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MARCO DOTTI, MD
MD
Neurology Physician
NPI: 1508916263IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
44230(WI)
Education
OTHER
Class of 1987
Research & Publications (20)
Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.
PMID 18829627·J Neurol Neurosurg Psychiatry·2009
8-other
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant.
PMID 19444543·J Neurol·2009
5-case
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
PMID 19105190·Hum Mutat·2009
8-other
Occurrence of ankylosing spondylitis and multiple sclerosis-like syndrome in a HLA-B27 positive patient.
PMID 19444380·Neurol Sci·2009
5-case
Apoptosis in CADASIL: an in vitro study of lymphocytes and fibroblasts from a cohort of Italian patients.
PMID 19180562·J Cell Physiol·2009
8-other
Two cases of hemichorea-hemiballism with nonketotic hyperglycemia: a new point of view.
PMID 19305947·Neurol Sci·2009
5-case
Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry.
PMID 18226551·Neuroimage·2008
8-other
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy.
PMID 18500496·J Neurol·2008
8-other
CSF levels of beta-amyloid 1-42, tau and phosphorylated tau protein in CADASIL.
PMID 18803653·Eur J Neurol·2008
8-other
Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
PMID 18842453·Clin Neurophysiol·2008
8-other
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia.
PMID 18813041·Anesthesiology·2008
8-other
Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.
PMID 17768021·Brain Dev·2008
5-case
Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
PMID 18803652·Eur J Neurol·2008
8-other
A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.
PMID 18022198·J Neurol Sci·2008
5-case
Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics.
PMID 18672073·Neuroimage·2008
8-other
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNA.
PMID 18603265·J Neurol Sci·2008
5-case
Brain structural damage in spinocerebellar ataxia type 2. A voxel-based morphometry study.
PMID 18311829·Mov Disord·2008
8-other
Brain structural damage in Friedreich's ataxia.
PMID 17634216·J Neurol Neurosurg Psychiatry·2008
8-other
MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome.
PMID 18080849·J Neurol·2008
8-other
The first cerebrotendinous xanthomatosis family from Argentina: a new mutation in CYP27A1 gene.
PMID 18227423·Neurology·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 824 ILLINOIS AVENUE
STEVENS POINT, WI 54481 - Phone
- (715) 342-7500
Quick Facts
- NPI
- 1508916263
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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