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DR. THOMAS F. BIRD M.D.
M.D.
Anesthesiology Physician
NPI: 1053397380Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
26355-020(WI)
Research & Publications (20)
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.
PMID 19139049·Hum Mol Genet·2009
8-other
A patient with Huntington's disease and long-surviving fetal neural transplants that developed mass lesions.
PMID 19057918·Acta Neuropathol·2009
5-case
Ultrastructure of spermatozoa of Solifuges (Arachnida, Solifugae): possible characters for their phylogeny?
PMID 18774581·Tissue Cell·2009
7-preclinical
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.
PMID 19567404·Hum Mol Genet·2009
8-other
Late onset Huntington Disease: clinical and genetic characteristics of 34 cases.
PMID 18977004·J Neurol Sci·2009
8-other
Detergent-insoluble EAAC1/EAAT3 aberrantly accumulates in hippocampal neurons of Alzheimer's disease patients.
PMID 18624794·Brain Pathol·2009
8-other
Progranulin plasma levels in the diagnosis of frontotemporal dementia.
PMID 19224898·Brain·2009
8-other
Trends in hospitalizations for neonatal jaundice and kernicterus in the United States, 1988-2005.
PMID 19171618·Pediatrics·2009
8-other
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
PMID 19451530·Neurology·2009
8-other
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.
PMID 19562355·Acta Neuropathol·2009
5-case
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.
PMID 18980218·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
PMID 18396105·Lancet Neurol·2008
8-other
An investigation of bacteriological and chemical water quality and the barriers to private well water sampling in a Southwestern Ontario Community.
PMID 18401117·J Water Health·2008
4-observational
Silver syndrome: The complexity of complicated hereditary spastic paraplegia.
PMID 18490616·Neurology·2008
8-other
Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.
PMID 18093156·Eur J 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
- 2323 N LAKE DR
MILWAUKEE, WI 53211 - Phone
- (414) 291-1000
Quick Facts
- NPI
- 1053397380
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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