Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life-Reference-Cited by-同舟云学术

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Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Published:2018-07-31 Issue:3 Volume:10 Page:264-273
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Çizmecioğlu Filiz Mine,Jones Jeremy Huw,Paterson Wendy Forsyth,Kherra Sakina,Kourime Mariam,McGowan Ruth,Shaikh M. Guftar,Donaldson Malcolm

Publisher

Galenos Yayinevi

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 20 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. Management of food socialization for children with Prader-Willi Syndrome: An exploration study in Malaysia;PLOS ONE;2024-08-30

2. The impact of premature birth on auditory-visual processes in very preterm schoolchildren;npj Science of Learning;2024-07-06

3. Genotype–phenotype characteristics of 57 patients with Prader–Willi syndrome: a single-center experience from Turkey;Clinical Dysmorphology;2024-06-18

4. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation;Frontiers in Endocrinology;2024-04-26

5. Feeding tube use and complications in Prader‐Willi syndrome: Data from the Global Prader‐Willi Syndrome Registry;American Journal of Medical Genetics Part A;2024-02

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