34 THIAMAZOL OR PROPILTHIOURACIL AND L-T4 COMBINATION THERAPY FOR INFANTS BORN TO MOTHER WITH GRAVES' DISEASE

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34 NOVEL MUTATIONS IN THE CYP11B1 GENE IN JAPANESEPATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 11β-HYDROXYIASE DEFICIENCY
'Nectosome' : a novel cytoplasmic vesicle containing nectin in the egg of the sea urchin, Temnopleurus hardwickii
FOMATION AND ACCUMULATION OF NECTIN-CONTAINING GRANULES DURING OOGENESIS IN THE SEA URCHIN, TEMNOPLEURUS HARDWICKI(Developmental Biology)(Proceedings of the Seventy-Third Annual Meeting of the Zoological Society of Japan)
Indocarbazostatins C and D, New Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells
Synthesis and Activity of Pyrimidinylpropenamide Antibiotics : The Alkyl Analogues of Sparsomycin(Organic Chemistry)
Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : II. Isolation, Physicochemical Properties and Structural Elucidation
Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : I. Screening, Taxonomy, Fermentation and Biological Activities
Indocardazostatin, a Novel Inhibitor of NGF-induced Neurite Outgrowth from Rat Pheochromocytoma PC12 Cells
Cloning of the Gene Cluster Responsible for the Biosynthesis of Brasilicardin A, a Unique Diterpenoid
Presence of Copalyl Diphosphate Synthase Gene in an Actinomycete Possessing the Mevalonate Pathway
A Protein of the basal lamina of the sea urchin embryo
TIMING OF CARDIOVERSION APPLICATION IN THYROTOXIC ATRIAL FIBRILLATION : Arrhythmia : FREE COMMUNICATIONS (Abstract) : 45 Annual Scientific Meeting, Japanese Circulation Society
Morphological and Biochemical Studies on Yolk Degradation in the Sea Urchin, Hemicentrotus pulcherrimus
34 THIAMAZOL OR PROPILTHIOURACIL AND L-T4 COMBINATION THERAPY FOR INFANTS BORN TO MOTHER WITH GRAVES' DISEASE
46 GENETIC ANALYSIS IN PATIENTS WITH CONGENITAL NEPHROGENIC DIABETES INSIPIDUS
48 DIAGNOSIS OF MILD CONGENIAL HYPOTHYROIDISM ETIOLOGY OF THE DISEASE AND CONFIRMATORY TEST PERFORMED BY COUNCIL MEMBERS OF THE JSPE FOR DIAGNOSIS OF THE DISEASE
54 TWO PUBERTAL BOYS WITH IMPAIRED GLUCOSE TOLERANCE AND THRIFTY PHENOTYPE
Persistent high TRAb values during pregnancy predict increased risk of neonatal hyperthyroidism following radioiodine therapy for refractory hyperthyroidism
100 ANALYSIS OF CYP21 GENE IN STEROID 21-HYDROXYLASE DEFICIENCY IN HIROSHIMA PREFECTURE
Evaluation of biventricular interaction in various cardiac diseases by pulsed Doppler echocardiography.
50 ASSOCIATION STUDY OF HUMAN MUT T HOMOLOGUE 1 GENE VAL83MET POLYMORPHISM WITH TYPE 1 DIABETES MELLrrus.
179 α-TUBULIN GENE EXPRESSION IN THE BRAIN OF rdw RATS WITH CONGENITAL HYPOTHYROIDISM

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