146 results on '"Yang, Aram"'
Search Results
2. Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review
3. A phase III clinical trial of GC1111 as an enzyme replacement therapy in previously untreated mucopolysaccharidosis type II (Hunter syndrome) patients: A double-blind, randomized, active-controlled (part 1) and open-labeled, historical placebo-controlled (part 2) study
4. Therapeutic potential of intracerebroventricular recombinant human heparan-N-sulfatase enzyme replacement therapy in MPS IIIA mice
5. Impact of Nontreatment Duration and Keratopathy on Major Adverse Cardiovascular Events in Fabry Disease: A Nationwide Cohort Study
6. Case of Chronic Active Epstein-Barr Virus Infection Developed Hemophagocytic Lymphohistiocytosis after COVID-19 Infection
7. Prader-Willi syndrome and growth hormone therapy: exploring the precise management of hypothalamic short stature: A review
8. Two-photon Photoemission of Organic Semiconductor Molecules on Ag(111)
9. Two-photon Photo-emission of Ultrathin Film PTCDA Morphologies on Ag(111)
10. The Ultrafast Dynamics of Image Potential State Electrons at the Dimethylsulfoxide/Ag(111) Interface
11. Determination of Band Curvatures by Angle-resolved Two-photon Photoemission in thin films of C(60) on Ag(111)
12. Impact of BMI on peak growth hormone responses to provocative tests and therapeutic outcome in children with growth hormone deficiency
13. Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial
14. Impact of 6-month triptorelin formulation on predicted adult height and basal gonadotropin levels in patients with central precocious puberty
15. Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III
16. Organization, Governance, and Affordable Housing Outcomes: Urbanized Neighborhoods in Ohio
17. Association Between Non-invasive Diagnostic Methods of Liver Fibrosis and Type 2 Diabetes in Pediatric Patients With Non-alcoholic Fatty Liver Disease
18. Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome
19. Measuring the Differentiated Impact of New Low-Income Housing Tax Credit (LIHTC) Projects on Households’ Movements by Income Level within Urban Areas
20. Identification of a likely pathogenic variant of YY1 in a patient with developmental delay
21. Ultrafast electron dynamics at metal interfaces: intraband relaxation of image state electrons of friction
22. Effect of COVID-19 on air pollution and respiratory viral infection of children in South Korea
23. The role of growth hormone device optimization in patient-reported outcomes: real-world evidence from South Korea
24. Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review
25. Coexistence of Growth Hormone Deficiency and Pituitary Microadenoma in a Child with Unique Mosaic Turner Syndrome: A Case Report and Literature Review
26. The role of growth hormone device optimisation in patient-reported outcomes: Real-world evidence from South Korea
27. Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center
28. Unusual Presentation of Kawasaki Disease with Multisystem Inflammation and Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2: A Case Report
29. A Case of Von Hippel-Lindau Disease Presented with Multiple Pancreatic Cysts and Medullary Hemangioblastoma
30. Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.
31. MOESM1 of Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial
32. Multisystem Inflammatory Syndrome in Children Related to COVID-19: the First Case in Korea
33. Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature
34. Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center
35. MON-248 Impact of Body Mass Index on Peak Growth Hormone Response to Provocative Testing and Therapeutic Outcome in Children with Growth Hormone Deficiency
36. A case of de novo 18p deletion syndrome with panhypopituitarism
37. Two-photon Photoemission of Organic Semiconductor Molecules on Ag(111)
38. Identification of a novel mutation in EXT2 in a fourth‐generation Korean family with multiple osteochondromas and overview of mutation spectrum
39. A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets
40. Etiological trends in male central precocious puberty
41. HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report
42. An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing
43. Prevalence and risk factors for type 2 diabetes mellitus with Prader–Willi syndrome: a single center experience
44. Further delineation of COG8-CDG: A case with novel compound heterozygous mutations diagnosed by targeted exome sequencing
45. Prevalence and Epidemiological Characteristics of Endoscopically Proven Reflux Esophagitis in Children in Korea
46. 2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
47. Introduction to the New Version of PWS Application and It's Use in Medical Practice
48. Clinical and endocrine characteristics and genetic analysis of Korean children with McCune–Albright syndrome: a retrospective cohort study
49. Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience.
50. Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion
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