Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
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Stress doses of glucocorticoids cannot prevent progression of all adrenal crises.Acute vitamin d toxicity in an infant.The Cubic Functions for Spline Smoothed L, S and M Values for BMI Reference Data of Japanese Children.Isolated neurosarcoidosis revealed by diabetes insipidus, visual loss and diplopia in a child patient: a diagnostic problemGuidelines for the treatment of childhood-onset Graves' disease in Japan, 2016Evaluation of growth hormone treatment efficacy in short Japanese children born small for gestational age: Five-year treatment outcome and impact on puberty.Hypothyroidism among pediatric patients with type 1 diabetes mellitus, from patients' characteristics to disease severityChildbirth and fertility preservation in childhood and adolescent cancer patients: a second national survey of Japanese pediatric endocrinologistsPartial lipodystrophy in patients who have undergone hematopoietic stem cell transplantation during childhood: an institutional cross-sectional survey.Skeletal Deformity Associated with SHOX DeficiencyRadiation exposure and the risk of pediatric thyroid cancer.Effect of growth hormone treatment on quality of life in Japanese children with growth hormone deficiency: an analysis from a prospective observational study.Tumors of bilateral streak gonads in patients with disorders of sex development containing y chromosome material.Type 1 diabetes and autoimmunity.Increased Secretion of Endogenous GH after Treatment with an Intranasal GH-releasing Peptide-2 Spray Does Not Promote Growth in Short Children with GH DeficiencyA novel deletion mutation of the arginine vasopressin receptor 2 gene in a Japanese infant with nephrogenic diabetes insipidus.Growth failure starts from early infancy in children with short stature at age 6A 45,X/46,XY DSD (Disorder of Sexual Development) case with an extremely uneven distribution of 46,XY cells between lymphocytes and gonads.Onset of puberty and near adult height in short children born small for gestational age and treated with GH: Interim analysis of up to 10 years of treatment in Japan.Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocolsAdvanced maternal age in Indian children with thyroid dysgenesis.Hyperthyroidism in children: treatment outcomes and preferences in Eastern India.Bone age: assessment methods and clinical applications.Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.Age at menarche and near final height after treatment with gonadotropin-releasing hormone agonist alone or combined with growth hormone in Korean girls with central precocious puberty.An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene.Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2Neonatal mass screening for 21-hydroxylase deficiency.Current concepts in perinatal mineral metabolismClassic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.Gonadal function, fertility, and reproductive medicine in childhood and adolescent cancer patients: a national survey of Japanese pediatric endocrinologists.Pheochromocytoma complicated by cyanotic congenital heart disease: a case reportGrowth standard charts for Japanese children with mean and standard deviation (SD) values based on the year 2000 national surveyWeight-for-height charts for Japanese children based on the year 2000 Report of School Health Statistics Research.A Japanese male patient with 'fibular aplasia, tibial campomelia and oligodactyly': an additional case report.H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase DeficiencyTurner syndrome with ulcerative colitis.
P1433
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P1433
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
description
czasopismo naukowe
@pl
journal
@en
revista científica
@es
wetenschappelijk tijdschrift
@nl
wissenschaftliche Fachzeitschrift
@de
name
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@ast
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@en
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@es
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@nl
type
label
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@ast
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@en
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@es
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@nl
altLabel
Clin Pediatr Endocrinol
@en
prefLabel
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@ast
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@en
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@es
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
@nl
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P3181
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P1156
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P1476
Clinical pediatric endocrinolo ...... ty for Pediatric Endocrinology
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