195 results on '"Orsini, Paola"'
Search Results
2. The genomic analysis brings a new piece to the molecular jigsaw of idiopathic erythrocytosis
3. Early spinal muscular atrophy treatment following newborn screening: A 20‐month review of the first Italian regional experience
4. Erythrocytosis with JAK2 GGCC_46/1 haplotype and without JAK2 V617F mutation is associated with CALR rs1049481_G allele
5. Nanopore sequencing approach for immunoglobulin gene analysis in chronic lymphocytic leukemia
6. A Rare Case of Concurrent 2q34q36 Duplication and 2q37 Deletion in a Neonate with Syndromic Features
7. Droplet Digital PCR Is a Robust Tool for Monitoring Minimal Residual Disease in Adult Philadelphia-Positive Acute Lymphoblastic Leukemia
8. TNFRSF13B gene mutation in familial acute myeloid leukemia: A new piece in the complex scenario of hereditary predisposition?
9. Mutational analysis in BCR-ABL1 positive leukemia by deep sequencing based on nanopore MinION technology
10. Droplet Digital PCR Is a Reliable Tool for Monitoring Minimal Residual Disease in Acute Promyelocytic Leukemia
11. Case report: biallelic DNMT3A mutations in acute myeloid leukemia
12. Droplet digital PCR for the quantification of Alu methylation status in hematological malignancies
13. Design and MinION testing of a nanopore targeted gene sequencing panel for chronic lymphocytic leukemia
14. BCR–ABL1 e6a2 transcript in chronic myeloid leukemia: biological features and molecular monitoring by droplet digital PCR
15. Horizontal Gaze Palsy with Progressive Scoliosis with Overlapping Epilepsy and Learning Difficulties: A Case Report
16. 12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature
17. Additional file 1 of The genomic analysis brings a new piece to the molecular jigsaw of idiopathic erythrocytosis
18. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report
19. Recombinant human TSH and ablation of post-surgical thyroid remnants in differentiated thyroid cancer: the effect of pre-treatment with furosemide and furosemide plus lithium
20. Percutaneous Laser Ablation in the Treatment of Toxic and Pretoxic Nodular Goiter
21. Droplet digital PCR assay for quantifying of CALR mutant allelic burden in myeloproliferative neoplasms
22. First prenatal case of Noonan syndrome with SOS2 mutation: Implications of early diagnosis for genetic counseling
23. A complex and cryptic intrachromosomal rearrangement generating the FIP1L1_PDGFRA in adult acute myeloid leukemia
24. Nanopore sequencing sheds a light on the FLT3 gene mutations complexity in acute promyelocytic leukemia
25. JAK2 Negative Erythrocytosis Associated with JAK2 GGCC_46/1 Haplotype, Calr rs1049481_G, and Normal Erythropoietin Level: Is This a New Entity?
26. Erythrocytosis with JAK2 GGCC_46/1 haplotype and without JAK2 V617F mutation is associated with CALR rs1049481_G allele
27. Nanopore Sequencing in Blood Diseases: A Wide Range of Opportunities
28. Recombinant human thyroid-stimulating hormone is effective for radioiodine ablation of post-surgical thyroid remnants
29. Assay of Free Thyroxine and Free Triiodothyronine in Fine-Needle Aspiration of Thyroid Nodules: a Useful and Low-Cost Assessment
30. Radioiodine Treatment with 30 mCi after Recombinant Human Thyrotropin Stimulation in Thyroid Cancer: Effectiveness for Postsurgical Remnants Ablation and Possible Role of Iodine Content in l-Thyroxine in the Outcome of Ablation
31. Additional file 3: of Droplet digital PCR for the quantification of Alu methylation status in hematological malignancies
32. Additional file 2: of Droplet digital PCR for the quantification of Alu methylation status in hematological malignancies
33. Additional file 4: of Droplet digital PCR for the quantification of Alu methylation status in hematological malignancies
34. Nanopore sequencing sheds a light on the FLT3 gene mutations complexity in acute promyelocytic leukemia.
35. Thyroid Nodules with Microfollicular Findings Reported on Fine-Needle Aspiration: Invariably Surgical Treatment?
36. Droplet Digital PCR for the Quantification of Alu Methylation Status in Hematological Malignancies
37. RARA and RARG gene downregulation associated with EZH2 mutation in acute promyelocytic-like morphology leukemia
38. Genomic BCR-ABL1 breakpoint characterization by a multi-strategy approach for “personalized monitoring” of residual disease in chronic myeloid leukemia patients
39. Overexpression of the LSAMP and TUSC7 genes in acute myeloid leukemia following microdeletion/duplication of chromosome 3
40. Erythrocytosis with JAK2GGCC_46/1 haplotype and without JAK2V617F mutation is associated with CALRrs1049481_G allele
41. A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome
42. Systemic Mastocytosis With Associated Chronic Lymphocytic Leukemia: A Matter Of Diseases Or Prognostic Factors
43. Droplet digital PCR analysis of NOTCH1 gene mutations in chronic lymphocytic leukemia
44. TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing
45. MYEOV gene overexpression in primary plasma cell leukemia with t(11;14)(q13;q32)
46. A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.
47. Visual Vignette
48. Droplet Digital PCR Analysis for Diagnosis and Minimal Residual Disease Monitoring in Adult Ph+ Acute Lymphoblastic Leukemia
49. Absolute quantification of the pretreatmentPML-RARAtranscript defines the relapse risk in acute promyelocytic leukemia
50. Myelodysplastic syndrome with 5q deletion following IgM monoclonal gammopathy, showing gene mutation MYD88 L265P
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.