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排序方式: 共有125条查询结果,搜索用时 14 毫秒
101.
In the clinical setting, noninvasive blood gas monitoring has become the standard of care over arterial punctures. Technology has provided ways to measure both arterial oxygen (PaO2) and arterial Carbon Dioxide (PaCO2). With the availability of noninvasive blood gas monitoring, patient care and comfort is improving, and cost savings are being implemented. Overall noninvasive monitoring can aid in the diagnosis of some pulmonary diseases and monitor patient progress. 相似文献
102.
A. Verrotti D. Laino V. E. Rinaldi A. Suppiej L. Giordano I. Toldo L. Margari P. Parisi R. Rizzo S. Matricardi R. Cusmai S. Grosso R. Gaggero N. Zamponi P. Pavone G. Capovilla M. Rauchenzauner C. Cerminara G. Di Gennaro M. Esposito P. Striano S. Savasta G. Coppola S. Siliquini F. Operto V. Belcastro F. Ragona G. L. Marseglia A. Spalice 《European journal of neurology》2016,23(2):241-246
103.
Patricia Validire Mathieu Capovilla Bernard Asselain Youlia Kirova Rémi Goudefroye Corine Plancher Alain Fourquet Manuela Zanni Philippe Gaulard Anne Vincent‐Salomon Didier Decaudin 《American journal of hematology》2009,84(3):133-139
The aims of this study were to define the initial pathological and clinical characteristics, and prognostic factors of patients with primary breast malignant lymphoma (PBL). All patients treated at the Institut Curie for lymphoma with breast involvement were reviewed. A pathological review of all cases was performed. Forty‐five cases were selected in whom 38 cases were of diffuse large B‐cell lymphoma. A complete analysis was then performed on these 38 patients. Twenty out of 28 cases (71%) of cases were Bcl‐2 positive and four out of 28 (14%) had a CD10 positive staining. Peculiar initial characteristics showed nodal involvement in 58% of the cases and two or more extra‐nodal sites in 31% of the cases. Among the 37 patients for whom all data were available, and according to the International Prognostic Index, 19 patients (51%) were classified in the low‐risk group, 5 cases (14%) in the low‐ to intermediate‐risk group, 6 patients (16%) in the intermediate‐ to high‐risk group, and 7 (19%) case in the high‐risk group. At the end of initial therapy, 34 patients (89%) achieved CR. With a median follow‐up of 96 months, 18 patients (47%) relapsed of whom 3 had a relapse in central nervous system site. The 5‐year disease‐free (DFS) and overall survivals (OS) were 54% and 61%, respectively. In multivariate analysis, the presence of 2 or more extranodal sites was prognostic for lower DFS (P = 0.0008) and OS (P = 0.09), and a performance status ≥1 was prognostic for lower OS (P = 0.005). Finally, when our series was compared with a historical series of 111 patients with aggressive nodal lymphomas, we observed significant lower survival rates in localized PBL (P < 0.03). Initial breast localization has a pejorative impact on the outcome of patients with Non‐Hodgkin's Lymphoma (NHL), with an impressive adverse influence of additional extranodal sites. These results suggest a specific management of NHL with breast involvement. Am. J. Hematol., 2009. © 2008 Wiley‐Liss, Inc. 相似文献
104.
Benign idiopathic partial epilepsies in infancy. 总被引:6,自引:0,他引:6
In infancy, partial epilepsies have been considered with suspicion for their probable association with brain lesions. Japanese authors first described partial epilepsies in infancy with a favorable outcome and called them benign partial epilepsy in infancy with complex partial seizures. Similar, but familial, cases with onset during the first year of life were described some years later and called benign infantile familial convulsions. Similar familial cases with subsequent choreoathetosis were described in 1997 and called infantile convulsions and choreoathetosis. Benign infantile convulsions have also been described in association with mild gastroenteritis. Interictal electroencephalography (EEG) was always normal in all of these forms. More recently, a new epileptic syndrome characterized by partial seizures with onset between ages 13 and 30 months, a benign outcome, and characteristic EEG abnormalities in the vertex regions during sleep has been described. There is also an early-onset benign childhood occipital seizure susceptibility syndrome that can start in infancy. 相似文献
105.
Traction on the septum during transoral septotomy for Zenker diverticulum improves the final outcome
106.
V. Torre E. Pasino M. Capovilla Dr. L. Cervetto 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1981,44(4):427-430
Summary Exposure of isolated toad retinae to phosphodiesterase inhibitors induced changes in the ionic permeability of rod cells. Under similar conditions intracellularly recorded light responses were observed also in the absence of external Na+. Hyperpolarizing photoresponses in Na+-free media required the presence of divalent cations among which Mg2+, Mn2+ and Ba2+ were the most effective.Supported by a fellowship of the Scuola Normale Superiore, Pisa 相似文献
107.
108.
Early myoclonic epileptic encephalopathy (E.M.E.E.) 总被引:1,自引:0,他引:1
B. Dalla Bernardina O. Dulac N. Fejerman C. Dravet G. Capovilla S. Bondavalli V. Colamaria J. Roger 《European journal of pediatrics》1983,140(3):248-252
The authors describe the electroclinical aspects and evolution of nine cases of myoclonic epileptic encephalopathy which began between two days and ten weeks of life. At onset it is associated with: myoclonic jerks, partial fits and periodic paroxysmal EEG abnormalities. Repeated spasms coexisting with partial fits and 'suppression-bursts' (both appearing later) complete the electroclinical picture. The neurological status (initially normal) progressively deteriorates leading within a few months to a decerebrate posture with opisthotonos. In spite of thorough neuroradiological, biochemical, cytological, metabolic, and ultrastructural investigations, the etiology remained unknown. However, the electroclinical and evolutive patterns are similar to those of some metabolic diseases (Polyodystrophy, Non-Ketotic Hyperglycinemia, etc.). All these observations display a homogeneous electroclinical pattern for which the authors propose the name of Early Myoclonic Epileptic Encephalopathy. This type deserves to be classified as a particular electroclinical entity among the epileptic encephalopathies of the first year of life; since its course is regularly downhill in all cases there may be a familial recurrence due to the possibility of a metabolic etiology. 相似文献
109.
Intermittent falls and fecal incontinence as a manifestation of epileptic negative myoclonus in idiopathic partial epilepsy of childhood 总被引:3,自引:0,他引:3
Capovilla G Rubboli G Beccaria F Meregalli S Veggiotti P Giambelli PM Meletti S Tassinari CA 《Neuropediatrics》2000,31(5):273-275
We report two children, suffering from idiopathic partial epilepsy, who started to present, in the same period of time, with epileptic negative myoclonus (ENM) in one lower limb and fecal incontinence (FI). Polygraphic recordings showed that ENM was associated with paroxysmal activities distributed over the vertex region. Both ENM and FI disappeared when ethosuximide treatment was started. We hypothesize that, in our patients, ENM in one lower limb and FI depended on a transitory impairment, caused by epileptic activity that altered the functionality of nearby cortical areas, located in fronto-mesial regions, involved in the control of the muscular tone of the lower limbs and of the pelvic floor muscles. 相似文献
110.
Capovilla M Durlach A Fourati E Beucher AB Eschard JP Dehoux E Le Noach J Cucherousset J 《Clinical rheumatology》2007,26(1):60-63
Synovial metastases are rare events. Only 37 cases diagnosed by synovial fluid cytologic examination and/or by microscopic
investigation of synovial biopsies have been previously reported in the literature. We report another case of shoulder chronic
arthritis due to a recurrence of rectal adenocarcinoma and review previous published observations. Generally, this condition
carries a poor prognosis with average patients survival of less than 5 months. The possibility of metastatic disease should
be considered when an elderly person or patient with a history of previous malignancy presents with a chronic arthritis. 相似文献