Prader–Willi syndrome in neonates: twenty cases and review of the literature in Southern China
暂无分享,去创建一个
W. Zhou | Ping Wang | Long-guang Huang | W. Yuan | Ning Zhao | Xiaowen Chen
[1] H. Deng,et al. Insulin sensitivity in a patient with Prader-Willi syndrome , 2015 .
[2] B. Whitman,et al. Prader-Willi syndrome and growth hormone therapy: take a deep breath and weigh the data. , 2013, The Journal of pediatrics.
[3] L. Gravina,et al. Change in Prevalence of Congenital Defects in Children With Prader-Willi Syndrome , 2013, Pediatrics.
[4] J. Hamilton,et al. Longitudinal evaluation of sleep-disordered breathing in children with Prader-Willi Syndrome during 2 years of growth hormone therapy. , 2013, The Journal of pediatrics.
[5] S. Reid,et al. Prader–Willi syndrome in Victoria: Mortality and causes of death , 2012, Journal of paediatrics and child health.
[6] C. D. de Korte,et al. Cardiac evaluation in children with Prader–Willi syndrome , 2012, Acta paediatrica.
[7] Jian-jun Yang,et al. Genetic diagnosis and weight loss surgery of a case of Prader-Willi syndrome , 2011 .
[8] E. Christ,et al. Regulation of whole body energy homeostasis with growth hormone replacement therapy and endurance exercise. , 2011, Physiological genomics.
[9] Hong Wang,et al. [Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome]. , 2010, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.
[10] Lu-yun Li,et al. [Identification of a cryptic 1p36.3 microdeletion in a patient with Prader-Willi-like syndrome features]. , 2010, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.
[11] J. Bryant,et al. Recombinant human growth hormone for the treatment of growth disorders in children: a systematic review and economic evaluation. , 2010, Health technology assessment.
[12] W. Jia,et al. Precise microdeletion detection of Prader-Willi Syndrome with array comparative genome hybridization. , 2010, Biomedical and environmental sciences : BES.
[13] M. Tauber,et al. Endocrine Disorders in Children with Prader-Willi Syndrome – Data from 142 Children of the French Database , 2010, Hormone Research in Paediatrics.
[14] J. Wit,et al. Efficacy and safety of long-term continuous growth hormone treatment in children with Prader-Willi syndrome. , 2009, The Journal of clinical endocrinology and metabolism.
[15] M. Tauber,et al. Recommendations for the diagnosis and management of Prader-Willi syndrome. , 2008, The Journal of clinical endocrinology and metabolism.
[16] H. Duivenvoorden,et al. Randomized controlled GH trial: effects on anthropometry, body composition and body proportions in a large group of children with Prader–Willi syndrome , 2008, Clinical endocrinology.
[17] H. Duivenvoorden,et al. Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader–Willi syndrome , 2008, Clinical endocrinology.
[18] M. Tauber,et al. Early Diagnosis and Multidisciplinary Care Reduce the Hospitalization Time and Duration of Tube Feeding and Prevent Early Obesity in PWS Infants , 2007, Hormone Research in Paediatrics.
[19] M. Tauber,et al. KIGS Highlights: Growth Hormone Treatment in Prader-Willi Syndrome , 2007, Hormone Research in Paediatrics.
[20] K. Õunap,et al. The neonatal phenotype of Prader–Willi syndrome , 2006, American journal of medical genetics. Part A.
[21] D. Allen,et al. Growth hormone improves mobility and body composition in infants and toddlers with Prader-Willi syndrome. , 2004, The Journal of pediatrics.
[22] K. Devriendt,et al. Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders , 2004, European Journal of Human Genetics.
[23] A. Crinò,et al. Neonatal hypotonia: don't forget the Prader‐Willi syndrome , 2003, Acta paediatrica.
[24] D. Allen,et al. Benefits of long-term GH therapy in Prader-Willi syndrome: a 4-year study. , 2002, The Journal of clinical endocrinology and metabolism.
[25] S. Schwartz,et al. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. , 2001, Pediatrics.
[26] K. Macdermot,et al. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females , 2001, Journal of medical genetics.
[27] K. Westerterp,et al. Energy expenditure at rest and during sleep in children with Prader-Willi syndrome is explained by body composition. , 2000, The American journal of clinical nutrition.
[28] M. Butler,et al. Prader-Willi syndrome: consensus diagnostic criteria. , 1993, Pediatrics.
[29] Suzanne B. Cassidy,et al. Prader-Willi syndrome , 1989, Genetics in Medicine.
[30] R. Wharton,et al. NEONATAL RESPIRATORY DEPRESSION AND DELAY IN DIAGNOSIS IN PRADER‐WILLI SYNDROME , 1989, Developmental medicine and child neurology.
[31] D. Schoeller,et al. ENERGY EXPENDITURE AND BODY COMPOSITION IN PRADER-WILLI SYNDROME , 1984, Pediatric Research.
[32] L. de Catte,et al. Can fetal ultrasound result in prenatal diagnosis of Prader-Willi syndrome? , 2011, Genetic counseling.
[33] U. Eiholzer,et al. A Comprehensive Team Approach to the Management of Patients with Prader-Willi Syndrome , 2004, Journal of pediatric endocrinology & metabolism : JPEM.