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PubPharm (130)
51
Validity and accuracy of body fat prediction equations using anthropometrics measurements in adolescents
enthalten in:
Eating and weight disorders
| 2020
von
Ripka, W.
|
Orsso, C.
|
Haqq, A.
| +3
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52
Current and emerging therapies for managing hyperphagia and obesity in Prader-Willi syndrome : A narrative review
enthalten in:
Obesity reviews : an official journal of the International Association for the Study of Obesity
| 2020
von
Tan, Q.
|
Orsso, C.
|
Deehan, E.
| +6
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53
Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion
enthalten in:
Genes
| 2020
von
Tan, Q.
|
Potter, K.
|
Burnett, L.
| +4
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54
Lean mass reference curves in adolescents using dual-energy x-ray absorptiometry (DXA)
enthalten in:
PloS one
| 2020
von
Ripka, W.
|
Orsso, C.
|
Haqq, A.
| +3
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55
Dietary macronutrient regulation of acyl and desacyl ghrelin concentrations in children with Prader‐Willi syndrome (PWS)
enthalten in:
Clinical Endocrinology
| 2020
von
Alsaif, M.
|
Pakseresht, M.
|
Mackenzie, M.
| +6
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56
Current and emerging therapies for managing hyperphagia and obesity in Prader‐Willi syndrome : A narrative review
enthalten in:
Obesity Reviews
| 2020
von
Tan, Q.
|
Orsso, C.
|
Deehan, E.
| +6
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57
Assessment of body composition in pediatric overweight and obesity : A systematic review of the reliability and validity of common techniques
enthalten in:
Obesity Reviews
| 2020
von
Orsso, C.
|
Silva, M.
|
Gonzalez, M.
| +4
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58
Are There Benefits to Growth with Supplementing Long-Chain PUFAs to Toddlers Born Prematurely?
enthalten in:
The Journal of nutrition
| 2019
von
Patel, D.
|
Orsso, C.
|
Haqq, A.
| +1
CommentOn: J Nutr. 2019 Dec 1;149(12):2182-2190. - PMID 31187863
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59
Metabolic implications of low muscle mass in the pediatric population : a critical review
enthalten in:
Metabolism: clinical and experimental
| 2019
von
Orsso, C.
|
Tibaes, J.
|
Rubin, D.
| +4
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60
Low muscle mass and strength in pediatrics patients : Why should we care?
enthalten in:
Clinical nutrition (Edinburgh, Scotland)
| 2019
von
Orsso, C.
|
Tibaes, J.
|
Oliveira, C.
| +5
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Orphanet journal of rare diseases
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