role of G?(olf) in familial and sporadic adult-onset primary Dystonia.
- Neuropathology of cervical Dystonia.
- Non-Parkinson movement Disorders: Five new things.
- Dab2IP GTPase Activating Protein Regulates Dendrite Development and Synapse Number in Cerebellum.
- Neural expression of the transcription factor THAP1 during development in rat.
- Genotype-phenotype correlations in THAP1 Dystonia: molecular foundations and description of new cases.
- Mutations in CIZ1 cause adult onset primary cervical Dystonia.
- Comprehensive motor testing in Fmr1-KO mice exposes temporal defects in oromotor coordination.
- Blepharospasm plus Cervical Dystonia with Predominant Anterocollis: A Distinctive Subphenotype of Segmental Craniocervical Dystonia?
- An African-American family with Dystonia.
- Animal models of Dystonia: Lessons from a mutant rat.
- The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary Dystonia.
- Adult-onset leg Dystonia due to a missense mutation in THAP1.
- Localization of N-methyl-norsalsolinol within rodent and human Brain.
- Effect of resistance training on blood oxidative stress in Parkinson Disease.
- Abnormal motor function and dopamine neurotransmission in DYT1 DeltaGAG transgenic mice.
- Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice.
- Opposite functions of histamine H1 and H2 receptors and H3 receptor in substantia nigra pars reticulata.
- Subdivisions of inferior temporal cortex in squirrel monkeys make dissociable contributions to visual learning and memory.
- Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong Gait disorder in waddles mice.
- Rodent models for Dystonia research: characteristics, evaluation, and utility.
- Dropped head presentation of mitochondrial myopathy.
- Localization of preganglionic neurons that innervate choroidal neurons of pterygopalatine ganglion.
- Epilepsia partialis continua mistaken for Parkinson's Disease.
- Secondary cervical Dystonia associated with structural lesions of the central nervous system.
- Lyme neuroborreliosis manifesting as an intracranial mass lesion.
- Spinal cord stimulation for the failed Back syndrome.
- Stabilization of the cervical spine in spondyloepiphyseal dysplasia congenita.
- Surgically treated cavernous angiomas of the Brain stem: report of two cases and review of the literature.
- Spontaneous rupture of the stomach in an adult.
- Upregulation of foreBrain proenkephalin mRNA subsequent to NMDA receptor blockade.
- Topographic distribution of connections from the primary motor cortex to the corpus striatum in Aotus trivirgatus.
- Tularemia presenting with Ataxia.
- Chronic treatment with pentazocine or SFK 10047 decrease proenkephalin mRNA levels in the rat striatum and nucleus accumbens.
- Isolation stress increases tyrosine hydroxylase mRNA in the locus coeruleus and midBrain and decreases proenkephalin mRNA in the striatum and nucleus accumbens.
- Genomic effects of cold and isolation stress on magnocellular vasopressin mRNA-containing cells in the hypothalamus of the rat.
- Focal Dystonia secondary to cavernous angioma of the basal ganglia: case report and review of the literature.
- The DYT1 carrier state increases energy demand in the olivocerebellar network.
- Elevation of striatal and accumbal preproenkephalin, preprotachykinin and preprodynorphin mRNA abundance subsequent to N-methyl-D-aspartate receptor blockade with MK-801.
- Paroxysmal kinesigenic Dystonia associated with a medullary hemorrhage.
- Regulation by dopaminergic neurotransmission of dopamine D2 mRNA and receptor levels in the striatum and nucleus accumbens of the rat.
- Acute treatment with the N-methyl-D-aspartate receptor antagonist MK-801: effect of concurrent administration of haloperidol or scopolamine on preproenkephalin mRNA le...
- SPECT abnormalities in generalized Dystonia.
- Regulation of the tyrosine hydroxylase and dopamine beta-hydroxylase genes by the transcription factor AP-2.
- Severe bilateral Tremor in a liver transplant recipient taking cyclosporine.
- Glial elements contribute to stress-induced torsinA expression in the CNS and Peripheral nervous system.
- Novel THAP1 sequence variants in primary Dystonia.
- Inferior olive serotonin and norepinephrine levels during development in the genetically dystonic rat.
- Blink reflex to supraorbital Nerve stimulation in the cat.
- Serotonergic modulation of eye blinks in cat and monkey.
- Abnormal cerebellar output in the genetically dystonic rat.
- Caytaxin deficiency disrupts signaling pathways in cerebellar cortex.
- Single-unit activity of cerebellar nuclear cells in the awake genetically dystonic rat.
- Parasympathetic innervation of the meibomian glands in rats.
- Selective elimination of cerebellar output in the genetically dystonic rat.
- Cerebellectomy eliminates the motor syndrome of the genetically dystonic rat.
- Abnormal spontaneous and harmaline-stimulated Purkinje cell activity in the awake genetically dystonic rat.
- Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat.
- Developmental expression of rat torsinA transcript and protein.
- Cloning, developmental regulation and neural localization of rat epsilon-sarcoglycan.
- Blink-related sensorimotor anatomy in the rat.
- Immunohistochemical detection of wheat germ agglutinin-horseradish peroxidase (WGA-HRP).
- Cerebral cortical control of orbicularis oculi motoneurons.
- Murine central and Peripheral nervous system transcriptomes: comparative gene expression.
- Caytaxin deficiency causes generalized Dystonia in rats.
- Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors.
- Regional distribution of tetrahydroisoquinoline derivatives in rodent, human, and Parkinson''s Disease brain.
- Impaired leg extensor strength in individuals with Parkinson Disease and relatedness to functional mobility.
- Meige syndrome: what''s in a name?
- High-throughput mutational analysis of TOR1A in primary Dystonia.
- Effects of moderate-volume, high-load lower-body resistance training on strength and function in persons with Parkinson''s Disease: a pilot study.
- Projections from the hypothalamic paraventricular nucleus and the nucleus of the solitary tract to prechoroidal neurons in the superior salivatory nucleus: Pathways co...
- Delayed-onset oromandibular Dystonia after a cerebellar hemorrhagic stroke.
- Cerebellar cortical output encodes temporal aspects of rhythmic licking movements and is necessary for normal licking frequency.
- Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse.
- Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6.
- Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6.
- Dystonia: phenomenology.
Schools
Louisiana State Univ School Of Medicine In New Orleans
University Of Al Hospital
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
- MRI (Magnetic Resonance Imaging)
- Non-Cosmetic Chemodenervation
Conditions Treated
- Alzheimer's Background: yellow;'>Background: yellow;'>Disease
- Anterior Horn Background: yellow;'>Background: yellow;'>Disease
- Ataxia
- Autonomic Background: yellow;'>Disorders
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Doctors Specialties
- Neurology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Cross Blue Shield
- Network S
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Coventry Health Care of Tennessee PPO
- First Health (Coventry Health Care) PPO
- GEHA
- Choice Care PPO
- Mail Handlers Benefit Plan (MHBP)
- MedHealthInsurance
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Mutual of Omaha
- POMCO Group
- Qualchoice PPO
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Awards
- Memphis Magazine: Top Doctors
- CMS Meaningful Use Stage 1 Certification
Education
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University of Tennessee -
University of Alabama Medical Center -
Louisiana State University School of Medicine in New Orleans
Hospital
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Le Bonheur Children's Hospital -
University of Tennessee Medical Center
Drug Facts
| NPI NUMBER | 1407813439 | |
| NPPES Provider LastName | LEDOUX | |
| NPPES Provider FirstName | MARK | |
| NPPES Provider ZIPCode | 381322113 | |
| NPPES Provider State | TN | |
| Specialty Description | Emergency Medicine | |
| Total Claim Count | 1759.0 | |
| Distinct Opioid Count | 2.0 | |
| Opioid Claim Count | 36.0 | |
| Percent Opioid Claims | 2.05 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1407813439 |
| Last Name Of The Provider | LEDOUX |
| First Name Of The Provider | MARK |
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