2008
DOI: 10.1111/j.1610-0387.2007.06568_supp.x
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Aufbau eines deutschsprachigen Netzwerks für Patienten mit kongenitalen melanozytären Nävi

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Cited by 3 publications
(2 citation statements)
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“…On the homepage patients or their parents are requested to fill out an electronic questionnaire with data of CMN with a diameter of 3 cm or more in newborns or 10 cm in adults being registered. The aim of this registry is to gain insight on frequency of CMN, their risk of malignancy and their clinical course (http://www.naevus-netzwerk.de) [Krengel S et al 2008].…”
Section: Treatmentmentioning
confidence: 99%
“…On the homepage patients or their parents are requested to fill out an electronic questionnaire with data of CMN with a diameter of 3 cm or more in newborns or 10 cm in adults being registered. The aim of this registry is to gain insight on frequency of CMN, their risk of malignancy and their clinical course (http://www.naevus-netzwerk.de) [Krengel S et al 2008].…”
Section: Treatmentmentioning
confidence: 99%
“…Auch zum Thema der kongenitalen melanozytären Nävi (KMN) und neurokutanen Melanozytose im Kindesalter gibt es interessante aktuelle Erkenntnisse aus Studien, die eine genauere Einschätzung der Krankheitscharakteristika erlauben . Im Gegensatz zu früheren Studien wird aktuell bei sehr großen KMN über ein Lebenszeit‐Melanomrisiko von < 10 % statt bis zu 30 % berichtet.…”
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