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1. Hindered settling of log-normally distributed particulate suspensions: theoretical models vs. Stokesian simulations

2. Buckling of a monolayer of plate-like particles trapped at a fluid-fluid interface

4. Hydrodynamic interactions change the buckling threshold of parallel flexible sheets in shear flow

5. Analysis and optimization of a multicascade method for the size fractionation of poly-dispersed particle systems via sedimentation or centrifugation

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

7. Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome (NODRS)

8. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

9. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

10. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

11. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

12. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

13. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

14. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

16. Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples

17. De novo variants in DENND5B cause a neurodevelopmental disorder

18. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

19. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

20. Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

22. Towards nanomechanical models of liquid-phase exfoliation of layered 2D nanomaterials: analysis of a $\pi$-peel model

23. Liquid exfoliation of multilayer graphene in sheared solvents: a molecular dynamics investigation

24. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

25. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

26. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

27. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

28. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

29. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

30. A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis

31. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

32. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

33. Racial and Ethnic Disparities in Health Care Usage and Death by Neighborhood Poverty Among Individuals With Congenital Heart Defects, 4 US Surveillance Sites, 2011 to 2013

34. De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects

35. SLC35A2‐CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals

36. Public Health Approach to Improve Outcomes for Congenital Heart Disease Across the Life Span

37. De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

38. Preventing birth defects, saving lives, and promoting health equity: an urgent call to action for universal mandatory food fortification with folic acid

42. Dynamical Theory of the Inverted Cheerios Effect

43. Breaking the Nanoparticle Loading–Dispersion Dichotomy in Polymer Nanocomposites with the Art of Croissant‑Making

44. De novo variants in DENND5B cause a neurodevelopmental disorder

45. Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980–2017

46. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

47. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

49. Dipolar Capillary Interactions between Tilted Ellipsoidal Particles Adsorbed at Fluid-Fluid Interfaces

50. Brief Report: Pediatrician Perspectives Regarding Genetic Evaluations of Children with Autism Spectrum Disorder

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