Mary Helen Michetti LMHC
Counselor/Therapist | Mental Health
8 PINETREE RD NANTUCKET MA, 02554About
Mary Michetti is an Addiction Medicine Physician in NANTUCKET, MA. Mary evaluates patients using many different procedures, in order to determine what treatments must be carried out in order to properly assess their symptoms. Addiction Medicine Physicians provide medical care in addition to consultation for each patient and their families.
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Expert Publications
Data provided by the National Library of Medicine- Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.
- Efficacy of an adeno-associated virus 8-pseudotyped vector in glycogen storage disease type II.
- Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease.
- Evasion of immune responses to introduced human acid alpha-glucosidase by liver-restricted expression in glycogen storage disease type II.
- Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.
- Enhanced efficacy of an AAV vector encoding chimeric, highly secreted acid alpha-glucosidase in glycogen storage disease type II.
- Enhanced response to enzyme replacement therapy in Pompe disease after the induction of immune tolerance.
- Correction of multiple striated muscles in murine Pompe disease through adeno-associated virus-mediated gene therapy.
- Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: a case study.
- A convenient LC-MS method for assessment of glucose kinetics in vivo with D-[13C6]glucose as a tracer.
- Gb(3)/creatinine biomarkers for Fabry disease: issues to consider.
- Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory.
- Impaired clearance of accumulated lysosomal glycogen in advanced Pompe disease despite high-level vector-mediated transgene expression.
- Immunomodulatory gene therapy prevents antibody formation and lethal hypersensitivity reactions in murine pompe disease.
- Quantification of the oxidative damage biomarker 2,3-dinor-8-isoprostaglandin-F(2alpha) in human urine using liquid chromatography-tandem mass spectrometry.
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