250 related articles for article (PubMed ID: 18799937)
1. Common acute lymphoblastic leukemia in a girl with genetically confirmed LEOPARD syndrome.
Laux D; Kratz C; Sauerbrey A
J Pediatr Hematol Oncol; 2008 Aug; 30(8):602-4. PubMed ID: 18799937
[TBL] [Abstract][Full Text] [Related]
2. Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive).
Uçar C; Calýskan U; Martini S; Heinritz W
J Pediatr Hematol Oncol; 2006 Mar; 28(3):123-5. PubMed ID: 16679933
[TBL] [Abstract][Full Text] [Related]
3. [PTPN11 gene mutation in LEOPARD syndrome].
Paradisi M; Pedicelli C; Ciasulli A; Pinto F; Conti E; Sarkozy A; Angelo C
Minerva Pediatr; 2005 Aug; 57(4):189-93. PubMed ID: 16172598
[TBL] [Abstract][Full Text] [Related]
4. PTPN11, RAS and FLT3 mutations in childhood acute lymphoblastic leukemia.
Yamamoto T; Isomura M; Xu Y; Liang J; Yagasaki H; Kamachi Y; Kudo K; Kiyoi H; Naoe T; Kojma S
Leuk Res; 2006 Sep; 30(9):1085-9. PubMed ID: 16533526
[TBL] [Abstract][Full Text] [Related]
5. Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.
Digilio MC; Pacileo G; Sarkozy A; Limongelli G; Conti E; Cerrato F; Marino B; Pizzuti A; Calabrò R; Dallapiccola B
Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):95-8. PubMed ID: 14991917
[TBL] [Abstract][Full Text] [Related]
6. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.
Ogata T; Yoshida R
Pediatr Endocrinol Rev; 2005 Jun; 2(4):669-74. PubMed ID: 16208280
[TBL] [Abstract][Full Text] [Related]
7. Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia.
Bentires-Alj M; Paez JG; David FS; Keilhack H; Halmos B; Naoki K; Maris JM; Richardson A; Bardelli A; Sugarbaker DJ; Richards WG; Du J; Girard L; Minna JD; Loh ML; Fisher DE; Velculescu VE; Vogelstein B; Meyerson M; Sellers WR; Neel BG
Cancer Res; 2004 Dec; 64(24):8816-20. PubMed ID: 15604238
[TBL] [Abstract][Full Text] [Related]
8. Multiple granular cell tumors are an associated feature of LEOPARD syndrome caused by mutation in PTPN11.
Schrader KA; Nelson TN; De Luca A; Huntsman DG; McGillivray BC
Clin Genet; 2009 Feb; 75(2):185-9. PubMed ID: 19054014
[TBL] [Abstract][Full Text] [Related]
9. Schizencephaly in LEOPARD syndrome.
Liang JS; Chien YH; Hwu WL; Yeh SJ; Peng SF
Pediatr Neurol; 2009 Jul; 41(1):71-3. PubMed ID: 19520282
[TBL] [Abstract][Full Text] [Related]
10. A novel PTPN11 mutation in LEOPARD syndrome.
Conti E; Dottorini T; Sarkozy A; Tiller GE; Esposito G; Pizzuti A; Dallapiccola B
Hum Mutat; 2003 Jun; 21(6):654. PubMed ID: 14961557
[TBL] [Abstract][Full Text] [Related]
11. Malignant diseases in Noonan syndrome and related disorders.
Hasle H
Horm Res; 2009 Dec; 72 Suppl 2():8-14. PubMed ID: 20029231
[TBL] [Abstract][Full Text] [Related]
12. Acute lymphoblastic leukemia developing in a patient with Noonan syndrome harboring a PTPN11 germline mutation.
Sakamoto K; Imamura T; Asai D; Goto-Kawashima S; Yoshida H; Fujiki A; Furutani A; Ishida H; Aoki Y; Hosoi H
J Pediatr Hematol Oncol; 2014 Mar; 36(2):e136-9. PubMed ID: 24072241
[TBL] [Abstract][Full Text] [Related]
13. Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome).
Kato H; Yoshida R; Tsukamoto K; Suga H; Eto H; Higashino T; Araki J; Ogata T; Yoshimura K
Int J Dermatol; 2010 Oct; 49(10):1146-51. PubMed ID: 20883402
[TBL] [Abstract][Full Text] [Related]
14. Mutations of PTPN11 are rare in adult myeloid malignancies.
Hugues L; Cavé H; Philippe N; Pereira S; Fenaux P; Preudhomme C
Haematologica; 2005 Jun; 90(6):853-4. PubMed ID: 15951301
[TBL] [Abstract][Full Text] [Related]
15. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
Tartaglia M; Niemeyer CM; Fragale A; Song X; Buechner J; Jung A; Hählen K; Hasle H; Licht JD; Gelb BD
Nat Genet; 2003 Jun; 34(2):148-50. PubMed ID: 12717436
[TBL] [Abstract][Full Text] [Related]
16. A novel PTPN11 missense mutation in a patient with LEOPARD syndrome.
Osawa R; Akiyama M; Yamanaka Y; Ujiie H; Nemoto-Hasebe I; Takeda A; Yanagi T; Shimizu H
Br J Dermatol; 2009 Nov; 161(5):1202-4. PubMed ID: 19659470
[No Abstract] [Full Text] [Related]
17. [LEOPARD syndrome].
Hansen LK; Risby K; Bygum A; Gerdes AM
Ugeskr Laeger; 2009 Jan; 171(4):247. PubMed ID: 19174044
[TBL] [Abstract][Full Text] [Related]
18. Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation.
Nemes E; Farkas K; Kocsis-Deák B; Drubi A; Sulák A; Tripolszki K; Dósa P; Ferenc L; Nagy N; Széll M
Arch Dermatol Res; 2015 Dec; 307(10):891-5. PubMed ID: 26377839
[TBL] [Abstract][Full Text] [Related]
19. LEOPARD syndrome: clinical diagnosis in the first year of life.
Digilio MC; Sarkozy A; de Zorzi A; Pacileo G; Limongelli G; Mingarelli R; Calabrò R; Marino B; Dallapiccola B
Am J Med Genet A; 2006 Apr; 140(7):740-6. PubMed ID: 16523510
[TBL] [Abstract][Full Text] [Related]
20. Leopard syndrome.
Porciello R; Divona L; Strano S; Carbone A; Calvieri C; Giustini S
Dermatol Online J; 2008 Mar; 14(3):7. PubMed ID: 18627709
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
