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There are 4988035 results for: content related to: Tremor as the first neurological manifestation of Sneddon's syndrome

  1. Tremor and white matter lesions in Klinefelter syndrome

    Movement Disorders

    Volume 25, Issue 12, 15 September 2010, Pages: 1993–1994, Ester Coutinho, José Pedro Pereira, Daniel Dias, Sara Cavaco, Cláudia Pinto, Rui Carvalho and Marina Magalhães

    Version of Record online : 28 JUL 2010, DOI: 10.1002/mds.23149

  2. Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

    Movement Disorders

    Volume 23, Issue 10, 30 July 2008, Pages: 1384–1390, Teresa Temudo, Elisabete Ramos, Karin Dias, Clara Barbot, Jose P. Vieira, Ana Moreira, Eulalia Calado, Ines Carrilho, Guiomar Oliveira, Antonio Levy, Maria Fonseca, Alexandra Cabral, Pedro Cabral, Joao P Monteiro, Luis Borges, Roseli Gomes, Manuela Santos, Jorge Sequeiros and Patricia Maciel

    Version of Record online : 30 MAY 2008, DOI: 10.1002/mds.22115

  3. Maple syrup disease presenting as paroxysmal dystonia

    Annals of Neurology

    Volume 56, Issue 5, November 2004, Pages: 749–750, Teresa Temudo, Esmeralda Martins, Fátima Poças, Romeu Cruz and Laura Vilarinho

    Version of Record online : 25 OCT 2004, DOI: 10.1002/ana.20288

  4. Atypical stereotypies and vocal tics in Rett syndrome: An illustrative case

    Movement Disorders

    Volume 23, Issue 4, 15 March 2008, Pages: 622–624, Teresa Temudo, Paula Freitas, Jorge Sequeiros, Patricia Maciel and Guiomar Oliveira

    Version of Record online : 16 JAN 2008, DOI: 10.1002/mds.21939

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    PORTUGUESE REAL-LIFE EXPERIENCE WITH IBRUTINIB OUTSIDE CLINICAL TRIALS – A MULTICENTER ANALYSIS

    Hematological Oncology

    Volume 35, Issue S2, June 2017, Pages: 383–384, S. Silva, E. Espada, J.A. Melo, M.P. Lima, A. Ionita, J.P. Carda, J. Andrade, M. Neves, R. Cabral, T. Mendes, C. Gaspar, D. Alves, F. Pina, A. Botelho de Sousa, H. Coelho, A. Montalvão, H. Vitória, F. Lima, J. Coutinho, P. Lúcio, J.E. Guimarães, M.L. Ribeiro, M. Gomes da Silva and J. Raposo

    Version of Record online : 7 JUN 2017, DOI: 10.1002/hon.2439_146

  6. Aplasia cutis congenita associated with congenital heart defect, not a coincidence?

    American Journal of Medical Genetics

    Volume 34, Issue 4, December 1989, Pages: 614–615, Heloisa Santos, Isabel Cordeiro and Isabel Menezes

    Version of Record online : 5 JUN 2005, DOI: 10.1002/ajmg.1320340437

  7. Two novel functional mutations in the Na+,K+-ATPase α2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes

    Clinical Genetics

    Volume 73, Issue 1, January 2008, Pages: 37–43, M-J Castro, B Nunes, B De Vries, C Lemos, KRJ Vanmolkot, JJMW Van Den Heuvel, T Temudo, J Barros, J Sequeiros, RR Frants, JB Koenderink, JM Pereira-Monteiro and AMJM Van Den Maagdenberg

    Version of Record online : 19 NOV 2007, DOI: 10.1111/j.1399-0004.2007.00918.x

  8. Contact allergy to gold sodium thiosulfate

    Contact Dermatitis

    Volume 37, Issue 2, August 1997, Pages: 78–81, Raquel Solva, Fåtima Pereira, Olivia Bordalo, Elvira Silva, Antónia Baarros, Margarida Gonço, Teresa Correla, Graça Pessoa, Armando Baptista and Manuela Pecegueiro

    Version of Record online : 11 APR 2006, DOI: 10.1111/j.1600-0536.1997.tb00043.x

  9. PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency

    Clinical Endocrinology

    Volume 65, Issue 4, October 2006, Pages: 479–485, Manuel C. Lemos, Leonor Gomes, Margarida Bastos, Valeriano Leite, Edward Limbert, Davide Carvalho, Conceição Bacelar, Mariana Monteiro, Fernando Fonseca, Ana Agapito, João J. Castro, Fernando J. Regateiro and Manuela Carvalheiro

    Version of Record online : 18 JUL 2006, DOI: 10.1111/j.1365-2265.2006.02617.x

  10. Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosis

    American Journal of Medical Genetics

    Volume 99, Issue 4, 1 April 2001, Pages: 331–334, Humberto Vassal, Dr. Ana Medeira, Isabel Cordeiro, Heloísa G. Santos, Sérgio Castedo, Célia Saraiva, Patricia Mendes da Silva and Carolino Monteiro

    Version of Record online : 8 MAR 2001, DOI: 10.1002/1096-8628(20010401)99:4<331::AID-AJMG1175>3.0.CO;2-W

  11. Identification of a novel nonsense mutation (Q24X) in the glucose-6-phosphatase gene of a Portuguese patient with GSD Ia (von Gierke disease)

    Human Mutation

    Volume 16, Issue 5, November 2000, Page: 449, Hugo Rocha, Aguinaldo Cabral and Laura Vilarinho

    Version of Record online : 27 OCT 2000, DOI: 10.1002/1098-1004(200011)16:5<449::AID-HUMU25>3.0.CO;2-L

  12. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 portuguese ataxia families

    American Journal of Medical Genetics

    Volume 81, Issue 2, 28 March 1998, Pages: 134–138, I. Silveira, P. Coutinho, P. Maciel, C. Gaspar, S. Hayes, A. Dias, J. Guimarães, L. Loureiro, J. Sequeiros and G.A. Rouleau

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980328)81:2<134::AID-AJMG3>3.0.CO;2-W

  13. You have full text access to this OnlineOpen article
    Synchronous brain and intravascular B-cell lymphoma after remission of an adult hemophagocytic syndrome

    Clinical Case Reports

    Volume 4, Issue 4, April 2016, Pages: 327–330, Válter R. Fonseca, Eduardo Espada, Ruth Geraldes, Santiago Ortiz, Rita Sousa, Dolores Lopez, Marisa Teixeira Silva and Rui Victorino

    Version of Record online : 16 FEB 2016, DOI: 10.1002/ccr3.507

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    Anti-C1q antibodies: association with nephritis and disease activity in systemic lupus erythematosus

    Journal of Clinical Laboratory Analysis

    Volume 23, Issue 1, 2009, Pages: 19–23, Carlos Geraldo Moura, Isabella Lima, Lúcio Barbosa, Daniel Athanazio, Eliana Reis, Mitermayer Reis, Rufus W. Burlingame and Mittermayer B. Santiago

    Version of Record online : 12 JAN 2009, DOI: 10.1002/jcla.20280

  15. Efficacy of hydroxyurea in the treatment of a patient with erythrodermic psoriasis and chronic myelogenous leukaemia

    Journal of the European Academy of Dermatology and Venereology

    Volume 9, Issue 3, December 1997, Pages: 266–268, Luis Miguel Taveira, Cristina Gonçalves, António Paiva, Manuela Selores, Madalena Sanches and António Massa

    Version of Record online : 28 JUL 2006, DOI: 10.1111/j.1468-3083.1997.tb00516.x

  16. BK virus encephalitis with thrombotic microangiopathy in an allogeneic hematopoietic stem cell transplant recipient

    Transplant Infectious Disease

    Volume 13, Issue 2, April 2011, Pages: 161–167, R. Lopes da Silva, I. Ferreira, G. Teixeira, D. Cordeiro, M. Mafra, I. Costa, J.M. Bravo Marques and M. Abecasis

    Version of Record online : 5 NOV 2010, DOI: 10.1111/j.1399-3062.2010.00581.x

  17. Methylxanthines cause a decrease of prolactin plasma levels in healthy non-pregnant women

    Human Psychopharmacology: Clinical and Experimental

    Volume 4, Issue 1, March 1989, Pages: 33–39, M. Casas, S. Ferre, J. Rodriguez and F. Jane

    Version of Record online : 13 OCT 2004, DOI: 10.1002/hup.470040106

  18. Ulcerative colitis in a Southern European country: A national perspective

    Inflammatory Bowel Diseases

    Volume 16, Issue 5, May 2010, Pages: 822–829, Francisco Portela, Fernando Magro, Paula Lago, José Cotter, Isabelle Cremers, João de Deus, Ana Vieira, Horácio Lopes, Paulo Caldeira, Luísa Barros, Jorge Reis, Laura Carvalho, Raquel Gonçalves, Mário J. Campos, Paula Ministro, Maria A. Duarte, Jorge Amil, Susana Rodrigues, Luís Azevedo and A. Costa-Pereira

    Version of Record online : 12 OCT 2009, DOI: 10.1002/ibd.21119

  19. LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients

    Clinical Genetics

    Volume 74, Issue 6, December 2008, Pages: 502–512, J Oliveira, R Santos, I Soares-Silva, P Jorge, E Vieira, ME Oliveira, A Moreira, T Coelho, JC Ferreira, MJ Fonseca, C Barbosa, J Prats, ML Aríztegui, ML Martins, T Moreno, K Heinimann, C Barbot, SI Pascual-Pascual, A Cabral, I Fineza, M Santos and E Bronze-da-Rocha

    Version of Record online : 12 AUG 2008, DOI: 10.1111/j.1399-0004.2008.01068.x

  20. Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions

    Clinical Endocrinology

    Volume 56, Issue 4, April 2002, Pages: 465–473, B. M. Cavaco, R. Domingues, M. C. Bacelar, H. Cardoso, L. Barros, L. Gomes, M. M. A. Ruas, A. Agapito, A. Garrão, A. A. J. Pannett, J. L. Silva, L. G. Sobrinho, R. V. Thakker and V. Leite

    Version of Record online : 14 MAY 2002, DOI: 10.1046/j.1365-2265.2002.01505.x