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Dinh NV Freeman H Granger J Wong S Johanson M 《International journal of sports medicine》2011,32(3):205-210
Limited ankle dorsiflexion passive range of motion (DF PROM) has been associated with lower extremity overuse injuries. Therefore, clinicians often prescribe stretching exercises to increase ankle DF PROM. However, there is limited evidence to indicate if any particular gastrocnemius stretching exercise results in greater improvement in DF PROM. The aim of this study was to determine if gastrocnemius stretching in non-weight bearing (NWB) or weight bearing (WB) results in a greater increase of ankle DF PROM. 28 healthy volunteers, aged 18-55 years, who exhibited less than 10 degrees of ankle DF PROM completed the study. Participants were randomized into 2 stretching groups: NWB and WB. Both groups completed a 3-week home gastrocnemius stretching program, consisting of 5 repetitions held for 30 s each, 2 times daily. Participants' ankle DF PROM was measured with a blinded standard goniometer in NWB and WB positions before and after participation in a 3-week home gastrocnemius stretching program. Two 3-way mixed model ANOVAs demonstrated no significant difference in ankle DF PROM between the NWB and WB groups for either the NWB measurement condition (p=0.49) or WB measurement condition (p=0.86). Gastrocnemius stretching exercises performed in NWB or WB were equally effective in increasing ankle DF PROM. 相似文献
124.
James N. Gladstone MD Kevin E. Wilk PT James R. Andrews MD 《Operative Techniques in Sports Medicine》1997,5(2):78-87
Nonoperative treatment is generally the choice for Type I and II acromioclavicular (AC) joint injuries. The situation issomewhat more controversial when Type III AC dislocations are considered, particularly with respect to athletes and heavy laborers. A number of recent studies have supported conservative treatment in these groups. There is general consensus as to the need for surgical intervention for Type IV, V, and VI AC injuries. Integral to any form of management, nonoperative or operative, is a rehabilitation program that addresses range of motion, strength, and neuromuscular control. We describe our program, which is divided into four phases: (1) Pain control and immediate protected range of motion and isometric exercises; (2) strengthening exercises using isotonic contractions and proprioceptive neuromuscular facilitation (PNF) exercises; (3) Unrestricted functional participation with the goal of increasing strength, power, endurance, and neuromuscular control; and (4) return to activity with sport specific functional drills. An athlete is ready to return to competitive sports once the following criteria are met: full range of motion (ROM), no pain or tenderness, satisfactory clinical exam, and demonstration of adequate strength on isokinetic testing. The unique considerations in a throwing athlete with an AC injury are also addressed. The primary goal of the nonoperative treatment protocol is to return the athlete to full activities as quickly and as safely as possible. 相似文献
125.
Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts 下载免费PDF全文
Nanna Witting PhD MD Thomas Krag PhD Ulla Werlauff PhD PT Morten Duno ErCL PhD Sofie Thuroe Oestergaard BSc Julia Rebecka Dahlqvist MD John Vissing MD 《Muscle & nerve》2018,57(6):1026-1030
Introduction: Mutation in the collagen XII gene (COL12A1) was recently reported to induce Bethlem myopathy. We describe a family affected by collagen XII‐related myopathy in 3 generations. Methods: Systematic interview, clinical examination, skin biopsies, and MRI of muscle were used. Results: The phenotype was characterized by neonatal hypotonia, contractures, and delayed motor development followed by resolution of contractures and a motor performance limited by reduced endurance. DNA analyses revealed a novel donor splice‐site mutation in COL12A1 (c.8100 + 2T>C), which segregated with clinical affection and abnormal collagen XII retention in fibroblasts. MRI disclosed a selective wasting of the rectus femoris muscle. Discussion: COL12A1 mutations should be considered in patients with a mild Bethlem phenotype who present with selective wasting of the rectus femoris, absence of the outside‐in phenomenon on MRI, and abnormal collagen XII retention in fibroblasts. Muscle Nerve 57 : 1026–1030, 2018 相似文献
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Kayla M.D. Cornett MSc Manoj P. Menezes MD PhD Rosemary R. Shy MD Isabella Moroni MD Emanuela Pagliano MD Davide Pareyson MD Timothy Estilow OTR/L Sabrina W. Yum MD Trupti Bhandari PT Francesco Muntoni MD FRCPCH Matilde Laura PhD Mary M. Reilly MD FRCP Richard S. Finkel MD Kate J. Eichinger DPT David N. Herrmann MBBCh Paula Bray PhD Mark Halaki PhD Michael E. Shy MD Joshua Burns PhD for the CMTPedS Study Group 《Annals of neurology》2017,82(3):353-359
128.
Reduced skeletal muscle satellite cell number alters muscle morphology after chronic stretch but allows limited serial sarcomere addition 下载免费PDF全文
Matthew C. Kinney MD Sudarshan Dayanidhi PT PhD Peter B. Dykstra BS John J. McCarthy PhD Charlotte A. Peterson PhD Richard L. Lieber PhD 《Muscle & nerve》2017,55(3):384-392
Introduction: Muscles add sarcomeres in response to stretch, presumably to maintain optimal sarcomere length. Clinical evidence from patients with cerebral palsy, who have both decreased serial sarcomere number and reduced satellite cells (SCs), suggests a hypothesis that SCs may be involved in sarcomere addition. Methods: A transgenic Pax7‐DTA mouse model underwent conditional SC depletion, and their soleii were then stretch‐immobilized to assess the capacity for sarcomere addition. Muscle architecture, morphology, and extracellular matrix (ECM) changes were also evaluated. Results: Mice in the SC‐reduced group achieved normal serial sarcomere addition in response to stretch. However, muscle fiber cross‐sectional area was significantly smaller and was associated with hypertrophic ECM changes, consistent with fibrosis. Conclusions: While a reduced SC population does not hinder serial sarcomere addition, SCs play a role in muscle adaptation to chronic stretch that involves maintenance of both fiber cross‐sectional area and ECM structure. Muscle Nerve 55 : 384–392, 2017 相似文献
129.
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French version 下载免费PDF全文
Antoine Dany PT PhD Amandine Rapin MD MSc Brice Lavrard MD Virginie Saoût MD Christian Réveillère PhD Guillaume Bassez MD PhD Vincent Tiffreau MD PhD Yann Péréon MD PhD Sabrina Sacconi MD PhD Bruno Eymard MD PhD Moustapha Dramé MD PhD Damien Jolly MD PhD Jean‐Luc Novella MD PhD Jean‐Benoit Hardouin PhD François C. Boyer MD PhD 《Muscle & nerve》2017,56(6):1085-1091
130.
Yeliz Salci PT PhD Ecem Karanfil PT Ayla Fil Balkan PT Ebru Çalik Kütükçü PT Ali Naim Ceren PT Fatma Ayvat PT MSc Can Ebru Bekircan-Kurt MD Kadriye Armutlu PT 《Muscle & nerve》2019,59(2):208-212
Introduction: We sought to evaluate the test–retest reliability and construct validity of the 6- and 2-minute walk tests (6mWT and 2mWT, respectively) in patients with myasthenia gravis (MG). Methods: Thirty-one patients with generalized MG were enrolled in this study. The 6mWT, 2mWT, MG-specific quality of life questionnaire Turkish version (MG-QoL15T), quantitative myasthenia gravis test (QMG), and pulmonary function tests were administered. Results: The intraclass correlation coefficients of 2mWT and 6mWT were 0.894 and 0.932, respectively. The 6mWT and 2mWT had moderate correlations with forced vital capacity, maximal inspiratory pressure, QMG score, and MG-QoL15T score (ρ for 6mWT: 0.579, 0.539, −0.572, and −0.474; ρ for 2mWT: 0.460, 0.446, −0.532, −0.457). Both tests had similar performances for predicting disease severity (area under the curve = 0.761 for 6mWT and 0.759 for 2mWT). Discussion: The 6mWT and 2mWT have excellent test–retest reliability as well as moderate construct validity for the evaluation of functional exercise capacity patients with MG. Muscle Nerve 59 :208–212, 2019 相似文献