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PubPharm (182)
1
Endocrine involvement in hepatic glycogen storage diseases : pathophysiology and implications for care
enthalten in:
Reviews in endocrine & metabolic disorders
| 2024
von
Rossi, A.
|
Simeoli, C.
|
Pivonello, R.
| +8
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2
Idiopathic pathological ketotic hypoglycemia : finding the needle in a haystack
enthalten in:
Hormone research in paediatrics
| 2024
von
Wolfsdorf, J.
|
Derks, T.
|
Drachmann, D.
| +3
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3
Repurposing empagliflozin in individuals with glycogen storage disease Ib : A value-based healthcare approach and systematic benefit-risk assessment
enthalten in:
Journal of inherited metabolic disease
| 2024
von
Derks, T.
|
Venema, A.
|
Köller, C.
| +9
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4
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin : Consensus from an international workshop
enthalten in:
Molecular genetics and metabolism
| 2024
von
Grünert, S.
|
Derks, T.
|
Mundy, H.
| +15
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5
Endogenous Glucose Production in Patients With Glycogen Storage Disease Type Ia Estimated by Oral D-[6,6-2H2]-glucose
enthalten in:
The Journal of clinical endocrinology and metabolism
| 2024
von
Rossi, A.
|
Oosterveer, M.
|
van Dijk, T.
| +5
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6
Repurposing empagliflozin in individuals with glycogen storage disease Ib : A value‐based healthcare approach and systematic benefit‐risk assessment
enthalten in:
Journal of Inherited Metabolic Disease
| 2024
von
Derks, T.
|
Venema, A.
|
Köller, C.
| +9
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7
Precision-cut liver slices as an ex vivo model to assess impaired hepatic glucose production
enthalten in:
ResearchSquare.com
| 2023
von
Bakker, B.
|
Kiyuna, L.
|
Krishnamurthy, K.
| +11
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8
A Delphi Survey Study to Formulate Statements on the Treatability of Inherited Metabolic Disorders to Decide on Eligibility for Newborn Screening
enthalten in:
International journal of neonatal screening
| 2023
von
Veldman, A.
|
Kiewiet, M.
|
Westra, D.
| +21
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9
Glycogen storage diseases
enthalten in:
Nature reviews. Disease primers
| 2023
von
Hannah, W.
|
Derks, T.
|
Drumm, M.
| +3
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10
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients
enthalten in:
BMC biology
| 2023
von
Odendaal, C.
|
Jager, E.
|
Martines, A.
| +9
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Journal of inherited metabolic disease
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Journal of Inherited Metabolic Disease
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Research Support, Non-U.S. Gov't
17
Acyl-CoA Dehydrogenase
17
EC 1.3.8.7
14
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Glycogen Storage Disease
11
Blood Glucose
11
Glucose
10
IY9XDZ35W2
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Endogenous Glucose Production
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empagliflozin
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EC 3.1.3.9
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Glucose-6-Phosphatase
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Glycogen storage disease type Ib
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