Search Results

Suggested Topics within your search.
Refine Results
  1. 1
    Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases

    Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases by Marianne de Vasconcelos Carvalho, José Romero Souto de Sousa, Filipe Paiva Correa de Melo, Tatiane Fonseca Faro, Ana Clara Nunes Santos, Silvia Costa Carvalho, Ana Paula Veras Sobral

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Anhydrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). A case report

    Anhydrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). A case report by Jair Carneiro Leão, Ana Micaeli Costa Ferreira, Valdir Bandeira, Fábia V. Figueirôa, Stephen Porter

    Published 2005
    Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Developmental disorders of the dentition: An update

    Developmental disorders of the dentition: An update by Ophir D. Klein, Snehlata Oberoi, Ann Huysseune, Mária Hovořáková, M Peterka, Renata Peterková

    Published 2013
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  4. 4
    Diffuse Gastrointestinal Polyposis with Ectodermal Changes

    Diffuse Gastrointestinal Polyposis with Ectodermal Changes by S. Jarnum, Herluf Jensen

    Published 1966
    Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Conventional Complete Denture in Patients with Ectodermal Dysplasia

    Conventional Complete Denture in Patients with Ectodermal Dysplasia by Larissa Soares Reis Vilanova, Alfonso Sánchez‐Ayala, Giselle Rodrigues Ribeiro, Camila Heitor Campos, Arcelino Farias‐Neto

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Limb abnormalities on trisomy 18: evidences for early diagnosis

    Limb abnormalities on trisomy 18: evidences for early diagnosis by Rafael Fabiano Machado Rosa, na Cardoso Manique Rosa, Marina Boff Lorenzen, Paulo Ricardo Gazzola Zen, Ceres Andréia Vieira de Oliveira, Carla Graziadio, Giorgio Adriano Paskulin

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Molecular basis of hypohidrotic ectodermal dysplasia: an update

    Molecular basis of hypohidrotic ectodermal dysplasia: an update by Wiesław H. Trzeciak, Ryszard Koczorowski

    Published 2015
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  8. 8
    Aplasia cutis congenita: approach to evaluation and management

    Aplasia cutis congenita: approach to evaluation and management by John Browning

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Identification of a New Splice Form of the EDA1 Gene Permits Detection of Nearly All X-Linked Hypohidrotic Ectodermal Dysplasia Mutations

    Identification of a New Splice Form of the EDA1 Gene Permits Detection of Nearly All X-Linked Hypohidrotic Ectodermal Dysplasia Mutations by Alex W. Monreal, Jonathan Zonana, Betsy Ferguson

    Published 1998
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Ectodermal dysplasias: a new clinical-genetic classification

    Ectodermal dysplasias: a new clinical-genetic classification by Manuela Priolo

    Published 2001
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    A Role for NF-κB Essential Modifier/IκB Kinase-γ (NEMO/IKKγ) Ubiquitination in the Activation of the IκB Kinase Complex by Tumor Necrosis Factor-α

    A Role for NF-κB Essential Modifier/IκB Kinase-γ (NEMO/IKKγ) Ubiquitination in the Activation of the IκB Kinase Complex by Tumor Necrosis Factor-α by Eric Tang, Cun-Yu Wang, Yue Xiong, Kun‐Liang Guan

    Published 2003
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    p63α Mutations Lead to Aberrant Splicing of Keratinocyte Growth Factor Receptor in the Hay-Wells Syndrome

    p63α Mutations Lead to Aberrant Splicing of Keratinocyte Growth Factor Receptor in the Hay-Wells Syndrome by Alexey Fomenkov, Yi‐Ping Huang, Özlem Topaloglu, Anna Brechman, Motonobo Osada, T E Fomenkova, Eugene Yuriditsky, Barry Trink, David Sidransky, Edward A. Ratovitski

    Published 2003
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    Compound Heterozygous Desmoplakin Mutations Result in a Phenotype with a Combination of Myocardial, Skin, Hair, and Enamel Abnormalities

    Compound Heterozygous Desmoplakin Mutations Result in a Phenotype with a Combination of Myocardial, Skin, Hair, and Enamel Abnormalities by Mỹ G. Mahoney, Sara Sadowski, Donna Brennan, Pekka Pikander, Pekka Saukko, James K. Wahl, Heikki Aho, Kristiina Heikinheimo, Leena Bruckner‐Tuderman, Andrzej Fertala, Juha Peltonen, Jouni Uitto, Sirkku Peltonen

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Orofacial Features of Hypohidrotic Ectodermal Dysplasia

    Orofacial Features of Hypohidrotic Ectodermal Dysplasia by Sibele Nascimento de Aquino, Lívia Máris Ribeiro Paranaíba, Mário Sérgio Oliveira Swerts, Daniella Reis Barbosa Martelli, Letízia Monteiro de Barros, Hercílio Martelli Júnior

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Role of TRAF3 and -6 in the Activation of the NF-κB and JNK Pathways by X-linked Ectodermal Dysplasia Receptor

    Role of TRAF3 and -6 in the Activation of the NF-κB and JNK Pathways by X-linked Ectodermal Dysplasia Receptor by Suwan K. Sinha, Sunny Zachariah, Herson I. Quiñones, Masahisa Shindo, Preet M. Chaudhary

    Published 2002
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  16. 16
    p63 in Skin Development and Ectodermal Dysplasias

    p63 in Skin Development and Ectodermal Dysplasias by Maranke I. Koster

    Published 2010
    Get full text
    Revisão
    Save to List
    Saved in:
  17. 17
    New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein

    New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein by Marjorie Hubeau, Flora Ngadjeua, Anne Puel, Laura Israël, Jacqueline Feinberg, Maya Chrabieh, Kiran Belani, Christine Bodemer, Isabelle Fabre, Alessandro Plebani, Stéphanie Boisson‐Dupuis, Capucine Pïcard, Alain Fischer, Alain Israël, Laurent Abel, Michel Véron, Jean‐Laurent Casanova, Fabrice Agou, Jacinta Bustamante

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    Congenital deformity of the paw in a captive tiger: case report

    Congenital deformity of the paw in a captive tiger: case report by Sheila Canevese Rahal, Reinaldo S Volpi, Carlos Roberto Teixeira, Vania MV Machado, Guilherme DP Soares, Carlos Neto, Kathleen Linn

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  19. 19
    SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

    SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice by Ippei Okada, Haruka Hamanoue, Koji Terada, Takaya Tohma, André Mégarbané, Éliane Chouery, Joelle Abou‐Ghoch, Nadine Jalkh, Özgür Çoğulu, Ferda Özkınay, Kyoji Horie, Junji Takeda, Tatsuya Furuichi, Shiro Ikegawa, Kiyomi Nishiyama, Satoko Miyatake, Akira Nishimura, Takeshi Mizuguchi, Norio Niikawa, Fumiki Hirahara, Tadashi Kaname, Koh-ichiro Yoshiura, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Takahisa Furukawa, Naomichi Matsumoto, Hirotomo Saitsu

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  20. 20
    A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia

    A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia by Bárbara Rivera, José Perea, Eduardo Vilar Sanchez, Manuel Villapun, E. Sánchez-Tomé, Fátima Mercadillo, Mercedes Robledo, Javier Benı́tez, Miguel Urioste

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: