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2. Erratum: LEOPARD syndrome and multiple granular cell tumors: An underreported association? Indian J Dermatol Venereol Leprol; 2016; 82(2):246. PubMed ID: 26924415 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Generalized lentiginosis, short stature, and multiple cutaneous nodules--quiz case. LEOPARD syndrome (LS) associated with multiple granular cell tumors (GCTs). Gunson TH; Hashim N; Sharpe GR Arch Dermatol; 2010 Mar; 146(3):337-42. PubMed ID: 20231512 [No Abstract] [Full Text] [Related]
5. Multiple cutaneous granular cell tumors, joint hypermobility and mild facial dysmorphism in a child. Muscardin LM; Paradisi M; Provini A; Cota C; Marzetti G Int J Dermatol; 2006 Jul; 45(7):847-50. PubMed ID: 16863524 [TBL] [Abstract][Full Text] [Related]
6. A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder. Watanabe Y; Yano S; Niihori T; Aoki Y; Matsubara Y; Yoshino M; Matsuishi T Brain Dev; 2011 Aug; 33(7):576-9. PubMed ID: 21093184 [TBL] [Abstract][Full Text] [Related]
7. LEOPARD syndrome: a new polyaneurysm association and an update on the molecular genetics of the disease. Yagubyan M; Panneton JM; Lindor NM; Conti E; Sarkozy A; Pizzuti A J Vasc Surg; 2004 Apr; 39(4):897-900. PubMed ID: 15071461 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. LEOPARD syndrome: a variant of Noonan syndrome strongly associated with hypertrophic cardiomyopathy. Carcavilla A; Santomé JL; Pinto I; Sánchez-Pozo J; Guillén-Navarro E; Martín-Frías M; Lapunzina P; Ezquieta B Rev Esp Cardiol (Engl Ed); 2013 May; 66(5):350-6. PubMed ID: 24775816 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Leopard syndrome and Chiari type I malformation: a case report and review of the literature. Beier AD; Barrett RJ; Burke K; Kole B; Soo TM Neurologist; 2009 Jan; 15(1):37-9. PubMed ID: 19131856 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. [Multiple lentigines syndrome. Apropos of 2 cases. Critical study of the leopard syndrome]. Colomb D; Morel JP Ann Dermatol Venereol; 1984; 111(4):371-81. PubMed ID: 6476721 [TBL] [Abstract][Full Text] [Related]
20. Multiple cutaneous granular cell tumors and neurofibromatosis in childhood. A case report and review of the literature. Martin RW; Neldner KH; Boyd AS; Coates PW Arch Dermatol; 1990 Aug; 126(8):1051-6. PubMed ID: 2166484 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]