251 related articles for article (PubMed ID: 7586657)
1. Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus.
Ahlbom BE; Dahl N; Zetterqvist P; Annerén G
Clin Genet; 1995 Aug; 48(2):85-9. PubMed ID: 7586657
[TBL] [Abstract][Full Text] [Related]
2. Café au Lait Macules and Associated Genetic Syndromes.
Anderson S
J Pediatr Health Care; 2020; 34(1):71-81. PubMed ID: 31831114
[TBL] [Abstract][Full Text] [Related]
3. Multiple café au lait spots in familial patients with MAP2K2 mutation.
Takenouchi T; Shimizu A; Torii C; Kosaki R; Takahashi T; Saya H; Kosaki K
Am J Med Genet A; 2014 Feb; 164A(2):392-6. PubMed ID: 24311457
[TBL] [Abstract][Full Text] [Related]
4. Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).
Zhang J; Li M; Yao Z
Mol Med Rep; 2016 Nov; 14(5):4023-4029. PubMed ID: 27666661
[TBL] [Abstract][Full Text] [Related]
5. Legius Syndrome and its Relationship with Neurofibromatosis Type 1.
Denayer E; Legius E
Acta Derm Venereol; 2020 Mar; 100(7):adv00093. PubMed ID: 32147744
[TBL] [Abstract][Full Text] [Related]
6. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
Sharland M; Taylor R; Patton MA; Jeffery S
J Med Genet; 1992 Mar; 29(3):188-90. PubMed ID: 1348095
[TBL] [Abstract][Full Text] [Related]
7. A severe form of Noonan syndrome and autosomal dominant café-au-lait spots - evidence for different genetic origins.
Nyström AM; Ekvall S; Strömberg B; Holmström G; Thuresson AC; Annerén G; Bondeson ML
Acta Paediatr; 2009 Apr; 98(4):693-8. PubMed ID: 19120036
[TBL] [Abstract][Full Text] [Related]
8. Familial café au lait spots: a variant of neurofibromatosis type 1.
Abeliovich D; Gelman-Kohan Z; Silverstein S; Lerer I; Chemke J; Merin S; Zlotogora J
J Med Genet; 1995 Dec; 32(12):985-6. PubMed ID: 8825931
[TBL] [Abstract][Full Text] [Related]
9. Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome.
Thiel C; Wilken M; Zenker M; Sticht H; Fahsold R; Gusek-Schneider GC; Rauch A
Am J Med Genet A; 2009 Jun; 149A(6):1263-7. PubMed ID: 19449407
[TBL] [Abstract][Full Text] [Related]
10. Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).
Coppin BD; Temple IK
J Med Genet; 1997 Jul; 34(7):582-6. PubMed ID: 9222968
[TBL] [Abstract][Full Text] [Related]
11. Mutation in NRAS in familial Noonan syndrome--case report and review of the literature.
Ekvall S; Wilbe M; Dahlgren J; Legius E; van Haeringen A; Westphal O; Annerén G; Bondeson ML
BMC Med Genet; 2015 Oct; 16():95. PubMed ID: 26467218
[TBL] [Abstract][Full Text] [Related]
12. Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.
Bahuau M; Flintoff W; Assouline B; Lyonnet S; Le Merrer M; Prieur M; Guilloud-Bataille M; Feingold N; Munnich A; Vidaud M; Vidaud D
Am J Med Genet; 1996 Dec; 66(3):347-55. PubMed ID: 8985499
[TBL] [Abstract][Full Text] [Related]
13. Pigmentary anomalies in the multiple lentigines syndrome: Is it distinct from LEOPARD syndrome?
Arnsmeier SL; Paller AS
Pediatr Dermatol; 1996; 13(2):100-4. PubMed ID: 9122064
[TBL] [Abstract][Full Text] [Related]
14. Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene.
Digilio MC; Conti E; Sarkozy A; Mingarelli R; Dottorini T; Marino B; Pizzuti A; Dallapiccola B
Am J Hum Genet; 2002 Aug; 71(2):389-94. PubMed ID: 12058348
[TBL] [Abstract][Full Text] [Related]
15. Vertical transmission of the neurofibromatosis/Noonan syndrome.
Quattrin T; McPherson E; Putnam T
Am J Med Genet; 1987 Mar; 26(3):645-9. PubMed ID: 3105315
[TBL] [Abstract][Full Text] [Related]
16. Hereditary spinal neurofibromatosis: a rare form of NF1?
Poyhonen M; Leisti EL; Kytölä S; Leisti J
J Med Genet; 1997 Mar; 34(3):184-7. PubMed ID: 9132486
[TBL] [Abstract][Full Text] [Related]
17. Partial unilateral lentiginosis with ipsilateral Lisch nodules and axillary freckling.
Chen W; Fan PC; Happle R
Dermatology; 2004; 209(4):321-4. PubMed ID: 15539896
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
Charrow J; Listernick R; Ward K
Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
[TBL] [Abstract][Full Text] [Related]
19. Novel phenotypes of NF1 patients from unrelated Chinese families with tibial pseudarthrosis and anemia.
Banerjee S; Lei D; Liang S; Yang L; Liu S; Wei Z; Tang JP
Oncotarget; 2017 Jun; 8(24):39695-39702. PubMed ID: 27980226
[TBL] [Abstract][Full Text] [Related]
20. Novel association of neurofibromatosis type 1-causing mutations in families with neurofibromatosis-Noonan syndrome.
Ekvall S; Sjörs K; Jonzon A; Vihinen M; Annerén G; Bondeson ML
Am J Med Genet A; 2014 Mar; 164A(3):579-87. PubMed ID: 24357598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]