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Year Number of Results
2015 1
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2018 1
2019 1
2020 3
2021 2
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Page 1
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Barraud S, Delemer B, Poirsier-Violle C, Bouligand J, Mérol JC, Grange F, Higel-Chaufour B, Decoudier B, Zalzali M, Dwyer AA, Acierno JS, Pitteloud N, Millar RP, Young J. Barraud S, et al. Among authors: zalzali m. Neuroendocrinology. 2021;111(1-2):99-114. doi: 10.1159/000506640. Epub 2020 Feb 20. Neuroendocrinology. 2021. PMID: 32074614
Long-term progression of non-invasive follicular thyroid neoplasm with papillary-like nuclear features: A single-center retrospective study of the French Marne-Ardennes thyroid cancer registry.
Richard C, Debreuve-Theresette A, Patey M, Brabencova E, Filieri C, Zalzali M, Schvartz C. Richard C, et al. Among authors: zalzali m. Ann Endocrinol (Paris). 2020 Feb;81(1):34-38. doi: 10.1016/j.ando.2019.12.001. Epub 2020 Jan 25. Ann Endocrinol (Paris). 2020. PMID: 32057425
Added value of 18F-fluorocholine positron emission tomography-computed tomography in presurgical localization of hyperfunctioning parathyroid glands after dual tracer subtraction scintigraphy failure: A retrospective study of 47 patients.
Morland D, Lalire P, Deguelte S, Zalzali M, Richard C, Dejust S, Boulagnon C, Ly S, Papathanassiou D, Delemer B. Morland D, et al. Among authors: zalzali m. Medicine (Baltimore). 2020 Jan;99(2):e18681. doi: 10.1097/MD.0000000000018681. Medicine (Baltimore). 2020. PMID: 31914064 Free PMC article.