98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency

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243 A CASE OF McCUNE-ALBRIGHT SYNDROME WITH NARROWING OPTIC CANAL : A TRIAL OF INTRAVENOUS PAMIDRONATE TREATMENT
Existence of Blood Group Related Antigens in Nuclear Heterochromatin in Mucous Cells of Human Cervical Glands.
Relationship between Lectin Binding Properties and the Expression of Blood Group ABH Antigens in Vascular Endothelia and Red Blood Cells from 18 Primate Species
Histochemical Demonstration of Mucin Type Glycoproteins in Human Tissues Using Lectin Staining Method in Combination with Exo-and Endo-Glycosidase Digestion Procedures
肺臓炭粉沈着--20年前との比較〔英文〕
Effects of Exoglycosidase Digestion upon Lectin Stainings in Human Pancreas
LOCALIZATION OF BLOOD GROUP ANTIGENS IN HUMAN PANCREAS WITH LECTIN-HORSERADISH PEROXIDASE CONJUGATES
Localization of blood group antigens in formalin-fixed, paraffin-embedded human salivary glands and pancreas with lectin-HRP conjugate
Spectrophotometric Studies for Complex Formation of Diammonium 1, 4, 10, 13-Tetraoxa-7, 16-diazacycrooctadecane-bis(N-carbodithioate) with Transitional Metal Ions under Coexistence of Alkali Metal Ion and Alkali Earth Metal Ion
Determination of Trace Amounts of Silver in High-Purity Aluminum by Graphite-Furnace Atomic Absorption Spectrometry after Solvent Extraction and Micro-Volume Back-Extraction
Determination of Trace Amounts of Molybdenum in Rainwater and Snow by Graphite-Furnace Atomic Absorption Spectrometry after Solvent Extraction and Micro-Volume Back-Extraction
Double Schottky Diode-Type Gas Sensor for Discriminative Detection of Phosphine and Hydrogen
Spectrophotometric Characterization of Diazacrown Ethers Having Two Carbodithioate Groups
Synthesis and Absolute Configuration of Optically Active Telluronium Salts
Appraisal of bone maturity age derived from broadband ultrasonic attenuation in Japanese children and adolescents
Mental Retardation in a Boy with Congenital Adrenal Hypoplasia : A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL
168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
145 Study of the levels of new tumor marker, Basic fetoprotein (BFP) in comparison with that of CA125, CA19-9 and SLX in the gynecological disease.
40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1
53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome
64 GNAS1 mutation in a Japanese boy with progressive osseous heteroplasia.
98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency
101 A female case of classical 3β-hydroxysteroid dehydrogenase deficiency with multicystic ovary and anovulatory menstruation : Evaluation of ovarian function after puberty
109 A case of allergy to gelatin included in the gonadotropin-releasing hormone analog "depot leuprorelin acetate"
(一般演題)(日本アフェレシス学会第22回関西地方会抄録)
Fatty degeneration of osteocytes of the fourth metatarsus in patients with idiopathic necrosis of the femoral head.
83 Analysis of suppressor of cytokine signaling-2 (SOCS-2) gene in overgrowth syndrome

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