Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1919 1
1920 1
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 21
2024 10

Text availability

Article attribute

Article type

Publication date

Search Results

656 results

Results by year

Filters applied: . Clear all
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.
Piebaldism is an uncommon autosomal dominantly inherited pigment anomaly characterized by a congenital white forelock and leukoderma on the frontal scalp, forehead, ventral trunk and extremities. ...Genetic analyses reveal a consistent genotype-phenotype relationship in
Piebaldism is an uncommon autosomal dominantly inherited pigment anomaly characterized by a congenital white forelock and leukoderma
Piebaldism.
Shah M, Patton E, Zedek D. Shah M, et al. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 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.
Our understanding of melanocyte development, Piebaldism, and Waardenburg syndrome has improved dramatically over the past decade. ...This review focuses on the current understanding of human melanocyte development and the evaluation and management of Piebaldism and …
Our understanding of melanocyte development, Piebaldism, and Waardenburg syndrome has improved dramatically over the past decade. ... …
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 in a 2-year-old girl.
López V, Jordá E. López V, et al. Dermatol Online J. 2011 Feb 15;17(2):13. Dermatol Online J. 2011. PMID: 21382296 Free article. Review.
Piebaldism is a rare autosomal dominant skin disorder characterized by a white forelock and depigmented patches of skin, generally located on the forehead, central chest and abdomen, upper arms, and lower extremities. ...
Piebaldism is a rare autosomal dominant skin disorder characterized by a white forelock and depigmented patches of skin, generally lo
Piebaldism.
More V, Sharma R, Thomas V. More V, et al. Indian Pediatr. 2011 Aug;48(8):665-6. Indian Pediatr. 2011. PMID: 21918288 No abstract available.
656 results