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RACHEL SPIEGEL, M.D.
M.D.
Family Medicine Physician
NPI: 1881905156IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
164866(NC)0101253879(VA)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF VIRGINIA SCHOOL OF MEDICINE
Class of 2010
Research & Publications (20)
Severe meningoencephalitis due to late reactivation of Varicella-Zoster virus in an immunocompetent child.
PMID 19494359·J Child Neurol·2010
5-case
Norms for change in episodic memory as a prerequisite for the diagnosis of mild cognitive impairment (MCI).
PMID 19254092·Neuropsychology·2009
8-other
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mapping.
PMID 19140180·Am J Med Genet A·2009
5-case
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
PMID 19525956·Nat Genet·2009
8-other
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations.
PMID 19157875·Neuromuscul Disord·2009
5-case
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews.
PMID 19259137·Eur J Hum Genet·2009
5-case
Impact of APOE status on cognitive maintenance in healthy elderly persons.
PMID 18615849·Int J Geriatr Psychiatry·2009
8-other
Late relapse of herpes simplex virus encephalitis in a child due to reactivation of latent virus: clinicopathological report and review.
PMID 18230840·J Child Neurol·2008
5-case
Very-late-onset Friedreich ataxia with disturbing head tremor and without spinal atrophy--a case report.
PMID 18361475·Mov Disord·2008
5-case
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis.
PMID 18439547·Am J Hum Genet·2008
8-other
Value of routine screening for bone demineralization in an urban population of patients with epilepsy.
PMID 18164901·Epilepsy Res·2008
8-other
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.
PMID 17372854·J Inherit Metab Dis·2007
5-case
Founder effect with variable age at onset in Arab families with Lafora disease and EPM2A mutation.
PMID 17509003·Epilepsia·2007
4-observational
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
PMID 17846997·Am J Hum Genet·2007
8-other
Pseudomonas stutzeri knee arthritis in a child: case report and review.
PMID 17909340·J Pediatr Orthop B·2007
5-case
Retrospective evaluation of an intensive method of treatment for children with pervasive developmental disorder.
PMID 17942455·Autism·2007
8-other
The variable clinical phenotype of liver glycogen synthase deficiency.
PMID 18341095·J Pediatr Endocrinol Metab·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2955 IVY RD STE 205
CHARLOTTESVILLE, VA 22903 - Phone
- (434) 243-4500
Quick Facts
- NPI
- 1881905156
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 16
- Publications
- 20
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