PubMed (cited) for id: 606526

Year	Number of Results
2001	1
2002	2
2003	1
2006	1
2007	1
2011	1
2012	2
2015	1
2018	2
2019	1
2020	1
2024	0

1

Griscelli syndrome type 3 in Ethiopian sisters resulting from a homozygous missense mutation in MLPH.

Dagnewu KY, Ayele A, Liu L, Pramanik R, Onoufriadis A, Abebe E, McGrath JA. Dagnewu KY, et al. Int J Dermatol. 2020 Mar;59(3):e55-e57. doi: 10.1111/ijd.14724. Epub 2019 Nov 13. Int J Dermatol. 2020. PMID: 31721180 No abstract available.

2

[Griscelli syndrome type 3: A new case].

Kassem Youssef H, Ramstein C, Ginglinger E, Chouta Ngaha F, Nojavan H, Michel C. Kassem Youssef H, et al. Ann Dermatol Venereol. 2018 Dec;145(12):785-789. doi: 10.1016/j.annder.2018.07.030. Epub 2018 Oct 30. Ann Dermatol Venereol. 2018. PMID: 30389201 Review. French.

3

New Insights into the Melanophilin (MLPH) Gene Affecting Coat Color Dilution in Rabbits.

Demars J, Iannuccelli N, Utzeri VJ, Auvinet G, Riquet J, Fontanesi L, Allain D. Demars J, et al. Genes (Basel). 2018 Aug 23;9(9):430. doi: 10.3390/genes9090430. Genes (Basel). 2018. PMID: 30142960 Free PMC article.

4

Griscelli Syndrome Type 3: Two New Cases and Review of the Literature.

Nouriel A, Zisquit J, Helfand AM, Anikster Y, Greenberger S. Nouriel A, et al. Pediatr Dermatol. 2015 Nov-Dec;32(6):e245-8. doi: 10.1111/pde.12663. Epub 2015 Sep 4. Pediatr Dermatol. 2015. PMID: 26337734 Review.

5

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

Cağdaş D, Ozgür TT, Asal GT, Tezcan I, Metin A, Lambert N, de Saint Basile G, Sanal O. Cağdaş D, et al. Eur J Pediatr. 2012 Oct;171(10):1527-31. doi: 10.1007/s00431-012-1765-x. Epub 2012 Jun 19. Eur J Pediatr. 2012. PMID: 22711375

6

Cellular and clinical report of new Griscelli syndrome type III cases.

Westbroek W, Klar A, Cullinane AR, Ziegler SG, Hurvitz H, Ganem A, Wilson K, Dorward H, Huizing M, Tamimi H, Vainshtein I, Berkun Y, Lavie M, Gahl WA, Anikster Y. Westbroek W, et al. Pigment Cell Melanoma Res. 2012 Jan;25(1):47-56. doi: 10.1111/j.1755-148X.2011.00901.x. Epub 2011 Oct 3. Pigment Cell Melanoma Res. 2012. PMID: 21883982 Free PMC article.

7

A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs.

Drögemüller C, Philipp U, Haase B, Günzel-Apel AR, Leeb T. Drögemüller C, et al. J Hered. 2007;98(5):468-73. doi: 10.1093/jhered/esm021. Epub 2007 May 22. J Hered. 2007. PMID: 17519392 Free article.

8

A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat.

Ishida Y, David VA, Eizirik E, Schäffer AA, Neelam BA, Roelke ME, Hannah SS, O'Brien SJ, Menotti-Raymond M. Ishida Y, et al. Genomics. 2006 Dec;88(6):698-705. doi: 10.1016/j.ygeno.2006.06.006. Epub 2006 Jul 24. Genomics. 2006. PMID: 16860533 Free article.

9

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. Ménasché G, et al. J Clin Invest. 2003 Aug;112(3):450-6. doi: 10.1172/JCI18264. J Clin Invest. 2003. PMID: 12897212 Free PMC article.

10

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Ménasché G, Gürgey A, Berkel I, de Saint Basile G. Sanal O, et al. J Clin Immunol. 2002 Jul;22(4):237-43. doi: 10.1023/a:1016045026204. J Clin Immunol. 2002. PMID: 12148598

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

12 results

Results by year