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GERMAN NERI, M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1407886898Individual
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
35-032276(OH)
Research & Publications (20)
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR.
PMID 19603064·Eur J Hum Genet·2010
8-other
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis.
PMID 19628475·Hum Mol Genet·2009
7-preclinical
The controlled deposition of metal oxides onto carbon nanotubes by atomic layer deposition: examples and a case study on the application of V2O4 coated nanotubes in gas sensing.
PMID 19421470·Phys Chem Chem Phys·2009
8-other
Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.
PMID 18805826·J Med Genet·2009
8-other
Management of recurrent otitis media with rapid maxillary expansion: our experience.
PMID 19455994·B-ENT·2009
8-other
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder.
PMID 19681062·Autism Res·2009
8-other
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
PMID 19215041·Am J Med Genet A·2009
6-review
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
PMID 18854871·Eur J Hum Genet·2009
8-other
A premature infant with Costello syndrome due to a rare G13C HRAS mutation.
PMID 19213030·Am J Med Genet A·2009
5-case
A missense mutation in CASK causes FG syndrome in an Italian family.
PMID 19200522·Am J Hum Genet·2009
8-other
Silent beginning: early silencing of the MED1/MBD4 gene in colorectal tumorigenesis.
PMID 19182514·Cancer Biol Ther·2009
8-other
Elements of morphology: standard terminology for the head and face.
PMID 19125436·Am J Med Genet A·2009
8-other
Correlation between GJB2 mutations and audiological deficits: personal experience.
PMID 18668259·Eur Arch Otorhinolaryngol·2009
8-other
Mesenchymal stromal cells multipotency and plasticity: induction toward the hepatic lineage.
PMID 19530515·Eur Rev Med Pharmacol Sci·2009
8-other
Delayed facial nerve paralysis post middle ear surgery: herpes simplex virus activation.
PMID 19456000·B-ENT·2009
5-case
Hypo-phosphorylation of salivary peptidome as a clue to the molecular pathogenesis of autism spectrum disorders.
PMID 19367726·J Proteome Res·2008
8-other
No reason yet to change diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes.
PMID 19047498·J Med Genet·2008
8-other
On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
PMID 18932124·Am J Med Genet C Semin Med Genet·2008
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 14601 DETROIT AVE STE 730
LAKEWOOD, OH 44107 - Phone
- (216) 226-3577
Quick Facts
- NPI
- 1407886898
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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