Response to Hannah-Shmouni and Stratakis
- PMID: 30283095
- DOI: 10.1038/s41436-018-0313-0
Response to Hannah-Shmouni and Stratakis
Comment on
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Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med. 2018 Jul;20(7):671-682. doi: 10.1038/gim.2018.28. Epub 2018 Apr 26. Genet Med. 2018. PMID: 30006586
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Growth hormone excess in neurofibromatosis 1.Genet Med. 2019 May;21(5):1254-1255. doi: 10.1038/s41436-018-0312-1. Epub 2018 Oct 4. Genet Med. 2019. PMID: 30283094 No abstract available.
References
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- Hannah-Shmouni F, Stratakis CA. Growth hormone excess in neurofibromatosis type 1. Genet Med. 2018; https://doi.org/10.1038/s41436-018-0312-1
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- Stewart DR, Korf BR, Nathanson KL, Stevenson DA, Yohay K. Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2018;20:671–82. - DOI
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- Eugster E. Gigantism. In: De Groot LJ, Chrousos G, Dungan K, eds. Endotext. South Darmouth, MA: MDText.com; 2018. https://www.ncbi.nlm.nih.gov/books/NBK279155/
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- Josefson JL, Listernick R, Charrow J, Habiby RL. Growth hormone excess in children with optic pathway tumors is a transient phenomenon. Horm Res Paediatr. 2016;86:35–38. - DOI
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- Sani I, Albanese A. Endocrine long-term follow-up of children with neurofibromatosis type 1 and optic pathway glioma. Horm Res Paediatr. 2017;87:179–88. - DOI
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