Publications by authors named "Merit Lamp"

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A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis?
Fabio Gotta, Merit Lamp, Alessandro Geroldi, Lucia Trevisan, Paola Origone

Ann Hum Genet· September 2020

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Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients.
Paola Origone, Alessandro Geroldi, Merit Lamp, Francesca Sanguineri, Claudia Caponnetto

Neurodegener Dis· October 2019

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Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise".
Marina Grandis, Alessandro Geroldi, Rossella Gulli, Fiore Manganelli, Fabio Gotta, Merit Lamp

Orphanet J Rare Dis· October 2018

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Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patients.
Merit Lamp, Paola Origone, Alessandro Geroldi, Simonetta Verdiani, Fabio Gotta

Neurobiol Aging· June 2018

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Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier.
Paola Origone, Fabio Gotta, Merit Lamp, Lucia Trevisan, Alessandro Geroldi

Cerebellum Ataxias· March 2018

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1993-2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa.
Paola Mandich, Merit Lamp, Fabio Gotta, Rossella Gulli, Ariela Iacometti

Mol Genet Genomic Med· September 2017

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Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance.
Alessandro Geroldi, Patrizia Lastella, Margherita Patruno, Fabio Gotta, Nicoletta Resta, Merit Lamp

Neuromuscul Disord· April 2017

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Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype.
Paola Origone, Jennifer Accardo, Simonetta Verdiani, Merit Lamp, Dario Arnaldi

Neurocase· January 2016

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Quiz page February 2015: renal colic in an adolescent.
Giorgina B Piccoli, Marco A Cimmino, Merit Lamp, Fabio Gotta, Federica N Vigotti

Am J Kidney Dis· February 2015

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Survivin promoter polymorphisms and autoantibodies in endometriosis.
Merit Lamp, Merli Saare, Ülle Kadastik, Helle Karro, Andres Salumets

J Reprod Immunol· December 2012

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Polymorphisms in ESR1, ESR2 and HSD17B1 genes are associated with fertility status in endometriosis.
Merit Lamp, Maire Peters, Eva Reinmaa, Kadri Haller-Kikkatalo, Tanel Kaart

Gynecol Endocrinol· June 2011

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Genetic variations in vascular endothelial growth factor but not in angiotensin I-converting enzyme genes are associated with endometriosis in Estonian women.
Merit Lamp, Merli Saare, Triin Laisk, Helle Karro, Ulle Kadastik

Eur J Obstet Gynecol Reprod Biol· November 2010

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Polymorphisms in MMP-2 and MMP-9 promoter regions are associated with endometriosis.
Merli Saare, Merit Lamp, Tanel Kaart, Helle Karro, Ülle Kadastik

Fertil Steril· September 2010

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