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Phase II study shows potential benefit of adenoviral vascular endothelial growth factor C (VEGF-C) and lymph node transfer in lymphedema.
Plast Reconstr Surg. 2024 Aug 12. doi: 10.1097/PRS.0000000000011675. Online ahead of print.
Plast Reconstr Surg. 2024.
PMID: 39137430
Myth-Busting the Zone-of-Injury Concept: A Prospective Study on the Vascular Response to High-Energy Lower Extremity Trauma.
Cepas A, Kiiski J, Majava M, Kholová I, Kaartinen I.
Cepas A, et al. Among authors: majava m.
Plast Reconstr Surg. 2024 Jul 1;154(1):190e-198e. doi: 10.1097/PRS.0000000000010980. Epub 2023 Aug 10.
Plast Reconstr Surg. 2024.
PMID: 37561997
Free PMC article.
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Retrospective cohort study of long-term outcomes and prognostic factors for survival after lower extremity amputation in patients with diabetes.
Vuorlaakso M, Kiiski J, Majava M, Helminen M, Kaartinen I.
Vuorlaakso M, et al. Among authors: majava m.
J Diabetes Complications. 2023 Jan;37(1):108377. doi: 10.1016/j.jdiacomp.2022.108377. Epub 2022 Dec 6.
J Diabetes Complications. 2023.
PMID: 36525903
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Missense and nonsense mutations in the alternatively-spliced exon 2 of COL2A1 cause the ocular variant of Stickler syndrome.
McAlinden A, Majava M, Bishop PN, Perveen R, Black GC, Pierpont ME, Ala-Kokko L, Männikkö M.
McAlinden A, et al. Among authors: majava m.
Hum Mutat. 2008 Jan;29(1):83-90. doi: 10.1002/humu.20603.
Hum Mutat. 2008.
PMID: 17721977
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A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies.
Majava M, Hoornaert KP, Bartholdi D, Bouma MC, Bouman K, Carrera M, Devriendt K, Hurst J, Kitsos G, Niedrist D, Petersen MB, Shears D, Stolte-Dijkstra I, Van Hagen JM, Ala-Kokko L, Männikkö M, Mortier GR.
Majava M, et al.
Am J Med Genet A. 2007 Feb 1;143A(3):258-64. doi: 10.1002/ajmg.a.31586.
Am J Med Genet A. 2007.
PMID: 17236192
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Novel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP) genes in high myopia.
Majava M, Bishop PN, Hägg P, Scott PG, Rice A, Inglehearn C, Hammond CJ, Spector TD, Ala-Kokko L, Männikkö M.
Majava M, et al.
Hum Mutat. 2007 Apr;28(4):336-44. doi: 10.1002/humu.20444.
Hum Mutat. 2007.
PMID: 17117407
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Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H.
Masmoudi S, et al. Among authors: majava m.
Eur J Hum Genet. 2003 Feb;11(2):185-8. doi: 10.1038/sj.ejhg.5200934.
Eur J Hum Genet. 2003.
PMID: 12634867
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