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American Journal of Medical Genetics|September 1, 1993
Mucolipidosis type IV: a mild form with late onsetS Reis, R N Sheffer, S Merin, et al.Journal of Pediatric Ophthalmology and Strabismus|March 1, 1980
Chediak-Higashi syndrome: ocular findingsD BenEzra, F Mengistu, G Cividalli, et al.The British Journal of Ophthalmology|July 9, 1999
Cone and rod dysfunction in the NARP syndromeI Chowers, T Lerman-Sagie, O N Elpeleg, et al.American Journal of Physical Anthropology|July 1, 1982
Comparison of ultrasound and skinfold measurements in assessment of subcutaneous and total fatnessG A Borkan, D E Hults, J Cardarelli, et al.The British Journal of Ophthalmology|December 1, 1982
Combined vitamin A and E therapy prevents retinal electrophysiological deterioration in abetalipoproteinaemiaS Bishara, S Merin, M Cooper, et al.The British Journal of Ophthalmology|August 1, 1989
Corneal subepithelial monoclonal kappa IgG deposits in essential cryoglobulinaemiaI Kremer, P Wright, S Merin, et al.American Journal of Industrial Medicine|November 20, 2002
Significance of radiation exposure from work-related chest X-rays for epidemiological studies of radiation workersJ Cardarelli, H Spitz, C Rice, et al.Clinical Nephrology|April 1, 1986
A family with retinitis pigmentosa and ESRD with late presentation, hypertension and absence of polyuria or salt wastingM M Friedlaender, D Rubinger, J Silver, et al.Journal of Medical Genetics|December 1, 1995
Familial café au lait spots: a variant of neurofibromatosis type 1D Abeliovich, Z Gelman-Kohan, S Silverstein, et al.American Journal of Medical Genetics|December 1, 1994
Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic toolS Elyakim, I Lerer, J Zlotogora, et al.Pageof 7