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/vufind/Search/Results?lookfor=%22Elias%2C+Abdallah+F%22&type=Person&sort=year
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PubPharm (59)
1
Ion Channels in Gliomas-From Molecular Basis to Treatment
enthalten in:
International journal of molecular sciences
| 2023
von
Elias, A.
|
Lin, B.
|
Piggott, B.
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2
Ensuring equity : Pharmacogenetic implementation in rural and tribal communities
enthalten in:
Frontiers in pharmacology
| 2022
von
Leitch, T.
|
Killam, S.
|
Brown, K.
| +10
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3
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
enthalten in:
American journal of human genetics
| 2021
von
Radio, F.
|
Pang, K.
|
Ciolfi, A.
| +98
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4
N-glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiency
enthalten in:
Journal of inherited metabolic disease
| 2020
von
Park, J.
|
Mealer, R.
|
Elias, A.
| +13
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5
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease
enthalten in:
Journal of inherited metabolic disease
| 2020
von
Friederich, M.
|
Elias, A.
|
Kuster, A.
| +18
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6
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease
enthalten in:
Journal of Inherited Metabolic Disease
| 2020
von
Friederich, M.
|
Elias, A.
|
Kuster, A.
| +18
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7
N‐glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiency
enthalten in:
Journal of Inherited Metabolic Disease
| 2020
von
Park, J.
|
Mealer, R.
|
Elias, A.
| +13
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8
SLC35A2-CDG : Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
enthalten in:
Human mutation
| 2019
von
Ng, B.
|
Sosicka, P.
|
Agadi, S.
| +66
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9
Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patients
enthalten in:
Journal of inherited metabolic disease
| 2019
von
Vals, M.
|
Ashikov, A.
|
Ilves, P.
| +24
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10
Philip D. Pallister of Montana
enthalten in:
American journal of medical genetics. Part A
| 2019
von
Opitz, J.
|
Mullen, P.
|
Elias, A.
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