Search

Your search keyword '"A. Bertoli"' showing total 18,895 results

Search Constraints

Start Over You searched for: Author "A. Bertoli" Remove constraint Author: "A. Bertoli"
18,895 results on '"A. Bertoli"'

Search Results

51. A Survey of Autoantibodies to Self Antigens in Graves' Disease Patients with Thyroid-Associated Ophthalmopathy

52. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes

53. The Double Chooz antineutrino detectors

56. Surgical clipping and endovascular treatments for small or very small anterior communicating artery aneurysms: A comparative pooled analysis

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

60. List of contributors

62. Bridging the gap to real-world for network intrusion detection systems with data-centric approach

64. At a glance: the largest Niemann-Pick type C1 cohort with 602 patients diagnosed over 15 years

65. A founder DBR1 variant causes a lethal form of congenital ichthyosis

66. A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts

68. Characteristics and outcomes of COVID-19 patients admitted to hospital with and without respiratory symptoms

70. A-star path planning simulation for UAS Traffic Management (UTM) application

77. De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues

79. Superconvergence of the Strang splitting when using the Crank-Nicolson scheme for parabolic PDEs with Dirichlet and oblique boundary conditions

80. Erratum to: Search for exclusive Higgs and Z boson decays to ϕγ and ργ with the ATLAS detector

82. Targeting PP2A-dependent autophagy enhances sensitivity to ruxolitinib in JAK2V617F myeloproliferative neoplasms

87. A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion

91. Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disorders

92. Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders

93. Long-term real-world evidence of CPX-351 of high-risk patients with AML identified high rate of negative MRD and prolonged OS

96. Prevalence of hepatitis D virus infection in Central Italy has remained stable across the last 2 decades with dominance of subgenotypes 1 and characterized by elevated viral replication

98. Artificial intelligence-based prediction models for acute myeloid leukemia using real-life data: A DATAML registry study

100. International retrospective natural history study of LMNA-related congenital muscular dystrophy

Catalog

Books, media, physical & digital resources