Zobrazeno 1 - 10
of 78
pro vyhledávání: '"L, Virgolini"'
Autor:
F, Silvestri, D, Russo, R, Fanin, L, Virgolini, G, Terrosu, A, Donini, F, Bresadola, M, Baccarani
Publikováno v:
Haematologica. 80(1)
The indications for splenectomy in hematological diseases are well known. In particular, they include idiopathic thrombocytopenic purpura (ITP), hereditary spherocytosis (HS) and Hodgkin's disease (HD) (as a part of subdiaphragmatic staging). We pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8215a911dbdaed1e3f97689a849425e
https://pubmed.ncbi.nlm.nih.gov/7758991
https://pubmed.ncbi.nlm.nih.gov/7758991
Publikováno v:
Haematologica. 79(4)
In recent years recombinant alpha-interferons (alpha-IFNs) have been widely used in the treatment of several hematological malignancies. Prolonged courses of IFN have been shown to induce autoantibodies and to support the exacerbation or even the dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce5e5aa38bb0765f2441037411abd479
https://pubmed.ncbi.nlm.nih.gov/7806093
https://pubmed.ncbi.nlm.nih.gov/7806093
Publikováno v:
Minerva medica. 84(3)
Gaucher's disease is a lipidosis caused by deficiency of the enzyme glucocerebrosidase (glucosylceramidase) with secondary accumulation of glucocerebrosides in macrophage lysosomes. Three clinical forms of the disease have been described with autosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::755194d3780468db62f44b8c6c03b6ef
https://pubmed.ncbi.nlm.nih.gov/8492969
https://pubmed.ncbi.nlm.nih.gov/8492969
Publikováno v:
Minerva medica. 84(3)
Gaucher's disease is the most frequent of lysosomal storage diseases. In a family study two affected sisters of a type I patient were identified. Two of them underwent splenectomy, so reaching hematological normalization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dce0ee884767249d742fda20a936168a
https://pubmed.ncbi.nlm.nih.gov/8492967
https://pubmed.ncbi.nlm.nih.gov/8492967
Autor:
L, Virgolini, A, De Maglio
Publikováno v:
Italian journal of orthopaedics and traumatology. 18(4)
A young woman treated with combined therapy (chemo- and radiotherapy) for Hodgkin's disease later developed avascular necrosis of the humeral heads. The unusual location of the aseptic necrosis, and particularly the fact that it occurred bilaterally,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95d9103f5d863297704a2283de05846c
https://pubmed.ncbi.nlm.nih.gov/1345650
https://pubmed.ncbi.nlm.nih.gov/1345650
Autor:
L, Virgolini, C, Gallizia
Publikováno v:
Recenti progressi in medicina. 81(10)
The mechanisms of paraneoplastic hypercalcemic syndromes are heterogeneous. Neoplastic hypercalcemia without bone metastatic disease is caused by parathyroid hormone related protein, whose action is comparable to parathyroid hormone. Growth transform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffad7b3129a823656bb77bc5f90acb2c
https://pubmed.ncbi.nlm.nih.gov/2291007
https://pubmed.ncbi.nlm.nih.gov/2291007
Publikováno v:
Clinical nuclear medicine. 15(2)
A patient presented with recurrent pheochromocytoma 10 years following the apparently successful surgical cure of a right adrenal pheochromocytoma. Conventional medical imaging techniques, (chest radiograph, abdominal ultrasound, and abdominal CT) su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98ce047dd2ae7d4744403d2b616453c2
https://pubmed.ncbi.nlm.nih.gov/1690098
https://pubmed.ncbi.nlm.nih.gov/1690098
Publikováno v:
Acta Haematologica. 55:181-191
A patient with a combined hereditary deficiency of factors VII and VIII is presented together with a family study. The main bleeding manifestations were easy bruising and bleeding after tooth extractions. No hemarthrosis was ever observed. The main l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dd0697f94edbe298847c273d4238c88
https://doi.org/10.1159/000208012
https://doi.org/10.1159/000208012
Publikováno v:
Haematologica. 70(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8aca76896048c287bee5b2d29e72ee32
https://pubmed.ncbi.nlm.nih.gov/3938432
https://pubmed.ncbi.nlm.nih.gov/3938432
Autor:
L, Virgolini
Publikováno v:
Minerva medica. 76(41)
Chronic neutrophilic leukemia is a rare form of myeloproliferative disorders, with only sixteen reports in literature. Neutrophilic leukocytosis, bone marrow myeloid hyperplasia, elevated leukocytic alkaline phosphatase and the absence of Ph1 are the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8953f2fbe2bc57ea3d1702ea2e6e6a5
https://pubmed.ncbi.nlm.nih.gov/3903551
https://pubmed.ncbi.nlm.nih.gov/3903551