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排序方式: 共有7425条查询结果,搜索用时 78 毫秒
991.
992.
Raúl Veiga Cabello Pilar Navarro Alonso Miguel Cantalejo Moreira Alberto Díaz Oca Jorge Cabezudo Pedrazo 《Seminarios de la Fundación Espa?ola de Reumatología》2009,10(2):56-63
Vertebra plana is a concept introduced by Calvé in 1925 to name a process characterized by the collapse of a single vertebra with no involvement of the discs, widening of the intervertebral space of at least one third compared with normal width, and an increase in the density of the collapsed vertebra. Because of its benign and self-limiting nature, this entity was originally thought to be an osteochondritis. Later publications did not corroborate this view and connected this entity initially with eosinophilic granuloma and subsequently with additional malignant infiltrating tumoral processes, in particular with Ewing's sarcoma and lymphomas, thus posing difficulties for its management. The initial concept was extended in 1990 to crushed and wedged vertebrae, including developmental abnormalities such as bone dysplasias. The present article provides a general review of vertebra plana, including the concept, etiology and pathogenesis of related processes, clinical findings and diagnosis. We also discuss the debate on the benign or malignant nature of vertebra plana and on the need for an immediate biopsy versus observation, as well as the therapeutic orientations. 相似文献
993.
F Ruiz Santiago G Soler Dorda J M Izago?ola de Miguel J Martín Marcos J Alonso Pérez J M Hidalgo Garrido J A Jiménez Ríos J M Navarro Bernal L Fernández Ollero 《Revista española de enfermedades digestivas》1992,81(2):131-133
Two cases of jejunojejunal intussusception in whom diagnosis was reached preoperatively by ultrasonography and small bowel follow-through meal are presented. We review the sonographic patterns of intussusception that allow the differential diagnosis with miscellaneous gastrointestinal abnormalities detected by ultrasound. 相似文献
994.
A case of fixed eruption caused by ciprofloxacin is reported. To our knowledge, no other cases have been published. Cross-sensitivity with another fluoroquinolonc has been demonstrated. 相似文献
995.
M. Blanco J. E. Blanco J. Blanco E. A. Gonzalez A. Mora C. Prado L. Fern��ndez M. Rio J. Ramos M. P. Alonso 《Epidemiology and infection》1996,117(2):251-257
From February to July of 1994, 328 faecal samples from 32 herds were collected and verotoxin-producing Escherichia coli (VTEC) found on 84% of the farms. The proportion of animals infected varied from 0-63%. VTEC were recovered from 52 (20%) of 257 cows and from 16 (23%) of 71 calves. Although the VTEC belonged to 25 different serogroups, 7 (O8, O20, O22, O77, O113, O126 and O162) accounted for 46% of strains. Nearly 45% of the strains. Nearly 45% of the 83 bovine VTEC strains belonged to serogroups associated with haemorrhagic colitis and haemolytic uraemic syndrome in humans. However, only 2 (2%) of 83 VTEC strains isolated from cattle belonged to enterohaemorrhagic E. coli (EHEC) serotypes (O26:H11 and O157:H7), and only 8 (10%) were positive for the attaching and effacing E. coli (eae) gene sequence. Polymerase chain reaction (PCR) showed that 17 (20%) of VTEC strains carried VT1 genes, 43 (52%) possessed VT2 genes, and 23 (28%) carried both VT1 and VT2 genes. Characterization of VTEC isolates revelated a heterogeneous population in terms of serogroup and toxin type in the positive herds. This study confirms that healthy cattle are a reservoir of VTEC, but, the absence of eae genes in most bovine VTEC strains suggests that they may be less virulent for humans than eae-positive EHEC. 相似文献
996.
Use of somatostatin analogue scintigraphy in the localization of recurrent medullary thyroid carcinoma 总被引:1,自引:0,他引:1
Lluís Bernà Ana Chico Xavier Matías-Guiu Eugenia Mato Ana Catafau Carmen Alonso Josefina Mora Didac Mauricio José Rodríguez-Espinosa Carina Marí Albert Flotats Juan-Carlos Martín Montserrat Estorch Ignasi Carrió 《European journal of nuclear medicine and molecular imaging》1998,25(11):1482-1488
Detection of recurrence of medullary thyroid carcinoma (MTC) remains a diagnostic problem. Increased serum tumour marker levels
frequently indicate recurrence while conventional imaging techniques (CIT) are non-diagnostic. In this study, we performed
indium-111 octreotide scintigraphy and CIT in a series of 20 patients with MTC presenting with elevated serum tumour markers
after surgery. 111In-octreotide whole-body studies detected 15 pathological uptake foci in 11 of the 20 patients studied and CIT detected 17
lesions in 11 of the 20 patients. Ten patients underwent reoperation, five of them with positive 111In-octreotide scintigraphy and CIT and two with positive isotopic exploration and negative CIT. Surgical findings demonstrated
that the results of isotopic study and CIT had been false-positive for MTC in one case (sarcoidosis). The six patients with
true-positive 111In-octreotide studies had significantly higher basal calcitonin (CT) and carcinoembryonic antigen (CEA) levels than the patients
with negative isotopic studies. The expression of somatostatin receptor (SSTR) subtypes by PC-PCR could be investigated in
four cases with a positive isotopic study. Among the three cases with a true-positive study, SSTR2, the SSTR subtype that
preferentially binds to the somatostatin analogue octreotide, was detected in two, SSTR5 was demonstrated in the three, and
SSTR3 was detected in one. No subtype of SSTR was detected in the case with a final diagnosis of sarcoidosis. We conclude
that 111In-octreotide has limited sensitivity in detecting recurrence in patients with MTC, although its sensitivity may improve with
high serum CT levels. This radionuclide imaging technique should be employed when conventional imaging techniques are negative
or inconclusive or when the presence of somatostatin receptors may provide the basis for treatment with somatostatin analogues.
Received 5 April and in revised form 27 July 1998 相似文献
997.
P. E. Jiménez Caballero C. de Diego Boguna E. Martin Correa M. Serviá Candela C. Marsal Alonso 《European journal of neurology》2008,15(9):991-994
Background and purpose: We report a novel mutation in exon 8 of the presenilin 1 (PSEN1) gene (V261L) associated with early-onset autosomal dominant Alzheimer's disease and spastic paraparesis.
Methods and results: The proband was a woman who developed insidious cognitive decline with predominant memory loss and gait disorder secondary to spasticity at the age of 40. Her brother and her mother had a similar disease in the fifth decade of life. The feature of amnestic presentation with spastic paraparesis is consistent with the majority of mutations in the exon 8 of the PSEN1 1 gene.
Conclusions: Screening for PSEN1 mutations is especially likely to be productive when directed toward persons with positive family history and with age at onset of under 60. 相似文献
Methods and results: The proband was a woman who developed insidious cognitive decline with predominant memory loss and gait disorder secondary to spasticity at the age of 40. Her brother and her mother had a similar disease in the fifth decade of life. The feature of amnestic presentation with spastic paraparesis is consistent with the majority of mutations in the exon 8 of the PSEN1 1 gene.
Conclusions: Screening for PSEN1 mutations is especially likely to be productive when directed toward persons with positive family history and with age at onset of under 60. 相似文献
998.
999.
1000.