117 related articles for article (PubMed ID: 2518512)
1. The neurofibromatosis-Noonan syndrome: genetic heterogeneity versus clinical variability. Case report and review of the literature.
Borochowitz Z; Berant N; Dar H; Berant M
Neurofibromatosis; 1989; 2(5-6):309-14. PubMed ID: 2518512
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Ullrich-Turner syndrome and neurofibromatosis-1.
Schorry EK; Lovell AM; Milatovich A; Saal HM
Am J Med Genet; 1996 Dec; 66(4):423-5. PubMed ID: 8989459
[TBL] [Abstract][Full Text] [Related]
4. Neurofibromatosis with fully expressed Noonan syndrome.
Abuelo DN; Meryash DL
Am J Med Genet; 1988 Apr; 29(4):937-41. PubMed ID: 3135755
[TBL] [Abstract][Full Text] [Related]
5. A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
Yazdizadeh M; Tapia JL; Baharvand M; Radfar L
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Sep; 98(3):316-20. PubMed ID: 15356469
[TBL] [Abstract][Full Text] [Related]
6. Noonan phenotype associated with neurofibromatosis.
Allanson JE; Hall JG; Van Allen MI
Am J Med Genet; 1985 Jul; 21(3):457-62. PubMed ID: 2411134
[TBL] [Abstract][Full Text] [Related]
7. Juvenile papillomatosis of the breast associated with neurofibromatosis 1.
Tan TY; Amor DJ; Chow CW
Pediatr Blood Cancer; 2007 Sep; 49(3):363-4. PubMed ID: 16883593
[No Abstract] [Full Text] [Related]
8. Reproductive failure in a patient with neurofibromatosis-Noonan syndrome.
Meschede D; Froster UG; Gullotta F; Nieschlag E
Am J Med Genet; 1993 Sep; 47(3):346-51. PubMed ID: 8135279
[TBL] [Abstract][Full Text] [Related]
9. [The neurofibromatosis-Noonan syndrome: 4 cases].
Bouloc A; Lemerrer M; Blanchet-Bardon C
Ann Dermatol Venereol; 1993; 120(11):763-5. PubMed ID: 8210104
[No Abstract] [Full Text] [Related]
10. 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]
11. Noonan's syndrome and neurofibromatosis.
Shuper A; Mukamel M; Mimouni M; Steinherz R
Arch Dis Child; 1987 Feb; 62(2):196-8. PubMed ID: 3103548
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Neurofibromatosis-Noonan syndrome or LEOPARD Syndrome? A clinical dilemma.
Tullu MS; Muranjan MN; Kantharia VC; Parmar RC; Sahu DR; Bavdekar SB; Bharucha BA
J Postgrad Med; 2000; 46(2):98-100. PubMed ID: 11013475
[TBL] [Abstract][Full Text] [Related]
15. Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?
Yang CC; Happle R; Chao SC; Yu-Yun Lee J; Chen W
J Am Acad Dermatol; 2008 Mar; 58(3):493-7. PubMed ID: 18280349
[TBL] [Abstract][Full Text] [Related]
16. [A patient with features of the Noonan syndrome and neurofibromatosis].
de Planque MM; van der Graaff L; Meinders AE
Ned Tijdschr Geneeskd; 1983 Sep; 127(37):1674-8. PubMed ID: 6415498
[No Abstract] [Full Text] [Related]
17. Juvenile papillomatosis of the breast in a male infant with Noonan syndrome, café au lait spots, and family history of breast carcinoma.
Pacilli M; Sebire NJ; Thambapillai E; Pierro A
Pediatr Blood Cancer; 2005 Dec; 45(7):991-3. PubMed ID: 15700254
[TBL] [Abstract][Full Text] [Related]
18. Neurofibromatosis 1/Noonan syndrome associated with Hashimoto's thyroiditis and vitiligo.
Yalcin B; Tamer E; Gür G; Oztas P; Polat MU; Alli N
Acta Derm Venereol; 2006; 86(1):80-1. PubMed ID: 16586003
[No Abstract] [Full Text] [Related]
19. 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]
20. Bilateral segmental neurofibromatosis: a case report and review.
Gonzalez G; Russi ME; Lodeiros A
Pediatr Neurol; 2007 Jan; 36(1):51-3. PubMed ID: 17162198
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
