124 related articles for article (PubMed ID: 25572376)
1. LEOPARD syndrome: you could be the first one to diagnose!
Urs P; Konde S; Chouta N; Raj S
J Indian Soc Pedod Prev Dent; 2015; 33(1):57-60. PubMed ID: 25572376
[TBL] [Abstract][Full Text] [Related]
2. LEOPARD Syndrome.
Ghosh SK; Majumdar B; Rudra O; Chakraborty S
Dermatol Online J; 2015 Oct; 21(10):. PubMed ID: 26632807
[TBL] [Abstract][Full Text] [Related]
3. Leopard syndrome.
Sarkozy A; Digilio MC; Dallapiccola B
Orphanet J Rare Dis; 2008 May; 3():13. PubMed ID: 18505544
[TBL] [Abstract][Full Text] [Related]
4. Do you know this syndrome? Leopard syndrome.
Cançado FH; Silva LC; Taitson PF; Andrade AC; Pithon MM; Oliveira DD
An Bras Dermatol; 2017; 92(1):127-129. PubMed ID: 28225973
[TBL] [Abstract][Full Text] [Related]
5. Oro-dental and craniofacial anomalies in LEOPARD syndrome.
Yam AA; Faye M; Kane A; Diop F; Coulybaly-Ba D; Tamba-Ba A; Mbaye NG; Ba I
Oral Dis; 2001 May; 7(3):200-2. PubMed ID: 11495198
[TBL] [Abstract][Full Text] [Related]
6. LEOPARD syndrome without hearing loss or pulmonary stenosis: a report of 2 cases.
Ramos-Geldres TT; Dávila-Seijo P; Duat-Rodríguez A; Noguera-Morel L; Ezquieta-Zubicaray B; Rosón-López E; Hernández-Martín A; Torrelo-Fernández A
Actas Dermosifiliogr; 2015 May; 106(4):e19-22. PubMed ID: 25544017
[TBL] [Abstract][Full Text] [Related]
7. A rare cause of dyspnoea: the LEOPARD syndrome.
Demir S; Karakaya Z; Sagay S
J Pak Med Assoc; 2013 Apr; 63(4):527-9. PubMed ID: 23905457
[TBL] [Abstract][Full Text] [Related]
8. Acute motor and sensory axonal neuropathy in LEOPARD syndrome.
Beukers RJ; van Bellegem AC; Gruppen M; Overweg-Plandsoen WC; Vermeulen M
Pediatr Neurol; 2010 Apr; 42(4):301-3. PubMed ID: 20304339
[TBL] [Abstract][Full Text] [Related]
9. A LEOPARD mimicking ST-elevation myocardial infarction.
Bagur R; Bertrand OF; Bataille Y; Noël B; Rodés-Cabau J
Am J Cardiol; 2011 Jul; 108(1):169-71. PubMed ID: 21529747
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. LEOPARD syndrome with recurrent PTPN11 mutation Y279C and different cutaneous manifestations: two case reports and a review of the literature.
Kalev I; Muru K; Teek R; Zordania R; Reimand T; Köbas K; Ounap K
Eur J Pediatr; 2010 Apr; 169(4):469-73. PubMed ID: 19768645
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Importance of cardiovascular examination in patients with multiple lentigines: two cases of LEOPARD syndrome with hypertrophic cardiomyopathy.
Jurko T; Jurko A; Krsiakova J; Jurko A; Minarik M; Mestanik M
Acta Clin Belg; 2019 Apr; 74(2):82-85. PubMed ID: 29717636
[TBL] [Abstract][Full Text] [Related]
14. Anaesthetic implications of LEOPARD syndrome.
Torres J; Russo P; Tobias JD
Paediatr Anaesth; 2004 Apr; 14(4):352-6. PubMed ID: 15078383
[TBL] [Abstract][Full Text] [Related]
15. An uncommon association between skin lesions and LEOPARD syndrome affected an old patient. Case report.
Onesti MG; Fioramonti P; Fino P; Carella S; Spinelli G; Miraglia E; Giustini S
Ann Ital Chir; 2011; 82(1):79-82. PubMed ID: 21657161
[TBL] [Abstract][Full Text] [Related]
16. LEOPARD syndrome: what are café noir spots?
Rodríguez-Bujaldón A; Vazquez-Bayo C; Jimenez-Puya R; Galan-Gutierrez M; Moreno-Gimenez J; Rodriguez-Garcia A; Tercedor J; Velez-Garcia A
Pediatr Dermatol; 2008; 25(4):444-8. PubMed ID: 18789084
[TBL] [Abstract][Full Text] [Related]
17. PTPN11 mutations in LEOPARD syndrome: report of four cases in Taiwan.
Lin IS; Wang JN; Chao SC; Wu JM; Lin SJ
J Formos Med Assoc; 2009 Oct; 108(10):803-7. PubMed ID: 19864201
[TBL] [Abstract][Full Text] [Related]
18. The First Vietnamese Patient of LEOPARD Syndrome due to a
Nguyen HT; Pham NN; Anh Vu H; Tran TNA
Case Rep Genet; 2021; 2021():8197435. PubMed ID: 34552798
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]