These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

54 related articles for article (PubMed ID: 26728819)

  • 1. LEOPARD syndrome and multiple granular cell tumors: An underreported association?
    Aragüés IH; Domínguez MC; Blanco VP; Zubicaray BE; Fernández RS
    Indian J Dermatol Venereol Leprol; 2016; 82(1):77-9. PubMed ID: 26728819
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 10. Anesthesia and LEOPARD syndrome: a review of forty-nine anesthetic exposures.
    Yeoh TY; Wittwer ED; Weingarten TN; Sprung J
    J Cardiothorac Vasc Anesth; 2014 Oct; 28(5):1243-50. PubMed ID: 24461361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 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]  

  • 15. 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]  

  • 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]
    of 3.