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4,144 results on '"Banka A"'

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1. New Strong Gravitational Lenses from the DESI Legacy Imaging Surveys Data Release 9

3. Overcoming Post-War Traumas and Confl icts through Dialogue in Distributed Cognition

6. A Systematic Review of Deep Graph Neural Networks: Challenges, Classification, Architectures, Applications & Potential Utility in Bioinformatics

7. Global Practice Patterns in the Evaluation of Non-Obstructive Azoospermia: Results of a World-Wide Survey and Expert Recommendations

8. Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies

10. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.

11. Structures, processes and outcomes between first referral and referral hospitals in low-income and middle-income countries: a secondary preplanned analysis of the FALCON and ChEETAh randomised trials

12. Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

14. Change Detection in Remote Sensing SAR Image Using a Ratio-Based Operator

17. ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy.

19. Evolution of Ion Wake Characteristics with Experimental Conditions

20. Correction: Opioid Agonist Maintenance Treatment Outcomes—The OPTIMUS International Consensus Towards Evidence-Based and Patient-Centred Care, an Interim Report

21. Opioid Agonist Maintenance Treatment Outcomes—The OPTIMUS International Consensus Towards Evidence-Based and Patient-Centred Care, an Interim Report

22. The Impact of Experience Versus Decision Aids on Patient Preference Toward Virtual Care

23. New Strong Gravitational Lenses from the DESI Legacy Imaging Surveys Data Release 9

24. Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.

25. Intravascularly infused extracellular matrix as a biomaterial for targeting and treating inflamed tissues

26. Cargo-free particles divert neutrophil-platelet aggregates to reduce thromboinflammation

29. Microbiology testing capacity and antimicrobial drug resistance in surgical-site infections: a post-hoc, prospective, secondary analysis of the FALCON randomised trial in seven low-income and middle-income countries

30. Discovery of DNA methylation signature in the peripheral blood of individuals with history of antenatal exposure to valproic acid

31. Fuzzy inference system using genetic algorithm and pattern search for predicting roof fall rate in underground coal mines

33. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

34. Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes

35. DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity

36. Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

37. Access to and quality of elective care: a prospective cohort study using hernia surgery as a tracer condition in 83 countries

38. The impact of inversions across 33,924 families with rare disease from a national genome sequencing project

39. Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

41. Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

43. Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

44. Polysalicylic Acid Polymer Microparticle Decoys Therapeutically Treat Acute Respiratory Distress Syndrome

45. A review on cone-beam computed tomography and its application in dentistry

46. Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

47. Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases

48. Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

49. Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt

50. Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

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