Dr. Michael G Sweeney M.D.
Internist
725 S Queen St Dover DE, 19904Rating
4/5
About
Dr. Michael Sweeney is an internist practicing in Dover, DE. Dr. Sweeney specializes in the medical treatment of adults. Internists can act as a primary physician or a consultant to a primary physician. They manage both common and rare diseases. Dr. Sweeney provides comprehensive care and manages treatment with surgeons as well. Internists establish long-term relationships with their patients and incorporate disease prevention and mental health care into their practice.
Education and Training
Georgetown Univ Sch of Med, Washington Dc 1982
University of Maryland School of Medicine 1978
Georgetown University School of Medicine 1982
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Phenotypic variation of a new P0 mutation in genetically identical twins.
- A family with Friedreich ataxia and onion-bulb formations at sural nerve biopsy.
- Increased risk of stroke in patients with the A12308G polymorphism in mitochondria.
- Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.
- Cardiac abnormalities in patients with Leber's hereditary optic neuropathy.
- Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A.
- Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation.
- Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy.
- Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplication.
- Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
- Prenatal diagnosis of mitochondrial DNA8993 T----G disease.
- Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutation.
- What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed.
- Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis.
- Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients.
Treatments
- Diabetes
- Eczema
- Dermatitis
- Obesity
- Allergies
- Type 2 Diabetes
- Contact Dermatitis
- Hay Fever (allergic Rhinitis)
- Pain
- Vascular Disease
Dr. Michael G Sweeney M.D.'s Practice location
Practice At 725 S Queen St
725 S Queen St -Dover, DE 19904Get Direction
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Nearest Hospitals
BAYHEALTH - MILFORD MEMORIAL HOSPITALl
21 WEST CLARKE AVENUE MILFORD DE 19963UNIVERSITY OF MD SHORE MEDICAL CTR AT CHESTERTOWNl
100 BROWN STREET CHESTERTOWN MD 21620