AmirIsraelArbisserMD

Ophthalmology • Bettendorf, IA

Eye surgeons associates, PC

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Office
777 Tanglefoot Ln
Eye Surgeons Associates Pc
Bettendorf, IA 52722
Phone+1 563-323-2020

Fax+1 563-328-5694
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Education & Training

University of Texas Health Science Center at HoustonResidency, Ophthalmology, 1976 - 1979
Baylor College of MedicineClass of 1974

Certifications & Licensure

IL State Medical License 1987 - 2026
IA State Medical License 1979 - 2025
FL State Medical License 2016 - 2025
TX State Medical License 1974 - 2024
American Board of Ophthalmology Ophthalmology

Awards, Honors, & Recognition

CMS Meaningful Use Stage 1 Certification NextGen Ambulatory EHR, NextGen Healthcare, 2012-2013
Fellow (FAAO) American Academy of Ophthalmology

Publications & Presentations

PubMed

13 citations
The Sabinas syndrome
R. Rodney Howell, Amir I. Arbisser, David S. Parsons, Charles I. Scott, Ursula Fraustadt, William R. Collie, Robert N. Marshall, Oscar Cavazos Ibarra> ;American Journal of Human Genetics. 1981 Nov 1
Mesoectodermal dysgenesis: familial iris anomaly.
John H Drouilhet, Amir I Arbisser, Malcolm L. Mazow> ;Journal of Pediatric Ophthalmology. 1977 Nov 1
19 citations
Ocular findings in mannosidosis.
Amir I. Arbisser, A. Linn Murphree, Charles A. Garcia> ;American Journal of Ophthalmology. 1976 Sep 1
11 citations
An approach to the problem of noncompliance in a pediatric outpatient clinic.
Frederic P. Anderson, Daniel S. Rowe, Val C. Dean, Amir Arbisser> ;American Journal of Diseases of Children. 1971 Aug 1
A syndrome manifested by brittle hair with morphologic and biochemical abnormalities, developmental delay and normal stature.
Arbisser, A. I., Scott, C. I., Howell, R. R., Ong, P. S., Cox, H. L.> ;Birth Defects Orig Artic Ser. 1976
Rapid karyotypic diagnosis of a case of trisomy 18 in the neonatal intensive care unit.
Arbisser, A., Moore, C. M., Adcock, E. W., Morriss, F. H.> ;South Med J. 1977 Mar
Ocular findings in acid lipase deficiency.
Arbisser, A., Arbisser, L. B., Garcia, C. A., Akhtar, M., Moore, C. M., Howell, R. R.> ;Monogr Hum Genet. 1978
Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVB.
Arbisser, A. I., Donnelly, K. A., Scott, C. I., DiFerrante, N., Singh, J., Stevenson, R. E., Aylesworth, A. S., Howell, R. R.> ;Am J Med Genet. 1977
Letter: Mannosidosis and maternal penicillamine therapy.
Arbisser, A. I., Scott, C. I., Howell, B. R.> ;Lancet. 1976 Feb 7
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