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Published/Copyright:
September 15, 2020
Published Online: 2020-09-15
Published in Print: 2020-09-25
©2020 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Original Articles
- Variability of clinical and biochemical phenotype in liver phosphorylase kinase deficiency with variants in the phosphorylase kinase (PHKG2) gene
- Reference intervals for thyroid-stimulating hormone (TSH) and free thyroxine (FT4) in infants’ day 14–30 of life and a comparison with other studies
- Importance of thyroid-stimulating hormone levels in liver disease
- Assessment of thyroid gland vascularity with superb microvascular imaging in healthy children and its relationship with potential factors
- A retrospective analysis of congenital anomalies in congenital hypothyroidism
- Impact of parental origin of X-chromosome on clinical and biochemical profile in Turner syndrome
- Readiness for transition to adult care in adolescents and young adults with Turner syndrome
- A new type of pubertal height reference based on growth aligned for onset of pubertal growth
- Role of urinary NGAL and KIM-1 as biomarkers of early kidney injury in obese prepubertal children
- Self-assessed puberty is reliable in a low-income setting in rural Pakistan
- Timing and regimen of puberty induction in children with hypogonadism: a survey on the practice in Arab countries
- How useful are anthropometric measurements as predictive markers for elevated blood pressure in adolescents in different gender?
- Association between handgrip strength and cardiovascular risk factors among Korean adolescents
- Case Reports
- A novel GNAS mutation inherited from probable maternal mosaicism causes two siblings with pseudohypoparathyroidism type 1A
- Two intronic variants of CYP11B1 and CYP17A1 disrupt mRNA splicing and cause congenital adrenal hyperplasia (CAH)
- Case report: a 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus
- Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives
- Severe diabetic ketoacidosis and coronavirus disease 2019 (COVID-19) infection in a teenage patient with newly diagnosed diabetes
Articles in the same Issue
- Frontmatter
- Original Articles
- Variability of clinical and biochemical phenotype in liver phosphorylase kinase deficiency with variants in the phosphorylase kinase (PHKG2) gene
- Reference intervals for thyroid-stimulating hormone (TSH) and free thyroxine (FT4) in infants’ day 14–30 of life and a comparison with other studies
- Importance of thyroid-stimulating hormone levels in liver disease
- Assessment of thyroid gland vascularity with superb microvascular imaging in healthy children and its relationship with potential factors
- A retrospective analysis of congenital anomalies in congenital hypothyroidism
- Impact of parental origin of X-chromosome on clinical and biochemical profile in Turner syndrome
- Readiness for transition to adult care in adolescents and young adults with Turner syndrome
- A new type of pubertal height reference based on growth aligned for onset of pubertal growth
- Role of urinary NGAL and KIM-1 as biomarkers of early kidney injury in obese prepubertal children
- Self-assessed puberty is reliable in a low-income setting in rural Pakistan
- Timing and regimen of puberty induction in children with hypogonadism: a survey on the practice in Arab countries
- How useful are anthropometric measurements as predictive markers for elevated blood pressure in adolescents in different gender?
- Association between handgrip strength and cardiovascular risk factors among Korean adolescents
- Case Reports
- A novel GNAS mutation inherited from probable maternal mosaicism causes two siblings with pseudohypoparathyroidism type 1A
- Two intronic variants of CYP11B1 and CYP17A1 disrupt mRNA splicing and cause congenital adrenal hyperplasia (CAH)
- Case report: a 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus
- Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives
- Severe diabetic ketoacidosis and coronavirus disease 2019 (COVID-19) infection in a teenage patient with newly diagnosed diabetes
