نتائج البحث - Tami Uster
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1
Clinical spectrum of early onset epileptic encephalopathies caused by <scp><i>KCNQ2</i></scp> mutation حسب Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Hiroshi Arai, Sumimasa Yamashita, Taku Nakagawa, Takanari Fujii, Kenji Sugai, Kaoru S. Imai, Tami Uster, David Chitayat, Shelly K. Weiss, Hirofumi Kashii, Ryosuke Kusano, Ayumi Matsumoto, Kazuyuki Nakamura, Yoshinobu Oyazato, Mari Maeno, Kiyomi Nishiyama, Hirofumi Kodera, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Kayoko Saito, Kiyoshi Hayasaka, Naomichi Matsumoto, Hirotomo Saitsu
منشور في 2013Artigo -
2
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen حسب U. Schwarze, Tim Cundy, Shawna M. Pyott, H. E. Christiansen, Madhuri Hegde, Ruud A. Bank, Gerard Pals, Arunkanth Ankala, Karen N. Conneely, Laurie Seaver, Suzanne M. Yandow, Ellen M. Raney, Dusica Babovic‐Vuksanovic, Joan M. Stoler, Ziva Ben‐Neriah, Reeval Segel, Sari Lieberman, Liesbeth Siderius, Aida I. Al‐Aqeel, Mark C. Hannibal, Lucas Hudgins, Elizabeth McPherson, Michele Clemens, Michael D. Sussman, Robert D. Steiner, John D. Mahan, Rosemarie Smith, Kwame Anyane‐Yeboa, Julia Wynn, Karen Chong, Tami Uster, Salim Aftimos, V. Reid Sutton, Elise Davis, In S. Kim, Mary Ann Weis, David R. Eyre, Peter H. Byers
منشور في 2012Artigo
أدوات البحث:
موضوعات ذات صلة
Internal medicine
Medicine
Anatomy
Anesthesia
Biology
Carbamazepine
Chemistry
Clobazam
Electroencephalography
Encephalopathy
Endocrinology
Epilepsy
Epileptic spasms
Gene
Genetics
Haploinsufficiency
Hypsarrhythmia
Levetiracetam
Missense mutation
Mutation
Osteogenesis imperfecta
Pediatrics
Phenotype
Phenytoin
Procollagen peptidase
Psychiatry
Status epilepticus
Type I collagen
Valproic Acid
West Syndrome