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PubPharm (52)
1
Longitudinal changes in acylated versus unacylated ghrelin levels may be involved in the underlying mechanisms of the switch in nutritional phases in Prader-Willi syndrome
enthalten in:
Hormone research in paediatrics
| 2023
von
Grootjen, L.
|
Diene, G.
|
Molinas, C.
| +7
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2
Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young Adults
enthalten in:
The Journal of clinical endocrinology and metabolism
| 2023
von
Nannette, G.
|
Bar, C.
|
Diene, G.
| +10
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3
Liraglutide for Weight Management in Children and Adolescents With Prader-Willi Syndrome and Obesity
enthalten in:
The Journal of clinical endocrinology and metabolism
| 2022
von
Diene, G.
|
Angulo, M.
|
Hale, P.
| +6
CommentIn: J Clin Endocrinol Metab. 2023 Jan 13;:. - PMID 36638011
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4
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
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5
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
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6
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
enthalten in:
Clinical epigenetics
| 2022
von
Mackay, D.
|
Bliek, J.
|
Kagami, M.
| +26
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7
Impact of Deprivation on Obesity in Children with PWS
enthalten in:
Journal of clinical medicine
| 2022
von
Grolleau, S.
|
Delagrange, M.
|
Souquiere, M.
| +4
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8
What underlies emotion regulation abilities? An innovative programme based on an integrative developmental approach to improve emotional competencies : Promising results in children with Prader-Willi syndrome
enthalten in:
Frontiers in psychiatry
| 2022
von
Famelart, N.
|
Diene, G.
|
Çabal-Berthoumieu, S.
| +4
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9
Low bone mass in Noonan syndrome children correlates with decreased muscle mass and low IGF-1 levels
enthalten in:
Bone
| 2021
von
Delagrange, M.
|
Rousseau, V.
|
Cessans, C.
| +9
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10
Diabetes Mellitus in Prader-Willi Syndrome : Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients
enthalten in:
Journal of clinical medicine
| 2021
von
Clerc, A.
|
Coupaye, M.
|
Mosbah, H.
| +7
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Medienart: E-Artikel
Medienart
52
Aufsätze
E-Artikel
52
E-Ressourcen
Zeitschriftentitel
14
Orphanet journal of rare diseases
5
The Journal of clinical endocrinology and metab...
3
BMC medical genetics
3
Clinical epigenetics
2
Journal of clinical medicine
2
Pediatric endocrinology reviews : PER
2
Pediatrics
2
PloS one
1
American journal of medical genetics. Part A
1
Archives of disease in childhood
1
BMC Medical Genetics
1
Bone
1
European journal of endocrinology
1
European journal of human genetics : EJHG
1
Frontiers in psychiatry
1
Frontiers of hormone research
1
Genetics in medicine : official journal of the ...
1
Handbook of clinical neurology
1
Hormone research in paediatrics
1
Journal of Neuroendocrinology
Alle anzeigen ...
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Thema
38
Journal Article
13
Research Support, Non-U.S. Gov't
12
Prader-Willi syndrome
8
Ghrelin
7
Oxytocin
5
12629-01-5
5
Growth Hormone
5
Human Growth Hormone
4
50-56-6
4
9002-72-6
4
Obesity
4
Prader–Willi syndrome
4
Review
3
Genetic testing
3
Imprinting disorders
3
Multi-locus imprinting disorder
3
Multi-locus testing
3
Overlapping phenotypes
3
Randomized Controlled Trial
3
Unexpected molecular diagnosis
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
19
2020-
24
2010-2019
9
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
51
Englisch
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