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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1971 | 1 |
2016 | 1 |
2020 | 1 |
2024 | 0 |
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Familial progressive hyperpigmentation.
Arch Dermatol. 1971 Jun;103(6):581-91 passim.
Arch Dermatol. 1971.
PMID: 4326548
No abstract available.
Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).
Zhang J, Li M, Yao Z.
Zhang J, et al.
Mol Med Rep. 2016 Nov;14(5):4023-4029. doi: 10.3892/mmr.2016.5760. Epub 2016 Sep 22.
Mol Med Rep. 2016.
PMID: 27666661
Free PMC article.
Review.
These disorders, which include Legius syndrome, Noonan syndrome with multiple lentigines or LEOPARD syndrome, and familial progressive hyperpigmentation) are difficult to distinguish from NF1 at early stages, using skin appearance alone. ...
These disorders, which include Legius syndrome, Noonan syndrome with multiple lentigines or LEOPARD syndrome, and familial progres …
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Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation.
Kato M, Yagami A, Tsukamoto T, Shinkai Y, Kato T, Kurahashi H.
Kato M, et al.
J Dermatol. 2020 Jun;47(6):669-672. doi: 10.1111/1346-8138.15313. Epub 2020 Mar 18.
J Dermatol. 2020.
PMID: 32189379
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