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A Phase 3, Open-Label, Single-Arm Trial of the Efficacy and Safety of Triptorelin 6-Month Formulation in Chinese Children with Central Precocious Puberty.
- Published in:
- Advances in Therapy, 2024, v. 41, n. 12, p. 4537, doi. 10.1007/s12325-024-02991-x
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- Article
An Evaluation of the Accuracy of a Flash Glucose Monitoring System in Children with Diabetes in comparison with Venous Blood Glucose.
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- Journal of Diabetes Research, 2019, p. 1, doi. 10.1155/2019/4845729
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- Article
Comorbidity in Adult Patients Hospitalized with Type 2 Diabetes in Northeast China: An Analysis of Hospital Discharge Data from 2002 to 2013.
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- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/1671965
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- Article
DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing.
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- Journal of Personalized Medicine, 2022, v. 12, n. 6, p. 872, doi. 10.3390/jpm12060872
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- Article
Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study.
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- Journal of Personalized Medicine, 2022, v. 12, n. 5, p. 771, doi. 10.3390/jpm12050771
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- Article
Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature.
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- Journal of Personalized Medicine, 2022, v. 12, n. 3, p. 407, doi. 10.3390/jpm12030407
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- Article
Long-term Pegylated GH for Children With GH Deficiency: A Large, Prospective, Real-world Study.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 8, p. 2078, doi. 10.1210/clinem/dgad039
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- Article
Longitudinal changes in body mass index, height, and weight in children with acute myeloid leukemia.
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- BMC Pediatrics, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12887-024-04740-z
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- Article
Clinical characteristics and genotype‐phenotype correlations of 130 Chinese children in a high‐homogeneity single‐center cohort with 5α‐reductase 2 deficiency.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1431
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- Article
Clinical and ALPL Gene Mutations Analysis in an Early Onset Chinese Odontohypophosphatasia Patient.
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- American Journal of Biomedical Sciences, 2014, v. 6, n. 4, p. 308, doi. 10.5099/aj140400308
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- Article
AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0-3).
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- SCIENCE CHINA Life Sciences, 2017, v. 60, n. 7, p. 700, doi. 10.1007/s11427-017-9084-9
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- Article
Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome.
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- SCIENCE CHINA Life Sciences, 2017, v. 60, n. 7, p. 692, doi. 10.1007/s11427-017-9079-7
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- Article
High Prevalence of Obesity but Low Physical Activity in Children Aged 9–11 Years in Beijing.
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- Diabetes, Metabolic Syndrome & Obesity: Targets & Therapy, 2021, v. 14, p. 3323, doi. 10.2147/DMSO.S319583
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- Article
Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China.
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- Journal of Diabetes Research, 2015, p. 1, doi. 10.1155/2016/6314368
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- Article
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance.
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- Frontiers in Endocrinology, 2020, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.582516
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- Article
Influence of disease course and comprehensive management on blood glucose level in children and adolescents with type 2 diabetes mellitus.
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- Journal of Diabetes Investigation, 2024, v. 15, n. 8, p. 1026, doi. 10.1111/jdi.14194
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- Article
Development of a Minimum Dataset for the Monitoring of Recombinant Human Growth Hormone Therapy in Children with Growth Hormone Deficiency: A GloBE-Reg Initiative.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 4, p. 365, doi. 10.1159/000533763
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- Article
The Effects of Genetic Variation in <i>FTO</i> rs9939609 on Obesity and Dietary Preferences in Chinese Han Children and Adolescents.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104574
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- Article
A single center study on the current state of blood glucose control and related factors analysis in children with type 1 diabetes mellitus from 2015 to 2019.
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- Chinese Journal of Diabetes Mellitus, 2021, v. 13, n. 5, p. 462, doi. 10.3760/cma.j.cn115791-20200921-00575
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- Article
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factor.
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- 2020
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- Publication type:
- journal article
Clinical characteristics and chromosome 11p15 imprinting analysis of Silver-Russell syndrome - a Chinese experience.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 11/12, p. 1113, doi. 10.1515/jpem-2013-0490
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- Article
Two case reports of severe pediatric hyperosmolar hyperglycemia and diabetic ketoacidosis accompanied with rhabdomyolysis and acute renal failure.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 11/12, p. 1227, doi. 10.1515/jpem-2014-0131
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- Article
Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families.
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- European Journal of Endocrinology, 2024, v. 191, n. 1, p. 87, doi. 10.1093/ejendo/lvae082
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- Article
Long-acting PEGylated growth hormone in children with idiopathic short stature.
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- European Journal of Endocrinology, 2022, v. 187, n. 5, p. 709, doi. 10.1530/EJE-22-0449
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- Article
Fulminant Type 1 Diabetes in Children: A Multicenter Study in China.
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- Journal of Diabetes Research, 2017, p. 1, doi. 10.1155/2017/6924637
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- Article
Editorial: Childhood Diabetes in Low- and Middle-Income Countries.
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- Frontiers in Endocrinology, 2022, v. 12, p. 1, doi. 10.3389/fendo.2021.830700
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- Article
Associations Between Sleep Duration, Wake-Up Time, Bedtime, and Abdominal Obesity: Results From 9559 Chinese Children Aged 7–18 Years.
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- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.735952
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- Article
Comparative evaluation of short-term biomarker response to treatment for growth hormone deficiency in Chinese children with growth hormone deficiency born small for or appropriate for gestational age: a randomized phase IV open-label study.
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- Therapeutic Advances in Endocrinology & Metabolism, 2013, v. 4, n. 2, p. 41, doi. 10.1177/2042018813484051
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- Article
Clinical evaluation of recombinant human growth hormone injection in children with growth hormone deficiency.
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- Frontiers of Medicine in China, 2009, v. 3, n. 2, p. 171, doi. 10.1007/s11684-009-0027-4
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- Article
Correction to: One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria.
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- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-022-02296-8
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- Article
One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria.
- Published in:
- 2021
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- Publication type:
- journal article
Sifrim–Hitz‐Weiss/CHD4‐related syndrome: A new case report.
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- Pediatric Investigation, 2023, v. 7, n. 2, p. 137, doi. 10.1002/ped4.12357
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- Article
Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency.
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- Pediatric Investigation, 2021, v. 5, n. 4, p. 249, doi. 10.1002/ped4.12302
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- Article
Characteristics of pediatric inpatients with primary and secondary hypertension.
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- Pediatric Investigation, 2021, v. 5, n. 1, p. 28, doi. 10.1002/ped4.12249
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- Article
Clinical features and predictors of remission in children under the age of 7 years with Graves' disease.
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- Pediatric Investigation, 2020, v. 4, n. 3, p. 198, doi. 10.1002/ped4.12219
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- Article
Efficacy and safety of octreotide treatment for diazoxide‐unresponsive congenital hyperinsulinism in China.
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- Pediatric Investigation, 2020, v. 4, n. 1, p. 29, doi. 10.1002/ped4.12175
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- Article
Central precocious puberty as a prelude to hypogonadism in a patient with Klinefelter syndrome.
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- Pediatric Investigation, 2019, v. 3, n. 2, p. 127, doi. 10.1002/ped4.12136
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- Article
Variant analysis of the chromodomain helicase DNA‐binding protein 7 in pediatric disorders of sex development.
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- Pediatric Investigation, 2019, v. 3, n. 1, p. 31, doi. 10.1002/ped4.12111
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- Article
Central precocious puberty as a prelude of gonad dysplasia.
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- Pediatric Investigation, 2019, v. 3, n. 1, p. 50, doi. 10.1002/ped4.12118
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- Article
Validity of web‐based self‐assessment of pubertal development against pediatrician assessments.
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- Pediatric Investigation, 2018, v. 2, n. 3, p. 141, doi. 10.1002/ped4.12050
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- Article
Persistent Müllerian duct syndrome: A case report and review.
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- Experimental & Therapeutic Medicine, 2017, v. 14, n. 6, p. 5779, doi. 10.3892/etm.2017.5281
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- Article
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases.
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- Experimental & Therapeutic Medicine, 2015, v. 10, n. 4, p. 1277, doi. 10.3892/etm.2015.2677
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- Publication type:
- Article
Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China.
- Published in:
- Disease Markers, 2015, p. 1, doi. 10.1155/2016/6314368
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- Publication type:
- Article
Clinical and genetic characteristics of hypophosphatasia in Chinese children.
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- 2021
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- Publication type:
- journal article
Clinical and molecular spectrum of 46,XY disorders of sex development that harbour MAMLD1 variations: case series and review of literature.
- Published in:
- 2020
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- Publication type:
- journal article
Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.
- Published in:
- 2019
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- Publication type:
- journal article
Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature.
- Published in:
- 2019
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- Publication type:
- journal article
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Short Stature: A Systematic Review and Meta-Analysis.
- Published in:
- JAMA Pediatrics, 2023, v. 177, n. 11, p. 1149, doi. 10.1001/jamapediatrics.2023.3566
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- Article
Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter Study.
- Published in:
- Frontiers in Pharmacology, 2019, p. N.PAG, doi. 10.3389/fphar.2019.00173
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- Article
Phenotype and Molecular Characterizations of 30 Children From China With NR5A1 Mutations.
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- Frontiers in Pharmacology, 2018, p. 1, doi. 10.3389/fphar.2018.01224
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- Article