163 related articles for article (PubMed ID: 29314428)
1. Mosaic NRASopathy n a child with giant melanocytic congenital naevus, epidermal hamartoma and bilateral nephroblastomatosis: clinical implication for follow-up.
Maridet C; Morice-Picard F; Gros A; Crivelli L; de la Fouchardière A; Vergier B; Taïeb A
J Eur Acad Dermatol Venereol; 2018 Jul; 32(7):e258-e260. PubMed ID: 29314428
[No Abstract] [Full Text] [Related]
2. Making a mountain out of a molehill: NRAS, mosaicism, and large congenital nevi.
Gerami P; Paller AS
J Invest Dermatol; 2013 Sep; 133(9):2127-30. PubMed ID: 23949765
[TBL] [Abstract][Full Text] [Related]
3. Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS.
Kinsler VA; Thomas AC; Ishida M; Bulstrode NW; Loughlin S; Hing S; Chalker J; McKenzie K; Abu-Amero S; Slater O; Chanudet E; Palmer R; Morrogh D; Stanier P; Healy E; Sebire NJ; Moore GE
J Invest Dermatol; 2013 Sep; 133(9):2229-36. PubMed ID: 23392294
[TBL] [Abstract][Full Text] [Related]
4. Mosaic NRAS Q61R mutation in a child with giant congenital melanocytic naevus, epidermal naevus syndrome and hypophosphataemic rickets.
Ramesh R; Shaw N; Miles EK; Richard B; Colmenero I; Moss C
Clin Exp Dermatol; 2017 Jan; 42(1):75-79. PubMed ID: 27900779
[TBL] [Abstract][Full Text] [Related]
5. [Neurocutaneous melanosis and multiple congenital melanocytic naevi are associated with post-zygotic N-ras mutations].
Dereure O
Ann Dermatol Venereol; 2014 Apr; 141(4):314-5. PubMed ID: 24703650
[No Abstract] [Full Text] [Related]
6. Amplification of mutated NRAS leading to congenital melanoma in neurocutaneous melanocytosis.
Salgado CM; Basu D; Nikiforova M; Hamilton RL; Gehris R; Jakacki R; Panigrahy A; Yatsenko S; Reyes-Múgica M
Melanoma Res; 2015 Oct; 25(5):453-60. PubMed ID: 26266759
[TBL] [Abstract][Full Text] [Related]
7. Hereditary spastic paraplegia masqueraded by congenital melanocytic nevus syndrome: Dual pathogenesis of germline non-mosaicism and somatic mosaicism.
Sakaguchi Y; Uehara T; Sasaki M; Fujimura K; Kishi K; Kosaki K; Takenouchi T
Eur J Med Genet; 2020 Apr; 63(4):103803. PubMed ID: 31698101
[TBL] [Abstract][Full Text] [Related]
8. Aggressive melanoma in an infant with congenital melanocytic nevus syndrome and multiple, NRAS and BRAF mutation-negative nodules.
de la Rosa Carrillo D; Vindenes H; Kinsler VA; Rønnestad A; Ringstad G; Müller LO; Tafjord S; Tønseth KA; Kvamme B; Clausen OPF
Pediatr Dermatol; 2018 Sep; 35(5):e281-e285. PubMed ID: 29999207
[TBL] [Abstract][Full Text] [Related]
9. Naevus spilus-type congenital melanocytic naevus associated with a novel NRAS codon 61 mutation.
Krengel S; Widmer DS; Kerl K; Levesque MP; Schiestl C; Weibel L
Br J Dermatol; 2016 Mar; 174(3):642-4. PubMed ID: 26302237
[No Abstract] [Full Text] [Related]
10. Genetic analyses of mosaic neurofibromatosis type 1 with giant café-au-lait macule, plexiform neurofibroma and multiple melanocytic nevi.
Hida T; Idogawa M; Okura M; Sugita S; Sugawara T; Sasaki Y; Tokino T; Yamashita T; Uhara H
J Dermatol; 2020 Jun; 47(6):658-662. PubMed ID: 32246533
[TBL] [Abstract][Full Text] [Related]
11. Oncogenic codon 13 NRAS mutation in a primary mesenchymal brain neoplasm and nevus of a child with neurocutaneous melanosis.
Shih F; Yip S; McDonald PJ; Chudley AE; Del Bigio MR
Acta Neuropathol Commun; 2014 Oct; 2():140. PubMed ID: 25330907
[TBL] [Abstract][Full Text] [Related]
12. Immunohistochemical detection of the c-met proto-oncogene product in the congenital melanocytic nevus of an infant with neurocutaneous melanosis.
Takayama H; Nagashima Y; Hara M; Takagi H; Mori M; Merlino G; Nakazato Y
J Am Acad Dermatol; 2001 Mar; 44(3):538-40. PubMed ID: 11209133
[TBL] [Abstract][Full Text] [Related]
13. Melanoma arising in a giant congenital melanocytic nevus with neuroblastoma RAS mutation.
Dudani P; Senthilnathan G; Wajid MA; Gupta AK; Kaushal S; Arora S; Shamim SA; Bhari N
Indian J Dermatol Venereol Leprol; 2021; 87(3):416-420. PubMed ID: 33871206
[No Abstract] [Full Text] [Related]
14. Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.
Kinsler VA; Krengel S; Riviere JB; Waelchli R; Chapusot C; Al-Olabi L; Faivre L; Haenssle HA; Weibel L; Jeudy G; Vabres P
J Invest Dermatol; 2014 Oct; 134(10):2658-2660. PubMed ID: 24751729
[No Abstract] [Full Text] [Related]
15. Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome.
Ulrich M; Tinschert S; Siebert E; Franke I; Tüting T; Ulrich J; Schanze D; Wieland I; Zenker M
Pigment Cell Melanoma Res; 2019 May; 32(3):470-473. PubMed ID: 30548225
[No Abstract] [Full Text] [Related]
16. Epidermal, sebaceous, and melanocytic nevoid proliferations are spectrums of mosaic RASopathies.
Luo S; Tsao H
J Invest Dermatol; 2014 Oct; 134(10):2493-2496. PubMed ID: 25219651
[TBL] [Abstract][Full Text] [Related]
17. Congenital Melanocytic Nevus Syndrome: A Case Series.
Recio A; Sánchez-Moya AI; Félix V; Campos Y
Actas Dermosifiliogr; 2017 Nov; 108(9):e57-e62. PubMed ID: 28110826
[TBL] [Abstract][Full Text] [Related]
18. Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis.
Takahashi H; Natsumeda M; Hara N; Koyama A; Shimizu H; Miyashita A; Satake D; Mouri Y; Tsukano J; Kawabe K; Tsukamoto Y; Okada M; Ogura R; Yuki A; Umezu H; Kakita A; Ikeuchi T; Oishi M
Acta Neuropathol Commun; 2024 Jan; 12(1):14. PubMed ID: 38254245
[TBL] [Abstract][Full Text] [Related]
19. Neurocutaneous Melanocytosis and Leptomeningeal Melanoma.
Mitre V; Heym K; Clark GD; Venkatramani R
J Pediatr Hematol Oncol; 2021 Mar; 43(2):e195-e197. PubMed ID: 31764519
[TBL] [Abstract][Full Text] [Related]
20. CSF cytology diagnosis of NRAS-mutated primary leptomeningeal melanomatosis with neurocutaneous melanosis.
Kolin DL; Geddie WR; Ko HM
Cytopathology; 2017 Jun; 28(3):235-238. PubMed ID: 27696542
[No Abstract] [Full Text] [Related]
[Next] [New Search]