Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Anita Hokken Koelega"'
Autor:
Elena G. Bochukova, Katherine Lawler, Sophie Croizier, Julia M. Keogh, Nisha Patel, Garth Strohbehn, Kitty K. Lo, Jack Humphrey, Anita Hokken-Koelega, Layla Damen, Stephany Donze, Sebastien G. Bouret, Vincent Plagnol, I. Sadaf Farooqi
Publikováno v:
Cell Reports, Vol 22, Iss 13, Pp 3401-3408 (2018)
Summary: Transcriptional analysis of brain tissue from people with molecularly defined causes of obesity may highlight disease mechanisms and therapeutic targets. We performed RNA sequencing of hypothalamus from individuals with Prader-Willi syndrome
Externí odkaz:
https://doaj.org/article/4798546d39bd4dc69ff2ac49075ed378
Autor:
Melitza S. M. Elizabeth, Anita Hokken-Koelega, Jenny A. Visser, Sjoerd D. Joustra, Laura C. G. de Graaff
Publikováno v:
Genes; Volume 13; Issue 4; Pages: 623
Genes, 13(4). MDPI
Genes, 13(4):623. Multidisciplinary Digital Publishing Institute (MDPI)
Genes, 13(4). MDPI
Genes, 13(4):623. Multidisciplinary Digital Publishing Institute (MDPI)
In recent years, variants in immunoglobulin superfamily member 1 (IGSF1) have been associated with congenital hypopituitarism. Initially, IGSF1 variants were only reported in patients with central hypothyroidism (CeH) and macroorchidism. Later on, IG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cc0df404f9e1f5394d7d3151473a9a9
https://doi.org/10.3390/genes13040623
https://doi.org/10.3390/genes13040623
Autor:
Anita Hokken-Koelega, Aart-Jan van der Lely, Berthold Hauffa, Gabriele Häusler, Gudmundur Johannsson, Mohamad Maghnie, Jesús Argente, Jean DeSchepper, Helena Gleeson, John W Gregory, Charlotte Höybye, Fahrettin Keleştimur, Anton Luger, Hermann L Müller, Sebastian Neggers, Vera Popovic-Brkic, Eleonora Porcu, Lars Sävendahl, Stephen Shalet, Bessie Spiliotis, Maithé Tauber
Publikováno v:
Endocrine Connections, Vol 5, Iss 6, Pp R44-R54 (2016)
Objective: Seamless transition of endocrine patients from the paediatric to adult setting is still suboptimal, especially in patients with complex disorders, i.e., small for gestational age, Turner or Prader–Willi syndromes; Childhood Cancer Surviv
Externí odkaz:
https://doaj.org/article/7a57380673164f058f26701f6ab3c4d0
Autor:
Melitza S M, Elizabeth, Anita, Hokken-Koelega, Jenny A, Visser, Sjoerd D, Joustra, Laura C G, de Graaff
Publikováno v:
Genes. 13(4)
In recent years, variants in immunoglobulin superfamily member 1 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58d53ba8cb20ecb85f19578255f4a57d
https://pubmed.ncbi.nlm.nih.gov/35456429
https://pubmed.ncbi.nlm.nih.gov/35456429
Publikováno v:
Yearbook of Paediatric Endocrinology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3705f830c13cac63312a1c2a2f582e16
https://doi.org/10.1530/ey.18.4.8
https://doi.org/10.1530/ey.18.4.8
Autor:
Jessie M. Hulst, Kirsten S de Fluiter, Jorine A. Roelants, Koen F. M. Joosten, Anita Hokken-Koelega, Victoria A A Beunders, Irwin K M Reiss, Marijn J. Vermeulen, Dimitris Rizopoulos, Vincent W. V. Jaddoe, Esther G. Neelis
Publikováno v:
Pediatric obesity, 16(6):e12752. Wiley-Blackwell for the International Association for the Study of Obesity
Pediatric Obesity
Pediatric Obesity
Background: Concerns are raised about the influence of rapid growth on excessive fat mass (FM) gain in early life and later cardiometabolic health of infants born preterm. Objectives: To study the association between postnatal weight gain trajectorie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dc86c9aae03384f8892e2ef2173a080
https://pure.eur.nl/en/publications/aa86751d-06f2-41e8-81ed-cfc0f4569b81
https://pure.eur.nl/en/publications/aa86751d-06f2-41e8-81ed-cfc0f4569b81
Autor:
Jenny A. Visser, Anita Hokken-Koelega, Alicia F. Juriaans, Layla Damen, Patric J.D. Delhanty, Stephany Hermina Donze, Lionne N. Grootjen, T. Martin Huisman
Publikováno v:
Clinical Endocrinology, 94(5), 774-785. Wiley-Blackwell Publishing Ltd
Clinical Endocrinology
Clinical Endocrinology
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a typical behavioural phenotype, with characteristics of autism spectrum disorder (ASD) like stubbornness, temper tantrums and compulsivity. It has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a90bc3b0117447e2cd365c6848ffee
https://pure.eur.nl/en/publications/d011a4ce-e518-46f5-9377-b0ffe6d33d31
https://pure.eur.nl/en/publications/d011a4ce-e518-46f5-9377-b0ffe6d33d31
Publikováno v:
European Journal of Endocrinology, 182(4), 405-411. Bioscientifica Ltd
Objective Children with Prader–Willi syndrome (PWS) have mild to moderate cognitive impairment. Short-term studies showed positive effects of growth hormone (GH) on cognitive development. This study investigated the effects of 8 years of GH on cogn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf15175bec342a7ea7006690757a870f
https://pure.eur.nl/en/publications/6da9212b-15eb-4055-b733-d2f5527e2078
https://pure.eur.nl/en/publications/6da9212b-15eb-4055-b733-d2f5527e2078
Autor:
Régine P.M. Steegers-Theunissen, Irene V. Koning, Jorine A. Roelants, Koen F. M. Joosten, Marijn J. Vermeulen, Anita Hokken-Koelega, Sten P. Willemsen, Irwin K M Reiss, Irene A.L. Groenenberg
Publikováno v:
Pediatric Obesity. 12:65-71
SummaryBackground The predisposition for obesity is suggested to originate in the prenatal period. Prenatal markers are needed to identify foetuses at risk for neonatal adiposity, as early marker of childhood obesity. Objective The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::298929d8a08e336a229340784d5447e9
https://doi.org/10.1111/ijpo.12231
https://doi.org/10.1111/ijpo.12231
Autor:
Anita Hokken-Koelega, Hartmut A. Wollmann, Joseph Heissler, Cecilia Camacho-Hübner, Nienke E Bakker, Anders Lindberg
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 102(5), 1702-1711. Endocrine Society
__Abstract__ This is the fifth thesis of our research group in the field of Prader-Willi syndrome (PWS) and encompasses 6 new studies embedded in the Dutch PWS Cohort study in children and adolescents with PWS. In 1887, sir Langdon Down described an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f631cf1821fdaa21124f9102e8ec3f1
https://doi.org/10.1210/jc.2016-2962
https://doi.org/10.1210/jc.2016-2962