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/vufind/Search/Results?lookfor=%22Tinloy%2C+Bradford%22&type=Person&sort=year
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PubPharm (13)
1
The future of value-based emergency care : Development of an emergency medicine MIPS value pathway framework
enthalten in:
Journal of the American College of Emergency Physicians open
| 2022
von
Gettel, C.
|
Tinloy, B.
|
Nedza, S.
| +4
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2
The future of value‐based emergency care : Development of an emergency medicine MIPS value pathway framework
enthalten in:
Journal of the American College of Emergency Physicians Open
| 2022
von
Gettel, C.
|
Tinloy, B.
|
Nedza, S.
| +4
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3
Opening of Psychiatric Observation Unit Eases Boarding Crisis
enthalten in:
Academic emergency medicine : official journal of the Society for Academic Emergency Medicine
| 2018
von
Parwani, V.
|
Tinloy, B.
|
Ulrich, A.
| +5
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4
Emergency department evaluation and treatment of the shoulder and humerus
enthalten in:
Emergency medicine clinics of North America
| 2015
von
Bonz, J.
|
Tinloy, B.
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5
Emergency department evaluation and treatment of the shoulder and humerus
enthalten in:
Emergency medicine clinics of North America
| 2015
von
Bonz, J.
|
Tinloy, B.
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6
Perioperative risk factors for major complications in pediatric surgery : a study in surgical risk assessment for children
enthalten in:
Journal of the American College of Surgeons
| 2011
von
Weinberg, A.
|
Huang, L.
|
Jiang, H.
| +7
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7
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility
enthalten in:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
| 2011
von
Domené, S.
|
Stanescu, H.
|
Wallis, D.
| +6
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8
A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome
enthalten in:
Molecular genetics and metabolism
| 2008
von
Westbroek, W.
|
Tuchman, M.
|
Tinloy, B.
| +8
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9
A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome
enthalten in:
Molecular genetics and metabolism
| 2008
von
Westbroek, W.
|
Tuchman, M.
|
Tinloy, B.
| +8
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10
Cellular defects in Chediak-Higashi syndrome correlate with the molecular genotype and clinical phenotype
enthalten in:
The Journal of investigative dermatology
| 2007
von
Westbroek, W.
|
Adams, D.
|
Huizing, M.
| +13
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1
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Emergency medicine clinics of North America
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The journal of investigative dermatology
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Research Support, N.I.H., Intramural
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Caspases
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ADGRL3 protein, human
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Acromioclavicular Joint - injuries
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Adaptor Proteins, Signal Transducing
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Clavicle - injuries
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Dislocations - diagnosis
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