24 results on '"Sun Shouyue"'
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2. Infertility risk assessment with ultrasound in congenital adrenal hyperplasia male patients
3. COVID-19 Rebound After VV116 vs Nirmatrelvir-Ritonavir Treatment
4. Nonclassic Adrenal Hyperplasia (NCAH) due to 21-hydroxylase deficiency: A cohort of 78 patients
5. Intensive insulin therapy combined with metformin is associated with reduction in both glucose variability and nocturnal hypoglycaemia in patients with type 2 diabetes
6. A Multiclassifier System to Identify and Subtype Congenital Adrenal Hyperplasia Based on Circulating Steroid Hormones
7. Surgical biopsies in patients with central diabetes insipidus and thickened pituitary stalks
8. Sequential Versus Continual Purified Urinary FSH/hCG in Men With Idiopathic Hypogonadotropic Hypogonadism
9. Untargeted LC/MS-Based Metabolic Phenotyping of Hypopituitarism in Young Males
10. Targeted gene panel sequencing for molecular diagnosis of congenital adrenal hyperplasia
11. Genetic Findings in a Cohort of Patients with Androgen Insensitivity Syndrome
12. Clinical and molecular characterization of thirty Chinese patients with congenital lipoid adrenal hyperplasia
13. Diabetic Ketoacidosis at Diagnosis Influences Complete Remission After Treatment With Hematopoietic Stem Cell Transplantation in Adolescents With Type 1 Diabetes
14. The Optimized Calculation Method for Insulin Dosage in an Insulin Tolerance Test (ITT): A Randomized Parallel Control Study
15. Creatine Metabolism and Carnitine Shuttle System as Potential Diagnostic and Prognostic Biomarkers of Gonadotropin Replacement Therapy in Young Males With Panhypopituitarism
16. Seven Novel DAX1 Mutations with Loss of Function Identified in Chinese Patients with Congenital Adrenal Hypoplasia
17. Phenotype-Genotype Correlation in Eight Chinese 17α-Hydroxylase/17,20 Lyase-Deficiency Patients with Five Novel Mutations of CYP17A1 Gene
18. Omentum Is Better Site Than Kidney Capsule for Growth, Differentiation, and Vascularization of Immature Porcine β-Cell Implants in Immunodeficient Rats
19. 17β-Hydroxysteroid dehydrogenase 3 deficiency: Three case reports and a systematic review
20. New, recurrent, and prevalent mutations: Clinical and molecular characterization of 26 Chinese patients with 17alpha-hydroxylase/17,20-lyase deficiency
21. A prevalent and three novel mutations in CYP11B1 gene identified in Chinese patients with 11-beta hydroxylase deficiency
22. A Network Investigation on Idiopathic Hypogonadotropic Hypogonadism in China
23. A Novel SRD5A2 Mutation with Loss of Function Identified in Chinese Patients with Hypospadias
24. Seven NovelDAX1Mutations with Loss of Function Identified in Chinese Patients with Congenital Adrenal Hypoplasia
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