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AMAAL STARLING, M.D.
M.D.
Neurology Physician
NPI: 1801058193IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
42240(AZ)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 2008
Research & Publications (20)
A family with McLeod syndrome and calpainopathy with clinically overlapping diseases.
PMID 16344536·Neurology·2005
5-case
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
PMID 15367920·Eur J Hum Genet·2004
8-other
Calpainopathy: how broad is the spectrum of clinical variability?
PMID 14645990·J Mol Neurosci·2003
8-other
Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
PMID 12210342·Am J Med Genet·2002
8-other
Emergence of multiclass drug-resistance in HIV-2 in antiretroviral-treated individuals in Senegal: implications for HIV-2 treatment in resouce-limited West Africa.
PMID 19143530·Clin Infect Dis·2009
8-other
A multi-exonic SPG4 duplication underlies sex-dependent penetrance of hereditary spastic paraplegia in a large Brazilian pedigree.
PMID 17895902·Eur J Hum Genet·2007
8-other
Dental indicators of health and stress in early Egyptian and Nubian agriculturalists: a difficult transition and gradual recovery.
PMID 17786997·Am J Phys Anthropol·2007
8-other
Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil.
PMID 16755493·Genet Mol Res·2006
8-other
Alterations in N-methyl-D-aspartate receptor sensitivity and magnesium blockade occur early in development in the R6/2 mouse model of Huntington's disease.
PMID 16211559·J Neurosci Res·2005
7-preclinical
Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13.
PMID 15852396·Ann Neurol·2005
5-case
Characteristics and presenting complaints of outpatients with undiagnosed HIV infection: potential utility in selecting subjects for HIV testing.
PMID 15602131·J Acquir Immune Defic Syndr·2004
8-other
Increased GABAergic function in mouse models of Huntington's disease: reversal by BDNF.
PMID 15505789·J Neurosci Res·2004
7-preclinical
[Executive functions in children with phenylketonuria: variations as a function of phenilalanine plasm level].
PMID 15273847·Arq Neuropsiquiatr·2004
8-other
Modulation of AMPA currents by D2 dopamine receptors in striatal medium-sized spiny neurons: are dendrites necessary?
PMID 15128399·Eur J Neurosci·2004
4-observational
NMDA receptor alterations in neurons from pediatric cortical dysplasia tissue.
PMID 15054078·Cereb Cortex·2004
3-trial
Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum.
PMID 14647208·Eur J Hum Genet·2003
8-other
The 10 autosomal recessive limb-girdle muscular dystrophies.
PMID 12921790·Neuromuscul Disord·2003
6-review
Evaluation of alternative reporter genes for the yeast two-hybrid system.
PMID 12917809·Genet Mol Res·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
- 13400 E SHEA BLVD
SCOTTSDALE, AZ 85259 - Phone
- (480) 301-8000
Quick Facts
- NPI
- 1801058193
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 18
- Publications
- 20
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