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Simultaneous ipsilateral elbow and forearm fractures in children: a retrospective review.

Emergency radiology

Taylor KA, Junewick JA.
PMID: 15290541
Emerg Radiol. 2002 Dec;9(6):314-6. doi: 10.1007/s10140-002-0224-9. Epub 2002 Nov 20.

The aim is to evaluate the incidence of simultaneous ipsilateral forearm fractures in pediatric patients who present with elbow fractures and to attempt to identify patients who might be at greater risk of this type of injury. All pediatric...

Cite
Taylor KA, Junewick JA. Simultaneous ipsilateral elbow and forearm fractures in children: a retrospective review. Emerg Radiol. 2002;9(6):314-6doi: 10.1007/s10140-002-0224-9.
Taylor, K. A., & Junewick, J. A. (2002). Simultaneous ipsilateral elbow and forearm fractures in children: a retrospective review. Emergency radiology, 9(6), 314-6. https://doi.org/10.1007/s10140-002-0224-9
Taylor, Kimberly A, and Junewick, Joseph A J. "Simultaneous ipsilateral elbow and forearm fractures in children: a retrospective review." Emergency radiology vol. 9,6 (2002): 314-6. doi: https://doi.org/10.1007/s10140-002-0224-9
Taylor KA, Junewick JA. Simultaneous ipsilateral elbow and forearm fractures in children: a retrospective review. Emerg Radiol. 2002 Dec;9(6):314-6. doi: 10.1007/s10140-002-0224-9. Epub 2002 Nov 20. PMID: 15290541.
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The Perils of Perfectionism.

AJR. American journal of roentgenology

Junewick J, Gunderman RB.
PMID: 31082274
AJR Am J Roentgenol. 2019 Oct;213(4):740-741. doi: 10.2214/AJR.19.21158. Epub 2019 May 13.

No abstract available.

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Junewick J, Gunderman RB. The Perils of Perfectionism. AJR Am J Roentgenol. 2019;213(4):740-741doi: 10.2214/AJR.19.21158.
Junewick, J., & Gunderman, R. B. (2019). The Perils of Perfectionism. AJR. American journal of roentgenology, 213(4), 740-741. https://doi.org/10.2214/AJR.19.21158
Junewick, Joseph, and Gunderman, Richard B. "The Perils of Perfectionism." AJR. American journal of roentgenology vol. 213,4 (2019): 740-741. doi: https://doi.org/10.2214/AJR.19.21158
Junewick J, Gunderman RB. The Perils of Perfectionism. AJR Am J Roentgenol. 2019 Oct;213(4):740-741. doi: 10.2214/AJR.19.21158. Epub 2019 May 13. PMID: 31082274.
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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

American journal of human genetics

Stolz JR, Foote KM, Veenstra-Knol HE, Pfundt R, Ten Broeke SW, de Leeuw N, Roht L, Pajusalu S, Part R, Rebane I, Õunap K, Stark Z, Kirk EP, Lawson JA, Lunke S, Christodoulou J, Louie RJ, Rogers RC, Davis JM, Innes AM, Wei XC, Keren B, Mignot C, Lebel RR, Sperber SM, Sakonju A, Dosa N, Barge-Schaapveld DQCM, Peeters-Scholte CMPCD, Ruivenkamp CAL, van Bon BW, Kennedy J, Low KJ, Ellard S, Pang L, Junewick JJ, Mark PR, Carvill GL, Swanson GT.
PMID: 34739836
Am J Hum Genet. 2021 Nov 04;108(11):2206. doi: 10.1016/j.ajhg.2021.09.018.

No abstract available.

Cite
Stolz JR, Foote KM, Veenstra-Knol HE, et al. Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders. Am J Hum Genet. 2021;108(11):2206doi: 10.1016/j.ajhg.2021.09.018.
Stolz, J. R., Foote, K. M., Veenstra-Knol, H. E., Pfundt, R., Ten Broeke, S. W., de Leeuw, N., Roht, L., Pajusalu, S., Part, R., Rebane, I., Õunap, K., Stark, Z., Kirk, E. P., Lawson, J. A., Lunke, S., Christodoulou, J., Louie, R. J., Rogers, R. C., Davis, J. M., Innes, A. M., Wei, X. C., Keren, B., Mignot, C., Lebel, R. R., Sperber, S. M., Sakonju, A., Dosa, N., Barge-Schaapveld, D. Q. C. M., Peeters-Scholte, C. M. P. C. D., Ruivenkamp, C. A. L., van Bon, B. W., Kennedy, J., Low, K. J., Ellard, S., Pang, L., Junewick, J. J., Mark, P. R., Carvill, G. L., & Swanson, G. T. (2021). Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders. American journal of human genetics, 108(11), 2206. https://doi.org/10.1016/j.ajhg.2021.09.018
Stolz, Jacob R, et al. "Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders." American journal of human genetics vol. 108,11 (2021): 2206. doi: https://doi.org/10.1016/j.ajhg.2021.09.018
Stolz JR, Foote KM, Veenstra-Knol HE, Pfundt R, Ten Broeke SW, de Leeuw N, Roht L, Pajusalu S, Part R, Rebane I, Õunap K, Stark Z, Kirk EP, Lawson JA, Lunke S, Christodoulou J, Louie RJ, Rogers RC, Davis JM, Innes AM, Wei XC, Keren B, Mignot C, Lebel RR, Sperber SM, Sakonju A, Dosa N, Barge-Schaapveld DQCM, Peeters-Scholte CMPCD, Ruivenkamp CAL, van Bon BW, Kennedy J, Low KJ, Ellard S, Pang L, Junewick JJ, Mark PR, Carvill GL, Swanson GT. Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders. Am J Hum Genet. 2021 Nov 04;108(11):2206. doi: 10.1016/j.ajhg.2021.09.018. PMID: 34739836; PMCID: PMC8595928.
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Showing 1 to 3 of 3 entries