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ANGELO FEDERICO, DO
DO
Surgery Physician
NPI: 1306539242Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
5151016258(MI)
Research & Publications (20)
Leukoencephalopathy in 21-beta hydroxylase deficiency: report of a family.
PMID 19427150·Brain Dev·2010
5-case
Intestinal permeability in patients with chronic liver diseases: Its relationship with the aetiology and the entity of liver damage.
PMID 19502117·Dig Liver Dis·2010
8-other
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
PMID 19105190·Hum Mutat·2009
8-other
A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency.
PMID 19223931·Eur J Hum Genet·2009
5-case
Apoptosis in CADASIL: an in vitro study of lymphocytes and fibroblasts from a cohort of Italian patients.
PMID 19180562·J Cell Physiol·2009
8-other
Robust phase recovery in temporal speckle pattern interferometry using a 3D directional wavelet transform.
PMID 19649089·Opt Lett·2009
8-other
Occurrence of ankylosing spondylitis and multiple sclerosis-like syndrome in a HLA-B27 positive patient.
PMID 19444380·Neurol Sci·2009
5-case
Cerebellar and pyramidal dysfunctions, palpebral ptosis and weakness as presenting symptoms of PARK-2.
PMID 18973255·Mov Disord·2009
5-case
Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.
PMID 18829627·J Neurol Neurosurg Psychiatry·2009
8-other
Neuropsychological and MRI measures predict short-term evolution in benign multiple sclerosis.
PMID 19641173·Neurology·2009
8-other
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population.
PMID 19084844·J Neurol Sci·2009
5-case
Two cases of hemichorea-hemiballism with nonketotic hyperglycemia: a new point of view.
PMID 19305947·Neurol Sci·2009
5-case
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant.
PMID 19444543·J Neurol·2009
5-case
Voxel-wise assessment of progression of regional brain atrophy in relapsing-remitting multiple sclerosis.
PMID 19286193·J Neurol Sci·2009
8-other
Neuromyotonia as paraneoplastic manifestation of bladder carcinoma.
PMID 19249799·J Neurol Sci·2009
5-case
Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy.
PMID 18984949·Cerebrovasc Dis·2008
4-observational
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
PMID 18946002·Neurology·2008
5-case
Phase retrieval of singular scalar light fields using a two-dimensional directional wavelet transform and a spatial carrier.
PMID 18830312·Appl Opt·2008
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
- 18101 OAKWOOD BLVD
DEARBORN, MI 48124 - Phone
- (313) 593-7795
Quick Facts
- NPI
- 1306539242
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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