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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. Erratum: maternal mortality in Cameroon: a university teaching hospital report. Pan African Medical Journal Pan Afr Med J; 2015; 22():377. PubMed ID: 26816561 [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]
10. Erratum to: Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome. Wang AT; Lim T; Jamison J; Bush L; Soorya LV; Tavassoli T; Siper PM; Buxbaum JD; Kolevzon A J Neurodev Disord; 2016; 8():8. PubMed ID: 26981159 [TBL] [Abstract][Full Text] [Related]
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12. Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome. Kolevzon A; Bush L; Wang AT; Halpern D; Frank Y; Grodberg D; Rapaport R; Tavassoli T; Chaplin W; Soorya L; Buxbaum JD Mol Autism; 2015; 6():31. PubMed ID: 26034557 [TBL] [Abstract][Full Text] [Related]
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14. Erratum: Genome-wide association studies of multiple sclerosis. Cotsapas C; Mitrovic M Clin Transl Immunology; 2018; 7(8):e1038. PubMed ID: 30128152 [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. Erratum: Elimination of large tumors in mice by mRNA-encoded bispecific antibodies. Stadler CR; Bähr-Mahmud H; Celik L; Hebich B; Roth AS; Roth RP; Karikó K; Türeci Ö; Sahin U Nat Med; 2017 Oct; 23(10):1241. PubMed ID: 28985209 [TBL] [Abstract][Full Text] [Related]
17. 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]
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