290 results on '"Donti, Emilio"'
Search Results
52. Genetica Medica
53. A case of acute myeloid leukemia with deletion of chromosome 7 following PBSC transplantation
54. THE ITALIAN CO-OPERATIVE STUDY GROUP ON CHRONIC MYELOID LEUKEMIA. A prospective study of alfa-interferon and autologous bene marrow transplantation in chronic myeloid leukaemia
55. A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy
56. Phenotype of in vitro human otosclerotic cells and its mpdulation by TGF beta
57. Germline PTPN11 mutation affecting exon 8 in a case of syndromic juvenile myelomonocytic leukemia
58. Studio citogenetico di un caso di carcinoma a cellule basali e revisione della letteratura
59. Cytogenetics and molecular genetics of myelodisplastic syndromes
60. Response to low-dose ARA-C + IFN alpha in advanced and second chronic phase chronic myeloid leukemia
61. FMR1, FMR2, and SLITRK2 deletion inside a paracentric inversion involving bands Xq27.3-q28 in a male and his mother
62. Heterozygous X-linked adrenoleukodystrophy-associated myelopathy mimicking primary progressive multiple sclerosis
63. Myostatin depletion: A therapy for Ehlers-Danlos syndrome?
64. Diagnosi prenatale precoce: esperienze del centro regionale umbro
65. Expression of aphidicolin- induced fragile sites in lymphocytes of patients with breast cancer
66. Interferon alpha-2b as therapy for patients with Ph‘-positive chronic myelogenous leukemia
67. Hot water epilepsy and Mccune–Albright syndrome: A case report
68. Studio della fragilità cromosomica in linfociti di pazienti con carcinoma mammario
69. Trisomy 4 in acute nonlymphocytic leukemia: Report of two cases and review of the literature
70. Effect of INF' therapy on secondary Ph'-positive clones
71. Cytoskeletal characteristics and functional response to PHT stimulation in human normal and otosclerotic bone cell cultures
72. Response to Imatinib or Imatinib Containing Regimens of Secondary Clones in Chronic Myeloid Leukemia Patients with Additional Chromosomal Abnormalities.
73. Five children with deletions of 1p34.3 encompassing AGO1 and AGO3.
74. 7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages.
75. The translocation breakpoint of acute promyelocytic leukemia lies within the retonoic acid receptor alpha locus
76. Characterization of the cytoskeleton in human normal and otosclerotic osteoblastic-like cells
77. Evolving modalities of treatment with Interferon alfa-2b for Ph'-positive chronic myelogenous leukaemia
78. In vitro bone-marrow cell cultures and cytogenetic analysis in a case of myelodysplasia
79. Morphology and cytoskeleton organization in human osteoblastic cells treated with interleukin-1
80. Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly.
81. Impact of Complete Kariotypic Remission (CKR) and Sokal Risk on Overall Survival in Chronic Myelogenous Leukemia (CML) Patients: A Monocentric Experience.
82. Philadelphia Chromosome (Ph’) Secondary Clones in Chronic Myeloid Leukemia (CML) Are Not Indicative of Resistance to IFNa- or Imatinib-Based Treatment Regimens.
83. Patterns of Clonal Evolution in Ph’-Positive Chronic Myelogenous Leukemia (CML) during Chronic Phase: Overall Incidence, Type, Multiplicity, Development Time, Effect on Subsequent Genetic Instability, Sokal Risk, Type of bcr/abl Transcript and Hematological Evolution.
84. Occurrence of the same chromosome abnormalities in Ph+and Ph?cells in chronic myeloid leukaemia. Evidence of a secondary origin of the Ph chromosome?
85. Interferon-alpha-2b as therapy for untreated and pretreated patients with Ph' positive chronic myeloid leukemia
86. Localization of the human HF.10 finger gene on a chromosome region (3p21p22) frequently deleted in human cancers
87. Mapping of chromosome 17 breakpoint in acute myeloid leukemias
88. L'interferone nel trattamento della leucemia mieloide cronica Philadelphia positiva
89. L'interferone alfa nella leucemia mieloide cronica
90. cDNA isolation, expression analysis and chromosomal localization of two human zinc finger genes
91. L'interferone α-2b nel trattamento della leucemia mieloide cronica Ph' positiva
92. Molecular Response of CML Patients to INFα Based Treatment or to STI Based Therapy.
93. Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories
94. Spontaneous expression of FRA3P in a patient with Nager syndrome
95. Glycosaminoglycan Metabolism and Cytokine Release in Normal and Otosclerotic Human Bone Cells Interleukin-1 Treated
96. Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis
97. Expression of aphidicolin-induced fragile sites in lymphocytes of patients with breast cancer
98. A new case of familial paracentric inversion of chromosome 2
99. EFFECT OF IFNα THERAPY ON SECONDARY Ph1‐POSITIVE CLONES
100. Trisomy 4 in acute nonlymphocytic leukemia
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