Back to Search
ANDREA GROPMAN, M.D.
M.D.
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1407848005Individual
Specialties, Licenses & Credentials
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
22096(DC)72510(TN)
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
22096(DC)
Pediatrics Physician
Pediatrics
Code: 208000000X
22096(DC)
Research & Publications (20)
Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.
PMID 19567648·Radiology·2009
8-other
1H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations.
PMID 18262815·Mol Genet Metab·2008
5-case
New developments in Smith-Magenis syndrome (del 17p11.2).
PMID 17351481·Curr Opin Neurol·2007
6-review
Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2).
PMID 16647992·Pediatr Neurol·2006
6-review
The neurological presentations of childhood and adult mitochondrial disease: established syndromes and phenotypic variations.
PMID 16120409·Mitochondrion·2004
8-other
Imaging of neurogenetic and neurometabolic disorders of childhood.
PMID 14984686·Curr Neurol Neurosci Rep·2004
6-review
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C.
PMID 19415691·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Children with infantile neuronal ceroid lipofuscinosis have an increased risk of hypothermia and bradycardia during anesthesia.
PMID 19608805·Anesth Analg·2009
8-other
Clinical NOE 13C MRS for neuropsychiatric disorders of the frontal lobe.
PMID 18829354·J Magn Reson·2008
8-other
A 2-year-old male with developmental delay, irritability, and failure to thrive.
PMID 18710135·Pediatr Ann·2008
5-case
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
PMID 17607705·Am J Med Genet A·2007
8-other
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.
PMID 17079881·Genet Med·2006
8-other
The common deletion found in patient reexamined after 33 years and comparison with complete mtDNA sequences of maternal relatives.
PMID 16172025·Mitochondrion·2005
5-case
Monitoring gamma-hydroxybutyric acid levels in succinate-semialdehyde dehydrogenase deficiency.
PMID 15048909·Ann Neurol·2004
8-other
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.
PMID 14735585·Am J Med Genet A·2004
5-case
Nck beta interacts with tyrosine-phosphorylated disabled 1 and redistributes in Reelin-stimulated neurons.
PMID 14517291·Mol Cell Biol·2003
7-preclinical
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
- 262 DANNY THOMAS PL
MEMPHIS, TN 38105 - Phone
- (901) 595-3300
Quick Facts
- NPI
- 1407848005
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 2
- Publications
- 20
Are you this provider?
Claim Your Profile