A Multicenter Italian Study on Prader-Willi Syndrome

Author:

Pozzan G. B.,Cerutti F.,Corrias A.,Maffeis C.,Tonini G.,De Simone M.,Crino A.,Sposito M.,Balsamo A.,Balestrazzi P.,De Toni T.,Brambilla P.,Livieri C.,Salvatoni A.,Vido L.,Pinelli L.,Lungarotti M. S.,Mazzanti L.,Iughetti L.,Gastaldi R.,Lorini R.,Seminara S.,Borrelli P.,Chiumello G.

Publisher

Springer Berlin Heidelberg

Reference10 articles.

1. Butler MG (1989) Hypopigmentation: A common feature of Prader- Labhart-Willi Syndrome. Am J Hum Genet 45: 140–146

2. Fear CN, Mutton DE, Berry AC, Heckmatt JZ, Dubowitz (1985) Chromosome 15 in Prader-Willi Syndrome. Develop Med Child Neurol 27: 305–311

3. Holm VA (1981) The diagnosis of Prader-Willi Syndrome. In Holm VA, Shulzbacher S, Pipes PL (eds) Prader-Willi Syndrome, University Park Press, Baltimore, p 27

4. Lamb AS, Johnson WM (1987) Premature coronary artery atherosclerosis in a patient with Prader-Willi Syndrome. Am J Med Genet 28: 873–880

5. Ledbetter DH, Greenberg F, Holm VA, Cassidy SB (1987) Conference report: second annual Prader-Willi scientific conference. Am J Hum Genet 28: 779–790

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Medical Considerations;Management of Prader-Willi Syndrome;2022

2. One-year results of growth hormone treatment of short stature in Prader-Willi syndrome;Acta Paediatrica;1997-11

3. Medical Considerations in Prader-Willi Syndrome;Management of Prader-Willi Syndrome

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