Advanced Search Title: Author: Topik: Mata Kuliah:  Penerbit:   Tahun terbit:  Jenis:   Format:  Lokasi:  All -- Ben & Nafsiah Mboi Collection BI Corner Frans Seda Collection Kees Bertens Collection Lab-Kom-FK Perpustakaan FK Perpustakaan PKBB Perpustakaan PKPM Perpustakaan Pusat (BSD) Perpustakaan Pusat (Semanggi) Perpustakaan RSAJ Pusat Penelitian HIV AIDS Fulltext:  All Hanya yang memiliki fulltext Hanya yang belum ada fulltext Search Hasil 1 - 20 dari 35 (0.109375 detik)   Select all      Kirim  Download A Method of Utrophin Up-regulation Through RNAi-mediated Knockdown of the Transcription Factor EN1   Author:  Q, Wang; D-H, Cao; C-L, Jin; C-K, Lin; H-W, Ma; Y-Y, Wu Artikel dari The Journal of International Medical Research vol. 39 no. 01 (Mar. 2011)  , page 161-171 An Introduction to medical terminology for health care   Author: Hutton, Andrew R. Edisi: 4th     Penerbit: New York: Churchill Livingstone     Tahun terbit: 2006     Jenis: Books - Textbook Autosomal recessive myosclerosis myopathy is a collagen VI disorder   Author:  Merlini, L.; Martoni, E.; Grumati, P. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 16 (Oct. 2008)  , page 1245-1253 Autosomal recessive Bethlem myopathy   Author:  Gualandi, F.; Urciuolo, A.; Martoni, E. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 73 no. 22 (Dec. 2009)  , page 1883-1891 Birth of Spinal Muscular Atrophy Unaffected Baby from Genetically At-risk Parents Following a Pre-implantation Genetic Screening: A Case Report (Article of International Journal of Reproductive BioMedicine (IJRM) Vol. 20, Iss. 9 October 2022 p. 779–786)   Author:  Polim, Arie Adrianus; Handayani, Nining; Nurputra, Dian Kesumapramudya; Lubis, Anggia Melanie; Sirait, Batara; Jakobus, Dennis; Boediono, Arief; Sini, Ivan Penerbit: Knowledge E Publishing     Tahun terbit: 2022     Jenis: Article - diterbitkan di jurnal ilmiah internasional CD8/MHC-I Complex is Specific but Not Sensitive for the Diagnosis of Polymyositis   Author:  Dai, T-J; Li, W.; Zhao, Q-W Artikel dari The Journal of International Medical Research vol. 38 no. 03 (May 2010)  , page 1049-1059 Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debré type   Author:  Maldergem, L. Van; Yuksel-Apak, M.; Kayserili, H. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 20 (Nov. 2008)  , page 1602-1608 Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathies   Author:  Lommel, M.; Cirak, S.; Willer, T. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 74 no. 02 (Jan. 2010)  , page 157-164 Dehydroepiandrosterone for myotonic dystrophy type 1   Author:  Penisson-Besnier, I.; Devillers, M.; Porcher, R. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 06 (Aug. 2008)  , page 407-412 DNA : The Secret of Life   Author:  Watson, James D.; Berry, Andrew Penerbit: New York: Alfred A. Knopf     Tahun terbit: 2003     Jenis: Books Dysphagia in spinal muscular atrophy type II   Author:  Engel-Hoek, L. van den; Erasmus, C. E.; Bruggen, H. W. van Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 73 no. 21 (Nov. 2009)  , page 1787-1791 Dystrophin Immunity in Duchenne's Muscular Dystrophy   Author:  Mendell, Jerry R.; Campbell, Katherine; Rodino-Klapac, Louise; Sahenk, Zarife Artikel dari The New England Journal of Medicine (keterangan: ada di Proquest) vol. 363 no. 15 (Oct. 2010)  , page 1429-1437 Essentials of human anatomy & physiology   Author:  Marieb, Elaine Nicpon; Keller, Suzanne M Penerbit: London: Longman Pearson Education     Tahun terbit: 2018     Jenis: Books - Textbook Etiology of musician’s dystonia   Author:  Schmidt, A.; Jabusch, H. -C.; Altenmuller, E.; Hagenah, J. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 72 no. 14 (Apr. 2009)  , page 1248-1254 Evaluation of narrative abilities in patients suffering from Duchenne Muscular Dystrophy   Author:  Marini, A.; Lorusso, M.L.; D’Angelo, M.G.; Civati, F.; Turconi, A.C.; Fabbro, F.; Bresolin, N. Artikel dari Brain and Language (Full Text) vol. 102 no. 1 (2007)  , page 1-12 Facioscapulohumeral Muscular Dystrophy   Author:  Statland, Jeffrey M.; Tawil, Rabi Artikel dari Continuum vol. 22 no. 06 (Dec. 2016)  , page 1916-1931 From Representation to Mediation : The Shaping of Collective Mobilization on Muscular Dystrophy in France   Author: Rabeharisoa, Vololona Artikel dari Social Science & Medicine (www.elsevier.com/locate/sosscimed) vol. 62 no. 3 (Feb. 2006)  , page 564-576 Illustrated anatomy of the head and neck   Author:  Fehrenbach, Margaret J.; Herring, Susan W. Edisi: 3rd     Penerbit: Philadelphia: W.B. Saunders     Tahun terbit: 2007     Jenis: Books - Textbook Lack of toxicity of alpha-sarcoglycan overexpression supports clinical gene transfer trial in LGMD2D   Author:  Rodino-Klapac, L. R.; J-S, Lee; Mulligan, R. C.; Clark, K. R.; Mendell, J. R. Artikel dari Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 04 (Jul. 2008)  , page 240-247 Men on the Margin: A Bourdieusian Examination of Living into Adulthood with Muscular Dystrophy   Author:  Gibson, Barbara E.; Young, Nancy L.; Upshur, Ross; McKeever, Patricia Artikel dari Social Science & Medicine (www.elsevier.com/locate/sosscimed) vol. 65 no. 3 (Aug. 2007)  , page 505-517  Awal  Sebelumnya  Berikutnya  Akhir Halaman   dari 2   Lompat

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