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山形大学 医学部循環･呼吸･腎臓内科学 | 論文
- Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women
- Association of the -381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss
- Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals
- Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene
- PJ-502 Regional abnormality of restitution properties cause electrical activation alternans and ventricular arrhythmia in chronic myocardial infarction(Arrhythmia, Basic 6 (A) : PJ84)(Poster Session (Japanese))
- A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density
- Fluctuation of Activation Sequence is Determinant of Ventricular Fibrillation in LQT2 (Arrhythmia, Basic 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- -0107-THE SIGNIFICANCE OF DIPYRIDAMOLE ELECTROCARDIOGRAPHIC TEST IN PATIENTS WITH CORONARY ARTERY DISEASE : A COMPARATIVE STUDY WITH TREADMILL ELECTROCARDIOGRAPHIC TEST
- RELATIONSHIP BETWEEN EXERCISE TESTS AND CARDIAC DEATH IN ISCHEMIC HEART DISEASE : Exercise Test, Rehabilitation : 53 Annual Scientific Meeting, Japanese Circulation Society
- -14-CLINICAL SIGNIFICANCE OF EXERCISE INDUCED SILENT MYOCARDIAL ISCHEMIA : Excercise Test : FREE COMMUNICATIONS(I) : PROCEEDINGS OF THE 53th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- THE CORRELATION OF THE TREADMILL EXERCISE TEST WITH CARDIAC HEMODYNAMICS IN PATIENTS WITH PREVEIOUS MYOCARDIAL INFARCTION
- THE BODY SURFACE DISTRIBUTION OF THE QT INTERVAL IN PATIENTS WITH PREVIOUS MYOCARDIAL INFARCTION AND NORMAL SUBJECTS
- -365- MECHANISMS OF EXERCISE-INDUCED R-WAVE INCREASE IN CORONARY ARTERY DISEASE : COMPARATIVE STUDY BETWEEN TREADMILL EXERCISE AND DIPYRIDAMOLE INFUSION STRESS
- Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japa
- Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene
- Familial Hypercholesterolemia with Cholesteryl Ester Traansfer Protein Deficiency
- Enhanced ^Tc-Sestamibi Washout in Patients with Coronary Spastic Angina
- Myocardial ^Tc-Sestamibi Washout in Patients with Dilated Cardiomyopathy : Comparisons with Endomyocardial Biopsy
- Ultrastructural localization of heparan sulfate-like immunoreactivity in spinal spheroids of motor neuron disease
- Hereditary Ceruloplasmin Deficiency - A New Type of Diabetes Mellitus