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/vufind/Search/Results?lookfor=%22Johnson%2C+Stephanie+R%22&type=Person&page=3
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PubPharm (26)
21
Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy
enthalten in:
Journal of pediatric endocrinology & metabolism : JPEM
| 2011
von
O'Connell, S.
|
Johnson, S.
|
Lewis, B.
| +8
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22
Structural chromosome disruption of the NR3C2 gene causing pseudohypoaldosteronism type 1 presenting in infancy
enthalten in:
The journal of pediatric endocrinology and metabolism
| 2011
von
O'Connell, S.
|
Johnson, S.
|
Lewis, B.
| +8
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23
A genome-wide linkage analysis of dementia in the Amish
enthalten in:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
| 2006
von
Hahs, D.
|
McCauley, J.
|
Crunk, A.
| +11
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24
Emotional enhancement of perceptual priming is preserved in aging and early-stage Alzheimer's disease
enthalten in:
Neuropsychologia
| 2005
von
LaBar, K.
|
Torpey, D.
|
Cook, C.
| +4
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25
Emotional enhancement of perceptual priming is preserved in aging and early-stage Alzheimer's disease
enthalten in:
Neuropsychologia
| 2005
von
Labar, K.
|
Torpey, D.
|
Cook, C.
| +4
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26
[P‐070] : Neurocognitive morbidity in patients with sickle cell disease: A risk for Alzheimer's disease?
enthalten in:
Alzheimer's & Dementia
| 2005
von
Johnson, S.
|
Feliu, M.
|
Edmonds, H.
| +2
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