001     304300
005     20250907022527.0
024 7 _ |a 10.1158/1078-0432.CCR-24-3860
|2 doi
024 7 _ |a pmid:40560659
|2 pmid
024 7 _ |a 1078-0432
|2 ISSN
024 7 _ |a 1557-3265
|2 ISSN
024 7 _ |a altmetric:179097620
|2 altmetric
037 _ _ |a DKFZ-2025-01836
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Wasserman, Jonathan D
|0 0000-0001-7088-8146
|b 0
245 _ _ |a Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex.
260 _ _ |a Philadelphia, Pa. [u.a.]
|c 2025
|b AACR
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1756967815_27123
|2 PUB:(DE-HGF)
|x Review Article
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Hereditary endocrine neoplasia syndromes comprise multiple entities associated with an increased risk for the development of endocrine and nonendocrine neoplasms and other systemic manifestations. These syndromes typically demonstrate autosomal dominant inheritance, and each syndrome is associated with a unique genetic predisposition to a distinct spectrum of tumor susceptibility. Moreover, genotype-phenotype associations within each syndrome may affect the spectrum, penetrance, and age of onset of associated tumors. As many endocrine tumors are benign and/or indolent, a careful approach to monitoring is necessary, wherein the nature, timing of initiation, and frequency of presymptomatic surveillance balance the goal of detecting tumors at a point in which intervention would limit tumor-associated morbidity against the physical, emotional, and financial burdens of surveillance. In this study, we summarize changes in knowledge and practice recommendations related to children with multiple endocrine neoplasia syndromes (types 1, 2A, 2B, 4, and 5), hyperparathyroidism-jaw tumor syndrome, and Carney complex since an initial summary in 2017. These updates reflect the evolving understanding of these complex genetic disorders and aim to improve patient care and outcomes.
536 _ _ |a 312 - Funktionelle und strukturelle Genomforschung (POF4-312)
|0 G:(DE-HGF)POF4-312
|c POF4-312
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Multiple Endocrine Neoplasia: diagnosis
|2 MeSH
650 _ 2 |a Multiple Endocrine Neoplasia: genetics
|2 MeSH
650 _ 2 |a Multiple Endocrine Neoplasia: epidemiology
|2 MeSH
650 _ 2 |a Carney Complex: diagnosis
|2 MeSH
650 _ 2 |a Carney Complex: genetics
|2 MeSH
650 _ 2 |a Carney Complex: epidemiology
|2 MeSH
650 _ 2 |a Child
|2 MeSH
650 _ 2 |a Genetic Predisposition to Disease
|2 MeSH
650 _ 2 |a Jaw Neoplasms: diagnosis
|2 MeSH
650 _ 2 |a Jaw Neoplasms: genetics
|2 MeSH
650 _ 2 |a Hyperparathyroidism: diagnosis
|2 MeSH
650 _ 2 |a Hyperparathyroidism: genetics
|2 MeSH
700 1 _ |a Schneider, Kami Wolfe
|0 0000-0003-0865-8010
|b 1
700 1 _ |a Achatz, Maria-Isabel
|0 0000-0001-6894-1219
|b 2
700 1 _ |a Nakano, Yoshiko
|0 0000-0001-5394-8194
|b 3
700 1 _ |a Zelley, Kristin
|0 0000-0003-0970-1850
|b 4
700 1 _ |a Gallinger, Bailey
|0 0000-0003-0039-3652
|b 5
700 1 _ |a Bauer, Andrew J
|0 0000-0002-3952-881X
|b 6
700 1 _ |a Becktell, Kerri D
|0 0000-0002-1935-5157
|b 7
700 1 _ |a Wassner, Ari J
|0 0000-0003-0894-9301
|b 8
700 1 _ |a Raiti, Laura
|0 0009-0000-8270-8894
|b 9
700 1 _ |a Doria, Andrea S
|0 0000-0003-3202-0447
|b 10
700 1 _ |a States, Lisa J
|0 0000-0003-0260-3975
|b 11
700 1 _ |a Stratakis, Constantine A
|0 0000-0002-4058-5520
|b 12
700 1 _ |a Brodeur, Garrett M
|0 0000-0002-6721-122X
|b 13
700 1 _ |a Diller, Lisa R
|0 0000-0002-4073-5509
|b 14
700 1 _ |a Kamihara, Junne
|0 0000-0002-2852-7387
|b 15
700 1 _ |a Malkin, David
|0 0000-0001-5752-9763
|b 16
700 1 _ |a Pajtler, Kristian
|0 P:(DE-He78)a7c1bbac024fa232d9c6b78443328d9d
|b 17
|u dkfz
700 1 _ |a Tamura, Chieko
|0 0000-0002-7496-4289
|b 18
700 1 _ |a Villani, Anita
|0 0000-0003-3283-2197
|b 19
700 1 _ |a Widjaja, Elysa
|0 0000-0003-0986-5476
|b 20
700 1 _ |a Das, Anirban
|0 0000-0001-7653-9529
|b 21
700 1 _ |a Rednam, Surya P
|0 0000-0001-8333-0758
|b 22
773 _ _ |a 10.1158/1078-0432.CCR-24-3860
|g Vol. 31, no. 17, p. 3628 - 3637
|0 PERI:(DE-600)2036787-9
|n 17
|p 3628 - 3637
|t Clinical cancer research
|v 31
|y 2025
|x 1078-0432
909 C O |o oai:inrepo02.dkfz.de:304300
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 17
|6 P:(DE-He78)a7c1bbac024fa232d9c6b78443328d9d
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-312
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Funktionelle und strukturelle Genomforschung
|x 0
914 1 _ |y 2025
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CLIN CANCER RES : 2022
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1110
|2 StatID
|b Current Contents - Clinical Medicine
|d 2024-12-27
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2024-12-27
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2024-12-27
915 _ _ |a IF >= 10
|0 StatID:(DE-HGF)9910
|2 StatID
|b CLIN CANCER RES : 2022
|d 2024-12-27
920 1 _ |0 I:(DE-He78)B062-20160331
|k B062
|l B062 Pädiatrische Neuroonkologie
|x 0
920 1 _ |0 I:(DE-He78)HD01-20160331
|k HD01
|l DKTK HD zentral
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)B062-20160331
980 _ _ |a I:(DE-He78)HD01-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21