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1دورية أكاديمية
المصدر: Slovenska pediatrija, Vol 31, Iss 1, Pp 18-24 (2024)
مصطلحات موضوعية: prader-willi syndrome (pws), comprehensive treatment, medical devices, dietary counselling, medications, behavioural strategies, Medicine, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: http://www.slovenskapediatrija.si/Portals/0/Clanki/2024/Slovpediatr-2024-1-03en.pdfTest; https://doaj.org/toc/1318-4423Test; https://doaj.org/toc/2712-3960Test
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2دورية أكاديمية
المؤلفون: Anna Maria Wędrychowicz, Katarzyna Doleżal-Ołtarzewska, Agata Zygmunt-Górska, Anna Urszula Kalicka-Kasperczyk, Katarzyna Tyrawa, Malgorzata Wojcik, Dominika Janus, Adrianna Kot, Agnieszka Lecka-Ambroziak, Elzbieta Petriczko, Joanna Wielopolska, Jerzy Starzyk
المصدر: Frontiers in Endocrinology, Vol 15 (2024)
مصطلحات موضوعية: Prader-Willi syndrome (PWS), hypothalamic-pituitary-adrenal axis (HPAA), central adrenal insufficiency (CAI), low-dose ACTH test (LDAT), glugacon stimulation test (GST), Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fendo.2024.1406931/fullTest; https://doaj.org/toc/1664-2392Test
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3دورية أكاديمية
المؤلفون: Simona F. Madeo, Luca Zagaroli, Sara Vandelli, Valeria Calcaterra, Antonino Crinò, Luisa De Sanctis, Maria Felicia Faienza, Danilo Fintini, Laura Guazzarotti, Maria Rosaria Licenziati, Enza Mozzillo, Roberta Pajno, Emanuela Scarano, Maria E. Street, Malgorzata Wasniewska, Sarah Bocchini, Carmen Bucolo, Raffaele Buganza, Mariangela Chiarito, Domenico Corica, Francesca Di Candia, Roberta Francavilla, Nadia Fratangeli, Nicola Improda, Letteria A. Morabito, Chiara Mozzato, Virginia Rossi, Concetta Schiavariello, Giovanni Farello, Lorenzo Iughetti, Vincenzo Salpietro, Alessandro Salvatoni, Mara Giordano, Graziano Grugni, Maurizio Delvecchio
المصدر: Frontiers in Endocrinology, Vol 15 (2024)
مصطلحات موضوعية: Prader-Willi syndrome (PWS), genotype-phenotype correlation, growth hormone (GH), metabolic syndrome, hypogonadism, bone metabolism, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fendo.2024.1382583/fullTest; https://doaj.org/toc/1664-2392Test
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4دورية أكاديمية
المؤلفون: Valentina Gigliucci, Marta Busnelli, Francesca Santini, Camilla Paolini, Alessandra Bertoni, Fabienne Schaller, Françoise Muscatelli, Bice Chini
المصدر: Frontiers in Neuroscience, Vol 17 (2023)
مصطلحات موضوعية: neurodevelopmental disorders (NDD), Schaaf-Yang Syndrome, Prader-Willi Syndrome (PWS), postnatal oxytocin treatment, oxytocin receptor expression, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fnins.2023.1026939/fullTest; https://doaj.org/toc/1662-453XTest
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5دورية أكاديمية
المؤلفون: Ahmed Abushahin, Amal Al-Naimi, Mutasim Abu-Hasan, Rania Arar, M. Lina Hayati, Antonisamy Belavendra, Ibrahim A. Janahi
مصطلحات موضوعية: Biomedical and clinical sciences, Cardiovascular medicine and haematology, Pharmacology and pharmaceutical sciences, Sleep-disordered breathing (SDB), Prader–Willi syndrome (PWS), growth hormone (GH), central sleep apnea (CSA)
الإتاحة: https://doi.org/10.1155/2023/9992668Test
https://figshare.com/articles/journal_contribution/Prevalence_of_Sleep-Disordered_Breathing_in_Prader_Willi_Syndrome/25250062Test -
6دورية أكاديمية
المؤلفون: Gigliucci, Valentina, Busnelli, Marta, Santini, Francesca, Paolini, Camilla, Bertoni, Alessandra, Schaller, Fabienne, Muscatelli, Françoise, Chini, Bice
المساهمون: Milan Center for Neuroscience (NeuroMi), Università degli Studi di Milano-Bicocca = University of Milano-Bicocca (UNIMIB), Institut de Neurobiologie de la Méditerranée Aix-Marseille Université (INMED - INSERM U1249), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
المصدر: ISSN: 1662-4548.
مصطلحات موضوعية: Prader-Willi Syndrome (PWS), postnatal oxytocin treatment, oxytocin receptor expression, neurodevelopmental disorders (NDD), Schaaf-Yang Syndrome, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]
العلاقة: hal-04133522; https://amu.hal.science/hal-04133522Test; https://amu.hal.science/hal-04133522/documentTest; https://amu.hal.science/hal-04133522/file/fnins-17-1026939.pdfTest
الإتاحة: https://doi.org/10.3389/fnins.2023.1026939Test
https://amu.hal.science/hal-04133522Test
https://amu.hal.science/hal-04133522/documentTest
https://amu.hal.science/hal-04133522/file/fnins-17-1026939.pdfTest -
7دورية أكاديمية
المؤلفون: Lawrence P. Richer, Qiming Tan, Merlin G. Butler, Hayford M. Avedzi, Darren S. DeLorey, Ye Peng, Hein M. Tun, Arya M. Sharma, Steven Ainsley, Camila E. Orsso, Lucila Triador, Michael Freemark, Andrea M. Haqq
المصدر: International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 8013
مصطلحات موضوعية: autonomic nervous system (ANS), childhood obesity, genetics, Prader–Willi syndrome (PWS)
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Molecular Genetics and Genomics; https://dx.doi.org/10.3390/ijms24098013Test
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8دورية أكاديمية
المؤلفون: Dajie Marschik-Zhang, Jun Wang, Xiushu Shen, Xiaoyun Zhu, Herong Gao, Hong Yang, Peter B. Marschik
المصدر: Journal of Clinical Medicine; Volume 12; Issue 3; Pages: 784
مصطلحات موضوعية: deep phenotyping, cross-condition comparison, infant, neuromotor function, motor development, Prechtl general movements assessment (GMA), motor optimality score-revised (MOS-R), Prader-Willi syndrome (PWS), cerebral palsy (CP)
وصف الملف: application/pdf
العلاقة: Mental Health; https://dx.doi.org/10.3390/jcm12030784Test
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9دورية أكاديمية
المؤلفون: Merlin G. Butler, Waheeda A. Hossain, Neil Cowen, Anish Bhatnagar
المصدر: International Journal of Molecular Sciences; Volume 24; Issue 2; Pages: 1220
مصطلحات موضوعية: Prader-Willi syndrome (PWS), high-resolution chromosomal microarray, PWS molecular genetic classes, typical 15q11-q13 deletion subtypes, maternal disomy 15 subclasses, atypical PWS genetic findings, DESTINY PWS
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Molecular Genetics and Genomics; https://dx.doi.org/10.3390/ijms24021220Test
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10دورية أكاديمية
المؤلفون: Merlin G. Butler
المصدر: International Journal of Molecular Sciences, Vol 24, Iss 5, p 4271 (2023)
مصطلحات موضوعية: Prader–Willi syndrome (PWS), PWS molecular genetic classes, typical 15q11-q13 Type I, Type II deletions, 15q11.2 BP1-BP2 deletion, clinical findings, Biology (General), QH301-705.5, Chemistry, QD1-999
العلاقة: https://www.mdpi.com/1422-0067/24/5/4271Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test; https://doaj.org/article/bb730d59c92041be84df5d20bcdbe601Test
الإتاحة: https://doi.org/10.3390/ijms24054271Test
https://doaj.org/article/bb730d59c92041be84df5d20bcdbe601Test