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Ophthalmology
|
April 1, 1981
Anterior segment and retinal pigmentary abnormalities in arteriohepatic dysplasia
J E Puklin, C A Riely, R M Simon, et al.
American Journal of Ophthalmology
|
December 1, 1973
GM1 gangliosidosis type I
M J Weiss, A E Krill, G Dawson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 18, 1975
Fabry disease: diagnosis by alpha-galactosidase activities in tears
D L Johnson, M A Del Monte, E Cotlier, et al.
Experimental Eye Research
|
September 1, 1981
Plasma tryptophan in humans with diabetic and senile cataracts
E Cotlier, Y R Sharma, J Zuckerman, et al.
Journal of the American Veterinary Medical Association
|
December 1, 1981
Nutritional cataracts in timber wolves
S J Vainisi, H F Edelhauser, E D Wolf, et al.
The New England Journal of Medicine
|
January 3, 1974
Letter: Diagnosis of Fabry's disease by tear alpha-galactosidase A
M A Del Monte, D L Johnson, E Cotlier, et al.
Bulletin Des Societes D'Ophtalmologie De France
|
February 1, 1981
[Ocular manifestations accompanying congenital biliary duct hypoplasia]
D A Lebuisson, F Herbet-Frileux, J J Aron, et al.
Archives of Internal Medicine
|
September 1, 1971
Macular cherry-red spot, corneal clouding, and beta-galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease
M F Goldberg, E Cotlier, L G Fichenscher, et al.
Ophthalmic Paediatrics and Genetics
|
July 1, 1988
Retinoblastoma: the Saudi Arabian experience
S Senft, A al-Kaff, G Bergqvist, et al.
AJR. American Journal of Roentgenology
|
December 1, 1980
Arteriohepatic dysplasia: radiologic features of a new syndrome
N S Rosenfield, M J Kelley, P S Jensen, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 100) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 100 results.
Ophthalmology
|
April 1, 1981
Anterior segment and retinal pigmentary abnormalities in arteriohepatic dysplasia
J E Puklin, C A Riely, R M Simon, et al.
American Journal of Ophthalmology
|
December 1, 1973
GM1 gangliosidosis type I
M J Weiss, A E Krill, G Dawson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 18, 1975
Fabry disease: diagnosis by alpha-galactosidase activities in tears
D L Johnson, M A Del Monte, E Cotlier, et al.
Experimental Eye Research
|
September 1, 1981
Plasma tryptophan in humans with diabetic and senile cataracts
E Cotlier, Y R Sharma, J Zuckerman, et al.
Journal of the American Veterinary Medical Association
|
December 1, 1981
Nutritional cataracts in timber wolves
S J Vainisi, H F Edelhauser, E D Wolf, et al.
The New England Journal of Medicine
|
January 3, 1974
Letter: Diagnosis of Fabry's disease by tear alpha-galactosidase A
M A Del Monte, D L Johnson, E Cotlier, et al.
Bulletin Des Societes D'Ophtalmologie De France
|
February 1, 1981
[Ocular manifestations accompanying congenital biliary duct hypoplasia]
D A Lebuisson, F Herbet-Frileux, J J Aron, et al.
Archives of Internal Medicine
|
September 1, 1971
Macular cherry-red spot, corneal clouding, and beta-galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease
M F Goldberg, E Cotlier, L G Fichenscher, et al.
Ophthalmic Paediatrics and Genetics
|
July 1, 1988
Retinoblastoma: the Saudi Arabian experience
S Senft, A al-Kaff, G Bergqvist, et al.
AJR. American Journal of Roentgenology
|
December 1, 1980
Arteriohepatic dysplasia: radiologic features of a new syndrome
N S Rosenfield, M J Kelley, P S Jensen, et al.
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of 10