Search Results - "Prader–Willi syndrome"

Potential of GLP-1 Analogs in Managing Hyperphagia and Obesity in Prader-Willi Syndrome: A Review of Efficacy and Safety by Olga Grelewicz, Adam Juśkiewicz, Elwira Servaas, Mateusz Haber, Paula Kula, Alicja Kotula, Adrianna Czachor, Natalia Kucy

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Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report by Tsuyoshi Murata, Toma Fukuda, Aya Kanno, Hyo Kyozuka, Akiko Yamaguchi, Hiromi Shimizu, Takafumi Watanabe, Keiya Fujimori

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Thyroid function in children with Prader-Willi syndrome in Southern China: a single-center retrospective case series by Xinjiang Huang, Xi Yin, Dongyan Wu, Yanna Cai, Xiuzhen Li, Wen Zhang, Chunhua Zeng, Xiaojian Mao, Li Liu

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Tailored management of life-threatening complications related to severe obesity in a young adult with Prader-Willi syndrome by Min-Sun Kim, Jiyeon Kim, Joongbum Cho, Sung Yoon Cho, Dong-Kyu Jin

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Endocrine problems in children with Prader-Willi syndrome: special review on associated genetic aspects and early growth hormone treatment by Dong-Kyu Jin

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Postural-motor development, spinal range of movement and caregiver burden in Prader-Willi syndrome-associated scoliosis: an observational study by Maria Chiara Maccarone, Mariarosa Avenia, Stefano Masiero

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Special Care Dentistry in a Patient with Prader-Willi Syndrome through the Use of Atraumatic Restorative Treatment under General Anesthesia by Caio Vinícius Gonçalves Roman-Torres, Sérgio Takashi Kussaba, Yasmin Comoti Vita Bantim, Roberta de Barros Antunes Almeida de Oliveira

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Inter- and intra-observer reliability of the "Assessment of Motor Repertoire- 3 to 5 Months" based on video recordings of infants with Prader-Willi syndrome by Jun Wang, Xiushu Shen, Hong Yang, Wei Shi, Xiaoyun Zhu, Herong Gao, Huanhuan Yin, Fanzhe Meng, Yun Wu

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Efficacy of denosumab therapy for a 21-year-old woman with Prader-Willi syndrome, osteoporosis and history of fractures: a case report by Uehara M, Nakamura Y, Takahashi J, Suzuki T, Iijima M, Arakawa Y, Ida K, Kosho T, Kato H

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A Case Of Prader-Willi Syndrome With Behavioural Disturbances: A Successful Multidisciplinary Management Approach / Nor Jannah Nasution Raduan ... [et al.] by Nasution Raduan, Nor Jannah Nasution Raduan, Salleh, Mohd Razali, Bahar, Norharlina, Md Tahir, Mohd Faiz, Md Rosli, Najwa Hanim

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Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report by Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu

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Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report by Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu

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Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome by Slater Howard R, Rowell Margaret, Francis David I, Northrop Emma, Albalwi Mohammed, Schüle Birgitt, Gardner RJ McKinlay, Francke Uta

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Evaluating the effect of recombinant human growth hormone treatment on sleep-related breathing disorders in toddlers with Prader-Willi syndrome: a one-year retrospective cohort study by Haiyan Guo, Jinrong Fu, Yufeng Zhou, Feihong Luo, Ruoqian Cheng

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Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome by Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

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Genetic Testing for Rare Diseases

Subjects: “…Prader-Willi syndrome…”
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Structure, Activity, and Function of Protein Methyltransferases

Subjects: “…Prader-Willi syndrome…”
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Cognitive and behavioral heterogeneity in genetic syndromes by Luiz F.L. Pegoraro, Carlos E. Steiner, Eloisa H.R.V. Celeri, Claudio E.M. Banzato, Paulo Dalgalarrondo

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Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders by Valery eGrinevich, Michel eDesarménien, Bice eChini, Maithé eTauber, Françoise eMuscatelli

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Cognitive and behavioral heterogeneity in genetic syndromes by Luiz F.L. Pegoraro, Carlos E. Steiner, Eloisa H.R.V. Celeri, Claudio E.M. Banzato, Paulo Dalgalarrondo

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