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PubPharm (130)
61
Risk Factors for Unhealthy Weight Gain and Obesity among Children with Autism Spectrum Disorder
enthalten in:
International journal of molecular sciences
| 2019
von
Dhaliwal, K.
|
Orsso, C.
|
Richard, C.
| +2
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62
Hormonal and metabolic effects of carbohydrate restriction in children with Prader-Willi syndrome
enthalten in:
Clinical endocrinology
| 2019
von
Irizarry, K.
|
Mager, D.
|
Triador, L.
| +3
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63
Dietary intake in youth with prader-willi syndrome
enthalten in:
American journal of medical genetics. Part A
| 2018
von
Mackenzie, M.
|
Triador, L.
|
Gill, J.
| +4
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64
Dietary intake in youth with prader‐willi syndrome
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2018
von
Mackenzie, M.
|
Triador, L.
|
Gill, J.
| +4
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65
The use of magnetic resonance imaging to characterize abnormal body composition phenotypes in youth with Prader-Willi syndrome
enthalten in:
Metabolism: clinical and experimental
| 2017
von
Orsso, C.
|
Mackenzie, M.
|
Alberga, A.
| +5
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66
Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome : A Case Study
enthalten in:
International journal of molecular sciences
| 2017
von
Bennett, J.
|
Hodgetts, S.
|
Mackenzie, M.
| +2
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67
Fecal Short-Chain Fatty Acid Variations by Breastfeeding Status in Infants at 4 Months : Differences in Relative versus Absolute Concentrations
enthalten in:
Frontiers in nutrition
| 2017
von
Bridgman, S.
|
Azad, M.
|
Field, C.
| +51
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68
Hormonal and Metabolic Responses to a Single Bout of Resistance Exercise in Prader-Willi Syndrome
enthalten in:
Hormone research in paediatrics
| 2017
von
Rubin, D.
|
Clark, S.
|
Haqq, A.
| +3
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69
The use of magnetic resonance imaging to characterize abnormal body composition phenotypes in youth with Prader–Willi syndrome
enthalten in:
Metabolism
| 2017
von
Orsso, C.
|
Mackenzie, M.
|
Alberga, A.
| +5
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70
Energy Metabolism Profile in Individuals with Prader-Willi Syndrome and Implications for Clinical Management : A Systematic Review
enthalten in:
Advances in nutrition (Bethesda, Md.)
| 2017
von
Alsaif, M.
|
Elliot, S.
|
MacKenzie, M.
| +3
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Orphanet journal of rare diseases
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Prader-Willi syndrome
12
Ghrelin
11
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11
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9
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