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885 results
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Autotransplantation of human carotid body cell aggregates for treatment of Parkinson's disease.
Arjona V, Mínguez-Castellanos A, Montoro RJ, Ortega A, Escamilla F, Toledo-Aral JJ, Pardal R, Méndez-Ferrer S, Martín JM, Pérez M, Katati MJ, Valencia E, García T, López-Barneo J. Arjona V, et al. Among authors: martin jm. Neurosurgery. 2003 Aug;53(2):321-8; discussion 328-30. doi: 10.1227/01.neu.0000073315.88827.72. Neurosurgery. 2003. PMID: 12925247 Clinical Trial.
Tympanostomy Tubes or Medical Management for Recurrent Acute Otitis Media.
Hoberman A, Preciado D, Paradise JL, Chi DH, Haralam M, Block SL, Kearney DH, Bhatnagar S, Muñiz Pujalt GB, Shope TR, Martin JM, Felten DE, Kurs-Lasky M, Liu H, Yahner K, Jeong JH, Cohen NL, Czervionke B, Nagg JP, Dohar JE, Shaikh N. Hoberman A, et al. Among authors: martin jm. N Engl J Med. 2021 May 13;384(19):1789-1799. doi: 10.1056/NEJMoa2027278. N Engl J Med. 2021. PMID: 33979487
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
Zhu N, Swietlik EM, Welch CL, Pauciulo MW, Hagen JJ, Zhou X, Guo Y, Karten J, Pandya D, Tilly T, Lutz KA, Martin JM, Treacy CM, Rosenzweig EB, Krishnan U, Coleman AW, Gonzaga-Juaregui C, Lawrie A, Trembath RC, Wilkins MR; Regeneron Genetics Center; PAH Biobank Enrolling Centers’ Investigators; NIHR BioResource for Translational Research - Rare Diseases; National Cohort Study of Idiopathic and Heritable PAH, Morrell NW, Shen Y, Gräf S, Nichols WC, Chung WK. Zhu N, et al. Among authors: martin jm. Genome Med. 2021 May 10;13(1):80. doi: 10.1186/s13073-021-00891-1. Genome Med. 2021. PMID: 33971972 Free PMC article.
Systematic review of sacroiliac joint motion and the effect of screw fixation.
Cardwell MC, Meinerz CM, Martin JM, Beck CJ, Wang M, Schmeling GJ. Cardwell MC, et al. Among authors: martin jm. Clin Biomech (Bristol, Avon). 2021 Apr 27;85:105368. doi: 10.1016/j.clinbiomech.2021.105368. Online ahead of print. Clin Biomech (Bristol, Avon). 2021. PMID: 33940477 Review.
Hereditary Epidermolysis Bullosa: A Case Series.
Guillen-Climent S, Fernández García L, García-Vázquez A, Martín JM. Guillen-Climent S, et al. Among authors: martin jm. Actas Dermosifiliogr. 2021 Apr 30:S0001-7310(21)00165-4. doi: 10.1016/j.ad.2020.08.015. Online ahead of print. Actas Dermosifiliogr. 2021. PMID: 33939986 Free article. English, Spanish. No abstract available.
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