582 results on '"Colombi, M"'
Search Results
102. Molecular characterization of two patients affected by the hallopeau-siemens variant of recessive epidemolysis bullosa dystrophica
103. Allelic deletion at chromosome 11p13 defines a tumour suppressor region between the catalase gene and D11S935 in human non-small cell lung carcinoma.
104. p53 protein accumulation and p53 gene alterations (RFLP, VNTR and p53 gene mutations) in non-invasive versus invasive human transitional bladder cancer
105. Role of different hematologic variables in defining the risk of malignant transformation in monoclonal gammopathy
106. Frequent TP53 gene alterations (mutation, allelic loss, nuclear accumulation) in primary non-small cell lung Cancer
107. Reviews
108. Uncommon clinical presentation of a lymphocytic lymphoma of intermediate differentiation in a patient with systemic sclerosis
109. Essential thrombocythemia and non-Hodgkin lymphoma: A case report
110. Altered fibronectin mRNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: hybridization analysis
111. Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts
112. Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica
113. Study of fibronectin expression in sections from human carcinomas
114. Study of fibronectin expression in tumour cells by dot-blot and hybridization: Quantitative evaluation by image analysis
115. The effect of dermatan sulfate on in vitro human plasma coagulation, platelet aggregation and βTG/PF4 release
116. Diagnosis and treatment of fungal infections in patients with hematologic malignancies.
117. Non interference by heparin with the cytostatic effect of adriamycin: an in vitro study on a human promyelocytic leukaemia cell line.
118. A pilot study on the use of the ProMACE-CytaBOM regimen as a first-line treatment of advanced follicular non-Hodgkin's lymphoma. Gruppo Italiano per lo Studio dei Linfomi.
119. Thrombotic and hemorrhagic complications in essential thrombocythemia. A retrospective study of 103 patients.
120. Trattamento di fistole profonde con rifamicina SV (Presentazione di quadri fistolografici).
121. Plasma cyclic nucleotide levels in acute leukemia patients
122. Genomic organisation and chromosomal localisation of the gene encoding human beta adducin
123. Thrombosis prevention with ticlopidine after femoropopliteal thromboendarterectomy
124. Acute gangrene of the scrotum and penis in four hematologic patients. The usefulness of hyperbaric oxygen therapy in one case.
125. Das Honorar
126. Cloning and expression of the facilitative glucose transporter GLUT10 in arterial tortuosity syndrome skin fibroblast rescue a control-like phenotype
127. Conjunctival hemorrhagic events associated with imatinib
128. Transformation enhancing factors in vitro and in vivo. Potential as cancer markers
129. Ocular toxocariasis: Case reports
130. Un caso paradigmatico di Sindrome di Marfan con una nuova mutazione nel gene FBN1
131. Further delineation of Loeys-Dietz syndrome type IV in a family with mild vascular involvement and a TGFB2 splicing mutation
132. Molecular characterization and transcriptome-wide expression profiling of two patients with spondyloepimetaphyseal dysplasia with joint laxity type 1
133. Classic Ehlers-Danlos sindrome: clinical and molecular characterization of 36 patients
134. Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome?
135. Diagnosi prenatale per sindrome delle arterie tortuose: identificazione di una nuova mutazione nel gene SLC2A10 in corso di gravidanza a rischio
136. Weekly administration of vincristine, cyclophosphamide, mitoxantrone and bleomycin (VEMB) in the treatment of elderly aggressive non Hodgkin's lymphoma
137. Le sindromi di Ehlers-Danlos
138. Ptosi viscerale generalizzata recidivante in una paziente con segni di connettivopatia ereditaria
139. WHOLE EXOME SEQUENCING (WES) IDENTIFYED COL6A5 VARIANTS IN FAMILIAL NEUROPATHIC CHRONIC ITCH
140. Characterization of a 24-year-old woman with osteogenesis imperfecta/Ehlers-Danlos syndrome overlapping phenotype due to the novel c.3469_3470del mutation in the COL1A1 gene
141. A pilot study of low-dose subcutaneous alemtuzumab therapy for patients with hemotherapy-refractory chronic lymphocytic leukemia
142. Sindrome di Ehlers-Danlos di tipo ipermobile: variabilità clinica in 50 pazienti italiani
143. Caratterizzazione di una famiglia italiana affetta da artrogriposi distale di tipo 2B e mutazione ricorrente p.R63H nel gene TNNT3
144. Rosai-Dorfman syndrome with extranodal localizations and response to glucocorticoids: a case report
145. Simulazione numerica delle conseguenze di un terremoto a Messina
146. Characterisation of a large duplication in the COL5A1 gene in a classic Ehlers-Danlos syndrome patient
147. Clinical and molecular characterization of a family with LDS type IV: identification of the first TGFB2 splice mutation
148. Italian validation of the functional difficulties questionnaire (FDQ-9) and its correlation with major determinants of quality of life in adults with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorder.
149. Expression of transformation markers and suppression of tumorigenicity in human cell hybrids
150. Low-dose heparin in thoracic surgery: Effect on blood coagulation and fibrinolysis system
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.