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L Nadler

Showing results (51-60 of 409) with videos related to

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Lancet (London, England)|March 17, 1979
Methylumbelliferyl-guanidinobenzoate reactive proteases in amniotic fluid: possible marker for cystic fibrosisM M Walsh, H L Nadler
Lancet (London, England)|July 12, 1980
Prenatal detection of cystic fibrosis on amniotic fluidH L Nadler, M M Walsh
The Journal of Laboratory and Clinical Medicine|September 1, 1975
Enzymic reduction of cystine and glutathione in cultivated human fibroblast from normal subjects and patients with cystinosisC I Kaye, H L Nadler
The Journal of Laboratory and Clinical Medicine|March 1, 1973
A fluorometric assay of alpha-glucosidase and its application in the study of Pompe's diseaseI S Salafsky, H L Nadler
American Journal of Obstetrics and Gynecology|December 15, 1971
Intracellular organelles and enzymes in cellfree amniotic fluidI S Salafsky, H L Nadler
Pediatric Research|March 1, 1974
Schilder's disease: abnormal cholesterol retention and accumulation in cultivated fibroblastsB K Burton, H L Nadler
Pediatric Research|September 1, 1975
Deficiency of arginine esterase in cystic fibrosis of the pancreas: demonstration of the proteolytic nature of the activityG J Rao, H L Nadler
Pediatrics|March 1, 1978
Clinical diagnosis of the inborn errors of metabolism in the neonatal periodB K Burton, H L Nadler
The New England Journal of Medicine|February 5, 1970
Deficiency of lysosomal acid phosphatase. A new familial metabolic disorderH L Nadler, T J Egan
Progress in Clinical and Biological Research|January 1, 1982
Soluble and membranous neutral beta-glucosidasesY Ben-Yoseph, H L Nadler
Pageof 41

Showing results (51-60 of 409) with videos related to

Sort By:
Pageof 41
Lancet (London, England)|March 17, 1979
Methylumbelliferyl-guanidinobenzoate reactive proteases in amniotic fluid: possible marker for cystic fibrosisM M Walsh, H L Nadler
Lancet (London, England)|July 12, 1980
Prenatal detection of cystic fibrosis on amniotic fluidH L Nadler, M M Walsh
The Journal of Laboratory and Clinical Medicine|September 1, 1975
Enzymic reduction of cystine and glutathione in cultivated human fibroblast from normal subjects and patients with cystinosisC I Kaye, H L Nadler
The Journal of Laboratory and Clinical Medicine|March 1, 1973
A fluorometric assay of alpha-glucosidase and its application in the study of Pompe's diseaseI S Salafsky, H L Nadler
American Journal of Obstetrics and Gynecology|December 15, 1971
Intracellular organelles and enzymes in cellfree amniotic fluidI S Salafsky, H L Nadler
Pediatric Research|March 1, 1974
Schilder's disease: abnormal cholesterol retention and accumulation in cultivated fibroblastsB K Burton, H L Nadler
Pediatric Research|September 1, 1975
Deficiency of arginine esterase in cystic fibrosis of the pancreas: demonstration of the proteolytic nature of the activityG J Rao, H L Nadler
Pediatrics|March 1, 1978
Clinical diagnosis of the inborn errors of metabolism in the neonatal periodB K Burton, H L Nadler
The New England Journal of Medicine|February 5, 1970
Deficiency of lysosomal acid phosphatase. A new familial metabolic disorderH L Nadler, T J Egan
Progress in Clinical and Biological Research|January 1, 1982
Soluble and membranous neutral beta-glucosidasesY Ben-Yoseph, H L Nadler
Pageof 41