(Q38058101)

27 August 2017

Piebaldism: A brief report and review of the literature (English)

1 reference

27 August 2017

1 reference

Saurabh Agarwal

1

1 reference

PMC publication ID

3481873

27 August 2017

Amit Ojha

series ordinal

2

1 reference

27 August 2017

1 May 2012

1 reference

Indian Dermatology Online Journal

27 August 2017

1 reference

27 August 2017

3

1 reference

27 August 2017

2

1 reference

27 August 2017

144-147

1 reference

Melanocyte transplant in piebaldism: case report

27 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Piebaldism: a case report and a concise review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

ALBINISM AMONG INDIANS IN ARIZONA AND NEW MEXICO

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Grover disease (transient acantholytic dermatosis) and piebaldism.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

A novel KIT mutation results in piebaldism with progressive depigmentation.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Long-term results of noncultured epidermal cellular grafting in vitiligo, halo naevi, piebaldism and naevus depigmentosus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Molecular basis of human piebaldism

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Piebaldism and neurofibromatosis type 1: family report.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3481873

Acquired pigmented macules in human piebald lesions. Ultrastructure of melanocytes in hypomelanotic skin

31 August 2018

1 reference

12 December 2020

Piebaldness with Hirschsprung's disease

1 reference

12 December 2020

Human piebaldism: relationship between phenotype and site of kit gene mutation

1 reference

12 December 2020

Repigmentation of leucodermic defects in piebaldism by dermabrasion and thin split-thickness skin grafting in combination with minigrafting

1 reference

12 December 2020

Association of piebaldism and neurofibromatosis type 1 in a girl

1 reference

12 December 2020

Piebaldism associated with congenital dyserythropoietic anemia type II (HEMPAS)

1 reference

12 December 2020

Piebaldism in diamond-blackfan anaemia: a new phenotype?

1 reference

12 December 2020

Partial albinism and deaf-mutism due to a recessive sex-linked gene

1 reference

12 December 2020

Identifiers

DOI

10.4103/2229-5178.96722

1 reference

27 August 2017

1 reference

PMC publication ID

3481873

27 August 2017

PubMed publication ID

23130293

1 reference

PMC publication ID

3481873