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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1986 1
1988 1
1993 1
1997 1
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2003 1
2004 1
2006 2
2007 1
2009 3
2010 2
2011 1
2012 1
2013 3
2014 1
2015 1
2016 2
2017 1
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Page 1
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.
Pezzini I, Geroldi A, Capponi S, Gulli R, Schenone A, Grandis M, Doria-Lamba L, La Piana C, Cremonte M, Pisciotta C, Nolano M, Manganelli F, Santoro L, Mandich P, Bellone E. Pezzini I, et al. Among authors: doria lamba l. Neuromuscul Disord. 2016 Jan;26(1):26-32. doi: 10.1016/j.nmd.2015.09.008. Epub 2015 Sep 16. Neuromuscul Disord. 2016. PMID: 26525999
A novel compound heterozygous mutation of C20orf54 gene associated with Brown-Vialetto-Van Laere syndrome in an Italian family.
Bandettini di Poggio M, Gagliardi S, Pardini M, Marchioni E, Monti Bragadin M, Reni L, Doria-Lamba L, Roccatagliata L, Ceroni M, Schenone A, Cereda C. Bandettini di Poggio M, et al. Among authors: doria lamba l. Eur J Neurol. 2013 Jul;20(7):e94-5. doi: 10.1111/ene.12163. Eur J Neurol. 2013. PMID: 23750839 No abstract available.
Brown-Vialetto-Van Laere syndrome: clinical and neuroradiological findings of a genetically proven patient.
Bandettini Di Poggio M, Monti Bragadin M, Reni L, Doria-Lamba L, Cereda C, Pardini M, Roccatagliata L, Rossi A, Schenone A. Bandettini Di Poggio M, et al. Among authors: doria lamba l. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Mar;15(1-2):141-4. doi: 10.3109/21678421.2013.837931. Epub 2013 Oct 1. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24079556
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect.
Di Maria E, Gulli R, Balestra P, Cassandrini D, Pigullo S, Doria-Lamba L, Bado M, Schenone A, Ajmar F, Mandich P, Bellone E. Di Maria E, et al. Among authors: doria lamba l. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1495-8. doi: 10.1136/jnnp.2003.028100. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377708 Free PMC article.
Intermittent-relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility.
Giribaldi G, Doria-Lamba L, Biancheri R, Severino M, Rossi A, Santorelli FM, Schiaffino C, Caruso U, Piemonte F, Bruno C. Giribaldi G, et al. Among authors: doria lamba l. Dev Med Child Neurol. 2012 May;54(5):472-6. doi: 10.1111/j.1469-8749.2011.04151.x. Epub 2011 Dec 5. Dev Med Child Neurol. 2012. PMID: 22142326 Free article.
20 results