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Nutritional phases in Prader-Willi syndrome
Miller, Jennifer L., Lynn, Christy H., Driscoll, Danielle C., Goldstone, Anthony P., Gold, June-Anne, Kimonis, Virginia, Dykens, Elisabeth, Butler, Merlin G., Shuster, Jonathan J., Driscoll, Daniel J.
Published in American journal of medical genetics. Part A (01.05.2011)
Published in American journal of medical genetics. Part A (01.05.2011)
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Obesity in Prader–Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches
Muscogiuri, G., Barrea, L., Faggiano, F., Maiorino, M. I., Parrillo, M., Pugliese, G., Ruggeri, R. M., Scarano, E., Savastano, S., Colao, A.
Published in Journal of endocrinological investigation (01.10.2021)
Published in Journal of endocrinological investigation (01.10.2021)
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Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome
Bieth, Eric, Eddiry, Sanaa, Gaston, Véronique, Lorenzini, Françoise, Buffet, Alexandre, Conte Auriol, Françoise, Molinas, Catherine, Cailley, Dorothée, Rooryck, Caroline, Arveiler, Benoit, Cavaillé, Jérome, Salles, Jean Pierre, Tauber, Maïthé
Published in European journal of human genetics : EJHG (01.02.2015)
Published in European journal of human genetics : EJHG (01.02.2015)
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Obesity management in Prader-Willi syndrome: current perspectives
Crinò, Antonino, Fintini, Danilo, Bocchini, Sarah, Grugni, Graziano
Published in Diabetes, metabolic syndrome and obesity (2018)
Published in Diabetes, metabolic syndrome and obesity (2018)
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Hormonal and metabolic effects of carbohydrate restriction in children with Prader‐Willi syndrome
Irizarry, Krystal A., Mager, Diana R., Triador, Lucila, Muehlbauer, Michael J., Haqq, Andrea M., Freemark, Michael
Published in Clinical endocrinology (Oxford) (01.04.2019)
Published in Clinical endocrinology (Oxford) (01.04.2019)
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Selective changes in vasopressin neurons and astrocytes in the suprachiasmatic nucleus of Prader–Willi syndrome subjects
Correa‐da‐Silva, Felipe, Berkhout, Jari B., Schouten, Pim, Sinnema, Margje, Stumpel, Constance T. R. M., Curfs, Leopold M. G., Höybye, Charlotte, Mahfouz, Ahmed, Meijer, Onno C., Pereira, Alberto M., Fliers, Eric, Swaab, Dick F., Kalsbeek, Andries, Yi, Chun‐Xia
Published in Journal of neuroendocrinology (01.05.2025)
Published in Journal of neuroendocrinology (01.05.2025)
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Evidence for Accelerated Biological Aging in Young Adults with Prader–Willi Syndrome
Donze, Stephany H, Codd, Veryan, Damen, Layla, Goedegebuure, Wesley J, Denniff, Matthew, Samani, Nilesh J, van der Velden, Janiëlle A E M, Hokken-Koelega, Anita C S
Published in The journal of clinical endocrinology and metabolism (01.06.2020)
Published in The journal of clinical endocrinology and metabolism (01.06.2020)
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The Italian registry for patients with Prader–Willi syndrome
Salvatore, Marco, Torreri, Paola, Grugni, Graziano, Rocchetti, Adele, Maghnie, Mohamad, Patti, Giuseppa, Crinò, Antonino, Elia, Maurizio, Greco, Donatella, Romano, Corrado, Franzese, Adriana, Mozzillo, Enza, Colao, Annamaria, Pugliese, Gabriella, Pagotto, Uberto, Lo Preiato, Valentina, Scarano, Emanuela, Schiavariello, Concetta, Tornese, Gianluca, Fintini, Danilo, Bocchini, Sarah, Osimani, Sara, De Sanctis, Luisa, Sacco, Michele, Rutigliano, Irene, Delvecchio, Maurizio, Faienza, Maria Felicia, Wasniewska, Malgorzata, Corica, Domenico, Stagi, Stefano, Guazzarotti, Laura, Maffei, Pietro, Dassie, Francesca, Taruscio, Domenica
Published in Orphanet journal of rare diseases (15.02.2023)
Published in Orphanet journal of rare diseases (15.02.2023)
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Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes
Kim, Soo-Jeong, Miller, Jennifer L, Kuipers, Paul J, German, Jennifer Ruth, Beaudet, Arthur L, Sahoo, Trilochan, Driscoll, Daniel J
Published in European journal of human genetics : EJHG (01.03.2012)
Published in European journal of human genetics : EJHG (01.03.2012)
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Differences in Bone Metabolism between Children with Prader–Willi Syndrome during Growth Hormone Treatment and Healthy Subjects: A Pilot Study
Gajewska, Joanna, Chełchowska, Magdalena, Szamotulska, Katarzyna, Klemarczyk, Witold, Strucińska, Małgorzata, Ambroszkiewicz, Jadwiga
Published in International journal of molecular sciences (01.09.2024)
Published in International journal of molecular sciences (01.09.2024)
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Circulating insulin‐like growth factor 1 levels are reduced in very young children with Prader–Willi syndrome independent of anthropometric parameters and nutritional status
Koizumi, Mikiko, Konishi, Ayako, Etani, Yuri, Ida, Shinobu, Kawai, Masanobu
Published in Clinical endocrinology (Oxford) (01.03.2022)
Published in Clinical endocrinology (Oxford) (01.03.2022)
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Hypothalamic neuropeptides and neurocircuitries in Prader Willi syndrome
Correa‐da‐Silva, Felipe, Fliers, Eric, Swaab, Dick F., Yi, Chun‐Xia
Published in Journal of neuroendocrinology (01.07.2021)
Published in Journal of neuroendocrinology (01.07.2021)
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Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader–Willi Syndrome
Richer, Lawrence P., Tan, Qiming, Butler, Merlin G., Avedzi, Hayford M., DeLorey, Darren S., Peng, Ye, Tun, Hein M., Sharma, Arya M., Ainsley, Steven, Orsso, Camila E., Triador, Lucila, Freemark, Michael, Haqq, Andrea M.
Published in International journal of molecular sciences (28.04.2023)
Published in International journal of molecular sciences (28.04.2023)
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Prader–Willi syndrome and early‐onset morbid obesity NIH rare disease consortium: A review of natural history study
Butler, Merlin G., Kimonis, Virginia, Dykens, Elisabeth, Gold, June A., Miller, Jennifer, Tamura, Roy, Driscoll, Daniel J.
Published in American journal of medical genetics. Part A (01.02.2018)
Published in American journal of medical genetics. Part A (01.02.2018)
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Central hypothyroidism improves with age in very young children with Prader‐Willi syndrome
Konishi, Ayako, Ida, Shinobu, Shoji, Yasuko, Etani, Yuri, Kawai, Masanobu
Published in Clinical endocrinology (Oxford) (01.03.2021)
Published in Clinical endocrinology (Oxford) (01.03.2021)
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Growth hormone therapy for Prader-Willi syndrome: challenges and solutions
Grugni, Graziano, Sartorio, Alessandro, Crinò, Antonino
Published in Therapeutics and clinical risk management (01.01.2016)
Published in Therapeutics and clinical risk management (01.01.2016)
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Anthropometric characteristics of newborns with Prader–Willi syndrome
Salvatoni, Alessandro, Moretti, Alex, Grugni, Graziano, Agosti, Massimo, Azzolini, Sara, Bonaita, Valentina, Cianci, Paola, Corica, Domenico, Crinò, Antonino, Delvecchio, Maurizio, Ferraris, Silvio, Greggio, Nella A., Iughetti, Lorenzo, Licenziati, Maria R., Madeo, Simona F., Nosetti, Luana, Pajno, Roberta, Rutigliano, Irene, Sacco, Michele, Salvatore, Silvia, Scarano, Emanuela, Trifirò, Giuliana, Wasniewska, Malgorzata
Published in American journal of medical genetics. Part A (01.10.2019)
Published in American journal of medical genetics. Part A (01.10.2019)
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