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F Iwata

Showing results (71-80 of 80) with videos related to

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Acta Paediatrica Japonica : Overseas Edition|May 16, 1998
Relationship between fat distribution and lipid and apolipoprotein profiles in young teenagersT Okada, Y Sato, H Yamazaki, et al.
American Journal of Human Genetics|November 5, 1997
Evidence for locus heterogeneity in Puerto Ricans with Hermansky-Pudlak syndromeS Hazelwood, V Shotelersuk, S C Wildenberg, et al.
Experimental Eye Research|April 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stressM G Nicolas, K Fujiki, K Murayama, et al.
The New England Journal of Medicine|May 1, 1998
Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome)W A Gahl, M Brantly, M I Kaiser-Kupfer, et al.
American Journal of Human Genetics|September 23, 2000
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.
Pediatric Research|January 7, 2000
Ocular nonnephropathic cystinosis: clinical, biochemical, and molecular correlationsY Anikster, C Lucero, J Guo, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|November 20, 2004
The WHO dose pole for the administration of praziquantel is also accurate in non-African populationsA Montresor, P Odermatt, S Muth, et al.
Nature Genetics|January 1, 1996
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporterD B Simon, C Nelson-Williams, M J Bia, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|August 1, 1997
[Usefulness of 7 day therapy with cefluprenam in the management of respiratory tract infections]K Shimada, M Ohmichi, H Sasaki, et al.
Molecular Vision|January 5, 1999
Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Acta Paediatrica Japonica : Overseas Edition|May 16, 1998
Relationship between fat distribution and lipid and apolipoprotein profiles in young teenagersT Okada, Y Sato, H Yamazaki, et al.
American Journal of Human Genetics|November 5, 1997
Evidence for locus heterogeneity in Puerto Ricans with Hermansky-Pudlak syndromeS Hazelwood, V Shotelersuk, S C Wildenberg, et al.
Experimental Eye Research|April 1, 1996
Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stressM G Nicolas, K Fujiki, K Murayama, et al.
The New England Journal of Medicine|May 1, 1998
Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome)W A Gahl, M Brantly, M I Kaiser-Kupfer, et al.
American Journal of Human Genetics|September 23, 2000
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.
Pediatric Research|January 7, 2000
Ocular nonnephropathic cystinosis: clinical, biochemical, and molecular correlationsY Anikster, C Lucero, J Guo, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|November 20, 2004
The WHO dose pole for the administration of praziquantel is also accurate in non-African populationsA Montresor, P Odermatt, S Muth, et al.
Nature Genetics|January 1, 1996
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporterD B Simon, C Nelson-Williams, M J Bia, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|August 1, 1997
[Usefulness of 7 day therapy with cefluprenam in the management of respiratory tract infections]K Shimada, M Ohmichi, H Sasaki, et al.
Molecular Vision|January 5, 1999
Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.
Pageof 8