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Cooper, Cynthia M
~ 18000  Ergebnisse:
Personensuche X
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1

The Kind Care Bundle: A Curriculum to Teach Medical Student..:

Cooper, Cynthia M. ; Gheihman, Galina
MedEdPORTAL.  , 2021
Link: https://doi.org/10.15766..
 
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2

Enhancing the Formal Preclinical Curriculum to Improve Medi..:

McKinley, Sophia K. ; Sell, Naomi M. ; Saillant, Noelle...
Journal of Surgical Education.  77 (2020)  4 - p. 788-798 , 2020
Link: https://doi.org/10.1016/..
 
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3

Medical students' perceptions and motivations prior to thei..:

McKinley, Sophia K. ; Kochis, Michael ; Cooper, Cynthia M....
The American Journal of Surgery.  218 (2019)  2 - p. 424-429 , 2019
Link: https://doi.org/10.1016/..
 
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4

Clinical application of a scale to assess genomic healthcar..:

McConkie‐Rosell, Allyn ; Schoch, Kelly ; Sullivan, Jennifer...
qt76z1t0c4.  , 2022
Link: https://escholarship.org..
 
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5

Endocannabinoid dysfunction in neurological disease: neuro-..:

Bainbridge, Matthew N ; Mazumder, Aloran ; Ogasawara, Daisuke...
qt1tp7967m.  , 2022
Link: https://escholarship.org..
 
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6

A novel DPH5-related diphthamide-deficiency syndrome causin..:

Shankar, Suma P ; Grimsrud, Kristin ; Lanoue, Louise...
qt9kg2s7vk.  , 2022
Link: https://escholarship.org..
 
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7

An autosomal dominant neurological disorder caused by de no..:

Ferdinandusse, Sacha ; McWalter, Kirsty ; te Brinke, Heleen...
https://research.vumc.nl/en/publications/fb984bc3-54bd-43df-883f-07db1704516c.  , 2021
Link: https://research.vumc.nl..
 
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8

An autosomal dominant neurological disorder caused by de no..:

Ferdinandusse, Sacha ; McWalter, Kirsty ; te Brinke, Heleen...
https://research.vumc.nl/en/publications/fb984bc3-54bd-43df-883f-07db1704516c.  , 2021
Link: https://research.vumc.nl..
 
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9

Correction to:An autosomal dominant neurological disorder c..:

Ferdinandusse, Sacha ; McWalter, Kirsty ; te Brinke, Heleen...
https://research.vumc.nl/en/publications/51c15301-9b33-479b-880d-cecb2f229a1f.  , 2021
Link: https://research.vumc.nl..
 
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10

IgG4‐related disease: Association with a rare gene variant ..:

Newman, John H ; Shaver, Aaron ; Sheehan, Jonathan H...
qt5m28j4dw.  , 2019
Link: https://escholarship.org..
 
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11

Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia an..:

Burrage, Lindsay C ; Reynolds, John J ; Baratang, Nissan Vida...
qt28k4m2m4.  , 2019
Link: https://escholarship.org..
 
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12

De Novo Pathogenic Variants in N-cadherin Cause a Syndromic..:

Accogli, Andrea ; Calabretta, Sara ; St-Onge, Judith...
qt113843xk.  , 2019
Link: https://escholarship.org..
 
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13

Heterozygous variants in MYBPC1 are associated with an expa..:

Shashi, Vandana ; Geist, Janelle ; Lee, Youngha...
qt44k6m8qw.  , 2019
Link: https://escholarship.org..
 
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14

Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ..:

Oláhová, Monika ; Yoon, Wan Hee ; Thompson, Kyle...
https://kclpure.kcl.ac.uk/portal/en/publications/09c5b802-d567-461f-94d5-b13e8de03804.  , 2018
Link: https://kclpure.kcl.ac.u..
 
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15

IRF2BPL Is Associated with Neurological Phenotypes:

Marcogliese, Paul C ; Shashi, Vandana ; Spillmann, Rebecca C...
qt2sb1c8bg.  , 2018
Link: https://escholarship.org..
 
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