286 results on '"Rabbani, Ali"'
Search Results
2. Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra
3. Relationship between a near Melanocortin-4 receptor gene variant and puberty timing in children is vague unlike obesity
4. Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry
5. Mesenchymal stem cell transplantation in newly diagnosed type-1 diabetes patients: a phase I/II randomized placebo-controlled clinical trial
6. The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial
7. On Bubble–Jet Interactions in Fluidized Beds
8. Novel disease-causing variants in a cohort of Iranian patients with metachromatic leukodystrophy and in silico analysis of their pathogenicity
9. Mapping a good society model in Ayatollah Khomeini’s religious political thought: Possibilities and challenges
10. Effects of the China-Pakistan Economic Corridor (CPEC) on the Economies of China and Pakistan
11. Supply Chain Networks Source of Knowledge Sharing: Impacts of Capability and Collaborative Innovation Activities on Innovation Performance
12. Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants
13. Role of vitamin D and vitamin D receptor gene polymorphisms on residual beta cell function in children with type 1 diabetes mellitus
14. TPP1 Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2
15. THE GROWTH AND DEVELOPMENT OF WEALTH FROM THE ISLAMIC SYSTEM
16. Design and numerical investigation of Savonius wind turbine with discharge flow directing capability
17. Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)
18. TPP1 Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2.
19. Tandem Mass Analysis of Amino Acids and Acylcarnitine Profiles in Neonates with Congenital Hypothyroidism
20. Evaluation of Effects of the COVID-19 Crisis on Disease Management in Children with Type 1 Diabete.
21. Determination of Bone Density by DEXA Method Based on Bone Age and its Comparison with Chronological Age in Chronic Patients
22. The consensus on the diagnosis and management of congenital 2 hypothyroidism in term neonates
23. Comparison of Once-daily Versus Twice-daily Injection of Insulin Detemir in Children with Type 1 Diabetes Mellitus
24. Inborn Errors of Metabolism in Iran: First Report from Iran Metabolic Registry.
25. Early and delayed puberty among Iranian children with obesity
26. Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra
27. Additional file 1 of Mesenchymal stem cell transplantation in newly diagnosed type-1 diabetes patients: a phase I/II randomized placebo-controlled clinical trial
28. In Memoriam Professor Gholamreza Walizadeh: The Chief Editor of Iranian Journal of Pediatrics and the Pioneer of Medical Writing in Iranian Pediatrics
29. COVID-19: A New Horizon in Congenital Heart Diseases
30. The Consensus on the Diagnosis and Management of Congenital 2 Hypothyroidism in Term Neonates.
31. Mesenchymal Stem Cell Transplantation in Newly Diagnosed Type-1 Diabetes Patients: A Phase I/II Randomized Placebo Controlled Clinical Trial
32. Litigation or Arbitration? Seven Factors to Consider.
33. Determination of carnitine ester profile in the children with type 1 diabetes: a valuable step towards a better management.
34. Exploring the breeding potential of Iranian emmer wheats to increase durum wheat tolerance to drought
35. Evaluation of serum IgA levels in Iranian patients with type 1 diabetes mellitus
36. TPP1Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2
37. HLA Typing of Patients with 21-Hydroxylase Deficiency in Iranian Children with Congenital Adrenal Hyperplasia
38. Meld Score: A Reliable Predictor of Mortality and Post Operative Complications in Patients with Chronic Liver Disease Undergoing Non-Transplant Surgeries
39. Efficacy and safety of Samtropin™ recombinant human growth hormone; a double-blind randomized clinical trial
40. Overweight and obesity and their associated factors in adolescents in Tehran, Iran, 2004–2005
41. Study of antibiotic resistance in patients of enteric perforation in a tertiary care hospital.
42. Prevalence of Factors Associated with Congenital Heart Disease
43. HLA-DRB, -DQA, and DQB alleles and haplotypes in Iranian patients with diabetes mellitus type I
44. Screening for celiac disease in diabetic children from Iran
45. Genetic Testing of Leukodystrophies Unraveling Extensive Heterogeneity in a Large Cohort: The Role of Five Common Diseases and Report of 38 Novel Variants
46. Factors affecting In-patient stay in patients operated for peptic ulcer perforation.
47. A 3-Year Single Surgeon Experience of the Arterial Switch Operation
48. The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants
49. Early and delayed puberty among Iranian children with obesity
50. Dyspnea and Cough: A Rare Report of the Kimura Disease
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