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Table representation of search results timeline featuring number of search results per year.

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1919 1
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1931 1
1946 2
1950 2
1951 1
1952 1
1954 2
1955 1
1956 2
1957 1
1959 1
1960 1
1961 3
1962 4
1964 1
1965 3
1967 2
1968 1
1969 3
1970 1
1971 1
1972 2
1974 3
1975 4
1976 10
1977 7
1978 3
1979 3
1980 1
1981 3
1982 3
1983 2
1984 5
1985 4
1986 12
1987 6
1988 9
1989 7
1990 5
1991 11
1992 14
1993 12
1994 16
1995 14
1996 10
1997 14
1998 15
1999 11
2000 13
2001 9
2002 13
2003 8
2004 17
2005 16
2006 16
2007 15
2008 15
2009 22
2010 24
2011 21
2012 27
2013 29
2014 25
2015 21
2016 20
2017 22
2018 15
2019 17
2020 32
2021 19
2022 20
2023 22
2024 17
2025 1

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665 results

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Page 1
Piebaldism.
Oiso N, Fukai K, Kawada A, Suzuki T. Oiso N, et al. J Dermatol. 2013 May;40(5):330-5. doi: 10.1111/j.1346-8138.2012.01583.x. Epub 2012 Jun 1. J Dermatol. 2013. PMID: 22670867 Review.
Genetic analyses reveal a consistent genotype-phenotype relationship in piebaldism. However, recently reported cases of piebaldism that are milder or severer than genetically expected indicate that other factors, such as a modifier gene of MC1R, influence skin and h …
Genetic analyses reveal a consistent genotype-phenotype relationship in piebaldism. However, recently reported cases of piebaldism …
Piebaldism.
Shah M, Patton E, Zedek D. Shah M, et al. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 31334958 Free Books & Documents.
Piebaldism is an autosomal dominant disorder affecting melanocyte migration and development characterized by isolated congenital leukoderma (white skin) and poliosis (white hair) in a distinct ventral midline pattern. The most common cause of piebaldism is a mutatio …
Piebaldism is an autosomal dominant disorder affecting melanocyte migration and development characterized by isolated congenital leuk …
Piebaldism in children.
Grob A, Grekin S. Grob A, et al. Cutis. 2016 Feb;97(2):90-2. Cutis. 2016. PMID: 26919497 Review.
Piebaldism is a rare autosomal-dominant disorder of melanocyte development characterized by congenital poliosis and stable patches of leukoderma. ...We present the case of a 14-year-old adolescent girl with piebaldism, along with a review of the pathogenesis, diagno …
Piebaldism is a rare autosomal-dominant disorder of melanocyte development characterized by congenital poliosis and stable patches of …
Piebaldism: an update.
Thomas I, Kihiczak GG, Fox MD, Janniger CK, Schwartz RA. Thomas I, et al. Int J Dermatol. 2004 Oct;43(10):716-9. doi: 10.1111/j.1365-4632.2004.02114.x. Int J Dermatol. 2004. PMID: 15485525 Review. No abstract available.
Piebaldism.
Bassi A, Berti S, Galeone M. Bassi A, et al. QJM. 2015 Nov;108(11):915. doi: 10.1093/qjmed/hcv101. Epub 2015 May 18. QJM. 2015. PMID: 25991872 No abstract available.
Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome.
Saleem MD. Saleem MD. Pediatr Dermatol. 2019 Jan;36(1):72-84. doi: 10.1111/pde.13713. Epub 2018 Dec 18. Pediatr Dermatol. 2019. PMID: 30561083 Review.
Melanocyte development is orchestrated by a complex interconnecting regulatory network of genes and synergistic interactions. Piebaldism and Waardenburg syndrome are neurocristopathies that arise from mutations in genes involved in this complex network. ...This review focu …
Melanocyte development is orchestrated by a complex interconnecting regulatory network of genes and synergistic interactions. Piebaldism …
Piebaldism.
Mosher DB, Fitzpatrick TB. Mosher DB, et al. Arch Dermatol. 1988 Mar;124(3):364-5. Arch Dermatol. 1988. PMID: 3345088 No abstract available.
Piebaldism.
Hazan C. Hazan C. Dermatol Online J. 2005 Dec 30;11(4):18. Dermatol Online J. 2005. PMID: 16403390 Free article.
The patient has a family history of a similar congenital pigment disorder, the pattern of which is indicative of the autosomal dominant disorder piebaldism....
The patient has a family history of a similar congenital pigment disorder, the pattern of which is indicative of the autosomal dominant diso …
[Piebaldism: a pigmentary anomaly to recognize: about a case and review of the literature].
El Kouarty H, Dakhama BS. El Kouarty H, et al. Pan Afr Med J. 2016 Nov 14;25:155. doi: 10.11604/pamj.2016.25.155.10499. eCollection 2016. Pan Afr Med J. 2016. PMID: 28292117 Free PMC article. Review. French.
Piebaldism is a rare autosomal dominant disorder characterized by an abnormal congenital skin pigmentation causing hypopigmented areas. ...We report the case of a 5-year old boy with piebaldism having a family history of dermatologic phenotype without other alterati …
Piebaldism is a rare autosomal dominant disorder characterized by an abnormal congenital skin pigmentation causing hypopigmented area …
Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development.
Spritz RA. Spritz RA. Semin Cutan Med Surg. 1997 Mar;16(1):15-23. doi: 10.1016/s1085-5629(97)80031-4. Semin Cutan Med Surg. 1997. PMID: 9125761 Review.
Disorders of melanocyte development are characterized by heterogeneous distribution of pigmentation, so-called 'white spotting,' typified by piebaldism and Waardenburg syndrome. It is now clear that these disorders of pigment cell development represent a subgroup of the ne …
Disorders of melanocyte development are characterized by heterogeneous distribution of pigmentation, so-called 'white spotting,' typified by …
665 results