Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

83 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
A fine balance: an autoregulatory gene therapy approach to treat obesity and achieve energy homeostasis.
Samson SL, Kohjima M, Chan L. Samson SL, et al. Gene Ther. 2009 Oct;16(10):1175-7. doi: 10.1038/gt.2009.88. Epub 2009 Jul 23. Gene Ther. 2009. PMID: 19626055 Free PMC article. No abstract available.
Gene therapy with neurogenin3, betacellulin and SOCS1 reverses diabetes in NOD mice.
Li R, Buras E, Lee J, Liu R, Liu V, Espiritu C, Ozer K, Thompson B, Nally L, Yuan G, Oka K, Chang B, Samson S, Yechoor V, Chan L. Li R, et al. Among authors: samson s. Gene Ther. 2015 Nov;22(11):876-82. doi: 10.1038/gt.2015.62. Epub 2015 Jul 14. Gene Ther. 2015. PMID: 26172077 Free PMC article.
Tubulin genes of the African trypanosome Trypanosoma brucei rhodesiense:nucleotide sequence of a 3.7-kb fragment containing genes for alpha and beta tubulins.
Kimmel BE, Samson S, Wu J, Hirschberg R, Yarbrough LR. Kimmel BE, et al. Among authors: samson s. Gene. 1985;35(3):237-48. doi: 10.1016/0378-1119(85)90002-2. Gene. 1985. PMID: 4043732
Role of Preablative Stimulated Thyroglobulin in Prediction of Nodal and Distant Metastasis on Iodine Whole-Body Scan.
Prabhu M, Samson S, Reddy A, Venkataramanarao SH, Chandrasekhar NH, Pillai V, Shetty V, Koriokose MA, Vaidhya B, Kannan S. Prabhu M, et al. Among authors: samson s. Indian J Nucl Med. 2018 Apr-Jun;33(2):93-98. doi: 10.4103/ijnm.IJNM_130_17. Indian J Nucl Med. 2018. PMID: 29643667 Free PMC article.
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice.
Studwell CM, Kelley EG; Undiagnosed Diseases Network, Sinsheimer JS, Palmer CGS, LeBlanc K. Studwell CM, et al. J Genet Couns. 2020 Oct 27. doi: 10.1002/jgc4.1329. Online ahead of print. J Genet Couns. 2020. PMID: 33108040
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science.
Schoch K, Esteves C, Bican A, Spillmann R, Cope H, McConkie-Rosell A, Walley N, Fernandez L, Kohler JN, Bonner D, Reuter C, Stong N, Mulvihill JJ, Novacic D, Wolfe L, Abdelbaki A, Toro C, Tifft C, Malicdan M, Gahl W, Liu P, Newman J, Goldstein DB, Hom J, Sampson J, Wheeler MT; Undiagnosed Diseases Network, Cogan J, Bernstein JA, Adams DR, McCray AT, Shashi V. Schoch K, et al. Genet Med. 2020 Oct 23. doi: 10.1038/s41436-020-00984-z. Online ahead of print. Genet Med. 2020. PMID: 33093671 Free article.
A Pituitary Society update to acromegaly management guidelines.
Fleseriu M, Biller BMK, Freda PU, Gadelha MR, Giustina A, Katznelson L, Molitch ME, Samson SL, Strasburger CJ, van der Lely AJ, Melmed S. Fleseriu M, et al. Among authors: samson sl. Pituitary. 2020 Oct 20. doi: 10.1007/s11102-020-01091-7. Online ahead of print. Pituitary. 2020. PMID: 33079318
Multidisciplinary management of acromegaly: A consensus.
Giustina A, Barkhoudarian G, Beckers A, Ben-Shlomo A, Biermasz N, Biller B, Boguszewski C, Bolanowski M, Bollerslev J, Bonert V, Bronstein MD, Buchfelder M, Casanueva F, Chanson P, Clemmons D, Fleseriu M, Formenti AM, Freda P, Gadelha M, Geer E, Gurnell M, Heaney AP, Ho KKY, Ioachimescu AG, Lamberts S, Laws E, Losa M, Maffei P, Mamelak A, Mercado M, Molitch M, Mortini P, Pereira AM, Petersenn S, Post K, Puig-Domingo M, Salvatori R, Samson SL, Shimon I, Strasburger C, Swearingen B, Trainer P, Vance ML, Wass J, Wierman ME, Yuen KCJ, Zatelli MC, Melmed S. Giustina A, et al. Among authors: samson sl. Rev Endocr Metab Disord. 2020 Dec;21(4):667-678. doi: 10.1007/s11154-020-09588-z. Epub 2020 Sep 10. Rev Endocr Metab Disord. 2020. PMID: 32914330 Review.
Maintenance of Acromegaly Control in Patients Switching From Injectable Somatostatin Receptor Ligands to Oral Octreotide.
Samson SL, Nachtigall LB, Fleseriu M, Gordon MB, Bolanowski M, Labadzhyan A, Ur E, Molitch M, Ludlam WH, Patou G, Haviv A, Biermasz N, Giustina A, Trainer PJ, Strasburger CJ, Kennedy L, Melmed S. Samson SL, et al. J Clin Endocrinol Metab. 2020 Oct 1;105(10):dgaa526. doi: 10.1210/clinem/dgaa526. J Clin Endocrinol Metab. 2020. PMID: 32882036 Free PMC article.
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
Schneeberger PE, Kortüm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D, Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M, Biskup S, Heller C, Maier EM, Javaher-Haghighi P, Bedeschi MF, Ajmone PF, Iascone M, Peeters H, Ballon K, Jaeken J, Rodríguez Alonso A, Palomares-Bralo M, Santos-Simarro F, Meuwissen MEC, Beysen D, Kooy RF, Houlden H, Murphy D, Doosti M, Karimiani EG, Mojarrad M, Maroofian R, Noskova L, Kmoch S, Honzik T, Cope H, Sanchez-Valle A; Undiagnosed Diseases Network, Gelb BD, Kurth I, Hempel M, Kutsche K. Schneeberger PE, et al. Brain. 2020 Aug 1;143(8):2437-2453. doi: 10.1093/brain/awaa204. Brain. 2020. PMID: 32761064
83 results
Jump to page
Feedback