Associate Professor of Medicine, Johns Hopkins University School of Medicine; Medical Director, Center for Inherited Heart Disease
Cardiology
Dr. Daniel Judge, MD
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Daniel Judge practices Cardiology. He attended Perelman School of Medicine at the University of Pennsylvania. He has 1 awards "CMS Meaningful Use Stage 1 Certification". Daniel Judge is a published MD. He has 19 papers published. The most current publication "Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells."
Publications
- Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
- Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
- Mitral Valve disease-morphology and mechanisms.
- Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.
- Yield of Serial Evaluation in At-Risk Family Members of Patients With ARVD/C.
- Sildenafil does not improve Cardiomyopathy in Duchenne/Becker muscular dystrophy.
- Novel and Highly Lethal NKX2.5 Missense Mutation in a Family With Sudden Death and Ventricular Arrhythmia.
- Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic Cardiomyopathy.
- A Pkd1-Fbn1 Genetic Interaction Implicates TGF-β Signaling in the Pathogenesis of Vascular Complications in Autosomal Dominant Polycystic Kidney Disease.
- Exercise Increases Age-Related Penetrance and Arrhythmic Risk in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated Desmosomal Mutation Carriers.
- Malignant Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy with a normal 12-lead electrocardiogram: A rare but underrecognized clinical entity.
- Mutation-Positive Arrhyhmogenic Right Ventricular Dysplasia/Cardiomyopathy: The Triangle of Dysplasia Displaced.
- LMNA-Associated Cardiocutaneous Progeria: An Inherited Autosomal Dominant Premature Aging Syndrome With Late Onset.
- A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial Syndrome.
- Prolonged RV endocardial activation duration: a novel marker of arrhythmogenic right ventricular dysplasia/Cardiomyopathy.
- Transthyretin cardiac amyloidosis: pathogenesis, treatments, and emerging role in Heart failure with preserved ejection fraction.
- Exercise has a Disproportionate Role in the Pathogenesis of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in Patients Without Desmosomal Mutations.
- Mutations in Alström protein impair terminal differentiation of cardiomyocytes.
Schools
University Of Pennsylvania School Of Medicine
Johns Hopkins University School Med
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
- Acute Venous Embolism Thrombosis
- Angina and Acute Coronary Syndrome
- Aortic Aneurysm
- Aortic Dissection
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Doctors Specialties
- Cardiology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Johns Hopkins University -
Perelman School of Medicine at the University of Pennsylvania
Hospital
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Johns Hopkins Hospital
Drug Facts
| NPI NUMBER | 1790726917 | |
| NPPES Provider LastName | JUDGE | |
| NPPES Provider FirstName | DANIEL | |
| NPPES Provider ZIPCode | 212870005 | |
| NPPES Provider State | MD | |
| Specialty Description | Cardiology | |
| Total Claim Count | 194.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1790726917 |
| Last Name Of The Provider | JUDGE |
| First Name Of The Provider | DANIEL |
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