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SANDRO CORTI, M.D.
M.D.
Neurology Physician
NPI: 1538503131IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
99195(MT)20702(NH)2020006664(MO)T3605(TX)MD473920(PA)4301111757(MI)ME144175(FL)
Hospitalist Physician
Hospitalist
Code: 208M00000X
ME144175(FL)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 2013
Research & Publications (20)
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.
PMID 19632744·Neurobiol Aging·2011
8-other
Clinical studies in stem cells transplantation for stroke: a review.
PMID 19485911·Curr Vasc Pharmacol·2010
6-review
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation.
PMID 17889967·Neurobiol Aging·2009
5-case
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
PMID 19000626·J Neurol Sci·2009
8-other
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.
PMID 19278689·J Neurol Sci·2009
1-meta
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
PMID 19236453·Eur J Neurol·2009
8-other
Aphasic and visual aura with increased vasogenic leakage: an atypical migrainosus status.
PMID 19573879·J Neurol Sci·2009
5-case
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies.
PMID 19091718·J Neurol Neurosurg Psychiatry·2009
5-case
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
PMID 19475721·Clin Genet·2009
8-other
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
PMID 19409522·Am J Hum Genet·2009
5-case
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
PMID 17888545·Neurobiol Aging·2009
8-other
Prevalence and characteristics of Shiga toxin-producing Escherichia coli in Swiss raw milk cheeses collected at producer level.
PMID 18565913·J Dairy Sci·2008
7-preclinical
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients.
PMID 18708572·J Neurol Neurosurg Psychiatry·2008
8-other
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy.
PMID 18769634·J Clin Invest·2008
7-preclinical
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion.
PMID 18804219·J Neurol Sci·2008
8-other
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
PMID 18946002·Neurology·2008
5-case
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency.
PMID 17936304·J Neurol Sci·2008
8-other
Absence of angiogenic genes modification in Italian ALS patients.
PMID 17113198·Neurobiol Aging·2008
8-other
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice.
PMID 17503505·Ann Neurol·2007
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 · 4 locations total
- Address
- 1250 S CEDAR CREST BLVD STE 405
ALLENTOWN, PA 18103 - Phone
- (610) 402-8420
Locations (4)
Quick Facts
- NPI
- 1538503131
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 9
- Locations
- 4
- Years in Practice
- 13
- Publications
- 20
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