Associate Professor, Medicine, University of Wisconsin Medical School
Cardiology
Dr. Giorgio Gimelli, MD
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Giorgio Gimelli is an expert in the field of Cardiology. He has 2 awards "Meaningful Use Stage 1 Certification" and "Fellow (FACC)". Giorgio Gimelli, MD is a published physician as well. He has 96 publications published. The latest was: Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome. He is registered with Medicare.
Publications
- Chronic Total Occlusion and Successful Drug-Eluting Stent Placement in Takayasu Arteritis Induced Renal Artery Stenosis.
- Diagnosis and Treatment of Peripheral Arterial Disease in CKD Patients.
- Pre PCI hospital antithrombotic therapy for ST elevation Myocardial infarction: striving for consensus.
- Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.
- T-cell apoptosis in ICF Syndrome.
- Late Acute thrombosis after coronary brachytherapy: when is the risk over?
- Satellite 2 methylation patterns in normal and ICF Syndrome cells and association of hypomethylation with advanced replication.
- Immediate and long-term clinical and angiographic results from Wiktor stent treatment for true bifurcation narrowings.
- A novel case of immunodeficiency, centromeric instability, and facial anomalies (the ICF Syndrome): immunologic and cytogenetic studies.
- Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation.
- Gene dosage of the spermidine/spermine N(1)-acetyltransferase ( SSAT) gene with putrescine accumulation in a patient with a Xp21.1p22.12 duplication and keratosis foll...
- A randomized comparison of direct stenting versus stenting with predilatation in native Coronary artery disease: results from the multicentric Crosscut study.
- Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman Syndrome patients with class II (BP2/3) deletions.
- Regional thrombolytic therapy and stent implantation in an Acutely occluded aortobifemoral bypass graft.
- Conservative vs. invasive treatment of aortocoronary saphenous vein graft Aneurysms: Treatment algorithm based upon a large series.
- Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?
- Molecular characterization of a t(2;6) balanced translocation that is associated with a complex phenotype and leads to truncation of the TCBA1 gene.
- A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studies.
- Vertebral Artery embolic protection via ipsilateral brachial approach during left subclavian Artery angioplasty and stenting--a case report.
- Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis.
- Treatment of an Angio-Seal-related vascular complication using the SilverHawk plaque excision system: a case report.
- Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.
- The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patie...
- Characterization of a recurrent 15q24 microdeletion Syndrome.
- Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation.
- Delayed complete Heart block secondary to jailed first septal perforator.
- Does detection of Carotid plaque affect physician behavior or motivate patients?
- How I do it: directional atherectomy for in-stent restenosis of a PTFE arteriovenous graft.
- How I do it: preferential use of the right external jugular vein for tunneled catheter placement.
- A recurrent 15q13.3 microdeletion Syndrome associated with mental retardation and seizures.
- Percutaneous closure of a large PDA in a 35-year-old man with elevated Pulmonary vascular resistance.
- Long-term survival using intra-Aortic balloon pump and percutaneous right ventricular assist device for biventricular mechanical support of cardiogenic shock.
- Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.
- How I do it: endovascular stent deployment using a novel technique that obviates the need for introducer-sheath upsizing.
- Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
- Hemodynamically supported percutaneous Coronary revascularization improves left ventricular function in patients with ischemic dilated cardiomyopathy at very high risk...
- A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms.
- Complex pathogenesis of Hirschsprung''s Disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11).
- The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma.
- An interesting case: retrograde blood flow from a LIMA sustaining hemodialysis via an AVF.
- Arterial interventions in arteriovenous access and chronic kidney Disease: a role for interventional nephrologists.
- Low-copy repeats on chromosome 22q11.2 show replication timing switches, DNA flexibility peaks and stress inducible asynchrony, sharing instability features with fragi...
- A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion Syndromes.
- Altered intra-nuclear organisation of heterochromatin and genes in ICF Syndrome.
- Array-CGH analysis in a patient with WAGR Syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation.
- Mutations in SOX17 are associated with Congenital anomalies of the kidney and the urinary tract.
- Microarray based analysis of an inherited terminal 3p26.3 deletion, containing only the CHL1 gene, from a normal father to his two affected children.
- Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies Syndrome type 2.
- A de novo balanced translocation t(7;12)(p21.2;p12.3) in a patient with Saethre-Chotzen-like phenotype downregulates TWIST and an osteoclastic protein-tyrosine phospha...
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
- West Syndrome associated with 14q12 duplications harboring FOXG1.
- A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko...
- Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF Syndrome).
- Correction for simultaneous catheter eccentricity and tilt in intravascular elastography.
- Carotid artery stenting in the first 100 consecutive patients: results and follow up.
- Mapping of the human COL5A1 gene to chromosome 9q34.3.
- Concomitant Turner Syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52.
- Roberts Syndrome: phenotypic variation, cytogenetic definition and heterozygote detection.
- Prenatal diagnosis of a partial 8p trisomy.
- Contiguous gene Syndromes due to deletions in the distal short arm of the human X chromosome.
- False-positive and false-negative findings on chorionic villus sampling.
- [New line of human neuroblastoma derived from bone marrow].
- The fetal pathology of the XXXXY-Syndrome.
- Dup(3)(p2----pter) in two families, including one infant with cyclopia.
- First trimester fetal karyotyping: one thousand diagnoses.
- Y-dependent polypeptides identified by two-dimensional gel electrophoresis of monozygotic X0 and XY fibroblasts.
- [A case of partial 9p monosomy].
- G-bands without pretreatment of slides, in chemically defined conditions.
- Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaic.
- A new biallelic DNA polymorphism of the human COL5A1 gene.
- Definitive assignment of the growth hormone-releasing factor gene to 20q11.2.
- Genotypic, phenotypic and biological characterization of a novel human lung adenocarcinoma cell line (LC 89)
- Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
- ICF Syndrome with variable expression in sibs.
- Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring Syndrome is caused by ring instability.
- Are the nail-patella Syndrome and the autosomal Goltz-like Syndrome the phenotypic expressions of different alleles at the COL5A1 locus?
- The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.
- The phenotype of a 45,X male with a Y/18 translocation.
- [18q Syndrome with deficiency of myelin basic protein (MBP)].
- Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres.
- Spectrum of clinical features associated with interstitial chromosome 22q11 deletions.
- Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome.
- Transmission of a fully functional human neocentromere through three generations.
- Frequency of silent myocardial ischemia following Coronary stenting.
- Primary versus rescue percutaneous coronary intervention in patients with Acute myocardial infarction.
- Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital Heart defects.
- A neocentromere in the DAZ region of the human Y chromosome.
- CENP-G in neocentromeres and inactive centromeres.
- Escape from gene silencing in ICF Syndrome: evidence for advanced replication time as a major determinant.
- Genetic variation in ICF Syndrome: evidence for genetic heterogeneity.
- Surgical and percutaneous Myocardial angiogenesis induction. Part I--laser revascularization.
- Intravascular ultrasound criteria for the assessment of the functional significance of intermediate Coronary artery stenoses and comparison with fractional flow reserve.
- Molecular characterisation of a supernumerary ring chromosome in a patient with VATER association.
- Endovascular treatment of a noninfected anastomotic juxtarenal aortic Aneurysm.
- Surgical and percutaneous Myocardial angiogenesis induction. Part II--neoangiogenesis.
Schools
Universita Degli Studi Di Genova Facolta Di Medicina E Chirurgia
Presby Med Center
Thomas Jefferson University Hospital
Procedures Preformed
- Ablation for Treatment of Cardiac Arrhythmias
- Cardiac Catheterization (incl. Coronary Angiography)
- Cardiac Imaging
- Cardiac MRI (Magnetic Resonance Imaging) of Heart or Chest
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Conditions Treated
- Aneurysm and Dissection of Heart
- Angina and Acute Coronary Syndrome
- Aortic Aneurysm
- Aortic Dissection
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Doctors Specialties
- Cardiology
- Interventional Cardiology
Accepted Insurances
Awards
- Meaningful Use Stage 1 Certification
- Fellow (FACC)
Education
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Thomas Jefferson University -
University of Pennsylvania -
University of Genoa Faculty of Medicine
Hospital
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Meriter UnityPoint Health -
University of Wisconsin Hospital and Clinics -
William S. Middleton Memorial Veterans Hospital
Drug Facts
| NPI NUMBER | 1629044706 | |
| NPPES Provider LastName | GIMELLI | |
| NPPES Provider FirstName | GIORGIO | |
| NPPES Provider ZIPCode | 537920001 | |
| NPPES Provider State | WI | |
| Specialty Description | Cardiology | |
| Total Claim Count | 1718.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1629044706 |
| Last Name Of The Provider | GIMELLI |
| First Name Of The Provider | GIORGIO |
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