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81.
Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina 下载免费PDF全文
Joshua R. Mann MD MPH Julie A. Royer MSPH Suzanne Mcdermott PhD James W. Hardin PhD Orgul Ozturk PhD Natalie Street MS CGC 《Muscle & nerve》2015,52(5):714-721
Introduction: Transitioning from adolescence to adulthood can be problematic for individuals with rare disabilities such as muscular dystrophy (MD). Methods: We identified a cohort of 220 individuals with MD and 440 matched comparison individuals and measured emergency room (ER) and inpatient (IP) encounters for the years 2000 through 2010, using all‐payer hospital discharge uniform billing data. We compared ER and IP use rates for people with and without MD, and for 15–19‐year‐olds with MD to 20–24‐year‐olds with MD. Results: ER and IP use rates were significantly higher among individuals with MD than the comparison group. In addition, ER and IP use rates were significantly higher in the 20–24‐year age group than in the 15–19‐year group. Conclusions: Additional research is needed to determine whether increased ER and IP use in young adults is attributable to difficulties in healthcare transition versus increased disease severity. Muscle Nerve 52: 714–721, 2015 相似文献
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Fetus in Fetu in Lieu of a Sacrococcygeal Teratoma: A Case Illuminating the Utility of Serial Prenatal Sonographic Examinations in Diagnosis 下载免费PDF全文
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Mary K. Ladd MA Beth N. Peshkin MS CGC Claudine Isaacs MD Gillian Hooker PhD ScM LCGC Shawna Willey MD Heiddis Valdimarsdottir PhD Tiffani DeMarco MS CGC Suzanne O'Neill PhD Savannah Binion BS Marc D. Schwartz PhD other members of the Surgery After Genetic Evaluation Study Group 《Journal of surgical oncology》2020,122(2):134-143
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A. Reghan Foley MD Yaqun Zou MD James E. Dunford PhD Jachinta Rooney PhD Goutam Chandra PhD Hui Xiong MD Volker Straub MD Thomas Voit MD Norma Romero MD PhD Sandra Donkervoort MS CGC Ying Hu MS Thomas Markello MD PhD Adam Horn PhD Leila Qebibo MD Jahannaz Dastgir DO Katherine G. Meilleur PhD Richard S. Finkel MD Yanbin Fan MD Kamel Mamchaoui PhD Stephanie Duguez PhD Isabelle Nelson PhD Jocelyn Laporte PhD Mariarita Santi MD Edoardo Malfatti MD PhD Thierry Maisonobe MD Philippe Touraine MD PhD Michio Hirano MD Imelda Hughes MD Kate Bushby MD Udo Oppermann PhD Johann Böhm PhD Jyoti K. Jaiswal PhD Tanya Stojkovic MD Carsten G. Bönnemann MD 《Annals of neurology》2020,88(2):332-347
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Sandra Donkervoort MS CGC Maria Papadaki BSc Josine M. de Winter MS Matthew B. Neu BS Janbernd Kirschner MD Véronique Bolduc PhD Michele L. Yang MD Melissa A. Gibbons MS CGC Ying Hu MS Jahannaz Dastgir DO Meganne E. Leach MSN APRN PPCNP‐BC Anne Rutkowski MD A. Reghan Foley MD Marcus Krüger MD Eric P. Wartchow BSc Elyshia McNamara BS Royston Ong BSc Kristen J. Nowak PhD Nigel G. Laing PhD Nigel F. Clarke PhD Coen A. C. Ottenheijm PhD Steven B. Marston MA DPhil DSc Carsten G. Bönnemann MD 《Annals of neurology》2015,78(6):982-994
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Stewart A. Factor DO N. Kyle Steenland PhD Donald S. Higgins MD Eric S. Molho MD Denise M. Kay PhD Jennifer Montimurro MS Ami R. Rosen MS CGC Cyrus P. Zabetian MD Haydeh Payami PhD 《Movement disorders》2011,26(12):2190-2195
Our aim was to examine disease‐related and genetic correlates of the development of psychotic symptoms in a large population of patients with Parkinson's disease. We studied 500 patients with Parkinson's disease from the NeuroGenetics Research Consortium using logistic regression models. Predictors were demographic, clinical (motor/nonmotor features), and genetic, measured as continuous or dichotomous variables. Continuous measures were divided into population‐based tertiles. Results are given as odds ratios (95% confidence intervals) for dichotomous variables and by ascending tertile for continuous variables. Psychotic symptoms were associated with increasing age: 4.86 (1.62–14.30) and 6.25 (2.09–18.74) (test for trend: P = 0.01); and duration of disease: 3.81 (1.23–11.76) and 5.33 (1.68–16.89) (test for trend: P = 0.03). For nonmotor features, we demonstrated positive trends with depression: 1.31 (0.47–3.61) and 5.01 (2.04–12.33) (test for trend: P < 0.0001); cognitive dysfunction: 0.69 (0.26–1.84) and 2.51 (1.00–6.29) (test for trend: P = 0.03); and an excess for those with sleep disorders: 2.00 (1.03–3.89) (P = 0.04). Psychotic symptoms were not associated with tremor or postural instability scores, but there was an association with freezing of gait: 3.83 (1.67–8.75) (P < 0.002). Psychotic symptoms were not associated with the presence of any examined polymorphisms in the apolipoprotein, alpha‐synuclein, or microtubule associated protein tau genes. This is the largest study to examine correlates of psychotic symptoms in Parkinson's disease. We discovered a novel association with freezing of gait. We demonstrated an association with depression and duration of disease, both of which were inconsistently related in previous studies, and confirmed the association with age, cognitive dysfunction, and sleep disorders. © 2011 Movement Disorder Society 相似文献
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Jean F. Jenkins PhD RN FAAN Cynthia Prows RN MSN Eileen Dimond RN MS Rita Monsen DSN MPH RN
Janet Williams RN CPNP CGC PhD FAAN 《Journal of Professional Nursing》2001,17(6):283-290
With the ongoing and increasingly rapid pace of genetic discoveries, nurses must be able to incorporate genetic knowledge into their everyday practices of promoting the genetic health of individuals, families, and communities. Although development of genetic health knowledge is in its infancy, nurses are currently expected to integrate information about genetic risks, testing, and treatments for clients throughout the clients' entire lifespan. All nurses must have an understanding of the relationship between genetics and health to appropriately identify and address genetic concerns in their clients. To fulfill these roles, nurses need to improve their knowledge base in genetics. This article provides recommendations for genetics curriculum in continuing and entry-level nursing education programs. These recommendations are outcomes of a research project involving genetics nurse experts as well as nurses new to the area of genetics, and a consensus workshop of nursing faculty involved in curriculum changes subsequent to an intensive genetics continuing education program. Nursing educators are beginning to recognize the importance of education of all nurses about genetics. If, however, all educators do not accept this responsibility, nurses will be left behind in designing and offering health care for the 21st century. 相似文献