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EUGENE ENGLE, M.D.
M.D.
Family Medicine Physician
NPI: 1366426835Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD019421E(PA)
Research & Publications (20)
Oculomotility disorders arising from disruptions in brainstem motor neuron development.
PMID 17502461·Arch Neurol·2007
6-review
Congenital fibrosis syndrome associated with central nervous system abnormalities.
PMID 12819981·Graefes Arch Clin Exp Ophthalmol·2003
5-case
Congenital fibrosis of the extraocular muscles type 1, distinctive conjunctival changes and intrapapillary disc colobomata.
PMID 19373680·Ophthalmic Genet·2009
5-case
Synergistic divergence: a distinct ocular motility dysinnervation pattern.
PMID 19578026·Invest Ophthalmol Vis Sci·2009
8-other
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome.
PMID 19541263·J AAPOS·2009
5-case
The measurement of body-image dissatisfaction-satisfaction: is rating importance important?
PMID 18463010·Body Image·2008
4-observational
Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome.
PMID 18653847·Science·2008
7-preclinical
Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome.
PMID 18455936·J AAPOS·2008
5-case
Abnormalities of the oculomotor nerve in congenital fibrosis of the extraocular muscles and congenital oculomotor palsy.
PMID 17389489·Invest Ophthalmol Vis Sci·2007
8-other
Two pedigrees segregating Duane's retraction syndrome as a dominant trait map to the DURS2 genetic locus.
PMID 17197532·Invest Ophthalmol Vis Sci·2007
8-other
Magnetic resonance imaging of innervational and extraocular muscle abnormalities in Duane-radial ray syndrome.
PMID 18055799·Invest Ophthalmol Vis Sci·2007
8-other
Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locus.
PMID 17197533·Invest Ophthalmol Vis Sci·2007
8-other
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
PMID 17511870·BMC Genet·2007
8-other
High-resolution magnetic resonance imaging demonstrates abnormalities of motor nerves and extraocular muscles in patients with neuropathic strabismus.
PMID 16678748·J AAPOS·2006
8-other
Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.
PMID 16525029·J Med Genet·2006
5-case
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
PMID 16815872·Brain·2006
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
- 80 DOE RUN RD
MANHEIM, PA 17545 - Phone
- (717) 664-0952
Quick Facts
- NPI
- 1366426835
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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