Dr. Alfred Ephraim Slonim M.D.
Geneticist | Molecular Genetic Pathology
2001 Marcus Ave Suite N210 New Hyde Park NY, 11042About
Dr. Alfred Slonim practices Genetic Medicine in New Hyde Park, NY. As a geneticist, Dr. Slonim performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Slonim carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
University of Melbourne Faculty of Medicine 1958
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review.
- Amino acid and hormonal response to long-term nocturnal nasogastric feeding therapy of glycogen storage disease type I (GSD-I).
- Amino acid and hormonal response to long-term nocturnal nasogastric feeding therapy of glycogen storage disease type I (GSD-I).
- A preliminary study of growth hormone therapy for Crohn's disease.
- Identification of two subtypes of infantile acid maltase deficiency.
- Successful treatment of severe type I glycogen storage disease with neonatal presentation by nocturnal intragastric feeding.
- Successful treatment of severe type I glycogen storage disease with neonatal presentation by nocturnal intragastric feeding.
- Combined biochemical and molecular diagnosis in blood of a common lipid myopathy.
- Type I glycogen storage disease: a metabolic basis for advances in treatment.
- Type I glycogen storage disease: a metabolic basis for advances in treatment.
- Effect of streptozotocin on red-blood-cell-reduced glutathione: modification by glucose, nicotinamide, and epinephrine.
- Effect of streptozotocin on red-blood-cell-reduced glutathione: modification by glucose, nicotinamide, and epinephrine.
- Biotinidase deficiency: novel mutations and their biochemical and clinical correlates.
- Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: pathognomonic finding of two-dimensional electrophoresis?
- Modification of the natural history of adult-onset acid maltase deficiency by nutrition and exercise therapy.
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