Maladie de Graves-Basedow et hyperprolactinémie chez une femme atteinte du syndrome de Noonan/neurofibromatose de type 1
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference22 articles.
1. The unsual association of three autoimmune disease in patients with Noonan syndrome;Amoroso;J Adolesc Health,2003
2. Endokrine Storungen bei Kindern mit Neurofibromatose von Reckinghausen;Andler;Monatsschr Kinderheikd,1979
3. Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndroma (NFNS);Baralle;Am J Med. Gent,2003
4. Von Recklinghausens disease: Clinicopathological study;Brasfield;Ann Surg,1987
5. Neurofibromatosis-Noonan syndrom;Buehning;Pediatr Dermatol,1995
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1. ‘If there were water we should stop and drink’: neurofibromatosis presenting with diabetes insipidus;BMJ Case Reports;2018-02-11
2. Thyroid Gland 18F-FDG Uptake in Neurofibromatosis Type 1;European Thyroid Journal;2018
3. Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?;Balkan Medical Journal;2017-12-01
4. Mutation of the NF1 Gene and the Associated Clinical Features in Family Members with Neurofibromatosis Type 1;The Korean Journal of Medicine;2016-05-01
5. Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors;Cancer Genetics and Cytogenetics;2008-04
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