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Clinical Genetics|October 27, 1998
Identification of two novel mutations in the OCRL1 gene in Japanese families with Lowe syndromeT Kubota, A Sakurai, K Arakawa, et al.The American Journal of the Medical Sciences|May 20, 1999
Multiple endocrine neoplasia type 1 concomitant with Prader-Willi syndrome: case report and genetic diagnosisK Nakajima, A Sakurai, T Kubota, et al.Rinsho Shinkeigaku = Clinical Neurology|September 19, 2002
[Genetic testing and bioethics]Y FukushimaNihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|September 1, 1990
[Breathlessness of the elderly and its managements]Y FukushimaActa Paediatrica Japonica : Overseas Edition|February 1, 1996
Noonan syndrome and its related disordersY FukushimaJournal of Human Genetics|September 25, 1998
Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1A Sakurai, S Shirahama, M Fujimori, et al.The Journal of Physiology|October 1, 1982
Blocking kinetics of the anomalous potassium rectifier of tunicate egg studied by single channel recordingY FukushimaFolia Psychiatrica Et Neurologica Japonica|January 1, 1977
A study on long-term prognosis of epilepsyY FukushimaFolia Psychiatrica Et Neurologica Japonica|January 1, 1981
A longitudinal study on epilepsy: with special reference to recurrence of seizure after long seizure-free periodY FukushimaThe Journal of Biological Chemistry|August 15, 1987
Inhibition by amine bases or by sodium ions and protection by divalent cations in the hydrolysis of phosphoenzyme of (Na,K)-ATPaseY FukushimaPageof 69