137 results on '"Loewenthal, Neta"'
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2. Early exposures and inherent factors in premature newborns are associated with type 1 diabetes
3. Correction to: Early exposures and inherent factors in premature newborns are associated with type 1 diabetes
4. Acute hyperglycaemia can impair driving skill in young type 1 diabetes mellitus patients
5. Thyroid function tests in newborns of mothers with hypothyroidism
6. Vitamin D deficiency in children with acute bronchiolitis: a prospective cross-sectional case- control study
7. Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred
8. GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysis
9. Hyperinsulinism / hyperammonemia syndrome caused by biallelic SLC25A36 mutation
10. GHRH-GH-IGF1 axis in pediatric Down syndrome: A systematic review and mini meta-analysis
11. Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation.
12. Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center
13. Correction to: Early exposures and inherent factors in premature newborns are associated with type 1 diabetes
14. Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3− secretion revealed by disease causing human mutation
15. Deep intronic variant in theARSBgene as the genetic cause for Maroteaux–Lamy syndrome ( MPS VI )
16. Feasibility Study of a Hybrid Closed-Loop System with Automated Insulin Correction Boluses
17. Vitamin D Deficiency in Children with Acute Bronchiolitis: A Prospective Cross-Sectional Case- Control Study
18. Varied Clinical Presentations of Seven Patients With Mutations in CYP11A1 Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc
19. Multiple Endocrine Deficiencies are Common in Hypoparathyroidism–Retardation–Dysmorphism Syndrome
20. Visits at the primary clinic do not reduce ketoacidosis rates at presentation in type 1 diabetes mellitus
21. The effect of vitamin D administration on vitamin D status and respiratory morbidity in late premature infants
22. Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy
23. Birth during the moderate weather seasons is associated with early onset of type 1 diabetes in the Mediterranean area
24. Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux–Lamy syndrome (MPS VI).
25. 1041-P: Feasibility Study of a Hybrid Closed-Loop System with Automated Correction Boluses
26. OR17-6 Parenteral Cephalosporins and Glucose During the Neonatal Period Are Associated with Pediatric Type 1 Diabetes Development
27. Combined Gestational Age- and Birth Weight–Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia
28. Visits at the primary clinic do not reduce ketoacidosis rates at presentation in type 1 diabetes mellitus.
29. Multiple Endocrine Deficiencies are Common in Hypoparathyroidism–Retardation–Dysmorphism Syndrome.
30. Long-term safety of α-1 antitrypsin therapy in children and adolescents with Type 1 diabetes
31. Exertional rhabdomyolysis in carbonic anhydrase 12 deficiency
32. Prevalence of early and late prematurity is similar among pediatric type 1 diabetes patients and the general population
33. Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 − secretion revealed by disease causing human mutation
34. Diagnosis, Management, and Possible Prevention of Hungry Bone Syndrome in an Adolescent with Primary Hyperparathyroidism and Vitamin D Deficiency.
35. Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3−secretion revealed by disease causing human mutation
36. Phosphoglucomutase-1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiency
37. Combined adrenal failure and testicular adrenal rest tumor in a patient with nicotinamide nucleotide transhydrogenase deficiency
38. Antenatal diagnosis and treatment of hypothyroid fetal goiter in an euthyroid mother: a case report and review of literature
39. Natural History and Clinical Manifestations of Hyponatremia and Hyperchlorhidrosis due to Carbonic Anhydrase XII Deficiency
40. Varied Clinical Presentations of Seven Patients With Mutations inCYP11A1Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc
41. The utility of basal serum LH in prediction of central precocious puberty in girls
42. Ethnic and Gender Inequities in the Evaluation of Referred Short Children
43. Testicular Expressed Genes Are Missing in Familial X-Linked Kallmann Syndrome due to Two Large Different Deletions in Daughter’s X Chromosomes
44. Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3− secretion revealed by disease causing human mutation.
45. Antenatal diagnosis and treatment of hypothyroid fetal goiter in an euthyroid mother: a case report and review of literature.
46. Nerve Growth Factor-Tyrosine Kinase A Pathway Is Involved in Thermoregulation and Adaptation to Stress: Studies on Patients with Hereditary Sensory and Autonomic Neuropathy Type IV
47. Use of health services and metabolic control among Bedouin and Jewish children with type I diabetes.
48. Ethnic Differences in Glycemic Control and Diabetic Ketoacidosis Rate Among Children with Diabetes Mellitus Type 1 in the Negev Area.
49. Refractory Hypoparathyroidism in a Child with Celiac Disease.
50. Decreased First Phase Insulin Response in Children with Congenital Insensitivity to Pain with Anhidrosis.
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