178 results on '"Näntö-Salonen, Kirsti"'
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2. Circulating CXCR5−PD-1hi peripheral T helper cells are associated with progression to type 1 diabetes
3. Inhaled Sargramostim Induces Resolution of Pulmonary Alveolar Proteinosis in Lysinuric Protein Intolerance
4. DNA methylation differences within INS , PTPN22 and IL2RA promoters in lymphocyte subsets in children with type 1 diabetes and controls
5. Urine Beta2-Microglobulin Is an Early Marker of Renal Involvement in LPI
6. Disorders of Amino Acid Transport at the Cell Membrane
7. Evaluation of plasma IL-21 as a potential biomarker for type 1 diabetes progression
8. Imbalance of plasma amino acids, metabolites and lipids in patients with lysinuric protein intolerance (LPI)
9. Dysfunction in macrophage toll-like receptor signaling caused by an inborn error of cationic amino acid transport
10. Transport Defects of Amino Acids at the Cell Membrane: Cystinuria, Lysinuric Protein Intolerance and Hartnup Disorder
11. Growth Hormone Therapy Is Safe and Effective in Patients with Lysinuric Protein Intolerance
12. Transport Defects of Amino Acids at the Cell Membrane: Cystinuria, Lysinuric Protein Intolerance and Hartnup Disorder
13. Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI)
14. Inhaled Sargramostim Induces Resolution of Pulmonary Alveolar Proteinosis in Lysinuric Protein Intolerance
15. Urine Beta2-Microglobulin Is an Early Marker of Renal Involvement in LPI
16. Nasal insulin to prevent type 1 diabetes in children with HLA genotypes and autoantibodies conferring increased risk of disease: a double-blind, randomised controlled trial
17. Carnitine deficiency and l-carnitine supplementation in lysinuric protein intolerance
18. Combined hyperlipidemia in patients with lysinuric protein intolerance
19. Long-term oral lysine supplementation in lysinuric protein intolerance
20. Nephropathy Advancing to End-Stage Renal Disease: A Novel Complication of Lysinuric Protein Intolerance
21. Virus infections among young children—the first year of the INDIS study
22. Human rhinoviruses in INDIS-study material—evidence for recovery of viable rhinovirus from fecal specimens
23. Hazards associated with pregnancies and deliveries in lysinuric protein intolerance
24. Impact of Intranasal Insulin on Insulin Antibody Affinity and Isotypes in Young Children With HLA-Conferred Susceptibility to Type 1 Diabetes
25. From Genetic Risk Awareness to Overt Type 1 Diabetes: Parental stress in a placebo-controlled prevention trial
26. The Diagnosis of Ectopic Focal Hyperinsulinism of Infancy with [18F]-Dopa Positron Emission Tomography
27. Noninvasive Diagnosis of Focal Hyperinsulinism of Infancy With [18F]-DOPA Positron Emission Tomography
28. Circulating Antiandrogenic Activity in Children with Congenital Adrenal Hyperplasia during Peroral Flutamide Treatment
29. Epitopes recognized by CBV4 responding T cells: effect of type 1 diabetes and associated HLA-DR-DQ haplotypes
30. Severe Persistent Hyperinsulinemic Hypoglycemia due to a De Novo Glucokinase Mutation
31. Oral supplementation corrects plasma lysine concentrations in lysinuric protein intolerance
32. Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase
33. FOXP3+ Regulatory T Cell Compartment Is Altered in Children With Newly Diagnosed Type 1 Diabetes but Not in Autoantibody-Positive at-Risk Children
34. The psychosocial self‐efficacy in adolescents with type 1 diabetes
35. Effector T Cell Resistance to Suppression and STAT3 Signaling during the Development of Human Type 1 Diabetes
36. Circulating CXCR5−PD-1hi peripheral T helper cells are associated with progression to type 1 diabetes.
37. Circulating CXCR5+PD-1+ICOS+ Follicular T Helper Cells Are Increased Close to the Diagnosis of Type 1 Diabetes in Children With Multiple Autoantibodies
38. Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population
39. Aineenvaihdunnan säätelyhäiriöt edeltävät tyypin 1 diabetesta
40. Dysregulation of lipid and amino acid metabolism precedes islet autoimmunity in children who later progress to type 1 diabetes
41. Circulating CXCR5+PD-1+ICOS+ Follicular T Helper Cells Are Increased Close to the Diagnosis of Type 1 Diabetes in Children With Multiple Autoantibodies.
42. Severe persistent hyperinsulinemic hypoglycemia due to a de novo glucokinase mutation.
43. DISTRIBUTION OF DIFFERENT COLLAGEN TYPES AND FIBRONECTIN IN NEUROFIBROMATOSIS TUMOURS
44. Dysregulation of lipid and amino acid metabolism precedes islet autoimmunity in children who later progress to type 1 diabetes
45. Impact of Repeated Dietary Counseling Between Infancy and 14 Years of Age on Dietary Intakes and Serum Lipids and Lipoproteins
46. Poor cognitive development and abdominal pain: Wilson's disease
47. Increased Aortic Intima-Media Thickness
48. Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic rickets
49. Serum Type III Procollagen in Children with Type I Hereditary Tyrosinemia
50. Gyrate Atrophy of the Choroid and Retina: Lymphocyte Ornithine-δ-Aminotransferase Activity in Different Mutations and Carriers
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