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DIANA ESCOLAR, MD
MD
Neurology Physician
NPI: 1215014543Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD20110(DC)
Research & Publications (20)
Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy.
PMID 17044012·Ann Neurol·2006
5-case
CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophy.
PMID 15984021·Ann Neurol·2005
3-trial
Collaborative translational research leading to multicenter clinical trials in Duchenne muscular dystrophy: the Cooperative International Neuromuscular Research Group (CINRG).
PMID 12206809·Neuromuscul Disord·2002
6-review
Clinical evaluator reliability for quantitative and manual muscle testing measures of strength in children.
PMID 11360262·Muscle Nerve·2001
8-other
Pharmacologic and genetic therapy for childhood muscular dystrophies.
PMID 11898513·Curr Neurol Neurosci Rep·2001
6-review
Clinical features of late-onset Pompe disease: a prospective cohort study.
PMID 18816591·Muscle Nerve·2008
4-observational
Pediatric sciatic neuropathies due to unusual vascular causes.
PMID 18658074·J Child Neurol·2008
5-case
A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy.
PMID 18335515·Ann Neurol·2008
3-trial
Reliable surrogate outcome measures in multicenter clinical trials of Duchenne muscular dystrophy.
PMID 16969838·Muscle Nerve·2007
3-trial
CINRG pilot trial of oxatomide in steroid-naïve Duchenne muscular dystrophy.
PMID 17459739·Eur J Paediatr Neurol·2007
2-rct
Challenges in drug development for muscle disease: a stakeholders' meeting.
PMID 17068768·Muscle Nerve·2007
7-preclinical
Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE.
PMID 16971696·Neurology·2006
5-case
Translating mighty mice into neuromuscular therapeutics: is bigger muscle better?
PMID 16723694·Am J Pathol·2006
7-preclinical
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
PMID 16478798·Brain·2006
8-other
Update on diagnosis and treatment of hereditary and acquired polyneuropathies in childhood.
PMID 16106624·Suppl Clin Neurophysiol·2004
6-review
Simulation of the visible spectra for edible virgin oils: potential uses.
PMID 15104819·Appl Spectrosc·2004
8-other
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13.
PMID 12811539·Hum Genet·2003
8-other
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome.
PMID 12796536·Neurology·2003
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
- 111 MICHIGAN AVE NW
WASHINGTON, DC 20010 - Phone
- (202) 884-2610
Quick Facts
- NPI
- 1215014543
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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