146 related articles for article (PubMed ID: 38189222)
1. Melanoma and LEOPARD Syndrome: Understanding the Role of PTPN11 Mutations in Melanomagenesis.
Palacios-Diaz RD; Pozuelo-Ruiz M; De Unamuno-Bustos B; Llavador-Ros M; Botella-Estrada R
Acta Derm Venereol; 2024 Jan; 104():adv14720. PubMed ID: 38189222
[No Abstract] [Full Text] [Related]
2. IMAGE CARDIO MED. A patient with LEOPARD syndrome and PTPN11 mutation.
Lehmann LH; Schaeufele T; Buss SJ; Balanova M; Hartschuh W; Ehlermann P; Katus HA
Circulation; 2009 Mar; 119(9):1328-9. PubMed ID: 19273734
[No Abstract] [Full Text] [Related]
3. Leopard syndrome caused by heterozygous missense mutation of Tyr 279 Cys in the PTPN11 gene in a sporadic case of Chinese Han.
Wang Y; Chen C; Wang DW
Int J Cardiol; 2014 Jul; 174(3):e101-4. PubMed ID: 24820750
[No Abstract] [Full Text] [Related]
4. Scalp melanoma in a woman with LEOPARD syndrome: possible implication of PTPN11 signaling in melanoma pathogenesis.
Cheng YP; Chiu HY; Hsiao TL; Hsiao CH; Lin CC; Liao YH
J Am Acad Dermatol; 2013 Oct; 69(4):e186-7. PubMed ID: 24034393
[No Abstract] [Full Text] [Related]
5. Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome.
Zhang J; Shen J; Cheng R; Ni C; Liang J; Li M; Yao Z
Mol Med Rep; 2016 Sep; 14(3):2639-43. PubMed ID: 27484170
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. 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]
9. Have You Ever Seen a LEOPARD?
Marchand L
Am J Med; 2019 Sep; 132(9):e711. PubMed ID: 31051144
[No Abstract] [Full Text] [Related]
10. PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience.
Keren B; Hadchouel A; Saba S; Sznajer Y; Bonneau D; Leheup B; Boute O; Gaillard D; Lacombe D; Layet V; Marlin S; Mortier G; Toutain A; Beylot C; Baumann C; Verloes A; Cavé H;
J Med Genet; 2004 Nov; 41(11):e117. PubMed ID: 15520399
[No Abstract] [Full Text] [Related]
11. Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations.
Östman-Smith I
Circ Genom Precis Med; 2023 Aug; 16(4):359-362. PubMed ID: 37325916
[No Abstract] [Full Text] [Related]
12. PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype".
Digilio MC; Sarkozy A; Pacileo G; Limongelli G; Marino B; Dallapiccola B
Eur J Pediatr; 2006 Nov; 165(11):803-5. PubMed ID: 16733669
[TBL] [Abstract][Full Text] [Related]
13. Pathogenesis of multiple lentigines in LEOPARD syndrome with PTPN11 gene mutation.
Motegi S; Yokoyama Y; Ogino S; Yamada K; Uchiyama A; Perera B; Takeuchi Y; Ohnishi H; Ishikawa O
Acta Derm Venereol; 2015 Nov; 95(8):978-84. PubMed ID: 25917897
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Structural insights into Noonan/LEOPARD syndrome-related mutants of protein-tyrosine phosphatase SHP2 (PTPN11).
Qiu W; Wang X; Romanov V; Hutchinson A; Lin A; Ruzanov M; Battaile KP; Pai EF; Neel BG; Chirgadze NY
BMC Struct Biol; 2014 Mar; 14():10. PubMed ID: 24628801
[TBL] [Abstract][Full Text] [Related]
16. Leopard syndrome: a report of five cases from one family in two generations.
Begić F; Tahirović H; Kardašević M; Kalev I; Muru K
Eur J Pediatr; 2014 Jun; 173(6):819-22. PubMed ID: 24401936
[TBL] [Abstract][Full Text] [Related]
17. Noonan syndrome with multiple lentigines with PTPN11 (T468M) gene mutation accompanied with solitary granular cell tumor.
Park SH; Lee SH
J Dermatol; 2017 Nov; 44(11):e280-e281. PubMed ID: 28681392
[No Abstract] [Full Text] [Related]
18. 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]
19. LEOPARD syndrome with partly normal skin and sex chromosome mosaicism.
Writzl K; Hoovers J; Sistermans EA; Hennekam RC
Am J Med Genet A; 2007 Nov; 143A(21):2612-5. PubMed ID: 17935252
[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]