985 results on '"Salih, Mustafa"'
Search Results
2. Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
3. Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
4. A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
5. Enhancing sustainable healthcare practices through energy-efficient wireless body area networks
6. A Study on the Role of Islamic Finance and Sustainable Development Goals
7. Entzündliche Myopathien
8. Environmental pollutants particulate matter (PM2.5, PM10), Carbon Monoxide (CO), Nitrogen dioxide (NO2), Sulfur dioxide (SO2), and Ozone (O3) impact on lung functions
9. IEEE 802.15.6 and LoRaWAN for WBAN in Healthcare: A Comparative Study on Communication Efficiency and Energy Optimization
10. Application of computational fluid dynamics simulations in food industry
11. Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
12. Geotechnical correlations of soil properties in Hilla City – Iraq
13. Salam As Banking Financing for Agriculture in Developing Countries: Lessons From Sudan
14. Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndrome
15. Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings.
16. IEEE 802.15.6 and LoRaWAN for WBAN in Healthcare: A Comparative Study on Communication Efficiency and Energy Optimization.
17. Peripheral Nerve Disorders
18. Movement Disorders in Childhood
19. Childhood Neuro-Ophthalmic Disorders
20. Inflammatory Myopathies
21. Myotonic Dystrophy and Periodic Paralyses
22. Metabolic Myopathies
23. Hereditary and Acquired Myopathies
24. Neuromuscular Transmission Disorders
25. Plexopathies and Radiculopathies
26. Cranial Nerve Disorders
27. Anterior Horn Cell Diseases
28. Approach to Motor Unit Diseases and the Floppy Infant Syndrome
29. Spinal Cord Disorders and Paraplegias
30. Disorders of Head Shape and Size
31. Childhood and Adolescent Epileptic Syndromes
32. Neurological Evaluation of Infants and Children
33. Neuroendocrine Disorders
34. Neurometabolic Disorders
35. Authenticity and quality of muscle foods : assessing consumer trust and fraud detection approaches
36. Effect of Air Pollutants Particulate Matter PM2.5, PM10, Carbon Monoxide (CO), Nitrogen Dioxide (NO2), Sulfur Dioxide (SO2), and Ozone (O3) on Fractional Exhaled Nitric Oxide (FeNO).
37. The morbid genome of ciliopathies: an update
38. Role of nano-capacitor on dielectric constant enhancement in PEO:NH4SCN:xCeO2 polymer nano-composites: Electrical and electrochemical properties
39. Design and Performance Optimization of WDM Lightwave System Using Optimum Modulation Formats
40. Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
41. A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report
42. Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
43. Autozygome and high throughput confirmation of disease genes candidacy
44. Genomic and phenotypic delineation of congenital microcephaly
45. Bi-allelic PRRT2variants may predispose to Self-limited Familial Infantile Epilepsy
46. Quality Control of Conventional X-Ray Machine at Najran University Hospital Radiology Department
47. Assessing the Impact of Using (FRP) Material for Strengthening the Holes in (RC) Beams.
48. Response of Several Maize Cultivars to Potassium Fertilizer Levels.
49. Bi-allelic variants inWDR47lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans
50. Review of Polymer Forms, Properties and Application in Medical Field
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