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S Merin

Showing results (61-70 of 76) with videos related to

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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.
The Journal of Pediatrics|April 1, 1974
Congenital corneal clouding with abnormal systemic storage bodies: a new variant of mucolipidosisE R Berman, N Livni, E Shapira, 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.
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.
Israel Journal of Medical Sciences|May 1, 1974
Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural studyH Stein, E R Berman, N Livni, 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.
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 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
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.
The Journal of Pediatrics|April 1, 1974
Congenital corneal clouding with abnormal systemic storage bodies: a new variant of mucolipidosisE R Berman, N Livni, E Shapira, 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.
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.
Israel Journal of Medical Sciences|May 1, 1974
Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural studyH Stein, E R Berman, N Livni, 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.
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.
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