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GALE JEANNIE HOBSON M.D.
M.D.
Family Medicine Physician
NPI: 1487893525IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
R0249(TX)25823(NE)
Education
BOSTON UNIVERSITY SCHOOL OF MEDICINE
Class of 2009
Research & Publications (20)
Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
PMID 19151366·J Child Neurol·2009
5-case
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.
PMID 19562355·Acta Neuropathol·2009
5-case
A large X-chromosomal deletion is associated with microphthalmia with linear skin defects (MLS) and amelogenesis imperfecta (XAI).
PMID 19610109·Am J Med Genet A·2009
5-case
Deletion of a splicing enhancer disrupts PLP1/DM20 ratio and myelin stability.
PMID 18835559·Exp Neurol·2008
7-preclinical
Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation.
PMID 17438221·Neurology·2007
5-case
Splice-site contribution in alternative splicing of PLP1 and DM20: molecular studies in oligodendrocytes.
PMID 16287154·Hum Mutat·2006
7-preclinical
Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect.
PMID 16374829·Ann Neurol·2006
5-case
PLP1 alternative splicing in differentiating oligodendrocytes: characterization of an exonic splicing enhancer.
PMID 16288477·J Cell Biochem·2006
7-preclinical
Search for memory effects in methane hydrate: structure of water before hydrate formation and after hydrate decomposition.
PMID 16268712·J Chem Phys·2005
8-other
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease.
PMID 15689360·Brain·2005
5-case
Supra-maximal effort and reaction and movement times in a non-compatible response time task.
PMID 16208301·J Sports Med Phys Fitness·2005
8-other
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.
PMID 16380909·Am J Hum Genet·2005
8-other
Team-referent attributions among sport performers.
PMID 16752446·Res Q Exerc Sport·2005
4-observational
A case of complicated spastic paraplegia 2 due to a point mutation in the proteolipid protein 1 gene.
PMID 15450775·J Neurol Sci·2004
5-case
Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy.
PMID 12601703·Ann Neurol·2003
4-observational
A PLP splicing abnormality is associated with an unusual presentation of PMD.
PMID 12325077·Ann Neurol·2002
7-preclinical
Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
PMID 12210342·Am J Med Genet·2002
8-other
A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.
PMID 11180600·Hum Mutat·2001
8-other
Evidence for neuroaxonal injury in patients with proteolipid gene mutations.
PMID 11723304·Neurology·2001
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
- 8288 S BROADWAY AVE
TYLER, TX 75703 - Phone
- (903) 606-7060
Quick Facts
- NPI
- 1487893525
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 17
- Publications
- 20
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