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There are 5410 results for: content related to: Consensus recommendations for the treatment of basal cell carcinomas in G orlin syndrome with topical methylaminolaevulinate-photodynamic therapy

  1. You have free access to this content
    Gorlin syndrome (nevoid basal cell carcinoma syndrome): Update and literature review

    Pediatrics International

    Volume 56, Issue 5, October 2014, Pages: 667–674, Katsunori Fujii and Toshiyuki Miyashita

    Version of Record online : 22 OCT 2014, DOI: 10.1111/ped.12461

  2. Gorlin Syndrome (Nevoid Basal Cell Carcinoma Syndrome)

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    Management of Genetic Syndromes

    Peter Farndon

    Published Online : 14 JAN 2005, DOI: 10.1002/0471695998.mgs023

  3. Complex karyotypic abnormality in ovarian fibroma associated with Gorlin syndrome

    American Journal of Medical Genetics

    Volume 112, Issue 1, 15 September 2002, Pages: 61–64, Lynn M. Smith, Ping Hu, Larry J. Meyer and Cheryl M. Coffin

    Version of Record online : 28 JUN 2002, DOI: 10.1002/ajmg.10607

  4. Deficient expression of aldehyde dehydrogenase 1A1 is consistent with increased sensitivity of Gorlin syndrome patients to radiation carcinogenesis

    Molecular Carcinogenesis

    Volume 54, Issue 6, June 2015, Pages: 473–484, Aaron T. Wright, Thierry Magnaldo, Ryan L. Sontag, Lindsey N. Anderson, Natalie C. Sadler, Paul D. Piehowski, Yannick Gache and Thomas J. Weber

    Version of Record online : 27 NOV 2013, DOI: 10.1002/mc.22115

  5. Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report

    Clinical Genetics

    Volume 82, Issue 1, July 2012, Pages: 71–76, H Roudgari, P A Farndon, A D Murray, C Hardy and Z Miedzybrodzka

    Version of Record online : 30 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01725.x

  6. Gorlin syndrome with ulcerative colitis in a Japanese girl

    American Journal of Medical Genetics Part A

    Volume 121A, Issue 1, 15 August 2003, Pages: 65–68, Katsunori Fujii, Toshiyuki Miyashita, Taku Omata, Kazuhiko Kobayashi, Jun-ichi Takanashi, Katsunori Kouchi, Masao Yamada and Yoichi Kohno

    Version of Record online : 1 APR 2003, DOI: 10.1002/ajmg.a.20082

  7. Co-occurrence of severe Goltz–Gorlin syndrome and pentalogy of Cantrell – Case report and review of the literature

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 1102–1105, Robert Smigiel, Aleksandra Jakubiak, Maria Paola Lombardi, Wojciech Jaworski, Ryszard Slezak, Dariusz Patkowski and Raoul C. Hennekam

    Version of Record online : 11 APR 2011, DOI: 10.1002/ajmg.a.33895

  8. Robert J. Gorlin, 1923–2006: A remembrance

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 23, 1 December 2006, Pages: 2516–2520, M. Michael Cohen Jr

    Version of Record online : 6 NOV 2006, DOI: 10.1002/ajmg.a.31555

  9. The use of imiquimod 5% cream for the treatment of basal cell carcinoma as observed in Gorlin's syndrome

    Clinical and Experimental Dermatology

    Volume 28, Issue s1, November 2003, Pages: 19–23, G. Micali, F. Lacarrubba, M. R. Nasca and R. De Pasquale

    Version of Record online : 17 OCT 2003, DOI: 10.1046/j.1365-2230.28.s1.7.x

  10. Molecular evidence of type 2 mosaicism in Gorlin syndrome

    British Journal of Dermatology

    Volume 169, Issue 6, December 2013, Pages: 1342–1345, A. Torrelo, A. Hernández-Martín, E. Bueno, I. Colmenero, I. Rivera, L. Requena, R. Happle and R. González-Sarmiento

    Version of Record online : 2 DEC 2013, DOI: 10.1111/bjd.12458

  11. You have free access to this content
    Robert J. Gorlin as a humorist

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 11, 1 June 2007, Pages: 1131–1134, M. Michael Cohen Jr.

    Version of Record online : 1 MAY 2007, DOI: 10.1002/ajmg.a.31814

  12. Nevoid Basal Cell Carcinoma (Gorlin) Syndrome

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    eLS

    Robert J Gorlin

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0006082

  13. Patched mutations and hairy skin patches: A new sign in Gorlin syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 23, 1 December 2006, Pages: 2625–2630, Louise C. Wilson, Ekundayo Ajayi-Obe, Birgitta Bernhard and Saskia M. Maas

    Version of Record online : 11 AUG 2006, DOI: 10.1002/ajmg.a.31374

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    Meier–Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2733–2742, Sonja A. de Munnik, Barto J. Otten, Jeroen Schoots, Louise S. Bicknell, Salim Aftimos, Jumana Y. Al-Aama, Yolande van Bever, Michael B. Bober, George F. Borm, Jill Clayton-Smith, Cheri L. Deal, Alaa Y. Edrees, Murray Feingold, Alan Fryer, Johanna M. van Hagen, Raoul C. Hennekam, Maaike C.E. Jansweijer, Diana Johnson, Sarina G. Kant, John M. Opitz, A. Radha Ramadevi, Willie Reardon, Alison Ross, Pierre Sarda, Constance T.R.M. Schrander-Stumpel, A. Erik Sluiter, I. Karen Temple, Paulien A. Terhal, Annick Toutain, Carol A. Wise, Michael Wright, David L. Skidmore, Mark E. Samuels, Lies H. Hoefsloot, Nine V.A.M. Knoers, Han G. Brunner, Andrew P. Jackson and Ernie M.H.F. Bongers

    Version of Record online : 28 SEP 2012, DOI: 10.1002/ajmg.a.35681

  15. Patched

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    Encyclopedia Of Molecular Medicine

    Allen E. Bale

    Published Online : 15 JAN 2002, DOI: 10.1002/0471203076.emm1095

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    The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes

    Human Mutation

    Volume 37, Issue 3, March 2016, Pages: 250–256, Miriam J. Smith, Jill E. Urquhart, Elaine F. Harkness, Emma K. Miles, Naomi L. Bowers, Helen J. Byers, Michael Bulman, Carolyn Gokhale, Andrew J. Wallace, William G. Newman and D. Gareth Evans

    Version of Record online : 11 JAN 2016, DOI: 10.1002/humu.22938

  17. Genetics of basal cell carcinoma

    Australasian Journal of Dermatology

    Volume 51, Issue 2, May 2010, Pages: 81–92, Sally E De Zwaan and Nikolas K Haass

    Version of Record online : 10 DEC 2009, DOI: 10.1111/j.1440-0960.2009.00579.x

  18. Meier-Gorlin syndrome (ear–patella–short stature syndrome) in an Italian patient: Clinical evaluation and analysis of possible candidate genes

    American Journal of Medical Genetics

    Volume 107, Issue 1, 1 January 2002, Pages: 48–51, Amnon Cohen, Roberta Mulas, Marco Seri, Alberto Gaiero, Graziella Fichera, Monica Marini, Maria Baffico and Gianni Camera

    Version of Record online : 26 OCT 2001, DOI: 10.1002/ajmg.10083

  19. Cardiac fibroma, anomalous pulmonary venous course, and persistent pneumonia in a patient with gorlin syndrome

    Pediatric Pulmonology

    Volume 49, Issue 1, January 2014, Pages: E7–E9, Benjamin T. Kopp, Kerry L. Rosen, Julie C. O'Donovan and Shahid Sheikh

    Version of Record online : 28 NOV 2012, DOI: 10.1002/ppul.22726

  20. Myelodysplastic Syndrome Occurring in a Patient with Gorlin Syndrome

    Pediatric Dermatology

    Volume 33, Issue 4, July/August 2016, Pages: e256–e257, Jamie L. Mull, Lisa M. Madden and Susan J. Bayliss

    Version of Record online : 31 MAY 2016, DOI: 10.1111/pde.12880