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TERRY HEIMAN-PATTERSON, MD
MD
Neurology Physician
NPI: 1437100559IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD021242E(PA)
CMS Specialties
PrimaryNEUROLOGY
Education
ALBANY MEDICAL COLLEGE OF UNION UNIVERSITY
Class of 1975
Research & Publications (17)
Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS.
PMID 16024047·J Neurol Sci·2005
4-observational
Lithium may slow progression of amyotrophic lateral sclerosis, but further study is needed.
PMID 18417448·Proc Natl Acad Sci U S A·2008
8-other
The ALSSQOL: balancing physical and nonphysical factors in assessing quality of life in ALS.
PMID 17101900·Neurology·2006
8-other
High-frequency chest wall oscillation in ALS: an exploratory randomized, controlled trial.
PMID 17000967·Neurology·2006
3-trial
Sensory testing in the assessment of laryngeal sensation in patients with amyotrophic lateral sclerosis.
PMID 16900807·Ann Otol Rhinol Laryngol·2006
4-observational
Effect of transgene copy number on survival in the G93A SOD1 transgenic mouse model of ALS.
PMID 15519671·Brain Res Mol Brain Res·2004
4-observational
A randomized, placebo-controlled trial of topiramate in amyotrophic lateral sclerosis.
PMID 12939417·Neurology·2003
3-trial
High-dose cyclophosphamide without stem-cell rescue for refractory CIDP.
PMID 12084892·Neurology·2002
8-other
GLT-1 glutamate transporter levels are unchanged in mice expressing G93A human mutant SOD1.
PMID 11790392·J Neurol Sci·2002
7-preclinical
Posttranslational modifications of recombinant myotube-synthesized human factor IX.
PMID 11133752·Blood·2001
4-observational
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM.
PMID 11694553·J Med Genet·2001
8-other
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
PMID 11685207·Nat Genet·2001
8-other
Elevated cortical extracellular fluid glutamate in transgenic mice expressing human mutant (G93A) Cu/Zn superoxide dismutase.
PMID 10737625·J Neurochem·2000
7-preclinical
Malignant hyperthermia-like episode in Becker muscular dystrophy.
PMID 11149452·Anesthesiology·2000
5-case
Patch clamp studies of the thr1313met mutant sodium channel causing paramyotonia congenita.
PMID 11054753·Muscle Nerve·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 3509 N BROAD ST
PHILADELPHIA, PA 19140 - Phone
- (215) 707-3040
Quick Facts
- NPI
- 1437100559
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 51
- Publications
- 17
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