Melanoma in congenital melanocytic naevi.

scientific article

Melanoma in congenital melanocytic naevi. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1111/BJD.15301
P932PMC publication ID5484991
P698PubMed publication ID28078671

P50authorNeil J. SebireQ38549176
Neil W BulstrodeQ56241474
P2093author name stringW K Chong
V A Kinsler
P O'Hare
T Jacques
J E Calonje
D Hargrave
O Slater
D Lomas
P2860cites workProliferative nodules arising within congenital melanocytic nevi: a histologic, immunohistochemical, and molecular analyses of 43 casesQ28307906
Acute Inhibition of MEK Suppresses Congenital Melanocytic Nevus Syndrome in a Murine Model Driven by Activated NRAS and Wnt SignalingQ30661575
High frequency of BRAFV600E mutation in acquired nevi and small congenital nevi, but low frequency of mutation in medium-sized congenital neviQ33243184
MEK inhibition appears to improve symptom control in primary NRAS-driven CNS melanoma in childrenQ33577613
Melanoma risk in congenital melanocytic naevi: a systematic reviewQ33997045
Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutationsQ33998283
Great Ormond Street Hospital for Children Registry for congenital melanocytic naevi: prospective study 1988-2007. Part 1-epidemiology, phenotype and outcomesQ34013879
Spectrum of central nervous system abnormalities in neurocutaneous melanocytosisQ34031334
New recommendations for the categorization of cutaneous features of congenital melanocytic nevi.Q34033621
High frequency of BRAF mutations in neviQ34160519
The incidence and significance of birthmarks in a cohort of 4,641 newbornsQ34266047
The incidence of birthmarks in the neonateQ34461050
Epidemiology of congenital pigmented naevi: I. Incidence rates and relative frequenciesQ34716617
Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naeviQ35571122
Genetic changes in neoplasms arising in congenital melanocytic nevi: differences between nodular proliferations and melanomasQ35789193
Classifying Melanocytic Tumors Based on DNA Copy Number ChangesQ35843508
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentQ36098992
Neurocutaneous melanosis presenting with hydrocephalus. Case report and review of the literatureQ36277580
Distinguishing melanocytic nevi from melanoma by DNA copy number changes: comparative genomic hybridization as a research and diagnostic toolQ36365473
Growth and hormone profiling in children with congenital melanocytic naeviQ36532499
Classification of neurological abnormalities in children with congenital melanocytic naevus syndrome identifies magnetic resonance imaging as the best predictor of clinical outcomeQ36532989
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRASQ36919636
Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemiaQ37406418
Proliferative nodules in a giant congenital melanocytic nevus-case report and review of the literatureQ37612007
Large congenital melanocytic nevi: therapeutic management and melanoma risk: a systematic reviewQ38062600
Molecular pathology of melanocytic tumorsQ38171606
Case reports of fatal or metastasizing melanoma in children and adolescents: a systematic analysis of the literatureQ38285394
Amplification of mutated NRAS leading to congenital melanoma in neurocutaneous melanocytosis.Q38844253
Age- and site-specific variation in the dermoscopic patterns of congenital melanocytic nevi: an aid to accurate classification and assessment of melanocytic nevi.Q40181923
Copy number abnormalities in new or progressive 'neurocutaneous melanosis' confirm it to be primary CNS melanomaQ42329085
Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.Q42882004
Metastatic melanoma in association with a giant congenital melanocytic nevus in an adult: controversial CGH findingsQ46907302
BRAF mutations are common somatic events in melanocytic neviQ47978923
NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi.Q54239316
BRAF mutations are also associated with neurocutaneous melanocytosis and large/giant congenital melanocytic nevi.Q54303127
Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi.Q54641558
Nevomelanocytic proliferations in the central nervous system of childrenQ72929418
Large congenital melanocytic nevi and the risk for development of malignant melanoma and neurocutaneous melanocytosisQ73031076
Chromosomal translocations as a mechanism of BRAF activation in two cases of large congenital melanocytic neviQ79777475
The association between large congenital melanocytic naevi and cutaneous melanoma: preliminary findings from an Internet-based registry of 379 patientsQ81406937
Complications of congenital melanocytic naevi in children: analysis of 16 years' experience and clinical practiceQ81727876
RAF around the edges--the paradox of BRAF inhibitorsQ83273681
The face in congenital melanocytic nevus syndromeQ83719724
Nodular lesions arising in a large congenital melanocytic naevus in a newborn with eruptive disseminated Spitz naeviQ84461504
Mitotically active proliferative nodule arising in a giant congenital melanocytic nevus: a diagnostic pitfallQ85952568
Naevus spilus-type congenital melanocytic naevus associated with a novel NRAS codon 61 mutationQ85959635
P275copyright licenseCreative Commons AttributionQ6905323
P6216copyright statuscopyrightedQ50423863
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectmelanomaQ180614
brain tumorQ233309
melanocytic nevusQ377568
skin neoplasmQ18921119
P5008on focus list of Wikimedia projectScienceSourceQ55439927
P304page(s)1131-1143
P577publication date2017-04-04
2017-05-01
P1433published inBritish Journal of DermatologyQ4970191
P1476titleMelanoma in congenital melanocytic naevi
P478volume176

Reverse relations

cites work (P2860)
Q89758976DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome
Q92180963Does the gene matter? Genotype-phenotype and genotype-outcome associations in congenital melanocytic naevi
Q92435505Giant Congenital Melanocytic Nevus Accompanied by an Intracranial Arachnoid Cyst
Q33577613MEK inhibition appears to improve symptom control in primary NRAS-driven CNS melanoma in children
Q64259715Melanoma arising in a Giant congenital melanocytic nevus: two case reports
Q64237658Melanoma subtypes: genomic profiles, prognostic molecular markers and therapeutic possibilities
Q64241169Neurocutaneous Melanosis in Association With Large Congenital Melanocytic Nevi in Children: A Report of 2 Cases With Clinical, Radiological, and Pathogenetic Evaluation
Q39267197Paediatric melanoma
Q92782658Paediatric melanoma: clinical update, genetic basis, and advances in diagnosis
Q89992208Surgical treatment of children and youth with congenital melanocytic nevi: self- and proxy-reported opinions
Q45955388The MeLiM Minipig: An Original Spontaneous Model to Explore Cutaneous Melanoma Genetic Basis.
Q100465050Transcriptional regulators and alterations that drive melanoma initiation and progression
Q57034868Use of sedation instead of general anaesthesia for screening MRI in congenital melanocytic naevi under the age of 1 year is a successful, safe, and economical first line approach
Q91864626cAMP-mediated regulation of melanocyte genomic instability: A melanoma-preventive strategy

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