170 results on '"Sedghi, Maryam"'
Search Results
2. How realistic is static traffic assignment? Analyzing automatic number-plate recognition data and image processing of real-time traffic maps for investigation
3. Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.
4. Understanding the impact of DIS3 cancer-associated mutations by in silico structure modeling
5. On genotype-phenotype relationship of dystrophinopathies among Iranian population
6. Site selection methodology for emergency centers in Silk Road based on compatibility with Asian Highway network using the AHP and ArcGIS (case study: I. R. Iran)
7. A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features
8. D5S351 and D5S1414 located at the spinal muscular atrophy critical region represent novel informative markers in the Iranian population
9. Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant
10. Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction
11. Structural and functional impact of missense mutations in TPMT: An integrated computational approach
12. Association of AHSG with alopecia and mental retardation (APMR) syndrome
13. Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants
14. Association of SOD2 rs2758339, rs5746136 and rs2842980 polymorphisms with increased risk of breast cancer: a haplotype-based case–control study.
15. Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population
16. Influence of social indices on demand and supply policies in petrol stations with congested queue
17. Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.
18. Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies
19. Experiences of caring cancer patients at home: The experiences of the healthcare professionals. : A qualitative literature review
20. Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome
21. An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
22. Upplevelser av att vårda cancerpatienter palliativt i hemmet: Sjukvårdspersonalens upplevelser. : En kvalitativ litteraturstudie
23. Infantile Neuroaxonal Dystrophy in Two Cases: Siblings with Different Presentations.
24. Interactive Data Driven Visualization for COVID-19 with Trends, Analytics and Forecasting
25. Therapeutic Effects of Adrenocorticotropic Hormone ACTH in Children with Severely Intractable Seizure
26. The Role of Emotional processing in Predicting Adaptability in Female Students Diagnosed with Oppositional Defiant Disorder
27. Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study
28. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
29. Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study
30. An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
31. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
32. The role of scheme cognitive and emotional processing in the predicting adjustment of students with defiance disorder coping
33. Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1
34. Clinical features of the myasthenic syndrome arising from mutations in GMPPB
35. A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) disease
36. Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families
37. Effects of early versus delayed excision and grafting on the return of the burned hand function
38. Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents
39. Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication
40. Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation
41. Mutations inGMPPBcause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies
42. Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population
43. Effects of terrain factors in 900 MHz GSM urban cells and a pathloss estimation approach
44. A performance evaluation of probabilistic vs. deterministic spiking neural network
45. Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1
46. Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries
47. A novel homozygous DPH1mutation causes intellectual disability and unique craniofacial features
48. Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran
49. Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset
50. Investigation ofTBX1gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects: Table 1
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