611 results on '"Grosso E"'
Search Results
2. On the distinctiveness of the electricity load profile
3. 2D Recurrent Neural Networks for Robust Visual Tracking of Non-Rigid Bodies
4. Blending 2D and 3D Face Recognition
5. 29MO Germline variants NGS characterization in patients with non-syndromic adrenocortical carcinoma
6. Real time detection of driver attention: Emerging solutions based on robust iconic classifiers and dictionary of poses
7. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
8. Does lesser trochanter implication affect hip flexion strength in proximal femur fracture?
9. GJB5 association with BRAF mutation and survival in cutaneous malignant melanoma
10. 2D Recurrent Neural Networks for Robust Visual Tracking of Non-Rigid Bodies
11. Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review
12. Targeting of the adaptor protein Tab2 as a novel approach to revert tamoxifen resistance in breast cancer cells
13. Genotype, phenotype and hormonal levels correlation in non-classical congenital adrenal hyperplasia
14. Producción de tomate y dinámica microbiológica del suelo de invernáculo al aplicar vermicompostas
15. Family-based whole exome sequencing allows a 25% diagnostic yield in patients with autism spectrum disorder
16. Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene
17. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations
18. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
19. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs
20. Laparoscopic cholecystectomy: Imaging of complications and normal postoperative CT appearance
21. Molecular Genetic Analysis of von Hippel-Lindau Disease by Denaturing High-Performance Liquid Chromatography
22. Treatment of the Pulmonary Involvement in the Patient with Tuberous Sclerosis Complex
23. A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA
24. Definition of the smallest pathological CAG expansion in SCA7
25. ESTRATÉGIAS E DESDOBRAMENTOS DE UMA URBANIZAÇÃO OLIGOPOLISTA EM PRIMAVERA DO LESTE, MATO GROSSO, BRASIL / STRATEGIES AND CONSEQUENCES OF AN OLIGOPOLISTIC URBANIZATION IN PRIMAVERA DO LESTE, MATO GROSSO, BRAZIL
26. Il regionalismo differenziato: potenzialià e aspetti problematici
27. 476 GJB5 association with BRAF mutation and survival in cutaneous melanoma
28. Fascia-iliaca compartment block vs intra-articular hip injection for preoperative pain management in intracapsular hip fractures: A blind, randomized, controlled trial
29. Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)
30. Erratum: Targeting of the adaptor protein Tab2 as a novel approach to revert tamoxifen resistance in breast cancer cells
31. Solution-Phase Parallel Synthesis of Aryloxyimino Amides via a Novel Multicomponent Reaction among Aromatic (Z)-Chlorooximes, lsocyanides, and Electron-Deficient Phenols
32. Teleradiology through iPad May Positively Affects the Quality of Health Care in a Paediatric Children Hospital
33. Identification of patients at high risk for hypocalcemia after total thyroidectomy
34. Solitary thyroid metastasis from colon cancer: a rare case report
35. A Decision Support System for the assisted diagnosis of brain tumors: a feasibility study for ¹⁸F-FDG PET preclinical studies
36. Prognostic Value of pre-therapy 18FDG PET/CT for the Outcome of 18FDG PET-guided SIB-IMRT in Patients with Head and Neck Cancer
37. Statistical Parametric Mapping for activation studies in rats
38. SPM for activation studies in rats on stress condition
39. 18FDG PET/CT Image-Guided Simultaneous Integrated Boost Intensity-Modulated Radiotherapy in Head and Neck cancer
40. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations
41. GERMLINE PROKINETICIN RECEPTOR 2 (PROKR2) VARIANTS ASSOCIATED WITH CENTRAL HYPOGONADISM CAUSE DIFFERENTAL MODULATION OF DISTINCT INTRACELLULAR PATHWAYS
42. Italian Study Group on Idiopathic Central Hypogonadism (ICH). Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways
43. Oligodontia segregating with a 7p21.2p21.1 ∼ Mb duplication in an Italian family with three affected siblings
44. A germline mismatch repair mutation possibly leading to a de novo NF1 germline mutation
45. Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders
46. Erythrocyte glutathione transferase: A non-antibody biomarker for systemic sclerosis, which correlates with severity and activity of the disease
47. Statistical voxel-based analysis of [F-18]FDG PET animal studies for the estimation of glucose metabolism in stress conditions
48. Labiopalatoschisi ed esadattilia bilaterale della mano associate ad una doppia delezione de novo sul cromosoma 4q32 e 4q34 che coinvolgono I geni PDGFC e FBXO8
49. 'A de novo X;8 translocation in a patient with psychomotor retardationand congenital cerebellar hypoplasia creates a PTK2-THOC2 fusion gene and knocks down THOC2 expression by transcriptional interference'
50. Delezione del gene ASTN2 (Astroactin-2), coinvolto nella migrazione neuronale, in due sorelle con ritardo psicomotorio
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